14_references 8.pdf - shodhganga
TRANSCRIPT
CHAPTER 8 REFERENCES
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 259
1 Y Kwon Handbook of essential pharmacokinetics pharmacodynamics and
drug metabolism for industrial scientists 2001 Springer publication New
York PP 35-45
2 L Edwards et al Principle and practice of pharmaceutical medicines 2 nd
edition2007 Wiley publication PP 85
3 W Foye et al Foyersquos Principles of medicinal chemistry sixth edition2007
Lippincott publication PP 300
4 C Ehrhardt et al Drug absorption studies in situ in vitro and in silico models
illustrated edition AAPS Press Springer publication 2008 PP 666
5 Y Qiu et al Developing solid oral dosage formspharmaceutical theory and
practice first edition 2009 Elsvier Publication USA PP 421-436
6 A Avdeef Absorption and drug development solubilitypermeability and
charge state John Wiley and sons Wiley interscience publication 2003 PP
20
7 Waiver of in vivo bioavailability and bioequivalence studies for immediate
release solid oral dosage forms based on a biopharmaceutics classification
system Guidance for industry USFDACDER Aug 2000
8 httpenwikipediaorgwikiBioavailability
9 Wagh et al Biopharmaceutical classification system International journal of
pharmacy and pharmaceutical sciences 2(1) 2010 PP 12-19
10 Banker and Rhodes Modern pharmaceutics 121 fourth edition Marcel
Dekker PP 84-86
11 Brahmankar and Jaiswal et al Biopharmaceutics and pharmacokinetics- a
treatise first edition Vallabh prakashan Delhi PP 18
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 260
12 httpwwwboomerorgcp3c22c2201html
13 Touitou and Barry Enhancement in drug delivery CRC press Taylor and
francis group 2006 PP 112
14 B Hancock et al Characteristics and significance of the amorphous state in
pharmaceutical systems Journal Pharmaceutical Sciences 86 1997 PP 1ndash12
15 M Grau et al Nanosuspensions of poorly soluble drugs ndash reproducibility of
small scale production Inetrnational Journal of Pharmaceutics 196 2000 PP
155ndash157
16 G Liversidge et al Particle size reduction for improvement of oral
bioavailability of hydrophobic drugs absolute oral bioavailability of
nanocrystalline danazol in beagle dogs Inetrnational Journal of
Pharmaceutics 125 1995 PP 91ndash97
17 J Hargrove et al Absorption of oral progesterone is influenced by vehicle and
particle size American Journal of Obstetrics and Gynecology 161 1989 PP
948ndash951
18 A Jounela et al Effect of particle size on the bioavailability of digoxin
European Journal of clinical Pharmacology 8 1975 PP 365ndash370
19 Y Ran et al Solubilization and Preformulation Studies on PG-300995 (an
anti-HIV drug) Journal of Pharmaceutical Sciences 94 (2) 2005 PP 297ndash
303
20 C Mbah Solubilization of valsartan by aqueous glycerol polyethylene glycol
and micellar solutions Pharmazie 61 (4) 2006 PP 322-324
21 R Chang et al Effect of Hydroxypropyl Beta-Cyclodextrin on Drug
Solubility in Water-Propylene Glycol Mixtures Drug Development and
Industrial Pharmacy 30 (3) 2004 PP 297ndash302
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 261
22 S Han et al Solubilization of Biphenyl Dimethyl Dicarboxylate by
Cosolvency Drug Development and Industrial Pharmacy 25 (11) 1999 PP
1193ndash1197
23 R Stancanelli et al The enhancement of isoflavones water solubility by
complexation with modified cyclodextrins A spectroscopic investigation with
implications in the pharmaceutical analysis Journal of Pharmaceutical and
biomedical analysis 44 (4) 2007 PP 980-984
24 S Gibaud et al Melarsoprolndashcyclodextrins inclusion complexes International
Journal of Pharmaceutics 306 ( 1-2) 2005 PP 107-121
25 S Wong et al Enhancement of the dissolution rate and oral absorption of a
poorly water soluble drug by formation of surfactant-containing
microparticles International Journal of Pharmaceutics 317 (1) 2006 PP 61-
68
26 Ryh-Nan Pan et al Enhancement of Dissolution and Bioavailability of
Piroxicam in Solid Dispersion Systems Drug Development and Industrial
Pharmacy 26 (9) 2000 PP 989 ndash 994
27 H Joshi et al Bioavailability enhancement of a poorly water-soluble drug by
solid dispersion in polyethylene glycolndash polysorbate 80 mixture International
Journal of Pharmaceutics 269 (1) 2004 PP 251-258
28 R Muller et al Emulsions and nanosuspensions for the formulation of poorly
soluble drugs Medpharm Scientific Publishers Stuttgart Germany 1998 PP
149ndash174
29 R Muller et al Nanosuspensions as Particulate Drug Formulations in
Therapy Rationale for Development and What We Can Expect for the Future
Advances in Drug Delivery Reviews 47 (1) 2001 PP 3ndash19
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 262
30 E Liversidge et al Nanosizing A Formulation Approach for Poorly Water-
Soluble Compounds European Journal of Pharmaceutical Sciences 18 (2)
2003 PP 113ndash120
31 P Lockman et al Nanoparticle Technology for Drug Delivery Across the
Blood-Brain Barrier Drug Development and Industrial Pharmacy 28 (1)
2002 PP 1ndash13
32 B Rabinow Nanosuspensions in Drug Delivery Nature Reviews Drug
discovery 3 (9) 2004 PP 785ndash796
33 V Patravale et al Nanosuspensions A Promising Drug Delivery Strategy
Journal of Pharmacy and Pharmacology 56 (7) 2004 PP 827ndash840
34 G Liversidge et al Particle Size Reduction for Improvement of Oral
Bioavailability of Hydrophobic Drugs I Absolute Oral Bioavailability of
Nanocrystalline Danazol in Beagle Dogs International Journal of
Pharmaceutics 125 (1)1995 PP 91ndash97
35 J Hecq et al Preparation and Characterization of Nanocrystals for Solubility
and Dissolution Rate Enhancement of Nifedipine International Journal of
Pharmaceutics 299 (1ndash2) 2005 PP 167ndash177
36 E Reverchon et al Production of Antibiotic Micro- and Nano-Particles by
Supercritical Antisolvent Precipitation Powder Technology 106 (1ndash2) 1999
PP 23ndash29
37 P Chattopadhyay et al Protein Nanoparticles Formation by Supercritical
Antisolvent with Enhanced Mass Transfer AIChE Journal 48 2002 PP
235ndash244
38 T Young et al Rapid Expansion from Supercritical to Aqueous Solution to
Produce Submicron Suspensions of Water-Insoluble Drugs Biotechnology
Progress 16 (3) 2000 PP 402ndash407
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 263
39 J Hu et al Rapid Dissolving High Potency Danazol Powders Produced by
Spray Freezing into Liquid Process International Journal of Pharmaceutics
271 (1ndash2) 2004 PP 145ndash154
40 J Hu et al Stable Amorphous Danazol Nanostructured Powders with Rapid
Dissolution Rates Produced by Spray Freezing into Liquid Drug Development
and Industrial Pharmacy 30 (7) 2004 PP 695ndash704
41 X Chen et al Rapid Dissolution of High Potency Danazol Powders Produced
by Evaporative Precipitation into Aqueous Solution Journal of
Pharmaceutical Sciences 93 (7) 2004 PP 1867ndash1878
42 JVaughn et al Supersaturation produces high bioavailability of amorphous
danazol particles formed by evaporative precipitation into aqueous solution
and spray freezing into liquid technologies Drug Development and Industrial
Pharmacy 32(5) 2006 PP 559-567
43 XChen et al Preparation of cyclosporine A nanoparticles by evaporative
precipitation into aqueous solution International Journal of Pharmaceutics
242 (1-2) 2002 PP 3-14
44 V Hoffarta et al Oral bioavailability of a low molecular weight heparin using
a polymeric delivery system Journal of Controlled Release 113 (1) 2006
PP 38-42
45 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science17 2008 PP
71-75
46 CPinto Reis et al Nanoencapsulation I Methods for preparation of drug
loaded polymeric nanoparticles Nanomedicine 2 2006 PP 8-21
47 TP Shakhtshneider et al The mechanochemical preparation of solid disperse
systems of ibuprofenndashpolyethylene glycol International Journal of
Pharmaceutics1301996 PP 25ndash32
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 264
48 M Sugimoto et al Improvement of dissolution characteristics and
bioavailability of poorly water-soluble drugs by novel cogrinding method
using water soluble-polymer International Journal of Pharmaceutics 160
1998 PP 11ndash19
49 M Vogt et al Cogrinding enhances the oral bioavailability of EMD 57033 a
poorly water soluble drug in dogs European Journal of Pharmaceutics and
Biopharmaceutics 68 (2) 2008 PP 338-345
50 C Pouton et al Formulation of self-emulsifying drug delivery systems
Advanced Drug Delivery Reviews 25 (1) 1997 PP 47-58
51 W Wu et al Enhanced bioavailability of silymarin by self-microemulsifying
drug delivery system European Journal of Pharmaceutics and
Biopharmaceutics 63 (3) 2006 PP 288-294
52 S Kapsi et al Processing factors in development of solid solution formulation
of itraconazole for enhancement of drug dissolution and bioavailability
International Journal of Pharmaceutics229 2001 PP 193ndash203
53 B Katzung et al Basic and clinical Pharmacology 11th
edition 2009
McGraw Hill Publication PP 167-188
54 FBarar Antihypertensive drugs Essentials of Pharmacotherapeutics 5th
edition 2009 SChand and Company Ltd PP 239-249
55 httpwwwrxlistcomdrugsalpha_ahtm
56 Atacand Product monograph Astrazeneca Canada 2008
57 H Matsunaga et al Solid state characterization of candesartan cilexetil (TCV
116) crystal structure and molecular mobilityChemical and Pharmaceutical
Bulletine 47(2) 1999 PP 182-186
58 httpwwwespacenetcomindexenhtm
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 265
59 httpwwwpatentlensnetdaisypatentlenspatentlenshtml
60 httpwwwsciruscom
61 United States pharmacopeia 32 NF 272009
62 DSubba Rao et al A stability indicating LC method for candesartan cilexetil
Chromatographia 66 (7-8) 2007 PP 499-507
63 SQutab et al Simple and sensitive LC-UV method for simultaneous analysis
of hydrochlorothiazide and candesartan cilexetil in pharmaceutical
formulations Acta Chromatographica 19 2007 PP 119-129
64 LZhang et al HPLC-UV simultaneous determination of candesartan cilexetil
and hydrochlorothiazide in compound candesartan cilexetil tablets Chienese
journal of Pharmaceutical Analysis 27 (4) 2007 PP 566-568
65 DDuchene et al Pharmaceutical uses of cyclodextrins and derivatives Drug
development and industrial pharmacy161990 PP 2487-2499
66 T Loftsson et al Pharmaceutical applications of cyclodextrinsdrug
solubilization and stabilization Journal of pharmaceutical sciences851996PP
1017-1025
67 RO Williams et al Characterization of an inclusion complex of cholesterol
and hydroxypropyl-β-Cyclodextrin European journal of pharmaceutics and
biopharmaceutics461998PP 355-360
68 JSzejtli Pastpresent and future of cyclodextrin research Pure and applied
chemistry 76(10)2004 PP 1825-1845
69 SBaboota et alCyclodextrins in drug delivery systems An update Latest
reviews 12003 retrieved from pharmainfonet
70 Innovative drug delivery technology for enhanced solubility and
stabilityCyDexIncOct 2004
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 266
71 GBettinetti et alInteraction of naproxen with noncrystalline acetyl beta and
acetyl gamma cyclodextrins in the solid and liquid stateEuropean Journal of
Pharmaceutical Sciences152002PP 21-29
72 CGazpio et al HPLC and solubility study of the interaction between pindolol
and cyclodextrinsJournal of Pharmaceutical and Biomedical Analysis37
2005PP 487-492
73 AMiro et alImprovement of gliquidone hypoglycaemic effect in rats by
cyclodextrin formulations European Journal of Pharmaceutical Sciences23
2004PP-57-64
74 BDevarakonda et al Comparison of the aqueous solubilization of practically
insoluble niclosamide by polyamidoamine dendrimers and cyclodextrins
International Journal of Pharmaceutics 3042005PP 193-209
75 SHiremath et alImproved dissolution rate of valdecoxib inclusion complexes
with hydroxyl propyl beta cyclodextrinIndian Journal of Pharmaceutical
Sciences692007PP 442-445
76 CHolvoet Development of an omeprazole parenteral formulation with
hydroxypropyl-beta-cyclodextrinPharmaceutical Development and
Technology12(3)2007PP 327-336
77 MChavanpatil et alEnhancement of nasal absorption of acyclovir via
cyclodextrins Journal of Inclusion phenomena and Macrocyclic
Chemistry44(1-4)2002 PP137-140
78 United States Patent 7259153ChangRong-KunDrug formulation and
delivery using crystalline methylated cyclodextrins
79 TLoftsson et al Cyclodextrins in drug delivery Expert opinion Drug
Delivery 2(2) 2005 PP 1-17
80 TLoftsson et al Self association of cyclodextrins and cyclodextrin complexes
Journal of Pharmaceutical Sciences 93(5)2004PP 1091-1099
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 267
81 MEsclusa-Diaz et al Preparation and evaluation of ketoconazole- beta
cyclodextrin multicomponent complexesInternational Journal of
Pharmaceutics1421996PP 183-187
82 K Connors et al The stability of cyclodextrin complexes in solution
Chemical Reviews 97 1997 PP 1325-1357
83 PChaudhari et al solubility enhancement of hydrophobic drugs using
synergistically interacting cyclodextrin and cosolventsCurrent science92(11)
2007PP 1586-1591
84 US patent 545721J Szejtli et al inclusion complexes of taxol or taxotere or
taxus extract formed with cyclodextrins its preparation and use
85 MAl Omari et alComparative study of the inclusion complexation of
pizotifen and ketotifen with native and modified cyclodextrinsJournal of
Solution Chemistry37(2)2008PP 249-264
86 MLinaresSolubilization of naphthaquinones by complexation with
hydroxypropyl β cyclodextrin International Journal of
Pharmaceutics1591997PP 13-18
87 MGuyot Physicochemical characterization and dissolution of norfloxacin-
cyclodextrin inclusion complexes and PEG solid dispersions International
journal of Pharmaceutics1231995PP 53-63
88 TNakate et al Imporvement of pulmonary absorption of cyclopeptide FK 224
in rats by co-formulating with beta cyclodextrin European Journal of
Pharmaceutics and Biopharmaceutics552003PP 147-154
89 HViernstein et alSolubility enhancement of low soluble biologically active
compounds-temperature and cosolvent dependent inclusion
complexationInternational Journal of Pharmaceutics 2562003PP 85-94
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 268
90 T Loftsson et alCyclodextrinsolubilization of benzodiazepinesformulation of
midazolam nasal sprayInternational Journal of Pharmaceutics2122001PP-
29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
inclusion complexes by phase solubility photostability physicochemical and
computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
93 H Archontaki et alStudy on inclusion complexes of bromazepam with beta
and beta hydroxypropylcyclodextrinsJournal of Pharmaceutical and
Biomedical analysis282002PP 761-769
94 O Aleem et al Effect of beta cyclodextrin and hydroxypropyl beta
cyclodextrins complexation on physicochemical properties and antimicrobial
activity of cefdinir Journal of Pharmaceutical and Biomedical analysis 47(3)
2008 PP 535-540
95 S RawatSolubility enhancement of celecoxib using beta cyclodextrin
inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
96 A Gil et al Evolution of the interaction of a new chemical entity eflucimibe
with gamma cyclodextrin during kneading processEuropean Journal of
Pharmaceutical Sciences 23 2004 PP 123-129
97 HAmmar et al Formulation and biological evaluation of glimepiride-
cyclodextrin-polymer systems International Journal of
Pharmaceutics3092006 PP 129-138
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 269
98 S Rawat et alEnhancement of Industrial absorption of few cox-2 inhibitors
through interaction with β-Cyclodextrins Journal of Pharmaceutical and
Biomedical Analysis 69 (4) 2007 PP529-534
99 H Hassan et al Enhacement of dissolution amount and in vivo bioavailability
of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
nicardipine-cyclodextrins inclusion compounds European Journal of
Pharmaceutical Sciences152007PP 79-88
101 OSolimann et al Amorphous spironolactone and hydroxypropylated
