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Potential of novel antiretrovirals to modulate expression and function of drug transporters in vitro
Author(s) -
Nadine Cécile Luise Zembruski,
Gabriele Büchel,
L. Jodicke,
Melanie Herzog,
Walter E. Haefeli,
Johanna Weiß
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/dkq501
Subject(s) - raltegravir , elvitegravir , abcg2 , multidrug resistance associated protein 2 , pharmacology , atp binding cassette transporter , maraviroc , transporter , efflux , p glycoprotein , biology , multiple drug resistance , chemistry , drug resistance , biochemistry , virology , viral load , microbiology and biotechnology , human immunodeficiency virus (hiv) , antiretroviral therapy , gene
The chemokine receptor antagonists maraviroc and vicriviroc and the integrase inhibitors elvitegravir and raltegravir are novel antiretroviral agents for the treatment of HIV-1 infections. ATP-binding cassette (ABC) transporters as modulators of the effectiveness and safety of therapy can mediate viral resistance and drug-drug interactions. To expand knowledge on drug-drug interactions of these antiretrovirals we investigated whether these compounds are substrates, inhibitors or inducers of important ABC transporters.

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