4.7 Article

Single and Multiple Dose Pharmacokinetics of Maraviroc in Saliva, Semen, and Rectal Tissue of Healthy HIV-negative Men

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JOURNAL OF INFECTIOUS DISEASES
卷 203, 期 10, 页码 1484-1490

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OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jir059

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资金

  1. Abbott
  2. Merck
  3. Pfizer
  4. Tibotec
  5. Gilead
  6. National Institutes of Health [R37 DK49381, R34 AI087065, K23 AI54980, K23 AI77355, P30 AI50410, UL1 RR025747, U19 AI31496]

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Methods. A pharmacokinetic study was performed in 12 HIV-negative men receiving maraviroc 300 mg twice daily for 8 days. Seven time-matched pairs of blood plasma (BP) and saliva samples were collected over 12 h on day 1 (PK1) and days 7 and 8 (PK2). One RT sample from each subject was collected during PK1 and PK2. Two SP samples were collected from each subject during PK1, and 6 SP samples were collected from each subject during PK2. Results. SP AUCs were similar to 50% lower than BP. However, protein binding in SP ranged from 4% to 25%, resulting in protein-free concentrations > 2-fold higher than BP. RT AUCs were 7.5- to 26-fold higher than BP. Maraviroc saliva AUCs were similar to 70% lower than BP, but saliva concentrations correlated with BP (r(2) = 0.58). Conclusions. More pharmacologically available maraviroc was found in SP than BP. High RT concentrations are promising for preventing rectal HIV acquisition. Saliva correlation with BP suggests that this may be useful for monitoring adherence. Clinical Trials Registration. NCT00775294.

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