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Cell disposition of raltegravir and newer antiretrovirals in HIV-infected patients: high inter-individual variability in raltegravir cellular penetration
Author(s) -
Aurélie Fayet Mello,
Thierry Buclin,
Céline Franc,
Sara Colombo,
S. Cruchon,
N. Guignard,
Jérôme Biollaz,
Amalio Telenti,
Laurent A. Décosterd,
Matthias Cavassini
Publication year - 2011
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkr151
Subject(s) - raltegravir , darunavir , maraviroc , etravirine , pharmacokinetics , pharmacology , chemistry , integrase inhibitor , ritonavir , chromatography , viral load , medicine , human immunodeficiency virus (hiv) , immunology , antiretroviral therapy
The site of pharmacological activity of raltegravir is intracellular. Our aim was to determine the extent of raltegravir cellular penetration and whether raltegravir total plasma concentration (C(tot)) predicts cellular concentration (C(cell)).

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