Journal Article

Intracellular and plasma pharmacokinetics of efavirenz in HIV-infected individuals

Lisa M. Almond, Patrick G. Hoggard, Damitha Edirisinghe, Saye H. Khoo and David J. Back

in Journal of Antimicrobial Chemotherapy

Published on behalf of British Society for Antimicrobial Chemotherapy

Volume 56, issue 4, pages 738-744
Published in print October 2005 | ISSN: 0305-7453
Published online September 2005 | e-ISSN: 1460-2091 | DOI: http://dx.doi.org/10.1093/jac/dki308
Intracellular and plasma pharmacokinetics of efavirenz in HIV-infected individuals

More Like This

Show all results sharing these subjects:

  • Medical Oncology
  • Critical Care

GO

Show Summary Details

Preview

Objectives: The site of action of efavirenz is inside HIV-infected cells. Measurement of intracellular (IC) concentrations of efavirenz may therefore provide further understanding of therapeutic failure, especially where virological rebound occurs despite adequate plasma levels, and a lack of detectable viral resistance. Here, we determined IC and plasma pharmacokinetics of efavirenz and their relationship with plasma protein binding and P-glycoprotein (P-gp, an active drug efflux transporter) expression.

Patients and methods: Venous blood samples from 10 HIV-infected patients receiving efavirenz (600 mg once a day plus two nucleoside reverse transcriptase inhibitors) were collected over the 24 h dosing interval. Plasma and peripheral blood mononuclear cells (PBMCs) were isolated. Plasma protein bound and unbound efavirenz were separated using ultrafiltration. IC (or cell-associated), total plasma and unbound plasma efavirenz levels were quantified using HPLC-UV. P-gp expression was measured by flow cytometry. Area under the concentration-time curves (AUC0–24) were then calculated using non-compartmental analyses and the IC accumulation expressed as a ratio of IC to plasma AUC0–24.

Results: The median (range) % unbound and IC accumulation ratio was 0.6% (0.4–1.5%) and 1.3 (0.7–3.3), respectively. There was a linear relationship between IC and total AUC0–24 (r2 = 0.59, P = 0.01) but not unbound AUC0–24 (r2 = 0.13, P = 0.75). An inverse correlation between IC AUC0–24 and % unbound was observed (r2 = 41, P = 0.05). There was no relationship between IC AUC0–24 and P-gp expression on the cell surface (r2 < 0.01, P = 0.98).

Conclusions: There was a direct relationship between % bound efavirenz in plasma and IC accumulation implying that the IC accumulation of efavirenz is related to binding to IC proteins or other cellular constituents. Studies investigating the unbound concentration of antiretrovirals inside the cell are now required.

Keywords: antiretrovirals; non-nucleoside reverse transcriptase inhibitors; NNRTIs

Journal Article.  5044 words.  Illustrated.

Subjects: Medical Oncology ; Critical Care

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.