cyclodextrin complexes with superior dissolution and
bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
102 Xianhong Wen et al Preparation and study the 12 inclusion complex of
carvedilol with beta cyclodextrin342004PP 517-523
103 KWaleczek et al Phase solubility study of pure (-)-α-bisabolol and camomile
essential oil with β cyclodextrin European Journal of Pharmaceutics and
Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
modeling studiesJournal of Inclusion Phenomena and Macrocyclic Chemistry
57(1-4) 2007 PP 503-510
105 Ning Li et alStudy of physicochemical properties of trimethoprim with
cyclodextrin in solution Journal of Pharmaceutical and Biomedical
Analysis382005 PP 370-374
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 270
106 CTimpe et al A novel solvent- based fluidised bed wet granulation process
for solid dispersionAmerical pharmaceutical review Nov2008PP 75-81
107 VYadav et alEnhancement of solubility and dissolution rate of BCS class II
pharmaceuticals by nonaqueous granulation techniqueInternational Journal of
Pharma Research and Development-online12 Feb 2008 PP 1-12
108 YJavadzadeh et alEnhancement of dissolution rate of piroxicam using
liquisolidcompactsII Farmaco602005 PP 361-365
109 YJavadzadeh et alLiquisolid technique as a new approach to sustain
propranolol hydrochloride release from tablet matricesInternational Journal of
Pharmaceutics3622008 PP 102-108
110 VYadav et alImprovement of solubility and dissolution of Indomethacin by
liquisolid and compaction granulationJournal of Pharmaceutical Sciences and
Research1(2)2009 PP 44-51
111 IDarwish et alDissolution rate enhancement of gibenclamide using liquisolid
tablet technologyActa Pharmaceutica522002PP 171-179
112 AYadav et alFormulation and evaluation of orodispersibleliquisolid
compacts of aceclofenacIndian Journal of Pharmacy Education and
Research44(3)2010 PP 227-235
113 SSpireas et alIn vitro release evaluation of hydrocortisone liquisolidtablets
Journal of Pharmaceutical Sciences871998 PP 867-872
114 AKarmarkar et alLiquisolid technology for dissolution rate enhancement or
sustaining releaseExpert opinion on drug delivery7(10)2010PP 1227-1234
115 ANokhodchi et al Drug release from liquisolid systems speed it up slow it
down Expert opinion on drug deliveryExpert opinion on drug
delivery8(2)2011PP 191-205
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 271
116 A Karmarkar LiquisolidtabletsA novel approach for drug delivery
International Journal of Health Research 2(1) 2009 PP 45-50
117 K Khaled et al In vivo evaluation of hydrochlorothiazide liquisolid tablets in
beagle dogsInternational Journal of Pharmaceutics 222 2001 PP 1-6
118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
124 SGubbi et al Formulation and characterization of atorvastatin calcium
liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 272
125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
126 B El- Houssieny et al Bioavailability and biological activity of liquisolid
compact formula of repaglinide and its effect on glucose tolerance in rabbits
Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
128 N Tiong et al Effects of liquisolid formulations on dissolution of naproxen
European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 273
135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
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187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
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fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
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spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
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3 W Foye et al Foyersquos Principles of medicinal chemistry sixth edition2007
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20
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release solid oral dosage forms based on a biopharmaceutics classification
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15 M Grau et al Nanosuspensions of poorly soluble drugs ndash reproducibility of
small scale production Inetrnational Journal of Pharmaceutics 196 2000 PP
155ndash157
16 G Liversidge et al Particle size reduction for improvement of oral
bioavailability of hydrophobic drugs absolute oral bioavailability of
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Pharmaceutics 125 1995 PP 91ndash97
17 J Hargrove et al Absorption of oral progesterone is influenced by vehicle and
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948ndash951
18 A Jounela et al Effect of particle size on the bioavailability of digoxin
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anti-HIV drug) Journal of Pharmaceutical Sciences 94 (2) 2005 PP 297ndash
303
20 C Mbah Solubilization of valsartan by aqueous glycerol polyethylene glycol
and micellar solutions Pharmazie 61 (4) 2006 PP 322-324
21 R Chang et al Effect of Hydroxypropyl Beta-Cyclodextrin on Drug
Solubility in Water-Propylene Glycol Mixtures Drug Development and
Industrial Pharmacy 30 (3) 2004 PP 297ndash302
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Cosolvency Drug Development and Industrial Pharmacy 25 (11) 1999 PP
1193ndash1197
23 R Stancanelli et al The enhancement of isoflavones water solubility by
complexation with modified cyclodextrins A spectroscopic investigation with
implications in the pharmaceutical analysis Journal of Pharmaceutical and
biomedical analysis 44 (4) 2007 PP 980-984
24 S Gibaud et al Melarsoprolndashcyclodextrins inclusion complexes International
Journal of Pharmaceutics 306 ( 1-2) 2005 PP 107-121
25 S Wong et al Enhancement of the dissolution rate and oral absorption of a
poorly water soluble drug by formation of surfactant-containing
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68
26 Ryh-Nan Pan et al Enhancement of Dissolution and Bioavailability of
Piroxicam in Solid Dispersion Systems Drug Development and Industrial
Pharmacy 26 (9) 2000 PP 989 ndash 994
27 H Joshi et al Bioavailability enhancement of a poorly water-soluble drug by
solid dispersion in polyethylene glycolndash polysorbate 80 mixture International
Journal of Pharmaceutics 269 (1) 2004 PP 251-258
28 R Muller et al Emulsions and nanosuspensions for the formulation of poorly
soluble drugs Medpharm Scientific Publishers Stuttgart Germany 1998 PP
149ndash174
29 R Muller et al Nanosuspensions as Particulate Drug Formulations in
Therapy Rationale for Development and What We Can Expect for the Future
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Soluble Compounds European Journal of Pharmaceutical Sciences 18 (2)
2003 PP 113ndash120
31 P Lockman et al Nanoparticle Technology for Drug Delivery Across the
Blood-Brain Barrier Drug Development and Industrial Pharmacy 28 (1)
2002 PP 1ndash13
32 B Rabinow Nanosuspensions in Drug Delivery Nature Reviews Drug
discovery 3 (9) 2004 PP 785ndash796
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Journal of Pharmacy and Pharmacology 56 (7) 2004 PP 827ndash840
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Bioavailability of Hydrophobic Drugs I Absolute Oral Bioavailability of
Nanocrystalline Danazol in Beagle Dogs International Journal of
Pharmaceutics 125 (1)1995 PP 91ndash97
35 J Hecq et al Preparation and Characterization of Nanocrystals for Solubility
and Dissolution Rate Enhancement of Nifedipine International Journal of
Pharmaceutics 299 (1ndash2) 2005 PP 167ndash177
36 E Reverchon et al Production of Antibiotic Micro- and Nano-Particles by
Supercritical Antisolvent Precipitation Powder Technology 106 (1ndash2) 1999
PP 23ndash29
37 P Chattopadhyay et al Protein Nanoparticles Formation by Supercritical
Antisolvent with Enhanced Mass Transfer AIChE Journal 48 2002 PP
235ndash244
38 T Young et al Rapid Expansion from Supercritical to Aqueous Solution to
Produce Submicron Suspensions of Water-Insoluble Drugs Biotechnology
Progress 16 (3) 2000 PP 402ndash407
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39 J Hu et al Rapid Dissolving High Potency Danazol Powders Produced by
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271 (1ndash2) 2004 PP 145ndash154
40 J Hu et al Stable Amorphous Danazol Nanostructured Powders with Rapid
Dissolution Rates Produced by Spray Freezing into Liquid Drug Development
and Industrial Pharmacy 30 (7) 2004 PP 695ndash704
41 X Chen et al Rapid Dissolution of High Potency Danazol Powders Produced
by Evaporative Precipitation into Aqueous Solution Journal of
Pharmaceutical Sciences 93 (7) 2004 PP 1867ndash1878
42 JVaughn et al Supersaturation produces high bioavailability of amorphous
danazol particles formed by evaporative precipitation into aqueous solution
and spray freezing into liquid technologies Drug Development and Industrial
Pharmacy 32(5) 2006 PP 559-567
43 XChen et al Preparation of cyclosporine A nanoparticles by evaporative
precipitation into aqueous solution International Journal of Pharmaceutics
242 (1-2) 2002 PP 3-14
44 V Hoffarta et al Oral bioavailability of a low molecular weight heparin using
a polymeric delivery system Journal of Controlled Release 113 (1) 2006
PP 38-42
45 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science17 2008 PP
71-75
46 CPinto Reis et al Nanoencapsulation I Methods for preparation of drug
loaded polymeric nanoparticles Nanomedicine 2 2006 PP 8-21
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systems of ibuprofenndashpolyethylene glycol International Journal of
Pharmaceutics1301996 PP 25ndash32
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Biopharmaceutics 68 (2) 2008 PP 338-345
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Biopharmaceutics 63 (3) 2006 PP 288-294
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of itraconazole for enhancement of drug dissolution and bioavailability
International Journal of Pharmaceutics229 2001 PP 193ndash203
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edition 2009
McGraw Hill Publication PP 167-188
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solubilization and stabilization Journal of pharmaceutical sciences851996PP
1017-1025
67 RO Williams et al Characterization of an inclusion complex of cholesterol
and hydroxypropyl-β-Cyclodextrin European journal of pharmaceutics and
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68 JSzejtli Pastpresent and future of cyclodextrin research Pure and applied
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72 CGazpio et al HPLC and solubility study of the interaction between pindolol
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73 AMiro et alImprovement of gliquidone hypoglycaemic effect in rats by
cyclodextrin formulations European Journal of Pharmaceutical Sciences23
2004PP-57-64
74 BDevarakonda et al Comparison of the aqueous solubilization of practically
insoluble niclosamide by polyamidoamine dendrimers and cyclodextrins
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75 SHiremath et alImproved dissolution rate of valdecoxib inclusion complexes
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Sciences692007PP 442-445
76 CHolvoet Development of an omeprazole parenteral formulation with
hydroxypropyl-beta-cyclodextrinPharmaceutical Development and
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cyclodextrins Journal of Inclusion phenomena and Macrocyclic
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78 United States Patent 7259153ChangRong-KunDrug formulation and
delivery using crystalline methylated cyclodextrins
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Delivery 2(2) 2005 PP 1-17
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82 K Connors et al The stability of cyclodextrin complexes in solution
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83 PChaudhari et al solubility enhancement of hydrophobic drugs using
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84 US patent 545721J Szejtli et al inclusion complexes of taxol or taxotere or
taxus extract formed with cyclodextrins its preparation and use
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Solution Chemistry37(2)2008PP 249-264
86 MLinaresSolubilization of naphthaquinones by complexation with
hydroxypropyl β cyclodextrin International Journal of
Pharmaceutics1591997PP 13-18
87 MGuyot Physicochemical characterization and dissolution of norfloxacin-
cyclodextrin inclusion complexes and PEG solid dispersions International
journal of Pharmaceutics1231995PP 53-63
88 TNakate et al Imporvement of pulmonary absorption of cyclopeptide FK 224
in rats by co-formulating with beta cyclodextrin European Journal of
Pharmaceutics and Biopharmaceutics552003PP 147-154
89 HViernstein et alSolubility enhancement of low soluble biologically active
compounds-temperature and cosolvent dependent inclusion
complexationInternational Journal of Pharmaceutics 2562003PP 85-94
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midazolam nasal sprayInternational Journal of Pharmaceutics2122001PP-
29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
inclusion complexes by phase solubility photostability physicochemical and
computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
93 H Archontaki et alStudy on inclusion complexes of bromazepam with beta
and beta hydroxypropylcyclodextrinsJournal of Pharmaceutical and
Biomedical analysis282002PP 761-769
94 O Aleem et al Effect of beta cyclodextrin and hydroxypropyl beta
cyclodextrins complexation on physicochemical properties and antimicrobial
activity of cefdinir Journal of Pharmaceutical and Biomedical analysis 47(3)
2008 PP 535-540
95 S RawatSolubility enhancement of celecoxib using beta cyclodextrin
inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
96 A Gil et al Evolution of the interaction of a new chemical entity eflucimibe
with gamma cyclodextrin during kneading processEuropean Journal of
Pharmaceutical Sciences 23 2004 PP 123-129
97 HAmmar et al Formulation and biological evaluation of glimepiride-
cyclodextrin-polymer systems International Journal of
Pharmaceutics3092006 PP 129-138
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98 S Rawat et alEnhancement of Industrial absorption of few cox-2 inhibitors
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99 H Hassan et al Enhacement of dissolution amount and in vivo bioavailability
of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
nicardipine-cyclodextrins inclusion compounds European Journal of
Pharmaceutical Sciences152007PP 79-88
101 OSolimann et al Amorphous spironolactone and hydroxypropylated
cyclodextrin complexes with superior dissolution and
bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
102 Xianhong Wen et al Preparation and study the 12 inclusion complex of
carvedilol with beta cyclodextrin342004PP 517-523
103 KWaleczek et al Phase solubility study of pure (-)-α-bisabolol and camomile
essential oil with β cyclodextrin European Journal of Pharmaceutics and
Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
modeling studiesJournal of Inclusion Phenomena and Macrocyclic Chemistry
57(1-4) 2007 PP 503-510
105 Ning Li et alStudy of physicochemical properties of trimethoprim with
cyclodextrin in solution Journal of Pharmaceutical and Biomedical
Analysis382005 PP 370-374
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106 CTimpe et al A novel solvent- based fluidised bed wet granulation process
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108 YJavadzadeh et alEnhancement of dissolution rate of piroxicam using
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109 YJavadzadeh et alLiquisolid technique as a new approach to sustain
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Pharmaceutics3622008 PP 102-108
110 VYadav et alImprovement of solubility and dissolution of Indomethacin by
