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JAC Advance Access published online on July 14, 2004

Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkh357
© 2004 by The British Society for Antimicrobial Chemotherapy
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Received December 22, 2003
Revised March 21, 2004
Accepted June 2, 2004

Original article

Lopinavir/ritonavir combined with twice-daily 400 mg indinavir: pharmacokinetics and pharmacodynamics in blood, CSF and semen

Adil Isaac 1*, Stephen Taylor 1, Patricia Cane 2, Erasmus Smit 3, Sarah E. Gibbons 4, David J. White 1, Susan M. Drake 1, Saye Khoo 4, David J. Back 4

1 Hawthorne House, Department of Genitourinary Medicine, Birmingham Heartlands Hospital, Birmingham B9 5SS, UK
2 Health Protection Agency, Birmingham Heartlands Hospital, Birmingham, Birmingham, UK; Antiviral Susceptibility Reference Unit, University of Birmingham, Birmingham, UK
3 Health Protection Agency, Birmingham Heartlands Hospital, Birmingham, Birmingham, UK
4 Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK

* To whom correspondence should be addressed. E-mail: Adilisaac{at}yahoo.com.


   Abstract

Objectives: To evaluate the steady-state blood plasma (BP), CSF and seminal plasma (SP) pharmacokinetics (PK) of twice-daily indinavir 400 mg and lopinavir/ritonavir.

Methods: Ten HIV-1-positive men on lopinavir/ritonavir participated in a PK study. PK sampling was performed before and 2 weeks after adding indinavir to lopinavir/ritonavir-containing regimens. BP, CSF and SP RNA levels, CD4 counts and blood chemistry were checked at baseline and 2 weeks after indinavir.

Results: At baseline: lopinavir parameters (n=10) in BP were within expected levels. Median lopinavir trough concentrations (n=5) in CSF and SP were below the limit of detection (BLD) (i.e. <10 ng/mL) and 248 ng/mL (range 96-2777), respectively. After indinavir: lopinavir Cmax, Cmin and AUC0-12 increased by 9%, 46% and 20%, respectively (P<0.32, P<0.32 and P<0.20). In two of four men lopinavir concentrations in CSF were detectable at 27 and 29 ng/mL. Median SP lopinavir concentration was 655 ng/mL (20-2734). Median indinavir PK parameters were Cmax 3365 ng/mL (range 2130-5194), Cmin 293 ng/mL (14-766), Tmax 2.25 h (1-3), AUC0-12 22452 ng/mL·h (11243-33661), and t1/2 2.8 h (1.4-3.7). Median indinavir concentrations in CSF and SP were 39 ng/mL (21-86) and 592 ng/mL (96-983). Two of eight men who initially had detectable BP viral load (VL) became BLD (<50 copies/mL) after the addition of indinavir, and in 2/4 men with low-level viraemia in SP (BPVL BLD) their SPVL became BLD after addition of indinavir.

Conclusions: Adding indinavir 400 mg twice daily to lopinavir/ritonavir-containing regimens did not significantly alter the median lopinavir PK parameters. However, wide interpatient variability in lopinavir concentrations was seen. In contrast plasma indinavir levels were >80 ng/mL in seven of eight plasma samples, and all CSF and semen samples collected.

Keywords: sanctuary sites; double boosted; protease inhibitors; drug interactions; HIV.
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