期刊
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
卷 51, 期 5, 页码 546-553出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAI.0b013e3181ae69c5
关键词
CCR5 antagonist; cervicovaginal; genital tract; maraviroc; pharmacokinetic; tissue; vaginal
Objective: To compare single- and multiple-dose maraviroc exposures in cervicovaginal fluid (CVF) and vaginal tissue (VT) with blood plasma (BP) and quantity maraviroc protein binding in CVF. Design: Open-label pharmacokinetic study. Methods: In 12 HIV-negative women, 7 paired CVF and BP samples were collected over 12 hours after I maraviroc dose. Subjects then received maraviroc twice daily for 7 days. After the last dose, subjects underwent CVF and BP sampling as on day 1, with additional sampling during terminal elimination. VT biopsies were obtained at steady state. Results: Day 1 and day 7 median maraviroc CVF AUC(T) were 1.9- and 2.7-fold higher, respectively, than BP. On day 1, 6 of 12 subjects had detectable maraviroc CVF concentrations within I hour; 12 of 12 were detectable within 2 hours, and all exceeded the protein-free IC90. On day 7, maraviroc CVF protein binding was 7.6% and the VT AUC(T) was 1.9-fold higher than BR Maraviroc CVF concentrations 72 hours after dose and BP concentrations 12 hours after dose were similar. Conclusions: Higher maraviroc exposure in the female genital tract rovides a pharmacologic basis for further evaluation of chemokine receptor 5 antagonists in HIV infection prophylaxis. This is the first study to report antiretroviral VT concentrations, CVF protein binding, and CVF terminal elimination.
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