In vitro LC-MS cocktail assays to simultaneously determine human cytochrome p450 activities

被引:43
作者
Dixit, Vaishali
Hariparsad, Niresh
Desai, Pankaj
Unadkat, Jashvant D. [1 ]
机构
[1] Univ Washington, Dept Pharmaceut, Seattle, WA 98195 USA
[2] Univ Cincinnati, Med Ctr, Dept Pharmacokinet & Biopharmaceut, Cincinnati, OH 45221 USA
关键词
cytochrome P450; CYP; in vitro cocktail; liquid chromatography-mass spectrometry; human hepatocytes; simultaneous; induction; microsomes;
D O I
10.1002/bdd.552
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Using liquid chromatography-mass spectrometry (LC-MS), two sensitive cocktail assays were developed, one to simultaneously determine activities of the cytochrome P450 enzymes, CYP1A2 (phenacitin), 2136 (bupropion), 2C8 (amodiaquine) and 2C19 (omperazole), and the other to determine simultaneously activities of CYP3A4/5 (testosterone), 2C9 (tolbutamide) and 2D6 (dextromethorphan). These cocktail assays are sensitive, require only a small amount of microsomal protein, employ selective and high turnover CYP substrates and do not require postincubation extraction. In each of these cocktails, no interactions were observed between the substrates. Combining the two cocktails into a single cocktail resulted in significant inhibition of CYP2D6 by amiodiaquine. These assays were used successfully to determine induction of CYP enzymes in microsomes, isolated from human hepatocytes treated (72h) with or without the prototypic inducer, rifampin. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:257 / 262
页数:6
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