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dc.contributor.authorRyu, J.-C.-
dc.contributor.authorSong, Y.-S.-
dc.contributor.authorKim, M.-
dc.contributor.authorCho, J.-H.-
dc.contributor.authorYun-Choi, H.S.-
dc.date.accessioned2024-01-21T22:35:56Z-
dc.date.available2024-01-21T22:35:56Z-
dc.date.created2021-09-02-
dc.date.issued1993-03-
dc.identifier.issn0253-6269-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/146100-
dc.description.abstract(±)-Higenamine is known as a cardiotonic principle of aconite root (root of Aconitum spp., Ranunculaceae). A simple and sensitive detection method for higenamine was developed by using gas chromatography-mass spectrometry (GC/MS). The recovery of higenamine after extraction and concentration with XAD-2 resin column was around 95% from rat biological fluids such as bile, plasma and urine. The limits of detection of higenamine in these biological fluids were approximately 0.1 ng/ml each. It has well been suggested that tetrahydroisoquinolines possessing catechol moiety such as higenamine should be subjected to the catechol-O-methyl transferase (COMT) activity in vivo. We detected two major peaks of presumed metabolites of higenamine in the total ion chromatogram obtained from the rat urine sample after the oral administration of (±)-higenamine. The scan mass spectrum of one of the metabolites coincided with those obtained from coclaurine (C6-O-methyl higenamine) and those of the other metabolite are suggestive of isococlaurine (C7-O-methyl higenamine). ? 1993, The Pharmaceutical Society of Korea. All rights reserved.-
dc.languageEnglish-
dc.subjectcardiotonic agent-
dc.subjectdrug metabolite-
dc.subjecthigenamine-
dc.subjectanimal experiment-
dc.subjectarticle-
dc.subjectderivatization-
dc.subjectdrug bile level-
dc.subjectdrug blood level-
dc.subjectdrug determination-
dc.subjectdrug urine level-
dc.subjectextraction-
dc.subjectgas chromatography-
dc.subjectmale-
dc.subjectmass spectrometry-
dc.subjectnonhuman-
dc.subjectoral drug administration-
dc.subjectrat-
dc.titleIdentification of higenamine and its metabolites in rat by gas chromatography/mass spectrometry-
dc.typeArticle-
dc.identifier.doi10.1007/BF02974485-
dc.description.journalClass1-
dc.identifier.bibliographicCitationArchives of Pharmacal Research, v.16, no.3, pp.213 - 218-
dc.citation.titleArchives of Pharmacal Research-
dc.citation.volume16-
dc.citation.number3-
dc.citation.startPage213-
dc.citation.endPage218-
dc.description.journalRegisteredClassscopus-
dc.identifier.scopusid2-s2.0-0027494746-
dc.type.docTypeArticle-
dc.subject.keywordPluscardiotonic agent-
dc.subject.keywordPlusdrug metabolite-
dc.subject.keywordPlushigenamine-
dc.subject.keywordPlusanimal experiment-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusderivatization-
dc.subject.keywordPlusdrug bile level-
dc.subject.keywordPlusdrug blood level-
dc.subject.keywordPlusdrug determination-
dc.subject.keywordPlusdrug urine level-
dc.subject.keywordPlusextraction-
dc.subject.keywordPlusgas chromatography-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusmass spectrometry-
dc.subject.keywordPlusnonhuman-
dc.subject.keywordPlusoral drug administration-
dc.subject.keywordPlusrat-
dc.subject.keywordAuthorCoclaurine-
dc.subject.keywordAuthorGas chromatography/Mass spectrometry-
dc.subject.keywordAuthorHigenamine-
dc.subject.keywordAuthorIsococlaume-
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