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dc.contributor.authorGabaldón, José Antonio
dc.contributor.authorNúñez Delicado, Estrella
dc.contributor.authorMercader Ros, María Teresa
dc.contributor.authorLucas Abellán, Carmen
dc.contributor.authorFortea Gorbe, María Isabel
dc.date.accessioned2017-07-24T11:44:24Z
dc.date.available2017-07-24T11:44:24Z
dc.date.issued2010
dc.identifier.citation37es
dc.identifier.isbn0308-8146
dc.identifier.urihttp://hdl.handle.net/10952/2386
dc.description.abstractThe beneficial effects from phenolic compounds have been attributed to their antioxidant activity. Differences in the chemical structure of flavonols and their degree of substitution will influence phenoxyl radical stability and, thereby, their antioxidant properties. Cyclodextrins (CDs) can be used as a flavonol complexation agent, since they act as a substrate reservoir in a dose-controlled manner. In the present paper, the effect of complexing flavonols, kaempferol, quercetin and myricetin with HP-b-CDs on their antioxidant capacity is studied by means of the oxygen radical absorbance capacity-fluorescein (ORAC-FL) assay. This complexation phenomenon increased the antioxidant activity of the three flavonols, which reached a maximum level when each flavonol had been complexed in the hydrophobic cavity of CDs. The antioxidant activity increased because of the flavonol was protected against rapid oxidation by free radicals.es
dc.language.isoenes
dc.publisherElsevier Ltdes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectFlavonols Antioxidant activity ORAC-FL Cyclodextrins Kaempferol Quercetin Myricetines
dc.titleEffect of HP-b-cyclodextrins complexation on the antioxidant activity of flavonolses
dc.typearticlees
dc.rights.accessRightsopenAccesses
dc.journal.titleFood Chemistryes
dc.volume.number118es
dc.issue.number769-773es
dc.description.disciplineCiencias de la Alimentaciónes


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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