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dc.contributor.authorLee, Su Hyeon-
dc.contributor.authorLee, Nanhee-
dc.contributor.authorHong, Youngmin-
dc.contributor.authorChung, Bong Chul-
dc.contributor.authorChoi, Man Ho-
dc.date.accessioned2024-01-20T02:33:50Z-
dc.date.available2024-01-20T02:33:50Z-
dc.date.created2021-09-04-
dc.date.issued2016-12-06-
dc.identifier.issn0003-2700-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/123325-
dc.description.abstractSulfated steroids can act as a latent form of active free steroids, coexisting with them in biological specimens. To evaluate the metabolic significance of free and sulfated steroid species, a simultaneous analysis of eight free steroids [cholesterol, pregnenolone, 17 alpha-hydroxypregnenolone, progesterone, 17 alpha-hydroxyprogesterone, dehydroepiandrosterone (DHEA), testosterone, and 17 beta-estradiol] and four biologically relevant sulfated steroids was developed and validated, using selected-ion and multiple-reaction monitoring modes coupled to polarity-switching liquid chromatography/mass spectrometry (LC/MS). All steroids were separated on a reversed-phase phenyl column (50 mm X 2 mm, 3 mu m) at a flow rate of 0.5 mL/min. The limits of quantification ranged from 0.1 to 50 ng/mL at extraction recoveries of 94.1-105.5%, while the precision and accuracy were 2.5-9.3% and 92.4-105.9%, respectively. Quantitative results obtained for samples from obese girls showed that the serum levels of DHEA sulfate were significantly increased (P = 0.004), along with the metabolic ratio representing DHEA sulfotransferase (P < 0.02). The developed novel LC/MS method can quantitatively profile both free and sulfated steroids in a single analytical run.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectDEHYDROEPIANDROSTERONE-SULFATE-
dc.subjectLC-MS/MS-
dc.subjectHUMAN SERUM-
dc.subjectBODY-FAT-
dc.subjectCHOLESTEROL-
dc.subjectOBESITY-
dc.subjectWEIGHT-
dc.subjectSEX-
dc.subjectCHILDREN-
dc.subjectHORMONES-
dc.titleSimultaneous Analysis of Free and Sulfated Steroids by Liquid Chromatography/Mass Spectrometry with Selective Mass Spectrometric Scan Modes and Polarity Switching-
dc.typeArticle-
dc.identifier.doi10.1021/acs.analchem.6b03183-
dc.description.journalClass1-
dc.identifier.bibliographicCitationANALYTICAL CHEMISTRY, v.88, no.23, pp.11624 - 11630-
dc.citation.titleANALYTICAL CHEMISTRY-
dc.citation.volume88-
dc.citation.number23-
dc.citation.startPage11624-
dc.citation.endPage11630-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000389556900053-
dc.identifier.scopusid2-s2.0-85030691436-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusDEHYDROEPIANDROSTERONE-SULFATE-
dc.subject.keywordPlusLC-MS/MS-
dc.subject.keywordPlusHUMAN SERUM-
dc.subject.keywordPlusBODY-FAT-
dc.subject.keywordPlusCHOLESTEROL-
dc.subject.keywordPlusOBESITY-
dc.subject.keywordPlusWEIGHT-
dc.subject.keywordPlusSEX-
dc.subject.keywordPlusCHILDREN-
dc.subject.keywordPlusHORMONES-
dc.subject.keywordAuthorsteroid sulfate-
dc.subject.keywordAuthormass spectrometry-
dc.subject.keywordAuthorreproductive steroid-
dc.subject.keywordAuthorobesity-
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