Development of GC-MS based cytochrome P450 assay for the investigation of multi-herb interaction

Authors
Oh, Hyun-ALee, HyunbeomKim, DonghakJung, Byung Hwa
Issue Date
2017-02-15
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Citation
ANALYTICAL BIOCHEMISTRY, v.519, pp.71 - 83
Abstract
As drug interactions with cytochrome P450 enzymes become increasingly important in the field of drug discovery, a high-throughput screening method for analysing the effects of a drug is needed. We have developed a simple and rapid simultaneous analytical method using a cocktail approach for measuring the activities of seven cytochrome P450 enzymes (CYP1A2, CYP2A6, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and CYP3A4). Human liver microsomes were used as a source for the seven cytochrome P450 enzymes, and a gas chromatography-mass spectrometry (GC-MS) was used for analysing their activities. Kinetic studies and inhibition assays of CYP enzymes were performed using known substrates and inhibitors for validating and comparing the reaction rates and time-dependent activities between methods using each substrate versus a method using a cocktail solution. The optimized cocktail method was successfully applied to evaluate the effects of the decoction of Socheongryong-tang (SCRT) on cytochrome P450 enzymes. Our cocktail method provides a simultaneous high-throughput activity assay using GC-MS for the first time. This method is applicable for analysing the drug interactions of various plant-derived mixtures. (C) 2016 Elsevier Inc. All rights reserved.
Keywords
HUMAN LIVER-MICROSOMES; IN-VITRO; MASS-SPECTROMETRY; DRUG-INTERACTION; LIQUID-CHROMATOGRAPHY; COCKTAIL APPROACH; INHIBITION ASSAY; CYP450 ENZYMES; LC-MS/MS; MEDICINE; HUMAN LIVER-MICROSOMES; IN-VITRO; MASS-SPECTROMETRY; DRUG-INTERACTION; LIQUID-CHROMATOGRAPHY; COCKTAIL APPROACH; INHIBITION ASSAY; CYP450 ENZYMES; LC-MS/MS; MEDICINE; GC-MS; Human liver microsomes; Cytochrome P450; Cocktail approach; Socheongryong-tang
ISSN
0003-2697
URI
https://pubs.kist.re.kr/handle/201004/123063
DOI
10.1016/j.ab.2016.12.015
Appears in Collections:
KIST Article > 2017
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