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Interaction Potential of Etravirine with Drug Transporters Assessed In Vitro
被引:29
|作者:
Zembruski, Nadine Cecile Luise
[1
]
Haefeli, Walter Emil
[1
]
Weiss, Johanna
[1
]
机构:
[1] Univ Heidelberg Hosp, Dept Clin Pharmacol & Pharmacoepidemiol, D-69120 Heidelberg, Germany
关键词:
MULTIDRUG-RESISTANCE PROTEIN-2;
P-GLYCOPROTEIN;
PROTEASE INHIBITORS;
PHARMACOKINETICS;
ATAZANAVIR;
RITONAVIR;
BLOCKERS;
RECEPTOR;
TMC125;
CELLS;
D O I:
10.1128/AAC.01527-10
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Etravirine is a novel nonnucleoside reverse transcriptase inhibitor (NNRTI) for the treatment of HIV-1 infections. ABC transporters potentially mediate clinically relevant drug-drug interactions. We assessed substrate characteristics and the inhibitory and inductive potential of etravirine on ABC transporters. Etravirine did not inhibit P-gp/ABCB1 and was not transported by the tested ABC transporters but was a potent inhibitor of BCRP/ABCG2. Etravirine induced several ABC transporters, especially BCRP/ABCG2. These data demonstrate that etravirine has the potential for drug-drug interactions by modulation of expression and function of several ABC transporters.
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页码:1282 / 1284
页数:3
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