A new method for the determination of free L-carnitine in serum samples based on high field single quantum coherence filtering H-1-NMR spectroscopy

dc.contributor.authorTsiafoulis, C. G.en
dc.contributor.authorExarchou, V.en
dc.contributor.authorTziova, P. P.en
dc.contributor.authorBairaktari, E.en
dc.contributor.authorGerothanassis, I. P.en
dc.contributor.authorTroganis, A. N.en
dc.date.accessioned2015-11-24T16:56:52Z
dc.date.available2015-11-24T16:56:52Z
dc.identifier.issn1618-2642-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10501
dc.rightsDefault Licence-
dc.subjectl-carnitineen
dc.subjectserumen
dc.subjecth-1-nmren
dc.subjectsingle quantum coherence filtering h-1-nmren
dc.subjectprotein precipitationen
dc.subjecttandem mass-spectrometryen
dc.subjectmagnetic-resonance-spectroscopyen
dc.subjectperformance liquid-chromatographyen
dc.subjecthigh-resolution nmren
dc.subjectseminal plasmaen
dc.subjectblood-serumen
dc.subjectacylcarnitinesen
dc.subjectmetabolitesen
dc.subjecturineen
dc.subjectquantificationen
dc.titleA new method for the determination of free L-carnitine in serum samples based on high field single quantum coherence filtering H-1-NMR spectroscopyen
heal.abstractThe rapid and accurate determination of specific metabolites present in biofluids is a very demanding task which is essential in both medicine and chemistry. l-carnitine (3-hydroxy-4-N-trimethylammonium butyrate) is an important metabolite which participates in a series of biological paths and therefore its determination is of diagnostic importance. A single quantum coherence filtering H-1 NMR methodology was used for the accurate and rapid determination of l-carnitine in human serum samples. The methodology is based on spectral simplification, and specifically on the distinction of the N-methyl proton signal of l-carnitine that is greatly overlapped in the H-1-NMR spectrum of serum. The quantitative results provided by the proposed method are in excellent agreement with those obtained by the enzymatic method, which is widely used. The proposed method is rapid (similar to 20 min of experimental time), selective, sensitive, and has good analytical characteristics (accuracy, reproducibility). Selected protein precipitation methods were also investigated and sample pretreatment with EtOH is suggested.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1007/s00216-010-4600-0-
heal.identifier.secondary<Go to ISI>://000286982900035-
heal.identifier.secondaryhttp://download.springer.com/static/pdf/260/art%253A10.1007%252Fs00216-010-4600-0.pdf?auth66=1381649373_a50270a6863e3a1399949181e6748752&ext=.pdf-
heal.journalNameAnal Bioanal Chemen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2011-
heal.publisherSpringer Verlag (Germany)en
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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