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dc.contributor.authorIslam, M. Nurul-
dc.contributor.authorYoo, Hye Hyun-
dc.contributor.authorLee, Jun-
dc.contributor.authorNam, Joo Won-
dc.contributor.authorSeo, Eun Kyoung-
dc.contributor.authorJin, Changbae-
dc.contributor.authorKim, Dong-Hyun-
dc.date.accessioned2024-01-20T22:31:51Z-
dc.date.available2024-01-20T22:31:51Z-
dc.date.created2021-09-03-
dc.date.issued2008-11-
dc.identifier.issn1060-3271-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/133023-
dc.description.abstractThe rhizomes of Anemarrhena asphodeloides Bunge (Liliaceae) are prescribed as crude drugs in herbal medication for the treatment of various diseases such as diabetes, inflammation, and platelet aggregation inhibition. A simple, sensitive, and precise reversed-phase liquid chromatographic method was developed to study the quantitative determination of 5 bioactive compounds from these rhizomes, namely, neomangiferin, mangiferin, isomangiferin, nyasol, and methylnyasol. Chromatographic analysis was performed on Capcell Pak C-18 column (150 x 4.6 mm, 3 mu m) with a mobile phase consisting of acetonitrile, methanol, and 0.1% formic acid at a flow rate of 1.00 mL/min. Quantitation was performed using a UV-visible detector at 260 nm. The method for the determination of reported medicinal agents was accurate and reproducible. Excellent linear behavior was observed over the investigated concentration range of 2.5-100.0 mu g/mL for neomangiferin; 1.5-60.0 mu g/mL for mangiferin; 0.5-20.0 mu g/mL for nyasol; and 0.2-20.0 mu g/mL for methylnyasol; correlation coefficient > 0.99. The intraday and interday precision over the concentration range of compounds was < 6.6% (relative standard deviation) and accuracy was between 94.9 and 109.3%. This method can be successfully applied for the analysis of medicinal compounds from the ethanolic extract of A. asphodeloides Bunge.-
dc.languageEnglish-
dc.publisherAOAC INT-
dc.subjectTANDEM MASS-SPECTROMETRY-
dc.subjectSWERTIA-MUSSOTII FRANCH-
dc.subjectRAT PLASMA-
dc.subjectCAPILLARY-ELECTROPHORESIS-
dc.subjectANTIDIABETIC ACTIVITY-
dc.subjectHYPOGLYCEMIC ACTIVITY-
dc.subjectACTIVE CONSTITUENTS-
dc.subjectMANGIFERIN-
dc.subjectIDENTIFICATION-
dc.subjectDIFFERENTIATION-
dc.titleSimultaneous Determination of Bioactive Xanthone Glycosides and Norlignans from Ethanolic Extract of Anemarrhena asphodeloides by Liquid Chromatography-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF AOAC INTERNATIONAL, v.91, no.6, pp.1271 - 1277-
dc.citation.titleJOURNAL OF AOAC INTERNATIONAL-
dc.citation.volume91-
dc.citation.number6-
dc.citation.startPage1271-
dc.citation.endPage1277-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000262118200006-
dc.identifier.scopusid2-s2.0-58449134302-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaFood Science & Technology-
dc.type.docTypeArticle-
dc.subject.keywordPlusTANDEM MASS-SPECTROMETRY-
dc.subject.keywordPlusSWERTIA-MUSSOTII FRANCH-
dc.subject.keywordPlusRAT PLASMA-
dc.subject.keywordPlusCAPILLARY-ELECTROPHORESIS-
dc.subject.keywordPlusANTIDIABETIC ACTIVITY-
dc.subject.keywordPlusHYPOGLYCEMIC ACTIVITY-
dc.subject.keywordPlusACTIVE CONSTITUENTS-
dc.subject.keywordPlusMANGIFERIN-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusDIFFERENTIATION-
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