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Evaluation of intermediate compounds in β-carboline alkaloids formation using model system including isotope labeled glycerol

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dc.contributor.authorLim, Kyung-Jik-
dc.contributor.authorShin, Han-Seung-
dc.date.accessioned2025-08-05T03:00:12Z-
dc.date.available2025-08-05T03:00:12Z-
dc.date.issued2025-11-
dc.identifier.issn0308-8146-
dc.identifier.issn1873-7072-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/58863-
dc.description.abstractβ-carbolines (βCs) such as norharman and harman are thermally formed in foods and have been associated with neurotoxic and mutagenic effects. This study explores glycerol-derived intermediates in βC formation, identifying 3-vinylindole as a key intermediate via isotope labeling. Model systems with labeled glycerol were used for carbon tracing. Quantitation and structural analysis were performed by HPLC, LC-MS/MS, and ESI-qTOF-MS/MS. In applied model system, formaldehyde levels increased from 33.77 to 77.12 mg/kg. Correspondingly, norharman concentrations rose from 98.59 to 680.19 μg/kg, demonstrating a dose-dependent relationship between glycerol content and βC formation. Time-resolved profiling showed 3-vinylindole peaked at 10 min and declined, while norharman concentration concurrently increased, supporting its role as a transient intermediate. Isotope tracing further confirmed a + 2 Da mass shift in 3-vinylindole, indicating the incorporation of glycerol-derived carbons. These findings elucidate a novel pathway for βC formation under thermal conditions and highlight glycerol's contribution to this process during food processing. © 2025 Elsevier Ltd-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier Ltd-
dc.titleEvaluation of intermediate compounds in β-carboline alkaloids formation using model system including isotope labeled glycerol-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.foodchem.2025.145522-
dc.identifier.scopusid2-s2.0-105011032830-
dc.identifier.wosid001541382800002-
dc.identifier.bibliographicCitationFood Chemistry, v.492, pp 1 - 11-
dc.citation.titleFood Chemistry-
dc.citation.volume492-
dc.citation.startPage1-
dc.citation.endPage11-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalResearchAreaNutrition & Dietetics-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.relation.journalWebOfScienceCategoryNutrition & Dietetics-
dc.subject.keywordPlusPICTET-SPENGLER REACTION-
dc.subject.keywordPlusHETEROCYCLIC AMINES-
dc.subject.keywordPlusMASS-SPECTROMETRY-
dc.subject.keywordPlusMAILLARD REACTION-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusTRYPTOPHAN-
dc.subject.keywordAuthorAldehydes-
dc.subject.keywordAuthorGlycerol-
dc.subject.keywordAuthorIndole-based intermediate-
dc.subject.keywordAuthorThermal reaction-
dc.subject.keywordAuthorβ-Carboline alkaloid-
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