Pharmacokinetics of a single 1g dose of azithromycin in rectal tissue in men.

Chlamydia is the most common bacterial sexually transmitted infection among men who have sex with men. Repeat infection following treatment with 1g azithromycin is common and treatment failure of up to 22% has been reported. This study measured the pharmacokinetics of azithromycin in rectal tissue i...

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Main Authors: Fabian Y S Kong, Thusitha W Rupasinghe, Julie A Simpson, Lenka A Vodstrcil, Christopher K Fairley, Malcolm J McConville, Jane S Hocking
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5370104?pdf=render
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author Fabian Y S Kong
Thusitha W Rupasinghe
Julie A Simpson
Lenka A Vodstrcil
Christopher K Fairley
Malcolm J McConville
Jane S Hocking
author_facet Fabian Y S Kong
Thusitha W Rupasinghe
Julie A Simpson
Lenka A Vodstrcil
Christopher K Fairley
Malcolm J McConville
Jane S Hocking
author_sort Fabian Y S Kong
collection DOAJ
description Chlamydia is the most common bacterial sexually transmitted infection among men who have sex with men. Repeat infection following treatment with 1g azithromycin is common and treatment failure of up to 22% has been reported. This study measured the pharmacokinetics of azithromycin in rectal tissue in men following a single 1g dose to assess whether azithromycin reaches the rectal site in adequate concentrations to kill chlamydia. Ten healthy men took a single oral dose of 1g azithromycin and provided nine self-collected swabs and one blood sample over 14 days. Participant demographics, medications, sexual behaviour, treatment side effects, lubricant use and douching practices were recorded with each swab. Drug concentration over time was determined using liquid chromatography-mass spectrometry and total exposure (AUC0-∞) was estimated from the concentration-time profiles. Following 1g of azithromycin, rectal concentrations peaked after a median of 24 hours (median 133mcg/g) and remained above the minimum inhibitory concentration for chlamydia (0.125mcg/mL) for at least 14 days in all men. AUC0-∞ was the highest ever reported in human tissue (13103((mcg/g).hr)). Tissue concentrations were not associated with weight (mg/kg), but data suggest that increased gastric pH could increase azithromycin levels and diarrhoea or use of water-based lubricants could decrease concentrations. High and sustained concentrations of azithromycin were found in rectal tissue following a single 1g dose suggesting that inadequate concentrations are unlikely to cause treatment failure. Factors effecting absorption (pH and diarrhoea) or drug depletion (douching and water-based lubricants) may be more important determinants of concentrations in situ.
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spelling doaj.art-dcc7e8c4edbc4c899498db1ebc82f6472022-12-21T17:56:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01123e017437210.1371/journal.pone.0174372Pharmacokinetics of a single 1g dose of azithromycin in rectal tissue in men.Fabian Y S KongThusitha W RupasingheJulie A SimpsonLenka A VodstrcilChristopher K FairleyMalcolm J McConvilleJane S HockingChlamydia is the most common bacterial sexually transmitted infection among men who have sex with men. Repeat infection following treatment with 1g azithromycin is common and treatment failure of up to 22% has been reported. This study measured the pharmacokinetics of azithromycin in rectal tissue in men following a single 1g dose to assess whether azithromycin reaches the rectal site in adequate concentrations to kill chlamydia. Ten healthy men took a single oral dose of 1g azithromycin and provided nine self-collected swabs and one blood sample over 14 days. Participant demographics, medications, sexual behaviour, treatment side effects, lubricant use and douching practices were recorded with each swab. Drug concentration over time was determined using liquid chromatography-mass spectrometry and total exposure (AUC0-∞) was estimated from the concentration-time profiles. Following 1g of azithromycin, rectal concentrations peaked after a median of 24 hours (median 133mcg/g) and remained above the minimum inhibitory concentration for chlamydia (0.125mcg/mL) for at least 14 days in all men. AUC0-∞ was the highest ever reported in human tissue (13103((mcg/g).hr)). Tissue concentrations were not associated with weight (mg/kg), but data suggest that increased gastric pH could increase azithromycin levels and diarrhoea or use of water-based lubricants could decrease concentrations. High and sustained concentrations of azithromycin were found in rectal tissue following a single 1g dose suggesting that inadequate concentrations are unlikely to cause treatment failure. Factors effecting absorption (pH and diarrhoea) or drug depletion (douching and water-based lubricants) may be more important determinants of concentrations in situ.http://europepmc.org/articles/PMC5370104?pdf=render
spellingShingle Fabian Y S Kong
Thusitha W Rupasinghe
Julie A Simpson
Lenka A Vodstrcil
Christopher K Fairley
Malcolm J McConville
Jane S Hocking
Pharmacokinetics of a single 1g dose of azithromycin in rectal tissue in men.
PLoS ONE
title Pharmacokinetics of a single 1g dose of azithromycin in rectal tissue in men.
title_full Pharmacokinetics of a single 1g dose of azithromycin in rectal tissue in men.
title_fullStr Pharmacokinetics of a single 1g dose of azithromycin in rectal tissue in men.
title_full_unstemmed Pharmacokinetics of a single 1g dose of azithromycin in rectal tissue in men.
title_short Pharmacokinetics of a single 1g dose of azithromycin in rectal tissue in men.
title_sort pharmacokinetics of a single 1g dose of azithromycin in rectal tissue in men
url http://europepmc.org/articles/PMC5370104?pdf=render
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