Full metadata record

DC Field Value Language
dc.contributor.authorOh, Hyun-A-
dc.contributor.authorLee, Hyunbeom-
dc.contributor.authorKim, Donghak-
dc.contributor.authorJung, Byung Hwa-
dc.date.accessioned2024-01-20T02:03:36Z-
dc.date.available2024-01-20T02:03:36Z-
dc.date.created2021-09-01-
dc.date.issued2017-02-15-
dc.identifier.issn0003-2697-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/123063-
dc.description.abstractAs 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.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectHUMAN LIVER-MICROSOMES-
dc.subjectIN-VITRO-
dc.subjectMASS-SPECTROMETRY-
dc.subjectDRUG-INTERACTION-
dc.subjectLIQUID-CHROMATOGRAPHY-
dc.subjectCOCKTAIL APPROACH-
dc.subjectINHIBITION ASSAY-
dc.subjectCYP450 ENZYMES-
dc.subjectLC-MS/MS-
dc.subjectMEDICINE-
dc.titleDevelopment of GC-MS based cytochrome P450 assay for the investigation of multi-herb interaction-
dc.typeArticle-
dc.identifier.doi10.1016/j.ab.2016.12.015-
dc.description.journalClass1-
dc.identifier.bibliographicCitationANALYTICAL BIOCHEMISTRY, v.519, pp.71 - 83-
dc.citation.titleANALYTICAL BIOCHEMISTRY-
dc.citation.volume519-
dc.citation.startPage71-
dc.citation.endPage83-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000392560300011-
dc.identifier.scopusid2-s2.0-85007110960-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusHUMAN LIVER-MICROSOMES-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusMASS-SPECTROMETRY-
dc.subject.keywordPlusDRUG-INTERACTION-
dc.subject.keywordPlusLIQUID-CHROMATOGRAPHY-
dc.subject.keywordPlusCOCKTAIL APPROACH-
dc.subject.keywordPlusINHIBITION ASSAY-
dc.subject.keywordPlusCYP450 ENZYMES-
dc.subject.keywordPlusLC-MS/MS-
dc.subject.keywordPlusMEDICINE-
dc.subject.keywordAuthorGC-MS-
dc.subject.keywordAuthorHuman liver microsomes-
dc.subject.keywordAuthorCytochrome P450-
dc.subject.keywordAuthorCocktail approach-
dc.subject.keywordAuthorSocheongryong-tang-
Appears in Collections:
KIST Article > 2017
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE