Determination of organochlorine pesticides and polychlorinated biphenyls in chicken eggs by matrix solid phase dispersion

dc.contributor.authorValsamaki, V. I.en
dc.contributor.authorBoti, V. I.en
dc.contributor.authorSakkas, V. A.en
dc.contributor.authorAlbanis, T. A.en
dc.date.accessioned2015-11-24T16:55:40Z
dc.date.available2015-11-24T16:55:40Z
dc.identifier.issn0003-2670-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10340
dc.rightsDefault Licence-
dc.subjectmatrix solid-phase dispersion (mspd)en
dc.subjectorganochlorine pesticides (ocs)en
dc.subjectpolychlorinated biphenyls (pcbs)en
dc.subjectchicken eggsen
dc.subjectchromatography-mass spectrometryen
dc.subjectperformance liquid-chromatographyen
dc.subjectelectron-capture detectionen
dc.subjectgas-chromatographyen
dc.subjectresiduesen
dc.subjectextractionen
dc.subjectsamplesen
dc.subjectfishen
dc.subjectchlorobiphenylsen
dc.subjectoptimizationen
dc.titleDetermination of organochlorine pesticides and polychlorinated biphenyls in chicken eggs by matrix solid phase dispersionen
heal.abstractA multiresidue method for the determination of 20 organochlorine pesticides (aldrin, endrin, dieldrin, alpha-BHC, beta-BHC, gamma-BHC, delta-BHC, alpha-chlordane, gamma-chlordane, 4,4'-DDE, 4,4'-DDT, 4,4'-DDD, endosulfan 1, endosulfan 11, endosulfan sulfate, endrin aldehyde, heptachlor, heptachlor epoxide, endrin ketone and methoxychlor) and eight PCB congeners (PCB 20, 28, 52, 101, 118, 138, 153, 180) in chicken eggs has been developed and validated. The samples were extracted by a simple and fast matrix solid-phase dispersion (MSPD) method using Florisil as the sorbent material and dichloromethane/hexane (1: 1) as the eluting system. Further purification of the extracts was conducted using a conventional clean-up procedure with concentrated sulphuric acid. Determination and quantitation of PCBs and OCs residues was carried out using a gas chromatograph equipped with an electron capture detector (GC-ECD). A mass spectrometric detector (GC-MS) in the selected ion monitoring (SIM) mode was used for confirmation purposes. The method detection limits were < 0.7 ng g(-1) for all PCBs and OCs and the relative standard deviations for analyses of samples fortified over the range of 10-200 ng g(-1) were < 8%. All compounds provided average recoveries (spiked at five concentration levels) ranging from 82% to 110%. The proposed method was used to analyze 30 commercial products taken from local markets in the course of a 3-month sampling campaign. (c) 2006 Elsevier B.V. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.aca.2006.03.050-
heal.identifier.secondary<Go to ISI>://000239524800029-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0003267006006234/1-s2.0-S0003267006006234-main.pdf?_tid=0dadce4cd0ccdea1b3a12813759f6463&acdnat=1333023457_0a43883b5bbac053d1a1166602aa5917-
heal.journalNameAnalytica Chimica Actaen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2006-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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