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Direct and metabolism-dependent cytochrome P45 inhibition assays for evaluating drug–drug interactions



Direct and metabolism-dependent cytochrome P45 inhibition assays for evaluating drug–drug interactions







We developed methods for evaluating the ntial inhibition of human cytochrome P45 (CYP) enzymes, including CYP1A2, CYP2A6, CYP2B6, CYP2?C9, CYP2?C19, CYP2D6, CYP2E1 and CYP3A4, using pooled human liver microsomes (HLMs). The CYP inhibition assay used substrate cocktail sets [set A: phenacetin for CYP1A2, coumarin for CYP2A6, (S)-(+)-mephenytoin for CYP2C19, dextromethorphan for CYP2D6 and midazolam for CYP3A4; set B: bupropion for CYP2B6, tolbutamide for CYP2C9, chlorzoxazone for CYP2E1, and testosterone for CYP3A4] with quantitation by liquid chromatography tandem mass spectrometry. A direct inhibition assay was performed with the substrate cocktails without ?-nicotinamide adenine dinucleotide phosphate (NADPH) pre-incubation, and a metabolism-dependent inhibition (MDI) assay was performed after 3?min of pre-incubation with NADPH in HLMs. MDI was identified based on the half-maximal inhibitory concentration (IC5) shifts. The IC5 values of the direct inhibitors determined using the probe substrate cocktails were in good agreement with previously reported values. Eight metabolism-dependent inhibitors including furafylline, 8-methoxypsoralen, tienilic acid, ticlopidine, fluoxetine, paroxetine, disulfiram and verapamil against CYP1A2, CYP2A6, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and CYP3A4, respectively, resulted in significant IC5 shifts (?2.5-fold) after pre-incubation. Thus, these CYP inhibition assays are considered to be useful tools for evaluating both direct inhibition and MDI at an early stage of the drug discovery and development process.

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