Effect of standard phenolic compounds and olive oil phenolic extracts on acrylamide formation in an emulsion system

dc.contributor.authorKotsiou, K.en
dc.contributor.authorTasioula-Margari, M.en
dc.contributor.authorCapuano, E.en
dc.contributor.authorFogliano, V.en
dc.date.accessioned2015-11-24T16:57:08Z
dc.date.available2015-11-24T16:57:08Z
dc.identifier.issn0308-8146-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10541
dc.rightsDefault Licence-
dc.subjectacrylamideen
dc.subjectemulsionen
dc.subjectphenolic compoundsen
dc.subjectsterilisation temperatureen
dc.subjectvirgin olive oilen
dc.subjectmodel systemsen
dc.subjectbamboo leavesen
dc.subjectantioxidanten
dc.subjectdegradationen
dc.subjectreductionen
dc.subjectoxidationen
dc.subjectbehavioren
dc.subjectkineticsen
dc.subjectcrispsen
dc.subjectbreaden
dc.titleEffect of standard phenolic compounds and olive oil phenolic extracts on acrylamide formation in an emulsion systemen
heal.abstractIn this work the effect of standard phenolic compounds such as trolox, phenolic acids (ferulic, gallic, protocatechuic and caffeic acid) and secoiridoids, extracted from virgin olive oil (VOO), on acrylamide formation in an emulsion system was investigated. The emulsion system was heated in an oil bath at different temperatures and for different periods of time. At 105 and 115 degrees C the generated amounts of acrylamide were negligible during the monitoring time. At 125 degrees C addition of standard phenolic compounds reduced acrylamide formation which was more pronounced at initial time of heating (20 min) reaching up to 70%. Protocatechuic and gallic acid were more effective than trolox, caffeic and ferulic acid in acrylamide reduction at the final time intervals of heating (30-60 min). On the contrary, addition of VOO extract in the emulsion system resulted in a remarkable increase of acrylamide level, which was ascribed to secoiridoids' structure containing aldehydic groups. (C) 2010 Elsevier Ltd. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.foodchem.2010.06.025-
heal.identifier.secondary<Go to ISI>://000282500000034-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0308814610007351/1-s2.0-S0308814610007351-main.pdf?_tid=e4fc4dc4-406e-11e3-b6c3-00000aab0f6b&acdnat=1383033258_0f250d8ce838e82aa5b93098e0c2cab4-
heal.journalNameFood Chemistryen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2011-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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