Determination of acrylamide and methacrylamide by normal

dc.contributor.authorPaleologos, E. K.en
dc.contributor.authorKontominas, M. G.en
dc.date.accessioned2015-11-24T16:55:31Z
dc.date.available2015-11-24T16:55:31Z
dc.identifier.issn0021-9673-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10319
dc.rightsDefault Licence-
dc.subjectacrylamideen
dc.subjectmethacrylamideen
dc.subjectacrylic aciden
dc.subjectmethacrylic aciden
dc.subjectnormal phase hplcen
dc.subjectuv detectionen
dc.subjectliquid-chromatographyen
dc.subjectmass-spectrometryen
dc.subjectmaillard reactionen
dc.subjectfoodsen
dc.subjectproductsen
dc.subjectgenotoxicityen
dc.subjectcarcinogenen
dc.titleDetermination of acrylamide and methacrylamide by normalen
heal.abstractA method using normal phase high performance liquid chromatography (NP-HPLC) with UV detection was developed for the analysis of acrylamide and methacrylamide. The method relies on the chromatographic separation of these analytes on a polar HPLC column designed for the separation of organic acids. Identification of acrylamide and methacrylamide is approached dually, that is directly in their protonated forms and as their hydrolysis products acrylic and methacrylic acid respectively, for confirmation. Detection and quantification is performed at 200 nm. The method is simple allowing for clear resolution of the target peaks from any interfering substances. Detection limits of 10 mu g L-1 were obtained for both analytes with the inter- and intra-day RSD for standard analysis lying below 1.0%. Use of acetonitrile in the elution solvent lowers detection limits and retention times, without impairing resolution of peaks. The method was applied for the determination of acrylamide and methacrylamide in spiked food samples without native acrylamide yielding recoveries between 95 and 103%. Finally, commercial samples of french and roasted fries, cookies, cocoa and coffee were analyzed to assess applicability of the method towards acrylamide, giving results similar with those reported in the literature. (C) 2005 Elsevier B.V. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.chroma.2005.04.037-
heal.identifier.secondary<Go to ISI>://000229945600004-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0021967305007958/1-s2.0-S0021967305007958-main.pdf?_tid=02d779699e0747e46c4d469839fdbfd6&acdnat=1333031370_92227a73c92084caa3770f152fa7ae8e-
heal.journalNameJournal of Chromatography Aen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2005-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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