Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Oh, Hyun-A | - |
dc.contributor.author | Lee, Hyunbeom | - |
dc.contributor.author | Kim, Donghak | - |
dc.contributor.author | Jung, Byung Hwa | - |
dc.date.accessioned | 2024-01-20T02:03:36Z | - |
dc.date.available | 2024-01-20T02:03:36Z | - |
dc.date.created | 2021-09-01 | - |
dc.date.issued | 2017-02-15 | - |
dc.identifier.issn | 0003-2697 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/123063 | - |
dc.description.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. | - |
dc.language | English | - |
dc.publisher | ACADEMIC PRESS INC ELSEVIER SCIENCE | - |
dc.subject | HUMAN LIVER-MICROSOMES | - |
dc.subject | IN-VITRO | - |
dc.subject | MASS-SPECTROMETRY | - |
dc.subject | DRUG-INTERACTION | - |
dc.subject | LIQUID-CHROMATOGRAPHY | - |
dc.subject | COCKTAIL APPROACH | - |
dc.subject | INHIBITION ASSAY | - |
dc.subject | CYP450 ENZYMES | - |
dc.subject | LC-MS/MS | - |
dc.subject | MEDICINE | - |
dc.title | Development of GC-MS based cytochrome P450 assay for the investigation of multi-herb interaction | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.ab.2016.12.015 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | ANALYTICAL BIOCHEMISTRY, v.519, pp.71 - 83 | - |
dc.citation.title | ANALYTICAL BIOCHEMISTRY | - |
dc.citation.volume | 519 | - |
dc.citation.startPage | 71 | - |
dc.citation.endPage | 83 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000392560300011 | - |
dc.identifier.scopusid | 2-s2.0-85007110960 | - |
dc.relation.journalWebOfScienceCategory | Biochemical Research Methods | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Analytical | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | HUMAN LIVER-MICROSOMES | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | MASS-SPECTROMETRY | - |
dc.subject.keywordPlus | DRUG-INTERACTION | - |
dc.subject.keywordPlus | LIQUID-CHROMATOGRAPHY | - |
dc.subject.keywordPlus | COCKTAIL APPROACH | - |
dc.subject.keywordPlus | INHIBITION ASSAY | - |
dc.subject.keywordPlus | CYP450 ENZYMES | - |
dc.subject.keywordPlus | LC-MS/MS | - |
dc.subject.keywordPlus | MEDICINE | - |
dc.subject.keywordAuthor | GC-MS | - |
dc.subject.keywordAuthor | Human liver microsomes | - |
dc.subject.keywordAuthor | Cytochrome P450 | - |
dc.subject.keywordAuthor | Cocktail approach | - |
dc.subject.keywordAuthor | Socheongryong-tang | - |
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