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Research1(2)2009 PP 44-51
111 IDarwish et alDissolution rate enhancement of gibenclamide using liquisolid
tablet technologyActa Pharmaceutica522002PP 171-179
112 AYadav et alFormulation and evaluation of orodispersibleliquisolid
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Research44(3)2010 PP 227-235
113 SSpireas et alIn vitro release evaluation of hydrocortisone liquisolidtablets
Journal of Pharmaceutical Sciences871998 PP 867-872
114 AKarmarkar et alLiquisolid technology for dissolution rate enhancement or
sustaining releaseExpert opinion on drug delivery7(10)2010PP 1227-1234
115 ANokhodchi et al Drug release from liquisolid systems speed it up slow it
down Expert opinion on drug deliveryExpert opinion on drug
delivery8(2)2011PP 191-205
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116 A Karmarkar LiquisolidtabletsA novel approach for drug delivery
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beagle dogsInternational Journal of Pharmaceutics 222 2001 PP 1-6
118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
124 SGubbi et al Formulation and characterization of atorvastatin calcium
liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
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125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
126 B El- Houssieny et al Bioavailability and biological activity of liquisolid
compact formula of repaglinide and its effect on glucose tolerance in rabbits
Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
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European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
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135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
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144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
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152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
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156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
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Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
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169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
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170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
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(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
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pharmaceutical sciences and drug research 2010 2 (2) 107-111
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of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
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delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
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glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
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(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
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197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
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PP 81-92
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metabolite in human plasma and urine by liquid chromatography and
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Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
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15 M Grau et al Nanosuspensions of poorly soluble drugs ndash reproducibility of
small scale production Inetrnational Journal of Pharmaceutics 196 2000 PP
155ndash157
16 G Liversidge et al Particle size reduction for improvement of oral
bioavailability of hydrophobic drugs absolute oral bioavailability of
nanocrystalline danazol in beagle dogs Inetrnational Journal of
Pharmaceutics 125 1995 PP 91ndash97
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particle size American Journal of Obstetrics and Gynecology 161 1989 PP
948ndash951
18 A Jounela et al Effect of particle size on the bioavailability of digoxin
European Journal of clinical Pharmacology 8 1975 PP 365ndash370
19 Y Ran et al Solubilization and Preformulation Studies on PG-300995 (an
anti-HIV drug) Journal of Pharmaceutical Sciences 94 (2) 2005 PP 297ndash
303
20 C Mbah Solubilization of valsartan by aqueous glycerol polyethylene glycol
and micellar solutions Pharmazie 61 (4) 2006 PP 322-324
21 R Chang et al Effect of Hydroxypropyl Beta-Cyclodextrin on Drug
Solubility in Water-Propylene Glycol Mixtures Drug Development and
Industrial Pharmacy 30 (3) 2004 PP 297ndash302
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Cosolvency Drug Development and Industrial Pharmacy 25 (11) 1999 PP
1193ndash1197
23 R Stancanelli et al The enhancement of isoflavones water solubility by
complexation with modified cyclodextrins A spectroscopic investigation with
implications in the pharmaceutical analysis Journal of Pharmaceutical and
biomedical analysis 44 (4) 2007 PP 980-984
24 S Gibaud et al Melarsoprolndashcyclodextrins inclusion complexes International
Journal of Pharmaceutics 306 ( 1-2) 2005 PP 107-121
25 S Wong et al Enhancement of the dissolution rate and oral absorption of a
poorly water soluble drug by formation of surfactant-containing
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68
26 Ryh-Nan Pan et al Enhancement of Dissolution and Bioavailability of
Piroxicam in Solid Dispersion Systems Drug Development and Industrial
Pharmacy 26 (9) 2000 PP 989 ndash 994
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solid dispersion in polyethylene glycolndash polysorbate 80 mixture International
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28 R Muller et al Emulsions and nanosuspensions for the formulation of poorly
soluble drugs Medpharm Scientific Publishers Stuttgart Germany 1998 PP
149ndash174
29 R Muller et al Nanosuspensions as Particulate Drug Formulations in
Therapy Rationale for Development and What We Can Expect for the Future
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Soluble Compounds European Journal of Pharmaceutical Sciences 18 (2)
2003 PP 113ndash120
31 P Lockman et al Nanoparticle Technology for Drug Delivery Across the
Blood-Brain Barrier Drug Development and Industrial Pharmacy 28 (1)
2002 PP 1ndash13
32 B Rabinow Nanosuspensions in Drug Delivery Nature Reviews Drug
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Journal of Pharmacy and Pharmacology 56 (7) 2004 PP 827ndash840
34 G Liversidge et al Particle Size Reduction for Improvement of Oral
Bioavailability of Hydrophobic Drugs I Absolute Oral Bioavailability of
Nanocrystalline Danazol in Beagle Dogs International Journal of
Pharmaceutics 125 (1)1995 PP 91ndash97
35 J Hecq et al Preparation and Characterization of Nanocrystals for Solubility
and Dissolution Rate Enhancement of Nifedipine International Journal of
Pharmaceutics 299 (1ndash2) 2005 PP 167ndash177
36 E Reverchon et al Production of Antibiotic Micro- and Nano-Particles by
Supercritical Antisolvent Precipitation Powder Technology 106 (1ndash2) 1999
PP 23ndash29
37 P Chattopadhyay et al Protein Nanoparticles Formation by Supercritical
Antisolvent with Enhanced Mass Transfer AIChE Journal 48 2002 PP
235ndash244
38 T Young et al Rapid Expansion from Supercritical to Aqueous Solution to
Produce Submicron Suspensions of Water-Insoluble Drugs Biotechnology
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40 J Hu et al Stable Amorphous Danazol Nanostructured Powders with Rapid
Dissolution Rates Produced by Spray Freezing into Liquid Drug Development
and Industrial Pharmacy 30 (7) 2004 PP 695ndash704
41 X Chen et al Rapid Dissolution of High Potency Danazol Powders Produced
by Evaporative Precipitation into Aqueous Solution Journal of
Pharmaceutical Sciences 93 (7) 2004 PP 1867ndash1878
42 JVaughn et al Supersaturation produces high bioavailability of amorphous
danazol particles formed by evaporative precipitation into aqueous solution
and spray freezing into liquid technologies Drug Development and Industrial
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precipitation into aqueous solution International Journal of Pharmaceutics
242 (1-2) 2002 PP 3-14
44 V Hoffarta et al Oral bioavailability of a low molecular weight heparin using
a polymeric delivery system Journal of Controlled Release 113 (1) 2006
PP 38-42
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polymer nanoparticles Reviews on Advanced Materials Science17 2008 PP
71-75
46 CPinto Reis et al Nanoencapsulation I Methods for preparation of drug
loaded polymeric nanoparticles Nanomedicine 2 2006 PP 8-21
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systems of ibuprofenndashpolyethylene glycol International Journal of
Pharmaceutics1301996 PP 25ndash32
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poorly water soluble drug in dogs European Journal of Pharmaceutics and
Biopharmaceutics 68 (2) 2008 PP 338-345
50 C Pouton et al Formulation of self-emulsifying drug delivery systems
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Biopharmaceutics 63 (3) 2006 PP 288-294
52 S Kapsi et al Processing factors in development of solid solution formulation
of itraconazole for enhancement of drug dissolution and bioavailability
International Journal of Pharmaceutics229 2001 PP 193ndash203
53 B Katzung et al Basic and clinical Pharmacology 11th
edition 2009
McGraw Hill Publication PP 167-188
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development and industrial pharmacy161990 PP 2487-2499
66 T Loftsson et al Pharmaceutical applications of cyclodextrinsdrug
solubilization and stabilization Journal of pharmaceutical sciences851996PP
1017-1025
67 RO Williams et al Characterization of an inclusion complex of cholesterol
and hydroxypropyl-β-Cyclodextrin European journal of pharmaceutics and
biopharmaceutics461998PP 355-360
68 JSzejtli Pastpresent and future of cyclodextrin research Pure and applied
chemistry 76(10)2004 PP 1825-1845
69 SBaboota et alCyclodextrins in drug delivery systems An update Latest
reviews 12003 retrieved from pharmainfonet
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stabilityCyDexIncOct 2004
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72 CGazpio et al HPLC and solubility study of the interaction between pindolol
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2005PP 487-492
73 AMiro et alImprovement of gliquidone hypoglycaemic effect in rats by
cyclodextrin formulations European Journal of Pharmaceutical Sciences23
2004PP-57-64
74 BDevarakonda et al Comparison of the aqueous solubilization of practically
insoluble niclosamide by polyamidoamine dendrimers and cyclodextrins
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75 SHiremath et alImproved dissolution rate of valdecoxib inclusion complexes
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Sciences692007PP 442-445
76 CHolvoet Development of an omeprazole parenteral formulation with
hydroxypropyl-beta-cyclodextrinPharmaceutical Development and
Technology12(3)2007PP 327-336
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cyclodextrins Journal of Inclusion phenomena and Macrocyclic
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78 United States Patent 7259153ChangRong-KunDrug formulation and
delivery using crystalline methylated cyclodextrins
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Delivery 2(2) 2005 PP 1-17
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82 K Connors et al The stability of cyclodextrin complexes in solution
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taxus extract formed with cyclodextrins its preparation and use
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Solution Chemistry37(2)2008PP 249-264
86 MLinaresSolubilization of naphthaquinones by complexation with
hydroxypropyl β cyclodextrin International Journal of
Pharmaceutics1591997PP 13-18
87 MGuyot Physicochemical characterization and dissolution of norfloxacin-
cyclodextrin inclusion complexes and PEG solid dispersions International
journal of Pharmaceutics1231995PP 53-63
88 TNakate et al Imporvement of pulmonary absorption of cyclopeptide FK 224
in rats by co-formulating with beta cyclodextrin European Journal of
Pharmaceutics and Biopharmaceutics552003PP 147-154
89 HViernstein et alSolubility enhancement of low soluble biologically active
compounds-temperature and cosolvent dependent inclusion
complexationInternational Journal of Pharmaceutics 2562003PP 85-94
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midazolam nasal sprayInternational Journal of Pharmaceutics2122001PP-
29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
inclusion complexes by phase solubility photostability physicochemical and
computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
93 H Archontaki et alStudy on inclusion complexes of bromazepam with beta
and beta hydroxypropylcyclodextrinsJournal of Pharmaceutical and
Biomedical analysis282002PP 761-769
94 O Aleem et al Effect of beta cyclodextrin and hydroxypropyl beta
cyclodextrins complexation on physicochemical properties and antimicrobial
activity of cefdinir Journal of Pharmaceutical and Biomedical analysis 47(3)
2008 PP 535-540
95 S RawatSolubility enhancement of celecoxib using beta cyclodextrin
inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
96 A Gil et al Evolution of the interaction of a new chemical entity eflucimibe
with gamma cyclodextrin during kneading processEuropean Journal of
Pharmaceutical Sciences 23 2004 PP 123-129
97 HAmmar et al Formulation and biological evaluation of glimepiride-
cyclodextrin-polymer systems International Journal of
Pharmaceutics3092006 PP 129-138
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98 S Rawat et alEnhancement of Industrial absorption of few cox-2 inhibitors
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Biomedical Analysis 69 (4) 2007 PP529-534
99 H Hassan et al Enhacement of dissolution amount and in vivo bioavailability
of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
nicardipine-cyclodextrins inclusion compounds European Journal of
Pharmaceutical Sciences152007PP 79-88
101 OSolimann et al Amorphous spironolactone and hydroxypropylated
cyclodextrin complexes with superior dissolution and
bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
102 Xianhong Wen et al Preparation and study the 12 inclusion complex of
carvedilol with beta cyclodextrin342004PP 517-523
103 KWaleczek et al Phase solubility study of pure (-)-α-bisabolol and camomile
essential oil with β cyclodextrin European Journal of Pharmaceutics and
Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
modeling studiesJournal of Inclusion Phenomena and Macrocyclic Chemistry
57(1-4) 2007 PP 503-510
105 Ning Li et alStudy of physicochemical properties of trimethoprim with
cyclodextrin in solution Journal of Pharmaceutical and Biomedical
Analysis382005 PP 370-374
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pharmaceuticals by nonaqueous granulation techniqueInternational Journal of
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108 YJavadzadeh et alEnhancement of dissolution rate of piroxicam using
liquisolidcompactsII Farmaco602005 PP 361-365
109 YJavadzadeh et alLiquisolid technique as a new approach to sustain
propranolol hydrochloride release from tablet matricesInternational Journal of
Pharmaceutics3622008 PP 102-108
110 VYadav et alImprovement of solubility and dissolution of Indomethacin by
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Research1(2)2009 PP 44-51
111 IDarwish et alDissolution rate enhancement of gibenclamide using liquisolid
tablet technologyActa Pharmaceutica522002PP 171-179
