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Hydrophillic Interaction Chromatography-tandem Mass Spectrometry Method for Identification and Quantitation of 5-MeO-DIPT and its Metabolites in Rat Urine

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dc.contributor.authorKim, Yoon-
dc.contributor.authorKim, Un Yong-
dc.contributor.authorIn, Moon Kyo-
dc.contributor.authorLee, Jaeick-
dc.contributor.authorKwon, Oh-Seung-
dc.contributor.authorYoo, Hye Hyun-
dc.date.accessioned2021-06-23T11:03:06Z-
dc.date.available2021-06-23T11:03:06Z-
dc.date.created2021-01-21-
dc.date.issued2011-04-
dc.identifier.issn0253-2964-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/38130-
dc.description.abstract5-Methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT), a psychoactive tryptamine derivative, is a hallucinogenic drug of abuse. In this study, 5-OH-DIPT and its metabolites were identified and the quantitative method was developed and validated by using hydrophilic interaction chromatography-tandem mass spectrometry (HILIC-MS/MS). Chromatographic separation was achieved on an Atlantis HILIC silica column (5 mu m, 100 x 2.1 mm). The metabolites of 5-MeO-DIPT in rat urine were characterized via Q1 scanning and product ion scanning. As a consequence, 5-MeO-IPT, 5-OH-DIPT, 6-OH-5-MeO-DIPT and their glucuronide conjugates were detected and identified as the metabolites of 5-MeO-DIPT. Subsequently, a quantitative method for 5-MeO-DIPT and its major metabolites, 5-MeO-IPT and 5-OH-DIPT, was developed in multiple reactions monitoring (MRM) mode. The calibration curves for all analytes evidenced good linearity over the concentration range of 11000 ng/mL with linear correlation co-efficients (r(2)) in excess of 0.99. The intra- and inter-day accuracy and precision were 92.2-110.2% and 1.5-9.9%, respectively.-
dc.language영어-
dc.language.isoen-
dc.publisher대한화학회-
dc.titleHydrophillic Interaction Chromatography-tandem Mass Spectrometry Method for Identification and Quantitation of 5-MeO-DIPT and its Metabolites in Rat Urine-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoo, Hye Hyun-
dc.identifier.doi10.5012/bkcs.2011.32.4.1158-
dc.identifier.scopusid2-s2.0-79954569828-
dc.identifier.wosid000290366200011-
dc.identifier.bibliographicCitationBulletin of the Korean Chemical Society, v.32, no.4, pp.1158 - 1164-
dc.relation.isPartOfBulletin of the Korean Chemical Society-
dc.citation.titleBulletin of the Korean Chemical Society-
dc.citation.volume32-
dc.citation.number4-
dc.citation.startPage1158-
dc.citation.endPage1164-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001545182-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlus5-METHOXY-N,N-DIISOPROPYLTRYPTAMINE-
dc.subject.keywordPlusPHENETHYLAMINES-
dc.subject.keywordPlusCONFIRMATION-
dc.subject.keywordPlusTRYPTAMINES-
dc.subject.keywordPlusFOXY-
dc.subject.keywordAuthor5-MeO-DIPT-
dc.subject.keywordAuthorHILIC-MS/MS-
dc.subject.keywordAuthorMetabolites-
dc.subject.keywordAuthorProfiling-
dc.subject.keywordAuthorQuantitation-
dc.identifier.urlhttp://koreascience.or.kr/article/JAKO201115037886521.page-
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