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dc.contributor.authorFiamegos, Y. C.en
dc.contributor.authorNanos, C. G.en
dc.contributor.authorStalikas, C. D.en
dc.date.accessioned2015-11-24T16:51:54Z-
dc.date.available2015-11-24T16:51:54Z-
dc.identifier.issn1570-0232-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9803-
dc.rightsDefault Licence-
dc.subjectamino acidsen
dc.subjectethylchloroformateen
dc.subjectderivatizationen
dc.subjecturineen
dc.subjectsingle-drop microextractionen
dc.subjectgcen
dc.subjectperformance liquid-chromatographyen
dc.subjectmass-spectrometryen
dc.subjectcapillary-electrophoresisen
dc.subjectsolvent microextractionen
dc.subjectflow-injectionen
dc.subjectderivativesen
dc.subjectsamplesen
dc.subjectionizationen
dc.subjectextractionen
dc.subjectproteinsen
dc.titleUltrasonic-assisted derivatization reaction of amino acids prior to their determination in urine by using single-drop microextraction in conjunction with gas chromatographyen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1016/j.jchromb.2004.09.013-
heal.identifier.secondary<Go to ISI>://000225413200010-
heal.identifier.secondaryhttp://ac.els-cdn.com/S1570023204007470/1-s2.0-S1570023204007470-main.pdf?_tid=ec76dfa6791f728baf9759077c46a46c&acdnat=1333040731_95684068eba08c9165befcde4429556b-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2004-
heal.abstractA derivatization-extraction method that avoids tedious preconcentration steps is established in order to determine amino acids accurately at nanogram levels. The method involves conversion of the analytes of concern to N(O,S)-ethoxycarbonyl amino acid ethyl esters and subsequent extraction by single-drop microextraction (SDME) followed by GC analysis. The reaction proceeds smoothly and rapidly under ultrasonication which removes the bubbles from the bulk solution. Precision is acceptable and 12 non-hydrolyzed amino acids can be determined in urine in this manner. As long as the extraction conditions are consistently applied, quantitative analysis can be performed accurately. The limits of detection were satisfactory in the range 0.010-0.025 mug/ml for GC-FID and 0.26-68 ng/ml for GC-MS(SIM) with 1 ml sample volume. (C) 2004 Elsevier B.V. All rights reserved.en
heal.publisherElsevieren
heal.journalNameJournal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciencesen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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