112 AYadav et alFormulation and evaluation of orodispersibleliquisolid
compacts of aceclofenacIndian Journal of Pharmacy Education and
Research44(3)2010 PP 227-235
113 SSpireas et alIn vitro release evaluation of hydrocortisone liquisolidtablets
Journal of Pharmaceutical Sciences871998 PP 867-872
114 AKarmarkar et alLiquisolid technology for dissolution rate enhancement or
sustaining releaseExpert opinion on drug delivery7(10)2010PP 1227-1234
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down Expert opinion on drug deliveryExpert opinion on drug
delivery8(2)2011PP 191-205
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International Journal of Health Research 2(1) 2009 PP 45-50
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beagle dogsInternational Journal of Pharmaceutics 222 2001 PP 1-6
118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
124 SGubbi et al Formulation and characterization of atorvastatin calcium
liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
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125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
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compact formula of repaglinide and its effect on glucose tolerance in rabbits
Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
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European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
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135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
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Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
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the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
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153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
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161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
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and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
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170 E Reverchon et al Rifampicine nanoparticles production by supercritical
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171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
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173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
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(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
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2007 PP 152-160
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390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
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2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
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of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
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glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
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192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
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(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
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corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
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Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
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200 APeepliwal et al Bioanalytical method development and its validation for
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PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
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23 R Stancanelli et al The enhancement of isoflavones water solubility by
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biomedical analysis 44 (4) 2007 PP 980-984
24 S Gibaud et al Melarsoprolndashcyclodextrins inclusion complexes International
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68
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149ndash174
29 R Muller et al Nanosuspensions as Particulate Drug Formulations in
Therapy Rationale for Development and What We Can Expect for the Future
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Soluble Compounds European Journal of Pharmaceutical Sciences 18 (2)
2003 PP 113ndash120
31 P Lockman et al Nanoparticle Technology for Drug Delivery Across the
Blood-Brain Barrier Drug Development and Industrial Pharmacy 28 (1)
2002 PP 1ndash13
32 B Rabinow Nanosuspensions in Drug Delivery Nature Reviews Drug
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33 V Patravale et al Nanosuspensions A Promising Drug Delivery Strategy
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Pharmaceutics 125 (1)1995 PP 91ndash97
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and Dissolution Rate Enhancement of Nifedipine International Journal of
Pharmaceutics 299 (1ndash2) 2005 PP 167ndash177
36 E Reverchon et al Production of Antibiotic Micro- and Nano-Particles by
Supercritical Antisolvent Precipitation Powder Technology 106 (1ndash2) 1999
PP 23ndash29
37 P Chattopadhyay et al Protein Nanoparticles Formation by Supercritical
Antisolvent with Enhanced Mass Transfer AIChE Journal 48 2002 PP
235ndash244
38 T Young et al Rapid Expansion from Supercritical to Aqueous Solution to
Produce Submicron Suspensions of Water-Insoluble Drugs Biotechnology
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40 J Hu et al Stable Amorphous Danazol Nanostructured Powders with Rapid
Dissolution Rates Produced by Spray Freezing into Liquid Drug Development
and Industrial Pharmacy 30 (7) 2004 PP 695ndash704
41 X Chen et al Rapid Dissolution of High Potency Danazol Powders Produced
by Evaporative Precipitation into Aqueous Solution Journal of
Pharmaceutical Sciences 93 (7) 2004 PP 1867ndash1878
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danazol particles formed by evaporative precipitation into aqueous solution
and spray freezing into liquid technologies Drug Development and Industrial
Pharmacy 32(5) 2006 PP 559-567
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242 (1-2) 2002 PP 3-14
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a polymeric delivery system Journal of Controlled Release 113 (1) 2006
PP 38-42
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polymer nanoparticles Reviews on Advanced Materials Science17 2008 PP
71-75
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loaded polymeric nanoparticles Nanomedicine 2 2006 PP 8-21
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Biopharmaceutics 63 (3) 2006 PP 288-294
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of itraconazole for enhancement of drug dissolution and bioavailability
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edition 2009
McGraw Hill Publication PP 167-188
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1017-1025
67 RO Williams et al Characterization of an inclusion complex of cholesterol
and hydroxypropyl-β-Cyclodextrin European journal of pharmaceutics and
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cyclodextrin formulations European Journal of Pharmaceutical Sciences23
2004PP-57-64
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Sciences692007PP 442-445
76 CHolvoet Development of an omeprazole parenteral formulation with
hydroxypropyl-beta-cyclodextrinPharmaceutical Development and
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cyclodextrins Journal of Inclusion phenomena and Macrocyclic
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delivery using crystalline methylated cyclodextrins
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Delivery 2(2) 2005 PP 1-17
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taxus extract formed with cyclodextrins its preparation and use
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Solution Chemistry37(2)2008PP 249-264
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hydroxypropyl β cyclodextrin International Journal of
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87 MGuyot Physicochemical characterization and dissolution of norfloxacin-
cyclodextrin inclusion complexes and PEG solid dispersions International
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complexationInternational Journal of Pharmaceutics 2562003PP 85-94
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midazolam nasal sprayInternational Journal of Pharmaceutics2122001PP-
29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
inclusion complexes by phase solubility photostability physicochemical and
computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
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and beta hydroxypropylcyclodextrinsJournal of Pharmaceutical and
Biomedical analysis282002PP 761-769
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2008 PP 535-540
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inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
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with gamma cyclodextrin during kneading processEuropean Journal of
Pharmaceutical Sciences 23 2004 PP 123-129
97 HAmmar et al Formulation and biological evaluation of glimepiride-
cyclodextrin-polymer systems International Journal of
Pharmaceutics3092006 PP 129-138
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of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
nicardipine-cyclodextrins inclusion compounds European Journal of
Pharmaceutical Sciences152007PP 79-88
101 OSolimann et al Amorphous spironolactone and hydroxypropylated
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bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
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essential oil with β cyclodextrin European Journal of Pharmaceutics and
Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
modeling studiesJournal of Inclusion Phenomena and Macrocyclic Chemistry
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105 Ning Li et alStudy of physicochemical properties of trimethoprim with
cyclodextrin in solution Journal of Pharmaceutical and Biomedical
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111 IDarwish et alDissolution rate enhancement of gibenclamide using liquisolid
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Research44(3)2010 PP 227-235
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Journal of Pharmaceutical Sciences871998 PP 867-872
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down Expert opinion on drug deliveryExpert opinion on drug
delivery8(2)2011PP 191-205
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beagle dogsInternational Journal of Pharmaceutics 222 2001 PP 1-6
118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
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of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
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liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
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International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
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Bioscience Trends 4 (1) 2010 PP 17-24
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European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
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133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
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136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
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Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
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145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
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the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
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2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
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microemulsifying drug delivery system European Journal of Pharmaceutics
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151 PZangPreparation and evaluation of self-microemulsifying drug delivery
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154 RHolm et al Examination of oral absorption and lymphatic transport of
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97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
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156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
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157 SNazzal et al Preparation and in vitro characterization of a eutectic based
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1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
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388-398
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164 S Wook Jun et al Preparation and characterization of
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and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
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170 E Reverchon et al Rifampicine nanoparticles production by supercritical
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(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
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antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
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(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
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2007 PP 152-160
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390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
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2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
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of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
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(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
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Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
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PP 247-253
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(15) 2003 PP 2581-2591
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and Research 4 (1) 2010 PP 60-63
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(3) 2010 PP345-354
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2002 PP 1ndash13
32 B Rabinow Nanosuspensions in Drug Delivery Nature Reviews Drug
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Pharmaceutics 125 (1)1995 PP 91ndash97
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and Dissolution Rate Enhancement of Nifedipine International Journal of
Pharmaceutics 299 (1ndash2) 2005 PP 167ndash177
36 E Reverchon et al Production of Antibiotic Micro- and Nano-Particles by
Supercritical Antisolvent Precipitation Powder Technology 106 (1ndash2) 1999
PP 23ndash29
37 P Chattopadhyay et al Protein Nanoparticles Formation by Supercritical
Antisolvent with Enhanced Mass Transfer AIChE Journal 48 2002 PP
235ndash244
38 T Young et al Rapid Expansion from Supercritical to Aqueous Solution to
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40 J Hu et al Stable Amorphous Danazol Nanostructured Powders with Rapid
Dissolution Rates Produced by Spray Freezing into Liquid Drug Development
and Industrial Pharmacy 30 (7) 2004 PP 695ndash704
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by Evaporative Precipitation into Aqueous Solution Journal of
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and spray freezing into liquid technologies Drug Development and Industrial
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precipitation into aqueous solution International Journal of Pharmaceutics
242 (1-2) 2002 PP 3-14
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a polymeric delivery system Journal of Controlled Release 113 (1) 2006
PP 38-42
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polymer nanoparticles Reviews on Advanced Materials Science17 2008 PP
71-75
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of itraconazole for enhancement of drug dissolution and bioavailability
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edition 2009
McGraw Hill Publication PP 167-188
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67 RO Williams et al Characterization of an inclusion complex of cholesterol
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cyclodextrin formulations European Journal of Pharmaceutical Sciences23
2004PP-57-64
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hydroxypropyl β cyclodextrin International Journal of
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cyclodextrin inclusion complexes and PEG solid dispersions International
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midazolam nasal sprayInternational Journal of Pharmaceutics2122001PP-
29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
inclusion complexes by phase solubility photostability physicochemical and
computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
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and beta hydroxypropylcyclodextrinsJournal of Pharmaceutical and
Biomedical analysis282002PP 761-769
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2008 PP 535-540
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inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
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with gamma cyclodextrin during kneading processEuropean Journal of
Pharmaceutical Sciences 23 2004 PP 123-129
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cyclodextrin-polymer systems International Journal of
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of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
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bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
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Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
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delivery8(2)2011PP 191-205
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118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
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of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
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liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
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International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
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Bioscience Trends 4 (1) 2010 PP 17-24
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European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
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133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
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136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
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145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
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148 P Postolache et al Cyclosporin bioavailability of two physically different oral
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2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
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151 PZangPreparation and evaluation of self-microemulsifying drug delivery
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154 RHolm et al Examination of oral absorption and lymphatic transport of
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97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
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156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
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157 SNazzal et al Preparation and in vitro characterization of a eutectic based
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International Journal of Pharmaceutics 286 2004 PP 147-156
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1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
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388-398
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165 H Hassan et al Enhancement of dissolution amount and in vivo
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International Journal of Pharmaceutics 301 2005 PP 199-208
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170 E Reverchon et al Rifampicine nanoparticles production by supercritical
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(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
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antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
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(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
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180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
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390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
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2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
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of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
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delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
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glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
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(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
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Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
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PP 247-253
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in human plasma and dosage forms using HPLC with a photodiode array
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(15) 2003 PP 2581-2591
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and Research 4 (1) 2010 PP 60-63
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40 J Hu et al Stable Amorphous Danazol Nanostructured Powders with Rapid
Dissolution Rates Produced by Spray Freezing into Liquid Drug Development
and Industrial Pharmacy 30 (7) 2004 PP 695ndash704
41 X Chen et al Rapid Dissolution of High Potency Danazol Powders Produced
by Evaporative Precipitation into Aqueous Solution Journal of
Pharmaceutical Sciences 93 (7) 2004 PP 1867ndash1878
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242 (1-2) 2002 PP 3-14
44 V Hoffarta et al Oral bioavailability of a low molecular weight heparin using
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PP 38-42
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polymer nanoparticles Reviews on Advanced Materials Science17 2008 PP
71-75
46 CPinto Reis et al Nanoencapsulation I Methods for preparation of drug
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drug delivery system European Journal of Pharmaceutics and
Biopharmaceutics 63 (3) 2006 PP 288-294
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of itraconazole for enhancement of drug dissolution and bioavailability
International Journal of Pharmaceutics229 2001 PP 193ndash203
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edition 2009
McGraw Hill Publication PP 167-188
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67 RO Williams et al Characterization of an inclusion complex of cholesterol
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cyclodextrin formulations European Journal of Pharmaceutical Sciences23
2004PP-57-64
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29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
inclusion complexes by phase solubility photostability physicochemical and
computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
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and beta hydroxypropylcyclodextrinsJournal of Pharmaceutical and
Biomedical analysis282002PP 761-769
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2008 PP 535-540
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inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
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with gamma cyclodextrin during kneading processEuropean Journal of
Pharmaceutical Sciences 23 2004 PP 123-129
97 HAmmar et al Formulation and biological evaluation of glimepiride-
cyclodextrin-polymer systems International Journal of
Pharmaceutics3092006 PP 129-138
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of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
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Pharmaceutical Sciences152007PP 79-88
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bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
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essential oil with β cyclodextrin European Journal of Pharmaceutics and
Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
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105 Ning Li et alStudy of physicochemical properties of trimethoprim with
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118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
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liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
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125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
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Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
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European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 273
135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
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145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
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microemulsifying drug delivery system European Journal of Pharmaceutics
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microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
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microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
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Pharmaceutics 167 1998 PP 155-164
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157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
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International Journal of Pharmaceutics 286 2004 PP 147-156
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1-14
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390
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and industrial Pharmacy 33 (2) 2007 PP 101-111
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PP 247-253
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(15) 2003 PP 2581-2591
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and Research 4 (1) 2010 PP 60-63
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Biopharmaceutics 63 (3) 2006 PP 288-294
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of itraconazole for enhancement of drug dissolution and bioavailability
International Journal of Pharmaceutics229 2001 PP 193ndash203
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edition 2009
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76 CHolvoet Development of an omeprazole parenteral formulation with
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87 MGuyot Physicochemical characterization and dissolution of norfloxacin-
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29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
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computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
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Biomedical analysis282002PP 761-769
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inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
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with gamma cyclodextrin during kneading processEuropean Journal of
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97 HAmmar et al Formulation and biological evaluation of glimepiride-
cyclodextrin-polymer systems International Journal of
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100 CFernandes et al Physicochemical characterization and in vitro dissolution of
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102 Xianhong Wen et al Preparation and study the 12 inclusion complex of
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Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
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105 Ning Li et alStudy of physicochemical properties of trimethoprim with
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119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
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120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
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Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
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International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
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European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
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135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
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SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
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SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
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161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
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and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
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168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
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170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
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antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
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174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
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(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
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of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
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2002 PP 53-61
190 wwweudragitevonikcom
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PP 247-253
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67 RO Williams et al Characterization of an inclusion complex of cholesterol
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68 JSzejtli Pastpresent and future of cyclodextrin research Pure and applied
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72 CGazpio et al HPLC and solubility study of the interaction between pindolol
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2004PP-57-64
74 BDevarakonda et al Comparison of the aqueous solubilization of practically
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87 MGuyot Physicochemical characterization and dissolution of norfloxacin-
