A Focused Multiple Reaction Monitoring (MRM) Quantitative Method for Bioactive Grapevine Stilbenes by Ultra-High-Performance Liquid Chromatography Coupled to Triple-Quadrupole Mass Spectrometry (UHPLC-QqQ)

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Campo DCValorIdioma
dc.contributorProteómica y Genómica Funcional de Plantases_ES
dc.contributor.authorHurtado-Gaitán, Elías-
dc.contributor.authorSellés-Marchart, Susana-
dc.contributor.authorMartínez Márquez, Ascensión-
dc.contributor.authorSamper-Herrero, Antonio-
dc.contributor.authorBru-Martinez, Roque-
dc.contributor.otherUniversidad de Alicante. Departamento de Agroquímica y Bioquímicaes_ES
dc.date.accessioned2017-03-14T08:31:47Z-
dc.date.available2017-03-14T08:31:47Z-
dc.date.issued2017-03-07-
dc.identifier.citationHurtado-Gaitán E, Sellés-Marchart S, Martínez-Márquez A, Samper-Herrero A, Bru-Martínez R. A Focused Multiple Reaction Monitoring (MRM) Quantitative Method for Bioactive Grapevine Stilbenes by Ultra-High-Performance Liquid Chromatography Coupled to Triple-Quadrupole Mass Spectrometry (UHPLC-QqQ). Molecules. 2017; 22(3):418. doi:10.3390/molecules22030418es_ES
dc.identifier.issn1420-3049-
dc.identifier.urihttp://hdl.handle.net/10045/64367-
dc.description.abstractGrapevine stilbenes are a family of polyphenols which derive from trans-resveratrol having antifungal and antimicrobial properties, thus being considered as phytoalexins. In addition to their diverse bioactive properties in animal models, they highlight a strong potential in human health maintenance and promotion. Due to this relevance, highly-specific qualitative and quantitative methods of analysis are necessary to accurately analyze stilbenes in different matrices derived from grapevine. Here, we developed a rapid, sensitive, and specific analysis method using ultra-high-performance liquid chromatography coupled to triple-quadrupole mass spectrometry (UHPLC-QqQ) in MRM mode to detect and quantify five grapevine stilbenes, trans-resveratrol, trans-piceid, trans-piceatannol, trans-pterostilbene, and trans-ε-viniferin, whose interest in relation to human health is continuously growing. The method was optimized to minimize in-source fragmentation of piceid and to avoid co-elution of cis-piceid and trans-resveratrol, as both are detected with resveratrol transitions. The applicability of the developed method of stilbene analysis was tested successfully in different complex matrices including cellular extracts of Vitis vinifera cell cultures, reaction media of biotransformation assays, and red wine.es_ES
dc.description.sponsorshipA.M.-M. acknowledges a grant from Conselleria d’Educacio, Cultura I Sport de la Generalitat Valenciana (FPA/2013/A/074). This work has been supported by grants from University of Alicante (VIGROB-105), the Spanish Ministry of Economy and Competitiveness (BIO2014-51861-R), and European funds for Regional development (FEDER).es_ES
dc.languageenges_ES
dc.publisherMDPIes_ES
dc.rights© 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.subjectUHPLCes_ES
dc.subjectMRMes_ES
dc.subjectResveratroles_ES
dc.subjectPiceides_ES
dc.subjectPiceatannoles_ES
dc.subjectEpsilon-viniferines_ES
dc.subjectPterostilbenees_ES
dc.subjectCell culturees_ES
dc.subjectBioconversiones_ES
dc.subjectWinees_ES
dc.subject.otherBioquímica y Biología Moleculares_ES
dc.titleA Focused Multiple Reaction Monitoring (MRM) Quantitative Method for Bioactive Grapevine Stilbenes by Ultra-High-Performance Liquid Chromatography Coupled to Triple-Quadrupole Mass Spectrometry (UHPLC-QqQ)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.3390/molecules22030418-
dc.relation.publisherversionhttp://dx.doi.org/10.3390/molecules22030418es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//BIO2014-51861-R-
Aparece en las colecciones:INV - Proteómica y Genómica Funcional de Plantas - Artículos de Revistas

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