fluoroquinolones medchem- oriental college of pharmacy
TRANSCRIPT
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BY:SONALI KANADE
KAUSHIK.N.KUCHERUCHA.J.KADMANEDIKSHA KANOJIYA
GUIDED BY : MR . AMJAD ALI
ORIENTAL COLLEGE OF PHARMACY , SANPADA,
NAVIMUMBAI.
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DEFINITION:
The fluoroquinolones are a family of broad spectrum,
systemic antibacterial agents that have been used widely as
therapy of respiratory and urinary tract infections.
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BackgroundIn 1962 nalidixic acid was discovered by
George Lesher during synthesis of chloroquine and was named as Quinolone.
Fluoroquinolones were derived by adding fluorine atom in nalidixic acid.
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Earlier quinolones were useful only for treatment of UTI.
Fluorinated derivatives achieve bactericidal levels in blood and tissues so they have improved antibacterial spectrum.
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1. SAFER TO USE
2.HIGH POTENCY
3.NEW FLUOROQUINOLONES ARE BROAD IN SPECTRUM
4.DEEP PENETRATION IN TISSUES (but dose not cross BBB. Can enter the cell i.e intracellular organism)
5.GOOD ORAL ABSORPTION
FLUOROQUINOLONES ARE FIVE STAR DRUGS !!!
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CLASSIFICATION
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Generations Drugs Spectrum
1st(Quinolone)
Nalidixic acid Gram -ve but not Pseudomonas species
2nd
NorfloxacinCiprofloxacin Ofloxacin
Gram -ve(including Pseudomonas species), some Gram+ (S. aureus) and some atypicals
3rd
Levofloxacin Sparfloxacin MoxifloxacinGatifloxacin
Same as 2nd generation with extended Gram +ve and atypical coverage
4th*Trovafloxacin Same as 3rd generation
with broad anaerobic coverage
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Structural relativity of fluoroquinolones
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First generation fluoroquinolones
Nalidixic acid
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ciprofloxacin Ofloxacin
Norfloxacin
Second generation fluoroquinolones
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Moxifloxacin Gatifloxacin
Levofloxacin Sparfloxacin
Third generation of fluoroquinolones
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Trovafloxacin
Fourth generation of fluoroquinolones
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SYNTHESIS OF CIPROFLOXACIN USE RETROSYNTHESIS TECHNIQUE IT WOULD MAKE YOUR
LIFE EASY.. !
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SYNTHESIS OF CIPROFLOXACIN
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CIPROFLOXACIN
SYNTHESIS (CONT..)
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Topoisomerase II : to convert the +ve supercoiling to –ve supercoiling. There by allowing the process of replication or the allows the action of DNA helicase to proceed.
Topoisomerase IV: to separate the entangled DNA so that its expression could be proceeded.
MECHANISM OF ACTION
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Fluoroquinolones blocks the ligase action where in has no effect on endoneuclease action of the enzyme. Thus what the bacteria left with is fragments of DNA which cannot be expressed.
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MECHANISM OF ACTION (cont..)Fluoroquinolones are bactericidal agents
They block bacterial DNA synthesis by inhibiting bacterial DNA gyrase and topoisomerase IV.
Inhibition of DNA gyrase prevents the relaxation of positively supercoiled DNA that is required for normal transcription and replication
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Cont….Inhibition of topoisomeraseIV interferes with
separation of replicated chromosomal DNA into the respective daughter cells during cell division.
They can enter cells easily via porins and are
used to treat intracellular pathogens (Legionella, pneumophila and Mycoplasma)
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RESISTANCE Resistance is due to • one or more point mutations in the
quinolone binding region of the target enzyme
OR to a change in the permeability of the organism
Resistance to one FQL confers cross
resistance to all members of the class.
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PharmacokinecticsWell absorbed orally with bioavailability 80-
95% almost equal to IVHalf life 3-10 hoursOral absorption impaired by divalent
actions(Antacids containing Mg, Ca or Al ).Most of fluoroquinolones eliminated by renal
mechanism so adjustment required in patients with creatinine clearance <50 ml/min.
Limited CSF penetration.
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Distribution [Conc] > serum:
Prostate tissueStoolBileLungKidneys NeutrophilsMacrophages
[Conc] < serum: Prostatic fluidBoneCSF
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Drug interactions Drugs increasing levels of FQL
FQL increasing the levels of :
Theophyline AntidepressantsNSAIDS Imipramine corticosteroids Caffene
TheophylineWarfarin (INR –monitored)
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Adverse effects.Generally safe antibioticsG.I.T-nausea,vomiting,diarrhea and antibiotic
associated colitis have been reported.CNS-confusion,insomnia,dizziness,anxiety,and
seizures(displacement of GABA from its receptors).
CVS-torsade de pointes,prolonged QTc interval.May damage growing cartilage resulting in
arthropathy(but that’s reversible so may b used in psudomonal infections in C.F where benefit outweighs the risk.)
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Cont.Tendonitis and tendon rupture is rare but
very serious.Phototoxicity-avoid excesive sun exposure.Leukopenia,eosinophilia (rare)Mild elevation in transaminases (rare)
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Contraindication Childrens (not absolute)PregnancyLactationEpilepsyQTc prolongation
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Commonly used Fluoroquinolones
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Ciprofloxacin 2nd generation fluoroquinoloneMainly effective against G –ve bacteria :Enterobacteriacae H. influenzae M. catarrhalisCampylobacter Pseudomonas N. gonorrheaeIntracellular pathogensM. Tuberculosis Mycoplasma ChlamydiaLegionella BrucellaNot effective against G+ and anaerobes
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Clinical uses1.Urinary tract infections (G- bacteria)2. Osteomyelitis due to P. aeruginosa 3. Gonorrhea4. Travellers’ diarrhea- ciprofloxacin
commonly used5. Tuberculosis6. Prostatitis7. Community- acquired pneumoniae 8. Diabetic foot infections ( P. aeruginosa )9.Anthrax
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Usual duration is 7-14 days Available forms
Brand name : ciproxin(bayer),cycin.
Oral Parentral Opthalmic 100 mg 200 mg iv 3mg/ml
solution250 mg 400 mg iv 3.3mg/mg
ointment500 mg
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Levofloxacin
3rd generation fluoroquinolone
Spectrum: Gram-ve, Gram+ve (S. aureus including MRSA & S. pneumoniae) and Legionella pneumophila, atypical resp. pathogens,
Mycobacterium tuberculosis
Indications:Chronic bronchitis and CAP• Nosocomial pneumonia Intra-abdominal infections
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Cont. Adverse reaction.Blood glucose disturbances in DM patientsQTC prolongation, torsades de pointes, arrhythmiasNausea, GI upset Interstitial nephritis
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Usual duration same 7-14 daysAvailable forms
Brand name:leflox,l-cyn,qumic
Oral Parentral Opthalmic 100 mg 5 mg/ml iv 5mg/ml
solution250 mg 25 mg/ml iv500mg
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REFERENCE:- http://www.DrNajeebLectures.comhttp://en.wikipedia.org/wiki/QuinoloneWilson and gisvolds textbook of Organic
Medicinal and Pharmaceutical Chemistry, by JhonH.Block and Jhon M. Beale. Eleventh edition. Pgno 247-252.
Foye’s principles of Medicinal chemistry, by Thomas L. lemke, David A williams.
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