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29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
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2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
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95 S RawatSolubility enhancement of celecoxib using beta cyclodextrin
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Biopharmaceutics 57 2004 PP 263-267
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97 HAmmar et al Formulation and biological evaluation of glimepiride-
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99 H Hassan et al Enhacement of dissolution amount and in vivo bioavailability
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100 CFernandes et al Physicochemical characterization and in vitro dissolution of
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101 OSolimann et al Amorphous spironolactone and hydroxypropylated
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102 Xianhong Wen et al Preparation and study the 12 inclusion complex of
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104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
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105 Ning Li et alStudy of physicochemical properties of trimethoprim with
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118 SSpirease et alEnhancement of prednisolone dissolution properties using
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188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
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2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
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Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
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125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
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2010 PP 135-142
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129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
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systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
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135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
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144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
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152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
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Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
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SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
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SPTM SVKMrsquoS NMIMS MUMBAI 266
71 GBettinetti et alInteraction of naproxen with noncrystalline acetyl beta and
acetyl gamma cyclodextrins in the solid and liquid stateEuropean Journal of
Pharmaceutical Sciences152002PP 21-29
72 CGazpio et al HPLC and solubility study of the interaction between pindolol
and cyclodextrinsJournal of Pharmaceutical and Biomedical Analysis37
2005PP 487-492
73 AMiro et alImprovement of gliquidone hypoglycaemic effect in rats by
cyclodextrin formulations European Journal of Pharmaceutical Sciences23
2004PP-57-64
74 BDevarakonda et al Comparison of the aqueous solubilization of practically
insoluble niclosamide by polyamidoamine dendrimers and cyclodextrins
International Journal of Pharmaceutics 3042005PP 193-209
75 SHiremath et alImproved dissolution rate of valdecoxib inclusion complexes
with hydroxyl propyl beta cyclodextrinIndian Journal of Pharmaceutical
Sciences692007PP 442-445
76 CHolvoet Development of an omeprazole parenteral formulation with
hydroxypropyl-beta-cyclodextrinPharmaceutical Development and
Technology12(3)2007PP 327-336
77 MChavanpatil et alEnhancement of nasal absorption of acyclovir via
cyclodextrins Journal of Inclusion phenomena and Macrocyclic
Chemistry44(1-4)2002 PP137-140
78 United States Patent 7259153ChangRong-KunDrug formulation and
delivery using crystalline methylated cyclodextrins
79 TLoftsson et al Cyclodextrins in drug delivery Expert opinion Drug
Delivery 2(2) 2005 PP 1-17
80 TLoftsson et al Self association of cyclodextrins and cyclodextrin complexes
Journal of Pharmaceutical Sciences 93(5)2004PP 1091-1099
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SPTM SVKMrsquoS NMIMS MUMBAI 267
81 MEsclusa-Diaz et al Preparation and evaluation of ketoconazole- beta
cyclodextrin multicomponent complexesInternational Journal of
Pharmaceutics1421996PP 183-187
82 K Connors et al The stability of cyclodextrin complexes in solution
Chemical Reviews 97 1997 PP 1325-1357
83 PChaudhari et al solubility enhancement of hydrophobic drugs using
synergistically interacting cyclodextrin and cosolventsCurrent science92(11)
2007PP 1586-1591
84 US patent 545721J Szejtli et al inclusion complexes of taxol or taxotere or
taxus extract formed with cyclodextrins its preparation and use
85 MAl Omari et alComparative study of the inclusion complexation of
pizotifen and ketotifen with native and modified cyclodextrinsJournal of
Solution Chemistry37(2)2008PP 249-264
86 MLinaresSolubilization of naphthaquinones by complexation with
hydroxypropyl β cyclodextrin International Journal of
Pharmaceutics1591997PP 13-18
87 MGuyot Physicochemical characterization and dissolution of norfloxacin-
cyclodextrin inclusion complexes and PEG solid dispersions International
journal of Pharmaceutics1231995PP 53-63
88 TNakate et al Imporvement of pulmonary absorption of cyclopeptide FK 224
in rats by co-formulating with beta cyclodextrin European Journal of
Pharmaceutics and Biopharmaceutics552003PP 147-154
89 HViernstein et alSolubility enhancement of low soluble biologically active
compounds-temperature and cosolvent dependent inclusion
complexationInternational Journal of Pharmaceutics 2562003PP 85-94
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 268
90 T Loftsson et alCyclodextrinsolubilization of benzodiazepinesformulation of
midazolam nasal sprayInternational Journal of Pharmaceutics2122001PP-
29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
inclusion complexes by phase solubility photostability physicochemical and
computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
93 H Archontaki et alStudy on inclusion complexes of bromazepam with beta
and beta hydroxypropylcyclodextrinsJournal of Pharmaceutical and
Biomedical analysis282002PP 761-769
94 O Aleem et al Effect of beta cyclodextrin and hydroxypropyl beta
cyclodextrins complexation on physicochemical properties and antimicrobial
activity of cefdinir Journal of Pharmaceutical and Biomedical analysis 47(3)
2008 PP 535-540
95 S RawatSolubility enhancement of celecoxib using beta cyclodextrin
inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
96 A Gil et al Evolution of the interaction of a new chemical entity eflucimibe
with gamma cyclodextrin during kneading processEuropean Journal of
Pharmaceutical Sciences 23 2004 PP 123-129
97 HAmmar et al Formulation and biological evaluation of glimepiride-
cyclodextrin-polymer systems International Journal of
Pharmaceutics3092006 PP 129-138
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SPTM SVKMrsquoS NMIMS MUMBAI 269
98 S Rawat et alEnhancement of Industrial absorption of few cox-2 inhibitors
through interaction with β-Cyclodextrins Journal of Pharmaceutical and
Biomedical Analysis 69 (4) 2007 PP529-534
99 H Hassan et al Enhacement of dissolution amount and in vivo bioavailability
of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
nicardipine-cyclodextrins inclusion compounds European Journal of
Pharmaceutical Sciences152007PP 79-88
101 OSolimann et al Amorphous spironolactone and hydroxypropylated
cyclodextrin complexes with superior dissolution and
bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
102 Xianhong Wen et al Preparation and study the 12 inclusion complex of
carvedilol with beta cyclodextrin342004PP 517-523
103 KWaleczek et al Phase solubility study of pure (-)-α-bisabolol and camomile
essential oil with β cyclodextrin European Journal of Pharmaceutics and
Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
modeling studiesJournal of Inclusion Phenomena and Macrocyclic Chemistry
57(1-4) 2007 PP 503-510
105 Ning Li et alStudy of physicochemical properties of trimethoprim with
cyclodextrin in solution Journal of Pharmaceutical and Biomedical
Analysis382005 PP 370-374
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106 CTimpe et al A novel solvent- based fluidised bed wet granulation process
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107 VYadav et alEnhancement of solubility and dissolution rate of BCS class II
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108 YJavadzadeh et alEnhancement of dissolution rate of piroxicam using
liquisolidcompactsII Farmaco602005 PP 361-365
109 YJavadzadeh et alLiquisolid technique as a new approach to sustain
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110 VYadav et alImprovement of solubility and dissolution of Indomethacin by
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111 IDarwish et alDissolution rate enhancement of gibenclamide using liquisolid
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112 AYadav et alFormulation and evaluation of orodispersibleliquisolid
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Research44(3)2010 PP 227-235
113 SSpireas et alIn vitro release evaluation of hydrocortisone liquisolidtablets
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114 AKarmarkar et alLiquisolid technology for dissolution rate enhancement or
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115 ANokhodchi et al Drug release from liquisolid systems speed it up slow it
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116 A Karmarkar LiquisolidtabletsA novel approach for drug delivery
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117 K Khaled et al In vivo evaluation of hydrochlorothiazide liquisolid tablets in
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118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
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2 (2) 2009 PP 382-386
124 SGubbi et al Formulation and characterization of atorvastatin calcium
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50-60
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125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
126 B El- Houssieny et al Bioavailability and biological activity of liquisolid
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Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
128 N Tiong et al Effects of liquisolid formulations on dissolution of naproxen
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373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
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132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
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133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
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Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
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135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
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136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
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144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
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enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
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152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
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Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
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160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
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169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
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SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 267
81 MEsclusa-Diaz et al Preparation and evaluation of ketoconazole- beta
cyclodextrin multicomponent complexesInternational Journal of
Pharmaceutics1421996PP 183-187
82 K Connors et al The stability of cyclodextrin complexes in solution
Chemical Reviews 97 1997 PP 1325-1357
83 PChaudhari et al solubility enhancement of hydrophobic drugs using
synergistically interacting cyclodextrin and cosolventsCurrent science92(11)
2007PP 1586-1591
84 US patent 545721J Szejtli et al inclusion complexes of taxol or taxotere or
taxus extract formed with cyclodextrins its preparation and use
85 MAl Omari et alComparative study of the inclusion complexation of
pizotifen and ketotifen with native and modified cyclodextrinsJournal of
Solution Chemistry37(2)2008PP 249-264
86 MLinaresSolubilization of naphthaquinones by complexation with
hydroxypropyl β cyclodextrin International Journal of
Pharmaceutics1591997PP 13-18
87 MGuyot Physicochemical characterization and dissolution of norfloxacin-
cyclodextrin inclusion complexes and PEG solid dispersions International
journal of Pharmaceutics1231995PP 53-63
88 TNakate et al Imporvement of pulmonary absorption of cyclopeptide FK 224
in rats by co-formulating with beta cyclodextrin European Journal of
Pharmaceutics and Biopharmaceutics552003PP 147-154
89 HViernstein et alSolubility enhancement of low soluble biologically active
compounds-temperature and cosolvent dependent inclusion
complexationInternational Journal of Pharmaceutics 2562003PP 85-94
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 268
90 T Loftsson et alCyclodextrinsolubilization of benzodiazepinesformulation of
midazolam nasal sprayInternational Journal of Pharmaceutics2122001PP-
29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
inclusion complexes by phase solubility photostability physicochemical and
computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
93 H Archontaki et alStudy on inclusion complexes of bromazepam with beta
and beta hydroxypropylcyclodextrinsJournal of Pharmaceutical and
Biomedical analysis282002PP 761-769
94 O Aleem et al Effect of beta cyclodextrin and hydroxypropyl beta
cyclodextrins complexation on physicochemical properties and antimicrobial
activity of cefdinir Journal of Pharmaceutical and Biomedical analysis 47(3)
2008 PP 535-540
95 S RawatSolubility enhancement of celecoxib using beta cyclodextrin
inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
96 A Gil et al Evolution of the interaction of a new chemical entity eflucimibe
with gamma cyclodextrin during kneading processEuropean Journal of
Pharmaceutical Sciences 23 2004 PP 123-129
97 HAmmar et al Formulation and biological evaluation of glimepiride-
cyclodextrin-polymer systems International Journal of
Pharmaceutics3092006 PP 129-138
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 269
98 S Rawat et alEnhancement of Industrial absorption of few cox-2 inhibitors
through interaction with β-Cyclodextrins Journal of Pharmaceutical and
Biomedical Analysis 69 (4) 2007 PP529-534
99 H Hassan et al Enhacement of dissolution amount and in vivo bioavailability
of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
nicardipine-cyclodextrins inclusion compounds European Journal of
Pharmaceutical Sciences152007PP 79-88
101 OSolimann et al Amorphous spironolactone and hydroxypropylated
cyclodextrin complexes with superior dissolution and
bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
102 Xianhong Wen et al Preparation and study the 12 inclusion complex of
carvedilol with beta cyclodextrin342004PP 517-523
