Analysis of malondialdehyde in biological matrices by capillary gas chromatography with electron-capture detection and mass spectrometry

dc.contributor.authorStalikas, C. D.en
dc.contributor.authorKonidari, C. N.en
dc.date.accessioned2015-11-24T16:49:19Z
dc.date.available2015-11-24T16:49:19Z
dc.identifier.issn0003-2697-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9466
dc.rightsDefault Licence-
dc.subjectfree and total malondialdehydeen
dc.subjectbiological samplesen
dc.subject2,4,6-trichlorophenylhydrazineen
dc.subjectgas chromatographyen
dc.subjectperformance liquid-chromatographyen
dc.subjectlow-density lipoproteinsen
dc.subjecthydroxy fatty-acidsen
dc.subjectlipid-peroxidationen
dc.subjectfree malonaldehydeen
dc.subjectlinoleic-aciden
dc.subjectoxidationen
dc.subjectaldehydesen
dc.subjectproductsen
dc.subjectderivatizationen
dc.titleAnalysis of malondialdehyde in biological matrices by capillary gas chromatography with electron-capture detection and mass spectrometryen
heal.abstractA gas chromatographic method is described for the quantification of free and total malondialdehyde (MDA) in biological materials, The procedure involves derivatization of the analyte with 2,4,6-trichlorophenylhydrazine, extraction with n-hexane, and separation of the cyclic derivatization product on a OV-5 gas chromatographic column. Concentration of the derivatization reagent, pH, reaction time, and temperature were investigated to determine the optimal derivatization conditions. Under these conditions, the method allows for the selective detection of free and total MDA at femtomole levels in several biological materials without any interferences. The procedure yields relative standard deviation values for the intra- and interassays in the range 3.3 and 3.9%, respectively, for the electron-capture and mass-selective (SIM mode) detection systems. Recoveries of MDA from spiked matrices reached 96%. The present method offers the advantage of the alternative use of either electron-capture or mass-selective detection, Furthermore it avoids overestimation of MDA since it employs mild conditions for sample processing and there is no need for preventing protein separation for the assessment of free MDA. (C) 2001 Academic Press.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1006/abio.2000.4951-
heal.identifier.secondary<Go to ISI>://000167283300014-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0003269700949510/1-s2.0-S0003269700949510-main.pdf?_tid=f93054e0b0f1ae3b57baf57980499762&acdnat=1333041001_50fd3a6d37323efefbe4dd3378172452-
heal.journalNameAnal Biochemen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2001-
heal.publisherAcademic Pressen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

Αρχεία

Φάκελος/Πακέτο αδειών

Προβολή: 1 - 1 of 1
Φόρτωση...
Μικρογραφία εικόνας
Ονομα:
license.txt
Μέγεθος:
1.74 KB
Μορφότυπο:
Item-specific license agreed upon to submission
Περιγραφή: