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The effect of ciprofloxacin and clarithromycin on sildenafil oral bioavailability in human volunteers

Sildenafil is the first oral therapeutic agent for the management of male erectile dysfunction. Its oral bioavailability is only 40% due to extensive presystemic elimination, mainly by CYP3A4. This study examined the effect of coadministration of ciprofloxacin or clarithromycin, which inhibit CYP3A4...

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Published in:Biopharmaceutics & drug disposition 2006-03, Vol.27 (2), p.103-110
Main Authors: Hedaya, Mohsen A., El-Afify, Dalia R., El-Maghraby, Gamal M.
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description Sildenafil is the first oral therapeutic agent for the management of male erectile dysfunction. Its oral bioavailability is only 40% due to extensive presystemic elimination, mainly by CYP3A4. This study examined the effect of coadministration of ciprofloxacin or clarithromycin, which inhibit CYP3A4, on the bioavailability and pharmacokinetics of sildenafil. Twelve healthy male volunteers received sildenafil alone or after pretreatment with the inhibitors in a balanced three‐way crossover design. The pharmacokinetic analysis showed that ciprofloxacin coadministration with sildenafil significantly increased the AUC from 1407 ± 380 to 2986 ± 917 µg h/l (90% confidence interval 119%–159%) and the Cmax from 287 ± 67 to 623 ± 192 µg/l (90% confidence interval 127%–152%). Similarly, clarithromycin coadministration increased sildenafil AUC from 1407 ± 380 to 3209 ± 762 µg h/l (90% confidence interval 127%–161%) and Cmax from 287 ± 67 to 694 ± 259 µg/l (90% confidence interval 132%–157%). Ciprofloxacin coadministration and clarithromycin coadministration with sildenafil did not affect the rate of sildenafil absorption significantly. These results indicate that coadministration of ciprofloxacin and clarithromycin significantly increased sildenafil bioavailability which can be attributed to the inhibitory effect of ciprofloxacin and clarithromycin on CYP3A4. Dose adjustment of sildenafil is thus necessary when administered with such drugs. Copyright © 2005 John Wiley & Sons, Ltd.
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Its oral bioavailability is only 40% due to extensive presystemic elimination, mainly by CYP3A4. This study examined the effect of coadministration of ciprofloxacin or clarithromycin, which inhibit CYP3A4, on the bioavailability and pharmacokinetics of sildenafil. Twelve healthy male volunteers received sildenafil alone or after pretreatment with the inhibitors in a balanced three‐way crossover design. The pharmacokinetic analysis showed that ciprofloxacin coadministration with sildenafil significantly increased the AUC from 1407 ± 380 to 2986 ± 917 µg h/l (90% confidence interval 119%–159%) and the Cmax from 287 ± 67 to 623 ± 192 µg/l (90% confidence interval 127%–152%). Similarly, clarithromycin coadministration increased sildenafil AUC from 1407 ± 380 to 3209 ± 762 µg h/l (90% confidence interval 127%–161%) and Cmax from 287 ± 67 to 694 ± 259 µg/l (90% confidence interval 132%–157%). Ciprofloxacin coadministration and clarithromycin coadministration with sildenafil did not affect the rate of sildenafil absorption significantly. These results indicate that coadministration of ciprofloxacin and clarithromycin significantly increased sildenafil bioavailability which can be attributed to the inhibitory effect of ciprofloxacin and clarithromycin on CYP3A4. Dose adjustment of sildenafil is thus necessary when administered with such drugs. 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Drug Dispos</addtitle><description>Sildenafil is the first oral therapeutic agent for the management of male erectile dysfunction. Its oral bioavailability is only 40% due to extensive presystemic elimination, mainly by CYP3A4. This study examined the effect of coadministration of ciprofloxacin or clarithromycin, which inhibit CYP3A4, on the bioavailability and pharmacokinetics of sildenafil. Twelve healthy male volunteers received sildenafil alone or after pretreatment with the inhibitors in a balanced three‐way crossover design. The pharmacokinetic analysis showed that ciprofloxacin coadministration with sildenafil significantly increased the AUC from 1407 ± 380 to 2986 ± 917 µg h/l (90% confidence interval 119%–159%) and the Cmax from 287 ± 67 to 623 ± 192 µg/l (90% confidence interval 127%–152%). Similarly, clarithromycin coadministration increased sildenafil AUC from 1407 ± 380 to 3209 ± 762 µg h/l (90% confidence interval 127%–161%) and Cmax from 287 ± 67 to 694 ± 259 µg/l (90% confidence interval 132%–157%). Ciprofloxacin coadministration and clarithromycin coadministration with sildenafil did not affect the rate of sildenafil absorption significantly. These results indicate that coadministration of ciprofloxacin and clarithromycin significantly increased sildenafil bioavailability which can be attributed to the inhibitory effect of ciprofloxacin and clarithromycin on CYP3A4. Dose adjustment of sildenafil is thus necessary when administered with such drugs. 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Drug treatments</topic><topic>Phosphodiesterase Inhibitors - administration &amp; dosage</topic><topic>Phosphodiesterase Inhibitors - pharmacokinetics</topic><topic>Piperazines - administration &amp; dosage</topic><topic>Piperazines - pharmacokinetics</topic><topic>Purines</topic><topic>sildenafil</topic><topic>Sildenafil Citrate</topic><topic>Sulfones</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hedaya, Mohsen A.</creatorcontrib><creatorcontrib>El-Afify, Dalia R.</creatorcontrib><creatorcontrib>El-Maghraby, Gamal M.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Biopharmaceutics &amp; drug disposition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hedaya, Mohsen A.</au><au>El-Afify, Dalia R.</au><au>El-Maghraby, Gamal M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of ciprofloxacin and clarithromycin on sildenafil oral bioavailability in human volunteers</atitle><jtitle>Biopharmaceutics &amp; drug disposition</jtitle><addtitle>Biopharm. Drug Dispos</addtitle><date>2006-03</date><risdate>2006</risdate><volume>27</volume><issue>2</issue><spage>103</spage><epage>110</epage><pages>103-110</pages><issn>0142-2782</issn><eissn>1099-081X</eissn><coden>BDDID8</coden><abstract>Sildenafil is the first oral therapeutic agent for the management of male erectile dysfunction. Its oral bioavailability is only 40% due to extensive presystemic elimination, mainly by CYP3A4. This study examined the effect of coadministration of ciprofloxacin or clarithromycin, which inhibit CYP3A4, on the bioavailability and pharmacokinetics of sildenafil. Twelve healthy male volunteers received sildenafil alone or after pretreatment with the inhibitors in a balanced three‐way crossover design. The pharmacokinetic analysis showed that ciprofloxacin coadministration with sildenafil significantly increased the AUC from 1407 ± 380 to 2986 ± 917 µg h/l (90% confidence interval 119%–159%) and the Cmax from 287 ± 67 to 623 ± 192 µg/l (90% confidence interval 127%–152%). Similarly, clarithromycin coadministration increased sildenafil AUC from 1407 ± 380 to 3209 ± 762 µg h/l (90% confidence interval 127%–161%) and Cmax from 287 ± 67 to 694 ± 259 µg/l (90% confidence interval 132%–157%). Ciprofloxacin coadministration and clarithromycin coadministration with sildenafil did not affect the rate of sildenafil absorption significantly. These results indicate that coadministration of ciprofloxacin and clarithromycin significantly increased sildenafil bioavailability which can be attributed to the inhibitory effect of ciprofloxacin and clarithromycin on CYP3A4. Dose adjustment of sildenafil is thus necessary when administered with such drugs. Copyright © 2005 John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>16372380</pmid><doi>10.1002/bdd.488</doi><tpages>8</tpages></addata></record>
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identifier ISSN: 0142-2782
ispartof Biopharmaceutics & drug disposition, 2006-03, Vol.27 (2), p.103-110
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source Wiley-Blackwell Read & Publish Collection
subjects Administration, Oral
Adult
Anti-Infective Agents - administration & dosage
Anti-Infective Agents - pharmacology
bioavailability
Biological and medical sciences
Biological Availability
Ciprofloxacin - administration & dosage
Ciprofloxacin - pharmacology
Clarithromycin - administration & dosage
Clarithromycin - pharmacology
CYP3A4 inhibitors
Cytochrome P-450 CYP3A
Cytochrome P-450 Enzyme Inhibitors
Cytochrome P-450 Enzyme System - metabolism
Drug Interactions
Humans
Liver - drug effects
Liver - enzymology
Male
Medical sciences
pharmacokinetic interactions
Pharmacology. Drug treatments
Phosphodiesterase Inhibitors - administration & dosage
Phosphodiesterase Inhibitors - pharmacokinetics
Piperazines - administration & dosage
Piperazines - pharmacokinetics
Purines
sildenafil
Sildenafil Citrate
Sulfones
title The effect of ciprofloxacin and clarithromycin on sildenafil oral bioavailability in human volunteers
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