references tablets: a novel approach to drug delivery...
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References
References
1. Sastry S, Nyshdham J, Fix J, (2000), Recent technological
advances in oral drug delivery: a review, AAPS Pharm Sci Tech, 3,
138-44.
2. Kaur T, Gill B, Kumar S, Gupta GD (2011), Mouth dissolving
tablets: A novel approach to drug delivery, International Journal of
Current Pharmamecutical Research, 3, 1-7.
3. Yeola B, Pisal S, Paradkar A, Mahadik K, (2000), New drug delivery
system for Elderly. Indian Drugs, 37(7), 312-8.
4. Chang R, Guo X, Burnside B, (2000), A review of fast dissolving
tablets, Pharm Tech, 52-4.
5. Kuchekar BS, Badhan AC, Mahajan HS, (2003), Mouth Dissolving
Tablets: A novel drug delivery system, Pharma Times, 35, 10-7.
6. Chien YW. Novel drug delivery systems. New York – Marcel Dekker
Inc., 2nd ed. 1992.p.139-140.
7. Buck JR, Peck GE, Banker GS. Drug development community,
1975; 1-8.
8. Bandari S, Mittapalli RK, Gannu R, Yamsani MR, (2008),
Orodispersible tablets: An overview, Asian J Pharm, 2(1), 2-11.
9. Jeong SH, Park K, (2008), Material properties for making fast
dissolving tablets by a compression method, Journal of Materials
Chemistry, 18, 3527–3535.
10. McLaughlin R, Banbury S, Crowley K, (2009), Orally Disintegrating
Tablets the Effect of Recent FDA Guidance on ODT Technologies
and Applications, Pharmaceutical Technology, 8(2), 161-172.
11. Bhowmik D, Chiranjib B, Krishnakanth P, Chandira RM. Fast
dissolving tablet: An overview. J Chem. Pharm. Res 2009;1:163-77.
12. Sharma S, (2008), New generation of tablet: Fast dissolving tablet,
Latest review, 6(5).
13. Kumari S, Visht S, Sharma PK, Yadav RK, (2010), Fast dissolving
Drug delivery system : Review Article, Journal of Pharmacy
Research, 3(6), 1444-1449.
References
14. Shukla D, Chakraborty S, Singh S, Mishra B, (2009), Mouth
Dissolving Tablets I: An Overview of Formulation Technology,
Scientia Pharmceutica, 76, 309-326.
15. Hirani JJ, Rathod DA, Vadalia KR, (2009), Orally Disintegrating
Tablets: A Review, Tropical Journal of Pharmaceutical Research,
8(2), 161-172.
16. Chang X, Guo BA, Burnside BA, Couch RA, (2000), review of fast
dissolving tablets, Pharmaceutical Technology, 24(6), 52-58.
17. Van Scoik KG, (1992), Solid Pharmaceutical Dosage in Tablet
Triturate form, 1992; US patent No 5,082,667.
18. Birader SS, Bhagavati ST, Kuppasad IJ, (2006), Fast dissolving
drug delivery systems: a brief overview, The International Journal of
Pharmacology, 4(2).
19. Sayeed A, Mohiuddin MH, (2011), Mouth dissolving tablets: An
Overview, International Journal of Research in Pharmaceutical and
Biomedical Sciences, 2(3), 959-970.
20. Panigrahi R, Behera S, (2010), A Review on Fast Dissolving
Tablets, Webmed Central Quality and patient safety, 1(9),
WMC00809.
21. Amarjit S, Rajesh J. United states Patent No.7122198. Fast
dissolving composition with prolonged sweet taste.
22. Vummaneni V, Chawla L, (2012), Mouth Dissolving Tablets: A
Review, Am J PharmTech Res, 2(3).
23. Rishi RK, (2004), Data Safety Monitoring Board, The Pharma
Review, 2, 32.
24. Prajapati BG, Ratnakar NA, (2009), Review on Recent patents on
Fast Dissolving Drug Delivery System, International Journal
PharmTech Research, 1(3), 790-798.
25. Shailesh S, Gupta GD, Bala R, Sharma N, Seth N, Goswami JP,
(2008), Orodispersible tablet: A review, 03, 29.
26. Abdelbary G, Prinderre P, Eouani C, Joachim J, Reynier JP,
Piccerelle P, (2004), The preparation of orally disintegrating tablets
using a hydrophilic waxy binder, International Journal of Pharma,
278(2), 423-33.
References
27. Bagul U, Gujar K, Patel N, Aphale S, Dhat S, (2010), Formulation
and Evaluation of Sublimed Fast Melt Tablets of Levocetirizine
Dihydrochloride, International Journal of Pharmamecutical
Sciences, 2(2), 76-80.
28. Kalia A, Khurana S, Bedi N, (2009), formulation and evaluation of
mouth dissolving tablets of oxcarbazepine, Int J pharm pharmace
sci, 1, 12-23.
29. Allen LV, Wang B, (2001), Process for making a particulate support
matrix for making a rapidly dissolving dosage form, US patent No
6,207,199.
30. Allen LV, Wang B, Davis JD, (2000), Method for Producing a
Rapidly Dissolving Dosage Form, US Patent No 6066 and 337.
31. Giri T, Tripathi D, Maunder R, (2010), Formulation aspects in the
development of Orodispersible tablets: an Overview, International
Journal Pharm and Pharm Sciences, 2(3), 38-42.
32. Arya A, Chandra A, Sharma V, Pathak K, (2010), Fast Dissolving
Oral Films: An Innovative Drug Delivery System and Dosage Form,
2(1), 576-583.
33. Lieberman HA, Lachman L, Schwartz JB, (1989), Pharmaceutical
dosage forms Tablets, New York, Marcel Deckker, Inc, 1, 131.
34. Reddy LH, Ghose B, Rajneesh, (2002), Fast dissolving drug
delivery systems: a review of the literature, Ind J Pharm Sci, 64(4),
331- 336.
35. Parakh SR, Gothoskar AV, (2003),A Review of Mouth Dissolving
Tablet, Pharma Tech, 92-100.
36. Babu GV, Kumar NR, Himasankar K, Seshasayana A, Murthy KV, (
2003),Nimesulide-modified gum karaya solid mixtures: preparation,
characterization and formulation development, Drug Dev Ind
Pharm, 29, 855-864.
37. Patel TS, Sengupta M, (2013),Fast Dissolving Tablet Technology –
A Review, WJPPS, 2(2), 485-508.
38. Vishwkarma DK, Tripathi AKB, Yogesh P, Maddheshiya B,
(2011),Review article on mouth dissolving film, Journal of Global
Pharma Technology, 3(1), 1-8.
References
39. Profile Resources at Business.com. Cima Labs - Profile. 2001, 27,
5.
40. Seager H, (1998), Drug-deliver Products and the Zydis Fast-
dissolving Dosage Form, J Pharm and Pharmacol, 50, 375-382.
41. Bhattacharya S, Pal TK, A review on Fast Dissolving Tablet
Technology, Pharmatutor.
42. Patel PB, Chaudhary A, Gupta GD, (2006), Fast Dissolving Drug
Delivery Systems: An Update, Pharmainfo.net, 4(4).
43. Jagani H, Patel R, Upadhyay P, Bhangale J, Kosalge S, (2011),
Fast dissolving tablets: present and future prospectus, J Advance
Pharm Healthcare Res, 2(1), 57-70.
44. Manivannan R, (2009),Oral disintegrating tablets: a future
compaction, International Journal of Pharmaceutical Research Dev-
Online, 1(10),1-10.
45. Chatap VK, (2007), Review on taste masking methods for bitter
drug, Pharmainfo Net, 5(1), 45.
46. Sohi H, Sultana Y, Khar RK, (2004),Taste masking technologies in
oral pharmaceutics: recent developments and approaches, Drug
Dev, Ind Pharm, 30(5), 429-48.
47. Reilly WJ, (2002), Remington: The science and practice of
pharmacy, 20th ed., Mack publishing company, 1018-20.
48. Saini S, Nanda A, Hooda M, Komal, Dhari J, (2011), Formulation
and evaluation of mouth dissolving anti-allergic tablets of
Levocitrizine dihydrochloride, J Chem Pharm Res, 3(5), 450-455.
49. Banker GS, Anderson GR, Lachman L, Liberman HA, Karnig JL,
(1987),The theory and practice of a industrial pharmacy, 3rdedition,
Varghese publishing house, Mumbai, 293.
50. Lachman L, Liberman H, Kanig J, (1976),The theory and practice of
industrial pharmacy, 2nd edn. Varghese Publishing House Mumbai,
pp. 297.
51. Amin AF, Shah T, Bhandani M, Patel M, (2007), Emerging trend in
the development of orally disintegrating tablet technology,
pharmainfo.net.
References
52. Younxia B, Sunada H, Yonezawa Y, Danjo K, (1999), Evaluation of
rapid disintegrating tablets prepared by Direct compression method,
Drug Dev Ind Pharm, 25(5), 571.
53. Zhang W, Wang Y, Gao X, Gao X, Peng S, Zheng Y, Okeke CI,
(2013), Optimization of Jiawei Qing’e Oral Fast Disintegrating
Tablets Based on Response Surface-Central Composite Design,
Chinese Herbal Medicines, 5(2), 138-144.
54. Sharma D, (2013), Formulation Development and Evaluation of
Fast Disintegrating Tablets of Salbutamol Sulphate for Respiratory
Disorders, ISRN Pharmaceutics, 1-8.
55. Reddy Mettu S, Reddy Veerareddy P, (2013), Formulation,
Evaluation and Pharmacokinetics of Flurbiprofen Fast Dissolving
Tablets, British Journal of Pharmaceutical Research, 3(4), 617-631.
56. Iyer SR, Sivakumar R, Siva P, Sajeeth CI, (2013), Formulation and
Evaluation of Fast Dissolving Tablets of Risperidone solid
dispersion, IJPCBS, 3(2), 388-397.
57. Elbary AA, Ali AA, Aboud HM, (2012), Enhanced dissolution of
meloxicam from orodispersible tablets prepared by different
methods, Bulletin Facult Pharmacy Cairo Univ, 07,001.
58. Roy H, Parida KR, Nandi S, Panda SK, Mohapatra DK, (2012),
Design of fast dissolving amlodipine besylate tablet formulations,
Asian J Pharm, 6, 51-9.
59. Thakre A, Bhople A, Jaiswal S, Chandewar A, Ghuge N, Wagh N,
Thakre S, Bari M, (2012), Formulation and Development of Oral
Fast Dissolving Tablet of Etoricoxib, Der Pharmacia Lettre, 4(4),
1169-1182.
60. Kaurav A, Jain S, Mishra S, Verma R, (2012), Formulation and
Evaluation of Fast Dissolving Tablet of Levocetrizine using Direct
Compression Technique, AJPER, 1(1), 32-41.
61. Sharma D, Chopra R, Bedi N, (2012), Development and evaluation
of paracetamol taste masked orally disintegrating tablets using
polymer coating technique, International Journal of Pharm Pharm
Sci, 4(3), 129-134.
References
62. Rane DR, Gulve HN, Patil VV, Thakare VM, Patil VR, (2012),
Formulation and evaluation of fast dissolving tablet of albendazole,
International Current Pharmaceutical Journal, 1(10), 311-316.
63. Patel K, Rajendra A, (2012), Design and Evaluation of Mouth
Dissolving Tablets of Anti Hypertensive Drug Telmisartan, Int J
Pharm Tech Res, 4(2), 715-724.
64. Sharma V, Singh L, Saxena P, Kumar JA, (2011), Formulation and
evaluation of mouth dissolving tablets of cefixime, IRJP, 2(5), 171-
174.)
65. Ganure Ashok L, Dangi Amish A , Patel Pinkal Kumar, Manish
Kumar Rai, Aravadiya Jigar P, (2011), Preparation and evaluation
of tramadol hydrochloride fast dispersible tablet by using
compression technique, IJPI’s Journal of Pharmaceutics and
Cosmetology, 1, 2.
66. Solanki SS, Dahima R, (2011), Formulation and evaluation of
aceclofenac mouth-dissolving tablet, J Adv Pharm Technol Res,
2(2), 128–131.
67. Masareddy R, Kokate A, Shah V, (2011), Development of
Orodispersible Tizanidine HCl Tablets Using Spray Dried
Coprocessed Exipient Bases, Indian J Pharm Sci, 2011; 73(4),
392–396.
68. Kumar DS, Reddy BA, Tiwari AK, Swetha B, Dey S, (2011),
Formulation and evaluation of mouth dissolving tablets of
Felodipine, AJPCR, 2011; 4(1).
69. Sharma V, Chopra H (2010), Formulation and Evaluation of Taste
Masked Mouth Dissolving Tablets of Levocetirizine Hydrochloride,
Iranian Journal of Pharmaceutical Research, 11(2), 457-463.
70. Keny RV, Desouza C, Lourenco CF, (2010), Formulation and
evaluation of Rizatriptan Benzoate mouth disintegrating tablets,
Indian J Pharm Sci, 72, 79-85.
71. Sawarikar PP, Sridhar BK, Shivkumar S, (2010), Formulation and
Evaluation of Fast Dissolving/Disintegrating Tablets of Isoxsuprine
Hydrochloride, Journal of Current Pharmaceutical Research, 3(1),
41-46.
References
72. Gnanaprakash K, Mallikarjuna Rao K, Chandra Sekhar KB,
Madhusudhana Chetty C, Alagusundaram M, Ramkanth S, (2009),
Formulation and evaluation of fast dissolving tablets of Valdecoxib,
International Journal of Pharm Tech Research, 1(4), 1387-1393.
73. Parikh R, Ranch KM, Koli AR, (2009), Formulation and optimization
of orodispersible tablets of Atenolol, International Journal of Pharm
tech Res, 1(4), 1559-63.
74. Zade PS, Kawtikwar PS, Sakarkar DM, (2009), Formulation,
evaluation and optimization of fast dissolving tablet containing
Tizanidine Hydrochloride, International Journal of Pharm Tech
Research, 1(1), 34-42.
75. Patel B, Patel D, Parmar R, Patel C, Serasiya T, Sanja SD, (2009),
Development and In vitro Evaluation of Fast Dissolving Tablets of
Glipizide, International Journal of Pharmacy and Pharma Sciences,
1(1), 145-50.
76. Parmar RB, Baria AH, Tank HM, Faldu SD, (2009), Formulation and
Evaluation of Domperidone Fast Dissolving Tablets, International
Journal of Pharm Tech Res, 1(3), 483-487.
77. Jain CP, Naruka PS, (2009), Formulation and Evaluation of Fast
dissolving tablet of Valsartan, International Journal of of Pharm,
1(1), 219-26.
78. Setty CM, Prasad DVK, Gupta VRM, Sa B, (2008), Development of
fast dispersible aceclofenac tablets: Effect of functionality of
superdisintegrant, International Journal of Pharmamecutical
Sciences, 180-185.
79. Dinesh BM, Patel YR, Patil UA, Rajani GP, Desai BG, (2007),
Formulation and evaluation of dispersible tablets of valdecoxib,
Pharma buzz , 2(10), 25-31.
80. Swamy PV, Areefulla SH, Shirsand AB, Gandra S, Prashanth B,
(2007), Orodispersible tablets of Meloxicam using disintegrant
blends for improved efficacy, Indian Journal of Pharm Sciences,
69(6), 836-840.
References
81. Malke S, Shidhaye S, Kadam VJ, (2007), Formulation and
evaluation of oxcarbazepine fast dissolve tablets, Indian Journal of
Pharm Sciences, 69(2), 211-14.
82. Shishu, Bhatti A, (2006), Fast Disintegrating tablets of Diazepam.
Indian drugs, 43(8), 643-648.
83. Kuno Y, Kojima M, Ando S, Nakagami H, (2005), Evaluation of
rapidly disintegrating tablets manufactured by phase transition of
sugar alcohols, J control Release, 105, 16-22.
84. Larry LA, (2005), Functionality comparison of 3 classes of
superdisintegrants in promoting Asprin tablet disintegration and
dissolution, AAPS Pharm Sci Tech, 6(4), 634-640.
85. Lalla JK, Mamania HM, (2004), Fast dissolving rofecoxib tablets,
India J Pharma Sci, 66(3), 350-3.
86. Mahajan HS, Kuchekar BS, Badhan AC, (2004), Mouth dissolving
tablets of Sumatriptan succinate, Indian Journal of Pharm Sciences,
66(2), 238-40.
87. Mahaejan HS, Kuchekar BS, Badhan AC, (2004), Mouth dissolving
tablets of Salbutamol sulphate: A novel drug delivery system, Indian
Drugs, 41(10), 592-98.
88. Kaushik D, Saini TR, Dureja H, (2004), development of melt in
mouth tablets by sublimation technique, Journal of pharmaceutical
research, 3(2), 35-37.
89. Induwade NH, Rayaguru TH, Nakhat PD, (2002), Novel approach-
Fast dissolving tablets, Indian Drugs, 39(8), 405-9.
90. Allen LV, Wang B, (1996), Process for making a particulate support
matrix for making a rapidly dissolving tablet, US patent No
5,587,180.
91. Madoria N, Maheshwari Y, Formulation, (2012), Optimization and
Characterization of Fast Dissolving Tablet of Celecoxib, Research
Journal of Pharmacy and Technology, 5(8), 1085-1088.
92. Pehlivan SB, Subasi B, Vural I, Unlu N, Capan Y, (2011),
Evaluation of drug-excipient interaction in the formulation of
celecoxib tablets, Acta Poloniae Pharmaceutica- Drug Research,
68(3), 423-433.
References
93. Gangawat LK, Sharma SK, Bisht R, (2011), Design and
development of fast dissolving Celecoxib tablet by solid dispersion
and camphor sublimation method using 32 full factorial design,
Pharm Tech, 1, 105-115.
94. Kumar S, (2010), Formulation and evaluation of Celecoxib
orodispensible tablets, RGUHS Journal of Pharmaceutical
Sciences, 11-21.
95. Tiwari V, kinikar DJ, Pillai K, Gokulan PD, (2010), Preparation and
Evaluation of Fast Dissolving Tablets of Celecoxib, Journal of
Current Pharmaceutical Research, 04, 4-10.
96. Dade BK, Chavala AK, (2010), Formulation of celecoxib in to
immediate release tablets, An International Journal of Advances In
Pharmaceutical Sciences, 1(2), 318-26.
97. Kadian SS, Kumar A, Dennis DM, Diwan A, (2010), Formulation
design and evaluation of floating matrix tablet of celecoxib by direct
compression, Int j ph sci, 2(2), 556-560.
98. Pandya VM, Patel DJ, Patel JK, Patel RP, (2009), Formulation,
Characterization and Optimization of Fast-Dissolve Tablets
Containing Celecoxib Solid Dispersion, Dissolution Technologies,
22-27.
99. Chandran S, Punnarao R, Saha RN, (2006), Development and In
vitro Evaluation of Oral Controlled Release Formulaitons of
Celecoxib Using Optimization Techniques, The Pharmaceutical
Society of Japan, 126(7), 505-514.
100. Jani P, Vadalia K, Bagdai H, Dedania R, Manseta P, (2012),
Formulation and evaluation of controlled release floating
microspheres of tolperisone hydrochloride, Asian J Pharm, 6, 190-
7.
101. Soni R, Patel M, Patel K, Patel N, (2012), Formulation & in vitro
evaluation of floating tablet of tolperisone hcl, IJPS, 3(4), 2477-
2492.
102. Martindale, (1993), The Extra Pharmacoepia, 30th edition, 1211.
103. Hofer D, Lohberger B, Steinecker B, Schmidt K, Quasthoff S,
Schreibmayer W, (2006), A comparative study of the action of
References
tolperisone on seven different voltage dependent sodium channel
isoforms, Eur J Pharmacol, 538 (1-3), 5–14.
104. Primo FT, Froehlich PE, (2005), Celecoxib Identification Methods,
Acta Farm Bonaerense, 24 (3), 421-5.
105. Krishnaveni G, Sathyannaryana PVV, (2012), A novel RP-HPLC
method for the quantification of Celecoxib in formulations, Research
Journal of Pharmaceutical, Biological and Chemical Sciences, 3(1),
340-346.
106. Yelland MJ, Nikles CJ, McNairn N, Del Mar CB, Schluter PJ, Brown
RM, (2007), Celecoxib compared with sustained release
paracetamol for osteoarthritis: a series of n-of-1 trials,
Rheumatology, 46(1), 135–40.
107. Tanaka R, Hirayama N, (2007), Structure of Tolperisone
hydrochloride, Analytical Sciences: X-ray Structure Analysis Online,
23, 85-89.
108. Kocsis P, Farkas S, Fodor L, Bielik N, Than M, Kolok S, Gere A,
Csejtei M, Tarnawa I, (2005), Tolperisone-type drugs inhibit spinal
reflexes via blockade of voltage-gated sodium and calcium
channels, J Pharmacol Exp Ther, 315 (3), 1237–1246.
109. Cims India, Update – 3, July – October 2011, pp 39.
110. Indian Pharmacopoeia, Vol. II, New Delhi, The Controller
Publication, Govt. of India, 2010, 1199.
111. British Pharmacopoeia, Vol. I, London, The British Pharmacopoeia
Commission, 2010, 672.
112. Japanese Pharmacopeia, 15th ed, Society of Japanese
Pharmacopeia, 2006, 1190-1191.
113. Welzig S, Rothenburger J, Kalz B, Gungl J, Gerdes K, (2010),
Tolperisone controlled release tablet, European patent, 2, 228 056
114. Gabrielsson J, lindberg NO, Lundstedt T, (2002), Multivariate
methods in pharmaceutical applications, Journal of Chernometrics,
16, 141-160,
115. Maryadele J O’ Neil, (2006), The Merck Index: An Encyclopedia of
chemicals, drugs and biologicals, 14th edition. New Jersey:
References
Published by Merck Research Laboratories, Division of Merck and
Co., Inc, Whitehouse station, 1698.
116. Murali M, Satyanarayana PV, (2011), Simple validated isocratic RP-
HPLC method for estimation of tolperisone in bulk and
pharmaceutical dosage form, Der Pharm Chemica, 3, 13-19.
117. Koladia BB, Vaghela VM, (2012), UV spectroscopic method for
quantitative estimation of tolperisone hydrochloride in bulk and
pharmaceutical dosage form, International Journal of PharmTech
Res, 4, 1317-22.
118. Liawruangrath S, Liawruangrath B, Pibool P, (2001), Simultaneous
determination of tolperisone and lidocaine by HPLC, J Pharm
Biomed Anal, 26, 865-72.
119. Sharma KK, Patel PU, (2012), First derivative spectroscopic
method for simultaneous estimation of paracetamol and tolperisone
in their combined dosage form, Journal of Pharmaceutical Sciences
and Biosciences Research, 2, 92-96.
120. Bombardier C, Laine L, Reicin A, Shapiro D, Burgos-Vargas R,
Davis B, Day R, Ferraz MB, Hawkey CJ, Hochberg MC, Kvien TK,
Schnitzer TJ, Weaver A, (2000), Comparison of upper
gastrointestinal toxicity of rofecoxib and naproxen in patients with
rheumatoid arthritis, VIGOR Study Group, New Eng J Med, 343,
1520-24.
121. Fung HB, Kuschenbaum HL, (1999), Clin Therap, 7, 1131-57.
122. Howard PA, Delafontaine P, (2004), Nonsteroidal anti-
Inflammatory drugs and cardiovascular risk, Journal of American
Coll Cardiol, 43, 519-25.
123. Lane JM, (2002), Antiinflammatory medications: selective COX-2
inhibitors, Journal American Academy of Orthopeadic Surgery, 10,
75-78.
124. Yazici AC, Baz K, Ikizoglu G, Kolturk A, Uzumlu H, Tataroglu C,
(2004), Celecoxib induced photoallaergic drug eruption,
International Journal of Dermatology, 43(6), 459 – 461.
References
125. Pentland AP, Schoggins JW, Scoh GA, Khan KNM, Han R, (1999),
Reduction of UV-induced skin tumors in hairless mice by selective
COX-2 inhibition, Carcinogenesis, 20(10), 1939 – 1944.
126. Lu Z, Xiong X, Zhang B, Lin G, Shi Y, Liu Z, Meng J, Zhou Y, Mei
Q, (2005), Evaluation of 2 celecoxib derivatives: analgesic effect
and selectivity to cyclooxygenase-2/1, Acta Pharmacologica Sinica,
26(12), 1505 – 1511.
127. Adegbolagun OM, Adelowo FA, (2011), Ultraviolet irradiation of
Celecoxib: Absence of adverse biological effect, Nigerian Journal
Pharm Sci, 10(1), 6 –15.
128. Nagarsenker MS, Joshi MS, (2005), Celecoxib-cyclodextrin
systems: characterization and evaluation of in vitro and in vivo
advantage, Drug Dev Ind Pharm, 31, 169-78.
129. Pehlivan SB, Suba B, Vural I, Unlu N, Capan Y, (2011), Evaluation
of drug-excipient interaction in the formulation of Celecoxib tablets,
Acta Poloniae Pharmaceutica n Drug Research, 68, 3, 423-433.
130. Baboota S, Agarwal SP, (2002), Inclusion complexation of
meloxicam with beta cyclodextrin, Indian J Pharm Sci, 64(4), 408–
411.
131. Fricker J, Varkalis J, Zwillich S, Adler R, Forester E, Recker DP,
Verburg KM, (2002), Valdecoxib is more efficacious than rofecoxib
in relieving pain associated with oral surgery, American Journal of
Therapy, 9(2), 89–97.
132. Camu F, Beecher T, Recker DP, Verburg KM, (2002), Valdecoxib, a
cox-2-specific inhibitor, is an efficacious, opioid-sparing analgesic in
patients undergoing hip arthroplasty, Am J Ther, 9(1), 43–51.
133. Dannhardt G, Kiefer W, (2001), Cyclooxygenase inhibitors - current
status and future prospects, European Journal of Medicinal
Chemistry, 36(2), 109–126.
134. McMurray RW, Hardy KJ, (2002), Cox-2 inhibitors: today and
tomorrow, Am J Med Sci, 323, 181.
135. Kornblum SS, Stoopak SB, (1973), A new tablet disintegrating
agent: crosslinked polyvinylpyrrolidone, Journalof Pharmaceutical
Sciences, 62, 43-49.
References
136. Rudnic EM, Lausier JM, Chilamkurti RN, Rhodes CT, (1980),
Studies of the utility of cross linked polyvinylpolypyrrolidine as a
tablet disintegrant, Drug Dev Ind Pharm, 6, 291- 309.
137. Gordon MS, Chowhan ZT, (1987), Effect of tablet solubility and
hygroscopicity on disintegrant efficiency in direct compression
tablets in terms of dissolution, Journal of Pharmaceutical Sciences,
76, 907–909.
138. Gordon MS, Rudraraju VS, (1993), Effect of the mode of super
disintegrant incorporation on dissolution in wet granulated tablets, J
Pharm Sci, 82, 220– 226.
139. Tagawa M, Chen R, Chen P, (2003), Effect of various disintegrants
on drug release behavior from tablets, J Pharm Sci Tech
Yakuzaigaku, 63(4), 238– 248.
140. Hipasawa N, Ishise S, Miyata M, Danjo K, (2004), Application of
nilvadipine solid dispersion to tablet formulation and manufacturing
using crospovidone and methylcellulose on dispersion carriers,
Chem Pharm Bull, 52(2), 244–247.
141. Schiermeier S, Schmidt PC, (2002), Fast dispersible ibuprofen
tablets, European Journalof Pharmaceutical Sciences, 15(3), 295–
305.
142. Thibert R, Hancock BC, (1996), Direct visualization of
superdisintegrant hydration using environmental scanning electron
microscopy, Journal of Pharmaceutical Sciences, 85, 1255–1258.
143. Caraballo I, Milan M, Rabasco AM, (1997), Influence of disintegrant
on the drug percolation threshold in tablets, Drug Dev Ind Pharm,
23(7), 665–669.
144. Yen SY, Chen CR, Lee MT, Chen LC, (1997), Investigation of
dissolution enhancement of nifedipine by deposition on
superdisintegrants, Drug Dev Ind Pharm, 23(3), 313–317.
145. Hirai N, Ishikawa K, Takahashi K, (2006), Improvement of the
agitation granulation method to prepare granules containing a high
content of a very hygroscopic drug, J Pharm Pharmacol, 56, 1437–
1441.
References
146. Newton JM, Razzo FN, (1975), Interaction of formulation factors
and dissolution fluid and the in vitro release of drug from hard
gelatin capsule, J Pharm Pharmacol, 27, 78.
147. Stewart AG, Grant DJW, Newton JM, (1979), The release of a
model low-dose drug (riboflavine) from hard gelatin capsule
formulations, J Pharm Pharmacol, 31, 1–6.
148. Chowhan ZT, Chi LH, (1986), Drug–excipient interactions resulting
from powder mixing III: solid state properties and their effect on
drug dissolution, J Pharm Sci, 75, 534–541.
149. Botzolakis JE, Augsburger LL, (1988), Disintegrating agents in hard
gelatin capsules part 1: mechanism of action, Drug Dev Ind Pharm,
14(1), 29–41.
150. Hannula AM, Marvola M, Jons M, (1989), Release of ibuprofen from
hard gelatin capsule formulations: effect of modern disintegrants,
Acta Pharm Fenn, 98, 189–196.
151. Marvola M,Hannula AM, Ojantakanen S, Westermarck E, Rajamaki
M, (1989), Effect of sodium bicarbonate and sodium starch
glycolate on the in vivo disintegration of hard gelatin capsules – a
radiological study in the dog, Acta Pharm Nord, 1, 355–362.
152. Khan KA, Rooke DJ, (1976), Effect of disintegrant type upon the
relationship between compressional pressure and dissolution
efficiency, J Pharm Pharmacol, 28, 633–636.
153. Rubinstein MH, Price EJ, (1977), In vivo evaluation of the effect of
five disintegrants on the bioavailability of frusemide from 40 mg
tablets, J Pharm Pharmacol, 29, 5.
154. Caramella C. The influence of disintegrants on the characteristics of
coated acetylsalicylic acid tablets. Farmaco (Prat) 1978; 33: 498–
507.
155. Gebre Mariam T, Winnemöller M, Schmidt PC, (1996), Evaluation
of the disintegration efficiency of a sodium starch glycolate
prepared from enset starch in compressed tablets, Eur J Pharm
Biopharm, 42(2), 124–132.
References
156. Cid E, Jaminet F, (1971), Influence of adjuvants on the dissolution
rate and stability of acetylsalicylic acid in compressed tablets, J
Pharm Belg, 26, 38–48.
157. Bolhuis GK, Van Kamp HV, Lerk CF, (1986), On the similarity of
sodium starch glycolate from different sources, Drug Dev Ind
Pharm, 12(4), 621–630.
158. Rudnic EM, Kanig JL, Rhodes CT, (1985), Effect of molecular
structure variation on the disintegrant action of sodium starch
glycolate, J Pharm Sci, 74, 647–650.
159. Bolhuis GK Arends-Scholte AW, Stuut GJ, de Vries JA, (1984),
Effect of variation of degree of substitution, crosslinking and purity
on the disintegrant efficiency of sodium starch glycolate, Acta
Pharm Technol, 30, 24–32.
160. Claudius JS, Neau SH, (1996), Kinetic and equilibrium
characterization of interactions between glycopeptide antibiotics
and sodium carboxymethyl starch, International Journal of
Pharmacy, 144, 71–79.
161. Claudius JS, Neau SH, (1998), The solution stability of vancomycin
in th presence and absence of sodium carboxymethyl starch, Int J
Pharm, 168, 41–48.
162. Kibbe AH, (2000), Handbook of pharmaceutical excipients:
Cellulose, silicified microcrystalline, American Public Health
Association, Washington.
163. Luukkonen P, Schaefer T, Hellen J, Juppo AM, Yliruusi J, (1999),
Rheological characterization of microcrystalline cellulose and
silicified microcrystalline cellulose wet masses using a mixer torque
rheometer, International Journal of Pharmaceutics, 188, 181–192.
164. Edge S, Steele F, Chen A, Tobyn M, Staniforth JN, (2000), The
mechanical properties of compacts of microcrystalline cellulose and
silicified microcrystalline cellulose, International Journal of
Pharmaceutics, 200, 67–72.
165. Van Veen B, Bolhuis GK, Wu YS, Zuurman K, Frijlink HW, (2005),
Compaction mechanism and tablet strength of unlubricated and
References
lubricated (silicified) microcrystalline cellulose, European Journal of
Pharmaceutics and Biopharmaceutics, 59, 133–138.
166. Sherwood BE, Becker JW, (1998), A new class of high functionality
excipients: Silicified microcrystalline cellulose, Pharmaceutical
Technology, 22, 78–88.
167. Guo M, Augsburger LL, (2003), Potential application of silicified
microcrystalline cellulose in direct-fill formulations for automatic
capsule-filling machines, Pharmaceutical Development and
Technology, 8, 47– 59.
168. Zografi G, Kontny MJ, Yang AYS, Brenner GS, (1984), Surface
area and water vapor sorption of microcrystalline cellulose,
International Journal of Pharmaceutics, 18, 99–116.
169. Hwang RC, Peck GR, (2001), A systematic evaluation of the
compression and tablets characteristics of various types of
microcrystalline cellulose, Pharmaceutical Technology, 24, 112–
132.
170. Muzikova J, Novakova P, (2007), A study of the properties of
compacts from silicified microcrystalline celluloses, Drug
Development and Industrial Pharmacy, 33, 775–781.
171. Fleming K, Gray DG, Matthews S, (2001), Cellulose Crystallites,
Chem Eur J, 7, 1831-1835.
172. Microcrystalline Cellulose, In: European Pharmacopoeia. 4 th
edition (2002), Strasbourg, France, Council of Europe.
173. Azizi Samir MAS, Alloin F, Dufresne A, (2005), A Review of Recent
Research into Cellulosic Whiskers, their Properties and their
Application in Nanocomposite Field, Biomacromolecules, 6, 612-
626.
174. Leppänen K, Anderson S, Torkkeli M, Knaapila M, Kotelnikova N,
Serimaa R, (009), Structure of Cellulose and Microcrystalline
Cellulose from Various Species, Cotton and Flax Studied by X-Ray
Scattering, Cellulose, 16, 999-1015.
175. Lachman L, Lieberman HA, Kanig JL, (1987), Tablet. In: Banker
GS, Anderson NR, editors. The Theory and Practice of Industrial
References
Pharmacy, 3rd Indian Ed. Bombay: Varghese Publishing House,
299–329.
176. Prabhu Halakatti K, Omer S, Gulgannavar SR, Kumar PP, (2010),
Formulation and evaluation of mouth disintegrating tablets of
famotidine by using Hibiscus Ros Sinensis mucilage and treated
agar, International Journal of Research in Ayurveda and Pharmacy,
1(2), 497–505.
177. Mehta KK, Patel HH, Patel ND, Vora CN, Patel NJ (2010),
Comparative evaluation of natural and synthetic superdisintegrant
for promoting nimesulide dissolution for fast dissolving technology,
International Journal of Pharmacy and Pharmaceutical Sciences,
2(3), 102–108.
178. Gokul Ghenge G, Pande SD, Ahmad A, Jejurkar L, Birari T, (2011),
Development and characterisation of fast disintegrating tablet of
amlodipine besylate using mucilage of plantago ovata as a natural
superdisintegrant, International Journal of PharmTech Research,
3(2), 938–945.
179. Prabakaran L, Sendhil D (2011), Formulation development of
patient friendly dosage form: all in one natural excipient as binder,
diluent and disintegrant, International Journal of Pharmacy and
Pharmaceutical Sciences, 3(2), 97–102.
180. Disintegration and dissolution tests. II. New Delhi: Controller of
Publications; 1996. Indian Pharmacopoeia; pp. A80–5. Appendix 7.
181. Klancke J, (2003), Dissolution testing of orally disintegrating
tablets, Diss Technol, 10, 6–8.
182. Jadhav SB, Kaudewar DR, Kaminwar GS, Jadhav AB, Kshirsagar
RV, Sakarkar DM, (2011), Formulation and evaluation of dispersible
tablets of diltiazem hydrochloride, International Journal of
PharmTech Research, 3(3), 1314–1321.
183. Metker V, Kumar A, Pathak N, Padhee K, Sahoo S, (2011),
Formulation and evaluation of orodispersible tablets of
lornoxicam, International Journal of Drug Development and
Research, 3(1), 281–285.
References
184. Arya A, Sharma S, Kumar J, Chandra A, Jaiswal P, (2010),
Formulation and evaluation of mouth dissolving tablets of ranitidine
HCL, International Journal of Pharm Tech Research, 2(2), 1574–
1577.
185. Kulkarni U, Rao NGR, (2011), Design and development of
Aceclofenac fast dissolving tablets by amorphous solid dispersion
technique using modified Marmelos gum,” International Journal of
Pharmaceutical Research and Development, 3(6), 201–210.
186. Setia A, Goyal N, Kansal S, (2011), Formulation and evaluation of
ciprofloxacin hydrochloride dispersible tablets using natural
substances as disintegrates, Pelagia Research Library Der
Pharmacia Sinica, 2(1), 36–39.
187. Abdul Ahad H, Sreenivsulu R, Reddy KK, Kavitha K, Sumapadmaja
B, Reddy VK, (2011), Isolation and characterization of Ficus indica
fruit mucilage, Journal of Pharmacy Research, 4(3), 726–727.
188. Kumar R, Patil S, Patil MB, Patil SR, Paschapur MS, (209),
Isolation and evaluation of disintegrant properties of fenugreek seed
mucilage, International Journal of PharmTech Research, 1(4), 982–
996.
189. Senthilnathan B, Rupenagunta A, (2011), Formulation development
and evaluation of venlafaxine hydrochloride orodispersible
tablets, International Journal of Pharmaceutical Sciences and
Research, 2(4), 913–921.
190. Anjankumar PB, Nazmuddin M, Kulkarni U, Hariprasanna RC,
(2011), Formulation and evaluation of lornoxicam fast dissolving
tablet, International Research Journal of Pharmacy, 2(4), 130–133.
191. Mohire NC, Yadav AV, (2010), Novel approach to formulate β-
cyclodextrin complexed mouth dissolving tablet of metronidazole
and its in-vitro evaluation, Journal of Pharmacy Research, 3(3),
662–667.
192. Nayak SM, Gopalkumar P, (2004), Design and optimization of fast
dissolving tablets for promethazine theoclate, Indian Drugs, 41,
554-6.
References
193. Gohel M, Patel M, Amin A, Agrwal R, Dave R, Bariya N, (2004),
Formulation design and optimization of mouth dissolve tablets of
nimesulide using vaccum drying technique, AAPS Pharm Sci Tech,
5, 1-6.
194. Kuchekar BS, Badhan AC, Mahajan HS, (2004), Mouth dissolving
tablets of salbutamol sulphate: A novel drug delivery system, Indian
Drugs, 41, 592-8.
195. Siddiqui MN, Garg G, Sharma PK, (2010), Fast dissolving tablets:
Preparation, characterization and evaluation: An overview.
International Journal of Pharmaceutical Sciences Review and
Research, 4(2), 87-96.
196. Puttalingaiah L, Kavitha K, Mani TT, (2011), Fast disintegrating
tablets: An Overview of Formulation, Technology and Evaluation.
Res J Pharmaceutical Biological Chem Sci, 2(2), 589-601.
197. Chaudhary Sunita A, Chaudhary Ankit B, Mehta Tejal A, (2010),
Excipients Updates for Orally Disintegrating Dosage Forms.
International Journal of Research Pharmaceutical Sciences,
1(2),103-107.
198. Goel Honey, Rai Parshuram, Rana Vikas, Tiwary Ashok K, (2008),
Orally Disintegrating Systems: Innovations in Formulation and
Technology. Recent Patents on Drug Delivery and Formulation, 2,
258-274.
199. Gupta A, Mishra AK , Gupta V , Bansal P, Singh R, Singh AK
(2010), Recent Trends of Fast Dissolving Tablet-An Overview of
Formulation Technology. International Journal of Pharmaceutical &
Biological Archives, 1(1):1-10.
200. Srivastava Saurabh, Bala Rajni, Joshi Baibhav, Rana AC, Singla
Vikas, (2012), Mouth dissolving tablet:Afuture compaction.
International Research Journal of Pharmacy, 3(8), 98-109.
201. Mishra B, Panigrahi D, Baghel S, (2005), Mouth dissolving tablets:
An overview of preparation techniques, evaluation and patented
technologies, J Pharm Res, 4, 33-8.
202. Gothoskar AV, Parakh SR, (2003), A Review of mouth dissolving
tablet technologies, Pharmaceutical Technology, 27, 92-100.
References
203. William RP, Ghosh TK, (2005), Orally disintegrating tablets.
Pharmaceutical Technology (Product, Technologies, and
Development issues in Oct 2005).
204. Wayne C, Dipan R, Ann D, (2006), Selecting superdisintegrants for
Orally Disintegrating Tablet, Formulations in Phrmaceutical
Technology, 08, 226-229.
205. Jadon RS, Vaidya VD, Khemariya P, Nayak S, (2009), Taste
Masking of Lornoxicam by Polymer Carrier System and Formulation
of Oral Disintegrating Tablets, IJDD, 1, 1-3
206. Biradar SS, (2006), Fast dissolving drug delivery systems: a brief
overview, The Internet Journal of Pharmacology, 4(2).
207. Ghosh T, Ghosh A, Prasad D, (2011), A Review on new generation
orodispersible tablets and its future prospective, International
Journal of Pharmacy and Pharmaceutical Sciences, 3(1), 1-7.
208. Agrawal VA, Rajurkar RM, Thonte S, Ingale RG, (2011), Fast
disintegrating tablets as a new drug delivery system: a review,
Pharmacophore, 2(1), 1-8.
209. Deshmekh KR, Vidyanand P, Shekhar V, Alok P, Pramod KD
(2011), A review on mouth dissolving tablet techniques, Int J Res
Ayurveda Pharm, 2(1), 66-74.
210. Monachandran PS, Sindhumol PG, Kiran TS (2011),
Superdisintegrants: An overview, J Pharm Sci Rev Res, 6(1), 105-
109.
211. Reeta RT, Mridul K (2011), An unlimited scope for novel
formulations as orally disintegrating systems: Present and future
prospects, J Appl Pharm Sci, 1(1), 13-19.
212. Ishikawa T, Mukai B, Shiraishi S, Naoki U, (1999), Preparation and
evaluation of tablets rapidly disintegrating in saliva containing bitter
taste masked granules by the compression method, Chem Pharm
Bull, 47(10), 1451-1454.
213. Yoshio K, Masazumi K, Shuichi A, Hiroaki N, (2008), Effect of
preparation method on properties of orally disintegrating tablets
made by phase transition, Int J Pharm, 355, 87–92.
References
214. Battue SK, Repay MA, Maunder S, Rio MY, (2007), Formulation
and evaluation of rapidly disintegrating tablet Fenoverine tablets:
Effect of superdisintegrants, Drug Dev Ind Pharm, 33, 1225-1232.
215. Bi Y, Sunada H, Yonezawa Y, Danjo K, Otsuka A, Iida K, (1996),
Preparation and evaluation of a compressed tablet rapidly
disintegrating in the oral cavity, Chem Pharm Bull (Tokyo), 44,
2121-2127.
216. Sreenivas SA, Gadad AP, Dandagi PM, Mastiholimath VS, Patil
MB, (2006), Formulation and Evaluation of Ondansetron HCl
Directly Compressed Mouth Disintegrating Tablets, Indian Drugs,
43, 35-37.
217. Kundu S, Sahoo PK, (2008), Recent trends in the developments of
orally disintegrating technology. Pharma Times, 40(4), 11-15.
218. Chakraborthy S, Khandai M, Singh SP, Patra N, (2008),
Comparative study on effect of natural and synthetic
superdisintegrant in the formulation of fast dissolving tablet,
International Journal of Green Pharmacy, 9, 22-25.
219. Gudas GK, Manasa B, Rajesham VV, Kumar SK, Prasanna
Kumari J, (2010), Formulation and evaluation of fast dissolving
tablets of Chlorpromazine HCl, J Pharm Sci Tech, 1, 99-102.
220. Kakade SM, Mannur VS, Ramani KB, Dhada AA, Naval CV,
Bhagwat A, (2010), Formulation and evaluation of mouth dissolving
tablets of losartan potassium by direct compression techniques, Int
J Res Phar Sci, 1(3), 290-295.
221. Mizumoto T, Masuda Y, Kajiyama A, Yanagisawa M, Nyshadham
JR, (2003), Tablets quickly disintegrating in the oral cavity and
process for producing the same, US Patent 6,589,554.
222. Yourong F, Shicheng Y, Seong HJ, Susumu K, Kinam P, (2004),
Orally Fast Disintegrating tablets: Developments, technologies,
Taste-masking and clinical studies, Critical review in therapeutic
drug carrier systems, 21(6), 433–475.
223. Percel PJ, Venkatesh GM, Vishnupad KS, (2001), Functional
coating of linezolid microcapsules for taste-masking and associated
formulation for oral administration, WO Patent 0,152,848.
References
224. Ishikawa T, Watanabe Y, Utoguchi N, Matsumoto M, (1999),
Preparation and evaluation of tablets rapidly disintegrating in saliva
containing bitter-taste-masked granules by the compression
method, Chem Pharm Bull, 47(10), 1451–1454.
225. Mishra DN, Bindal M, Singh SK, Kumar SGV, (2005), Rapidly
disintegrating oral tablets of meloxicam, Indian Drugs, 42(10), 685-
687.
226. Morita Y, Tsushima Y, Yasui M, Termoz R, Ajioka J, Takayama K,
(2002), Evaluation of the disintegration time of rapidly disintegrating
tablets via a novel utilizing a CCD camera. Chem & Pharma
Bulletin, 50(9), 1181–1186.
227. Ashwini KG, Choudhary RK, Chaitanya CH, (2011), Enhancement
of Solubility and Dissolution Rate of Irbesartan by Solid Dispersion
Technique, Asian Journal of Pharmceutical Clinical Research, 4(2),
364.
228. Jadhav SB, Kaudewar DR, Kaminwar GS, Jadhav AB, Kshirsagar
RV, Sakarkar DM, (2011), Formulation and evaluation of dispersible
tablets of diltiazem hydrochloride, International Journal of
PharmTech Research, 3(3), 1314–1321.
229. Metker V, Kumar A, Pathak N, Padhee K, Sahoo S, (2011),
Formulation and evaluation of orodispersible tablets of
lornoxicam, International Journal of Drug Development and
Research, 3(1), 281–285.
230. Mizumoto T, Masuda Y, Fukui M, (1996), Intrabuccally dissolving
compressed moldings and production process thereof, US Patent
5,576,014.
231. Milovac J, Kovacic M, Kopitar Z, Urbancic-Smerkolj J, Lenardic A,
Zorz M, (1991), Dispersible tablets of dihydroergotoxine
methanesulfonate and of acid addition salts thereof, US Patent
5,047,247.
232. Yourong F, Shicheng Yang, Seong HJ, Susumu K, Kinam P,
(2004), Orally Fast Disintegrating Tablets: Developments,
Technologies, Taste-Masking and Clinical Studies, Critical
Reviews™ in Therapeutic Drug Carrier Systems, 21(6), 433–475.
References
233. Parkash V, Maan S, DeepikaYadav SK, Hemlata, Jogpal V, (2011),
Fast disintegrating tablets: Opportunity in drug delivery system, J
Advanced pharma Techno & Res, 2(4), 223-35.
234. Kulkarni U, Rao R, (2011), Design and development of aceclofenac
fast dissolving tablets by amorphous solid dispersion technique
using modified Aegle marmelos gum. Int J Pharma Res Dev, 3(6),
201-210.
235. Mathur P, Saroha K, (2010), Mouth dissolving tablets: An overview
on future compaction in oral formulation technologies, Der
Pharmacia Sinica, 1(1), 179-187.
236. Aithal K, Harish NM, Rathnanand M, Shirwaikar A, Dutta M, (2006),
Once daily fast dissolving tablets of granisetron hydrochloride
formulation and in vitro evaluation. Indian Drugs, 43(7), 576-581.
237. Sharma Deepak, Kumar Dinesh, Singh Mankaran, Singh Gurmeet,
Rathore MS, (2012), Fast Disintegrating Tablets: A New Era in
Novel Drug Delivery System & New Market Oppor- tunities.Journal
of Drug Delivery & Therapeutics, 2(3), 74-86.
238. Arya A, Sharma S, Kumar J, Chandra A, Jaiswal P, (2010),
Formulation and evaluation of mouth dissolving tablets of ranitidine
HCL, International Journal of Pharm Tech Research, 2(2), 1574–
1577.
239. Senthilnathan B, Rupenagunta A, (2011), Formulation development
and evaluation of venlafaxine hydrochloride orodispersible
tablets, International Journal of Pharmaceutical Sciences and
Research, 2(4), 913–921.
240. Yoshio K, Masazumi K, Shuichi A, Hiroaki N, (2005), Evaluation of
rapidly disintegrating tablets manufactured by phase transition of
sugar alcohols, J Control Release, 105, 16-22.
241. Mohire NC, Yadav AV, (2010), Novel approach to formulate β-
cyclodextrin complexed mouth dissolving tablet of metronidazole
and its in-vitro evaluation, Journal of Pharmacy Research, 3(3),
662–667.
References
242. Nayak SM, Gopalkumar P, (2004), Design and optimization of fast
dissolving tablets for promethazine theoclate, Indian Drugs, 41,
554-6.
243. Gohel M, Patel M, Amin A, Agrwal R, Dave R, Bariya N, (2004),
Formulation design and optimization of mouth dissolve tablets of
nimesulide using vaccum drying technique, AAPS Pharm Sci Tech,
5, 1-6.
244. Camu F, Beecher T, Recker DP, Verburg KM, (2002), Valdecoxib, a
cox-2-specific inhibitor, is an efficacious, opioid-sparing analgesic in
patients undergoing hip arthroplasty, American Journal Therapy,
9(1), 43–51.
245. Dannhardt G, Kiefer W, (2001), Cyclooxygenase inhibitors - current
status and future prospects, European Journal of Medicinal
Chemistry, 36(2), 109–126.
246. McMurray RW, Hardy KJ, (2002), Cox-2 inhibitors: today and
tomorrow, Am J Med Sci, 323, 181.