103 KWaleczek et al Phase solubility study of pure (-)-α-bisabolol and camomile
essential oil with β cyclodextrin European Journal of Pharmaceutics and
Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
modeling studiesJournal of Inclusion Phenomena and Macrocyclic Chemistry
57(1-4) 2007 PP 503-510
105 Ning Li et alStudy of physicochemical properties of trimethoprim with
cyclodextrin in solution Journal of Pharmaceutical and Biomedical
Analysis382005 PP 370-374
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 270
106 CTimpe et al A novel solvent- based fluidised bed wet granulation process
for solid dispersionAmerical pharmaceutical review Nov2008PP 75-81
107 VYadav et alEnhancement of solubility and dissolution rate of BCS class II
pharmaceuticals by nonaqueous granulation techniqueInternational Journal of
Pharma Research and Development-online12 Feb 2008 PP 1-12
108 YJavadzadeh et alEnhancement of dissolution rate of piroxicam using
liquisolidcompactsII Farmaco602005 PP 361-365
109 YJavadzadeh et alLiquisolid technique as a new approach to sustain
propranolol hydrochloride release from tablet matricesInternational Journal of
Pharmaceutics3622008 PP 102-108
110 VYadav et alImprovement of solubility and dissolution of Indomethacin by
liquisolid and compaction granulationJournal of Pharmaceutical Sciences and
Research1(2)2009 PP 44-51
111 IDarwish et alDissolution rate enhancement of gibenclamide using liquisolid
tablet technologyActa Pharmaceutica522002PP 171-179
112 AYadav et alFormulation and evaluation of orodispersibleliquisolid
compacts of aceclofenacIndian Journal of Pharmacy Education and
Research44(3)2010 PP 227-235
113 SSpireas et alIn vitro release evaluation of hydrocortisone liquisolidtablets
Journal of Pharmaceutical Sciences871998 PP 867-872
114 AKarmarkar et alLiquisolid technology for dissolution rate enhancement or
sustaining releaseExpert opinion on drug delivery7(10)2010PP 1227-1234
115 ANokhodchi et al Drug release from liquisolid systems speed it up slow it
down Expert opinion on drug deliveryExpert opinion on drug
delivery8(2)2011PP 191-205
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 271
116 A Karmarkar LiquisolidtabletsA novel approach for drug delivery
International Journal of Health Research 2(1) 2009 PP 45-50
117 K Khaled et al In vivo evaluation of hydrochlorothiazide liquisolid tablets in
beagle dogsInternational Journal of Pharmaceutics 222 2001 PP 1-6
118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
124 SGubbi et al Formulation and characterization of atorvastatin calcium
liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 272
125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
126 B El- Houssieny et al Bioavailability and biological activity of liquisolid
compact formula of repaglinide and its effect on glucose tolerance in rabbits
Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
128 N Tiong et al Effects of liquisolid formulations on dissolution of naproxen
European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 273
135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
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SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
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SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 268
90 T Loftsson et alCyclodextrinsolubilization of benzodiazepinesformulation of
midazolam nasal sprayInternational Journal of Pharmaceutics2122001PP-
29-40
91 K Yap et al Characterization of the 13-Cis-retinoic acidcyclodextrin
inclusion complexes by phase solubility photostability physicochemical and
computational analysis European Journal of pharmaceutical sciences 25
2005PP 49-56
92 P Tayade et al Study of freeze ndashdried quercetin-cyclodextrin binary systems
by DSC X-ray Diffraction and SEM analysis Journal of pharmaceutical and
biomedical analysis34 2004PP 333-339
93 H Archontaki et alStudy on inclusion complexes of bromazepam with beta
and beta hydroxypropylcyclodextrinsJournal of Pharmaceutical and
Biomedical analysis282002PP 761-769
94 O Aleem et al Effect of beta cyclodextrin and hydroxypropyl beta
cyclodextrins complexation on physicochemical properties and antimicrobial
activity of cefdinir Journal of Pharmaceutical and Biomedical analysis 47(3)
2008 PP 535-540
95 S RawatSolubility enhancement of celecoxib using beta cyclodextrin
inclusion complexesEuropean Journal of pharmaceutics and
Biopharmaceutics 57 2004 PP 263-267
96 A Gil et al Evolution of the interaction of a new chemical entity eflucimibe
with gamma cyclodextrin during kneading processEuropean Journal of
Pharmaceutical Sciences 23 2004 PP 123-129
97 HAmmar et al Formulation and biological evaluation of glimepiride-
cyclodextrin-polymer systems International Journal of
Pharmaceutics3092006 PP 129-138
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 269
98 S Rawat et alEnhancement of Industrial absorption of few cox-2 inhibitors
through interaction with β-Cyclodextrins Journal of Pharmaceutical and
Biomedical Analysis 69 (4) 2007 PP529-534
99 H Hassan et al Enhacement of dissolution amount and in vivo bioavailability
of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
nicardipine-cyclodextrins inclusion compounds European Journal of
Pharmaceutical Sciences152007PP 79-88
101 OSolimann et al Amorphous spironolactone and hydroxypropylated
cyclodextrin complexes with superior dissolution and
bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
102 Xianhong Wen et al Preparation and study the 12 inclusion complex of
carvedilol with beta cyclodextrin342004PP 517-523
103 KWaleczek et al Phase solubility study of pure (-)-α-bisabolol and camomile
essential oil with β cyclodextrin European Journal of Pharmaceutics and
Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
modeling studiesJournal of Inclusion Phenomena and Macrocyclic Chemistry
57(1-4) 2007 PP 503-510
105 Ning Li et alStudy of physicochemical properties of trimethoprim with
cyclodextrin in solution Journal of Pharmaceutical and Biomedical
Analysis382005 PP 370-374
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 270
106 CTimpe et al A novel solvent- based fluidised bed wet granulation process
for solid dispersionAmerical pharmaceutical review Nov2008PP 75-81
107 VYadav et alEnhancement of solubility and dissolution rate of BCS class II
pharmaceuticals by nonaqueous granulation techniqueInternational Journal of
Pharma Research and Development-online12 Feb 2008 PP 1-12
108 YJavadzadeh et alEnhancement of dissolution rate of piroxicam using
liquisolidcompactsII Farmaco602005 PP 361-365
109 YJavadzadeh et alLiquisolid technique as a new approach to sustain
propranolol hydrochloride release from tablet matricesInternational Journal of
Pharmaceutics3622008 PP 102-108
110 VYadav et alImprovement of solubility and dissolution of Indomethacin by
liquisolid and compaction granulationJournal of Pharmaceutical Sciences and
Research1(2)2009 PP 44-51
111 IDarwish et alDissolution rate enhancement of gibenclamide using liquisolid
tablet technologyActa Pharmaceutica522002PP 171-179
112 AYadav et alFormulation and evaluation of orodispersibleliquisolid
compacts of aceclofenacIndian Journal of Pharmacy Education and
Research44(3)2010 PP 227-235
113 SSpireas et alIn vitro release evaluation of hydrocortisone liquisolidtablets
Journal of Pharmaceutical Sciences871998 PP 867-872
114 AKarmarkar et alLiquisolid technology for dissolution rate enhancement or
sustaining releaseExpert opinion on drug delivery7(10)2010PP 1227-1234
115 ANokhodchi et al Drug release from liquisolid systems speed it up slow it
down Expert opinion on drug deliveryExpert opinion on drug
delivery8(2)2011PP 191-205
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 271
116 A Karmarkar LiquisolidtabletsA novel approach for drug delivery
International Journal of Health Research 2(1) 2009 PP 45-50
117 K Khaled et al In vivo evaluation of hydrochlorothiazide liquisolid tablets in
beagle dogsInternational Journal of Pharmaceutics 222 2001 PP 1-6
118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
124 SGubbi et al Formulation and characterization of atorvastatin calcium
liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 272
125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
126 B El- Houssieny et al Bioavailability and biological activity of liquisolid
compact formula of repaglinide and its effect on glucose tolerance in rabbits
Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
128 N Tiong et al Effects of liquisolid formulations on dissolution of naproxen
European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 273
135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 269
98 S Rawat et alEnhancement of Industrial absorption of few cox-2 inhibitors
through interaction with β-Cyclodextrins Journal of Pharmaceutical and
Biomedical Analysis 69 (4) 2007 PP529-534
99 H Hassan et al Enhacement of dissolution amount and in vivo bioavailability
of itraconazole by complexation with beta cyclodextrin using supercritical
carbon dioxideJournal of Pharmaceutical and Biomedical
Analysis452007PP 243-250
100 CFernandes et al Physicochemical characterization and in vitro dissolution of
nicardipine-cyclodextrins inclusion compounds European Journal of
Pharmaceutical Sciences152007PP 79-88
101 OSolimann et al Amorphous spironolactone and hydroxypropylated
cyclodextrin complexes with superior dissolution and
bioavailabilityInternational Journal of Pharmaceutics1491997PP73-83
102 Xianhong Wen et al Preparation and study the 12 inclusion complex of
carvedilol with beta cyclodextrin342004PP 517-523
103 KWaleczek et al Phase solubility study of pure (-)-α-bisabolol and camomile
essential oil with β cyclodextrin European Journal of Pharmaceutics and
Biopharmaceutics55(2)2003PP 247-251
104 AAbdoh et alInclusion complexes of diclofenac with natural and modified
cyclodextrins explored through phase solubility1HNMR and molecular
modeling studiesJournal of Inclusion Phenomena and Macrocyclic Chemistry
57(1-4) 2007 PP 503-510
105 Ning Li et alStudy of physicochemical properties of trimethoprim with
cyclodextrin in solution Journal of Pharmaceutical and Biomedical
Analysis382005 PP 370-374
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 270
106 CTimpe et al A novel solvent- based fluidised bed wet granulation process
for solid dispersionAmerical pharmaceutical review Nov2008PP 75-81
107 VYadav et alEnhancement of solubility and dissolution rate of BCS class II
pharmaceuticals by nonaqueous granulation techniqueInternational Journal of
Pharma Research and Development-online12 Feb 2008 PP 1-12
108 YJavadzadeh et alEnhancement of dissolution rate of piroxicam using
liquisolidcompactsII Farmaco602005 PP 361-365
109 YJavadzadeh et alLiquisolid technique as a new approach to sustain
propranolol hydrochloride release from tablet matricesInternational Journal of
Pharmaceutics3622008 PP 102-108
110 VYadav et alImprovement of solubility and dissolution of Indomethacin by
liquisolid and compaction granulationJournal of Pharmaceutical Sciences and
Research1(2)2009 PP 44-51
111 IDarwish et alDissolution rate enhancement of gibenclamide using liquisolid
tablet technologyActa Pharmaceutica522002PP 171-179
112 AYadav et alFormulation and evaluation of orodispersibleliquisolid
compacts of aceclofenacIndian Journal of Pharmacy Education and
Research44(3)2010 PP 227-235
113 SSpireas et alIn vitro release evaluation of hydrocortisone liquisolidtablets
Journal of Pharmaceutical Sciences871998 PP 867-872
114 AKarmarkar et alLiquisolid technology for dissolution rate enhancement or
sustaining releaseExpert opinion on drug delivery7(10)2010PP 1227-1234
115 ANokhodchi et al Drug release from liquisolid systems speed it up slow it
down Expert opinion on drug deliveryExpert opinion on drug
delivery8(2)2011PP 191-205
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 271
116 A Karmarkar LiquisolidtabletsA novel approach for drug delivery
International Journal of Health Research 2(1) 2009 PP 45-50
117 K Khaled et al In vivo evaluation of hydrochlorothiazide liquisolid tablets in
beagle dogsInternational Journal of Pharmaceutics 222 2001 PP 1-6
118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
124 SGubbi et al Formulation and characterization of atorvastatin calcium
liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 272
125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
126 B El- Houssieny et al Bioavailability and biological activity of liquisolid
compact formula of repaglinide and its effect on glucose tolerance in rabbits
Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
128 N Tiong et al Effects of liquisolid formulations on dissolution of naproxen
European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 273
135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 270
106 CTimpe et al A novel solvent- based fluidised bed wet granulation process
for solid dispersionAmerical pharmaceutical review Nov2008PP 75-81
107 VYadav et alEnhancement of solubility and dissolution rate of BCS class II
pharmaceuticals by nonaqueous granulation techniqueInternational Journal of
Pharma Research and Development-online12 Feb 2008 PP 1-12
108 YJavadzadeh et alEnhancement of dissolution rate of piroxicam using
liquisolidcompactsII Farmaco602005 PP 361-365
109 YJavadzadeh et alLiquisolid technique as a new approach to sustain
propranolol hydrochloride release from tablet matricesInternational Journal of
Pharmaceutics3622008 PP 102-108
110 VYadav et alImprovement of solubility and dissolution of Indomethacin by
liquisolid and compaction granulationJournal of Pharmaceutical Sciences and
Research1(2)2009 PP 44-51
111 IDarwish et alDissolution rate enhancement of gibenclamide using liquisolid
tablet technologyActa Pharmaceutica522002PP 171-179
112 AYadav et alFormulation and evaluation of orodispersibleliquisolid
compacts of aceclofenacIndian Journal of Pharmacy Education and
Research44(3)2010 PP 227-235
113 SSpireas et alIn vitro release evaluation of hydrocortisone liquisolidtablets
Journal of Pharmaceutical Sciences871998 PP 867-872
114 AKarmarkar et alLiquisolid technology for dissolution rate enhancement or
sustaining releaseExpert opinion on drug delivery7(10)2010PP 1227-1234
115 ANokhodchi et al Drug release from liquisolid systems speed it up slow it
down Expert opinion on drug deliveryExpert opinion on drug
delivery8(2)2011PP 191-205
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 271
116 A Karmarkar LiquisolidtabletsA novel approach for drug delivery
International Journal of Health Research 2(1) 2009 PP 45-50
117 K Khaled et al In vivo evaluation of hydrochlorothiazide liquisolid tablets in
beagle dogsInternational Journal of Pharmaceutics 222 2001 PP 1-6
118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
124 SGubbi et al Formulation and characterization of atorvastatin calcium
liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 272
125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
126 B El- Houssieny et al Bioavailability and biological activity of liquisolid
compact formula of repaglinide and its effect on glucose tolerance in rabbits
Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
128 N Tiong et al Effects of liquisolid formulations on dissolution of naproxen
European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 273
135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 271
116 A Karmarkar LiquisolidtabletsA novel approach for drug delivery
International Journal of Health Research 2(1) 2009 PP 45-50
117 K Khaled et al In vivo evaluation of hydrochlorothiazide liquisolid tablets in
beagle dogsInternational Journal of Pharmaceutics 222 2001 PP 1-6
118 SSpirease et alEnhancement of prednisolone dissolution properties using
liquisolidcompacts International Journal of Pharmaceutics1661998PP 177-
188
119 YJavadzadeh et al Liquisolid technique for dissolution rate enhancement of a
high dose water-insoluble drug International Journal of Pharmaceutics 341
2007 PP 26-34
120 S Tayel et al Improvement of dissolution properties of carbamazepine
through application of the liquisolid tablet technique European Journal of
Pharmaceutics and Biopharmaceutics 69 (1) 2008 PP 342-347
121 R Fahmy et al Enhancement of famotidine dissolution rate through liquisolid
tablets formulationin vitro and in vivo evaluation European Journal of
Pharmaceutics and Biopharmaceutics 69 (3) 2008 PP 993-1003
122 BAkinlade et alLiquisolid systems to improve the dissolution of furosemide
Scientia Pharmaceutica 78 2010 PP 325-344
123 SGubbi et al Liquisolid technique for enhancement of dissolution properties
of bromhexinehydrochlorideResearch Journal of Pharmacy and Technology
2 (2) 2009 PP 382-386
124 SGubbi et al Formulation and characterization of atorvastatin calcium
liquisolidcompacts Asian Journal of Pharmaceutical Sciences 5 (2) 2010 PP
50-60
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 272
125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
126 B El- Houssieny et al Bioavailability and biological activity of liquisolid
compact formula of repaglinide and its effect on glucose tolerance in rabbits
Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
128 N Tiong et al Effects of liquisolid formulations on dissolution of naproxen
European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 273
135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 272
125 K El-Say et al Formulation and evaluation of rofecoxib liquisolid tablets
International Journal of Pharmaceutical Sciences Review and Research 3 (1)
2010 PP 135-142
126 B El- Houssieny et al Bioavailability and biological activity of liquisolid
compact formula of repaglinide and its effect on glucose tolerance in rabbits
Bioscience Trends 4 (1) 2010 PP 17-24
127 httpwwwaapsjorgabstractsAM_2008AAPS2008-000649PDF
128 N Tiong et al Effects of liquisolid formulations on dissolution of naproxen
European Journal of Pharmaceutics and Biopharmaceutics 73 (3) 2009 PP
373-384
129 Material safety data sheet Tween 20 Cayman Chemical Company 30th
June
2005
130 Santosh Kumar K et al Solubility enhancement of a drug by using liquisolid
technique International Journal of Pharma and biosciences 1(3) 2010 PP 1-5
131 A Kulkarniet al Liquisolid systems A review International Journal of
Pharmaceutical Sciences and Nanotechnology 3 (1) 2010 PP 795-802
132 S Emmadi et al Formulation and pharmacodynamics evaluation of liquisolid
compact Latin American Journal of Pharmacy 29 (8) 2010 PP 1303-1310
133 A Date et al Design and evaluation of self-nanoemulsifying drug delivery
systems (SNEDDS) for cefpodoximeproxetil International Journal of
Pharmaceutics329 (1-2) 2007 PP 166-172
134 Y Ito et alOral solid gentamicin preparation using emulsifier and adsorbent
Journal Of Controlled Release 105 2005 PP 23-31
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 273
135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 273
135 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self-emulsifying formulations of halofantrine Journal of Controlled
Release 105 2005 PP 23-31
136 Y Ito et alPreparation and evaluation of oral solid heparin using emulsifier
and adsorbent for in vitro and in vivo studies International journal of
Pharmaceutics 37 2006 PP 114-119
137 S Shafiq et al Development and bioavailability assessment of ramipril
nanoemulsion formulation European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 227-243
138 M Grove et al Bioavailability of seocalcitol IIIAdministration of lipid based
formulations to minipigs in the fasted and fed state European Journal of
Pharmaceutical Sciences 31 2007 PP 8-15
139 L Djekic et al The influence of cosurfactants and oils on the formation of
pharmaceutical microemulsions based on PEG-8 capryliccapricglycerides
International Journal of Pharmaceutics 352 2008 PP 231-239
140 P Li et al Effect of combined use of nonionic surfactant on formation of oil-
in-water microemulsions International Journal of Pharmaceutics 288 2005
PP 27-34
141 E Taha et al Preparation and in vitro characterization of self ndashnanoemulsified
drug delivery system (SNEDDS) of all-trans-retinol acetate International
Journal of Pharmaceutics 285 2004 PP 109-119
142 R Sachan et al Selfmicroemulsifying drug delivery system A novel approach
for enhancement of bioavailability International journal of Pharm Tech
Research 2(3) July-Sept 2010 PP 1738-1745
143 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 274
144 C Goddeeris et al Correlation between digestion of lipid phase of SMEDDS
and release of the anti ndashHIV drg UC 781 and the anti-mycotic drug
enilconazole from SMEDDS European Journal of Pharmaceutics and
Biopharmaceutics 66 2007 PP 173-181
145 M Cirri et al Liquid spray formulations of xibornol by using self
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 2007 PP 84-91
146 PNepal et al Preparation and in vitro-in vivo evaluation of Witepsol H 35
based self-nanoemulsifying drug delivery systems (SNEDDS) of coenzyme
Q10 European Journal of Pharmaceutical Sciences39 2010 PP 224-232
147 Q Jing et al HPLC determination of anetholetrithione and its application to
the pharmacokinetics in rabbits Journal of Pharmaceutical and Biomedical
Analysis 42 2006 PP 613-617
148 P Postolache et al Cyclosporin bioavailability of two physically different oral
formulations European review for medical and pharmacological sciences 6
2002 PP 127-131
149 B Kang et al Development of self microemulsifying drug delivwry systems
(SMEDDS) for oral bioavailability enhancement of simvastatin in beagle
dogs International Journal of Pharmaceutics 274 (1) 2004 PP 65-73
150 Wei Wu et al Enhanced bioavailability of silymarin by self ndash
microemulsifying drug delivery system European Journal of Pharmaceutics
and Biopharmaceutics63 2006 PP 288-294
151 PZangPreparation and evaluation of self-microemulsifying drug delivery
system of oridonin International Journal of Pharmaceutics 3552008PP 269-
276
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 275
152 Jong Soo Woo Reduced food effect and enhanced bioavailability of a self
microemulsifying formulation of itraconazole in healthy volunteers European
Journal of pharmaceutical sciences 33 2008 PP 159-165
153 MCirri et al Liquid spray formulations of xibornol by using self-
microemulsifying drug delivery systems International Journal of
Pharmaceutics 340 (1-2) 2007 PP 84-9
154 RHolm et al Examination of oral absorption and lymphatic transport of
halofantrine in a triple-cannulated canine model after administration in self-
microemulsifying drug delivery systems(SMEDDS) containing structured
triglycerides European Journal of Pharmaceutical Sciences 20 2003 PP 91-
97
155 Shui-Mei Khoo et al Formulation design and bioavailability assessment of
lipidic self ndashemulsifying formulations of halofantrine International Journal of
Pharmaceutics 167 1998 PP 155-164
156 APatel et al Preparation and in vivo evaluation of SMEDDS (Self-
Microemulsifying Drug Delivery system) containing finofibrate The AAPS
Journal 9 (3) 2007 Article 41 PP E344-E352
157 SNazzal et al Preparation and in vitro characterization of a eutectic based
semisolid self-nanoemulsified drug delivery system(SNEDDS) of ubiquinone
mechanism and progress of emulsion formation International Journal of
Pharmaceutics 235 2002 PP 247-265
158 Bok Ki Kang et al Controlled release of paclitaxel from microemulsion
containing PLGA and evaluation of anti-tumor activity in vitro and in vivo
International Journal of Pharmaceutics 286 2004 PP 147-156
159 ANarang et al Stable drug encapsulation in micelles and microemulsions
International journal of Pharmaceutics 345 2007 PP 9-25
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 276
160 I Pasquali et al Supercritical fluid technologiesAn innovative approach for
manipulating the solid ndashstate of pharmaceuticals Advanced Drug Delivery
Reviews 60 2008 PP 399-410
161 F Maulvi et al Supercritical technology A promising approach to enhance
drug solubility Journal of pharmaceutical sciences and research 4 2009 PP
1-14
162 T Yasuji et al Particle design of poorly water soluble drug substances using
supercritical fluid technologies Advanced drug delivery reviews 60 2008 PP
388-398
163 E Reverchon et al Production of micro and nano particles by supercritical
antisolvent precipitation Powder Technology 106 (1-2) 1999 PP 23-29
164 S Wook Jun et al Preparation and characterization of
simvastatinhydroxypropyl beta cyclodextrins inclusion complex using
supercritical Antisolvent(SAS) process European Journal of Pharmaceutics
and biopharmaceutics 66 (3) 2007 PP 413-421
165 H Hassan et al Enhancement of dissolution amount and in vivo
bioavailability of itraconazole by complexation with beta cyclodextrin using
supercritical carbon dioxide Journal of Pharmaceutical and biomedical
analysis (article accessed online)
166 M Kim et al Micronization of cilostazol using supercritical Antisolvent
(SAS) process Effect of process parameters Powder Technology 177 (2)
2007 PP 64-70
167 DWong et al Improved physicochemical characteristics of felodipine solid
dispersionparticles by supercritical anti solvent precipitation process
International Journal of Pharmaceutics 301 2005 PP 199-208
168 C Kalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and engineering Chemistry research 44
(24) 2005 PP 9339-9346
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 277
169 I Kikic et al Supercritical antisolvent precipitation of atenolol The influence
of organic solvent and of the processing approach The Journal of Supercritical
Fluids 38 (3) 2006 PP 434-441
170 E Reverchon et al Rifampicine nanoparticles production by supercritical
antisolvent precipitation International Journal of Pharmaceutics 243 (1-2)
2002 PP 83-91
171 CKalogiannis et al Production of amoxicillin microparticles by supercritical
antisolvent precipitation Industrial and Engineering Chemical Research 44
(24) 2005 PP 9339-9346
172 E Reverchon et al Supercritical antisolvent precipitation of cephalosporins
Powder Technology 164 (3) 2006 PP 139-146
173 Y Chang et al Micronization of sulfamethoxazole using supercritical
antisolvent process Journal of Materials Science 43 (7) 2007 PP 2328-2335
174 M Kim et al Preparation characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent
(SAS) process European Journal of Pharmaceutics and Biopharmaceutics 69
(2) 2008 PP 454-465
175 J Kim et al Physicochemical properties and oral bioavailability of amorphous
atorvastatin hemi-calcium using spray drying and SAS process International
Journal of Pharmaceutics 359 (1-2) 2008 PP 211-219
176 Hee June Park et al Recrystallization of fluconazole using supercritical
antisolvent (SAS) process International Journal of pharmaceutics 328 (2)
2007 PP 152-160
177 I Aranaz Functional characterization of chitin and chitosan Current chemical
Biology 3 2009 PP 203-230
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 278
178 S Dhawan et al Evaluation of mucoadhesive properties of chitosan
microspheres prepared by different methods AAPS Pharm Sci Tech 2004 5
(4) article 67
179 X Shu et al Chitosangelatin microspheres prepared by modified
emulsification and ionotropic gelation Journal of Microencapsulation 18 (2)
2001 PP 237-245
180 Mohanraj et al Nanoparticles reviewTropical Journal of pharmaceutical
Research June 2006 5 (1) PP 561-573
181 Rafeeq et al Development and characterization chitosan nanoparticles loaded
with isoniazide for the treatment of tuberculosis Research Journal of
Pharmaceutical Biological and Chemical sciences Oct ndashDec 2010 PP 383-
390
182 Dustgani et al Preparation of chitosan nanoparticles loaded by dexamethasone
sodium phosphate Iranian Journal of Pharmaceutical SciencesSpring 2008 4
(2) PP 111-114
183 P Saha et al Formulation and evaluation of chitosan based ampicillin
trihydrate nanoparticles Tropical Journal of Pharmaceutical Research 9 (5)
2010 PP 483-488
184 S Jing et al Preparation of influenza vaccinechitosanmicroparticles by ionic
gelation method Chemical Journal of Chinese Universities 29 (11) 2008 PP
2308-2311
185 Lopez-Leon et al Physicochemical characterization of chitosan nanoparticles
electrokinetic and stability behaviour Journal of colloid and interface science
283 (2005) PP 344-351
186 R Rao et al Preparation and characterization of ionotropic chitosan
microparticles for controlled release of aceclofenac International journal of
pharmaceutical sciences and drug research 2010 2 (2) 107-111
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 279
187 SKunjachanUnderstanding the mechanism of ionic gelation for synthesis of
chitosan nanoparticles using qualitative techniques Asian Journal of
Pharmaceutics 4 2010 PP 148-153
188 RPignatello et al Ocular Tolerability of Eudragit RS 100 and RL 100
nanosuspensions as carriers for ophthalmic controlled drug delivery Journal
of Pharmaceutical sciences 91 (12) 2002 PP 2636-2641
189 RPignatello et al Eudragit RS 100 nanosuspensions for ophthalmic controlled
delivery of ibuprofen European Journal Of Pharmaceutical Sciences16(1-2)
2002 PP 53-61
190 wwweudragitevonikcom
191 CDora et al Development and characterization of nanoparticles of
glibenclamide by solvent displacement method Acta Poloniae Pharmaceutica
67 (3) 2010 PP 283-290
192 SMudgal et al Design and development of 5-flurouracil loaded biodegradable
microspheres International Journal of Research in Ayurveda and Pharmacy 1
(1) 2010 PP 160-168
193 PDevrajan et al Preparation and in vitroin vivo evaluation of gliclazide
loaded eudragit nanoparticles as sustained release carriers Drug Development
and industrial Pharmacy 33 (2) 2007 PP 101-111
194 httpwwwpharmagatewaynetSearchAdvancedaspxq=Eudragit20L-100
195 H Eerikainen et al Preparation of polymeric nanoparticles containing
corticosteroid by a novel aerosol flow reactor method International Journal of
Pharmaceutics 263 2003 PP 69-83
196 MGonzalez et al Nanoencapsulation of acetyl salicylic acid within enteric
polymer nanoparticles Reviews on Advanced Materials Science 17 2008 PP
71-75
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354
REFERENCES
SPTM SVKMrsquoS NMIMS MUMBAI 280
197 M Gupta et al Nanoparticulate drug delivery system of cyclosporine
International Journal of Pharmacy and pharmaceutical Sciences 1 (2) 2009
PP 81-92
198 H Stenhoff et al Determination of candesartan cilexetilcandesartan and a
metabolite in human plasma and urine by liquid chromatography and
fluorometricdetection Journal of Chromatography BBiomedical Sciences and
Applications 731 (2) 1999 PP 411-417
199 M Levi et al Direct analysis of valsartan or candesartan in human plasma and
urines by on-line solid phase extraction coupled to electrospray tandem mass
spectrometry Journal of Chromatography B 877 (10) 2009 PP 919-926
200 APeepliwal et al Bioanalytical method development and its validation for
determination of candesartan cilexetil by high performance liquid
chromatography with UV detection ActaPharmaceutica Sciencia 52 2010
PP 247-253
201 N Erk Simultaneous analysis of candesartan cilexetil and hydrochlorothiazide
in human plasma and dosage forms using HPLC with a photodiode array
detector Journal of Liquid Chromatography and Related Technologies 26
(15) 2003 PP 2581-2591
202 A Sakur et al Determination of candesartan cilexetil in tablets by
spectrofluorimetry International Journal of Pharmaceutical Sciences Review
and Research 4 (1) 2010 PP 60-63
203 S Mehta et al LC and LC-MSTOF studies on stress degradation behavior of
candesartan cilexetil Journal of Pharmaceutical and Biomedical Analysis 52
(3) 2010 PP345-354