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dc.contributor.authorJung, Hyun-Jin-
dc.contributor.authorLee, Won-Yong-
dc.contributor.authorYoo, Young Sook-
dc.contributor.authorChung, Bong Chul-
dc.contributor.authorChoi, Man Ho-
dc.date.accessioned2024-01-20T19:03:03Z-
dc.date.available2024-01-20T19:03:03Z-
dc.date.created2021-09-02-
dc.date.issued2010-06-03-
dc.identifier.issn0009-8981-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/131338-
dc.description.abstractBackground: A database-dependent gas chromatography-mass spectrometry (GC-MS) based approach was developed for non-targeted metabolite profiling, focusing on 232 steroids, 24 fatty acids, 10 eicosanoids, 10 cannabinoids and 22 steroid-fatty acid esters in biological specimens. Methods: This method, used to search for potent biomarkers in lipid metabolism, included MS based analysis combined with high-temperature gas chromatographic (HTGC) separation of biological metabolites, statistical clustering and an in-house database (DB) searching. Results: The HTGC technique showed better detectability of high lipophilic compounds, particularly steroid-fatty acid esters, which generally have poor chromatographic properties on a conventional GC column. The in-house DB search consisted of the retention index and mass spectrum corresponding to each compound selected. The method was applied to tissue samples obtained from cardiac hypertrophy-induced mice. Increased levels of palmitic, linoleic, oleic, and stearic acids and cholesterol were detected and identified. Conclusions: This data-dependent non-targeted metabolite profiling technique could be more effective in biomarker studies associated with the steroid and lipid metabolism than commercially available DBs. (C) 2010 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectLIPOTOXIC CARDIOMYOPATHY-
dc.subjectLIPID ANALYSIS-
dc.subjectMETABOLOMICS-
dc.subjectURINE-
dc.subjectDISEASE-
dc.subjectCORTICOSTEROIDS-
dc.subjectHYPERTROPHY-
dc.subjectEXPRESSION-
dc.subjectESTROGENS-
dc.subjectSYSTEMS-
dc.titleDatabase-dependent metabolite profiling focused on steroid and fatty acid derivatives using high-temperature gas chromatography-mass spectrometry-
dc.typeArticle-
dc.identifier.doi10.1016/j.cca.2010.02.068-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCLINICA CHIMICA ACTA, v.411, no.11-12, pp.818 - 824-
dc.citation.titleCLINICA CHIMICA ACTA-
dc.citation.volume411-
dc.citation.number11-12-
dc.citation.startPage818-
dc.citation.endPage824-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000277864200007-
dc.identifier.scopusid2-s2.0-79951972384-
dc.relation.journalWebOfScienceCategoryMedical Laboratory Technology-
dc.relation.journalResearchAreaMedical Laboratory Technology-
dc.type.docTypeArticle-
dc.subject.keywordPlusLIPOTOXIC CARDIOMYOPATHY-
dc.subject.keywordPlusLIPID ANALYSIS-
dc.subject.keywordPlusMETABOLOMICS-
dc.subject.keywordPlusURINE-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusCORTICOSTEROIDS-
dc.subject.keywordPlusHYPERTROPHY-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusESTROGENS-
dc.subject.keywordPlusSYSTEMS-
dc.subject.keywordAuthorMetabolite profiling-
dc.subject.keywordAuthorSteroid-
dc.subject.keywordAuthorFatty acid-
dc.subject.keywordAuthorEicosanoids-
dc.subject.keywordAuthorGC-MS-
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