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dc.contributor.authorGhandforoush-Sattari, M
dc.contributor.authorMashayekhi, S
dc.contributor.authorNemati, M
dc.contributor.authorRoutledge, PA
dc.date.accessioned2018-08-26T08:14:59Z
dc.date.available2018-08-26T08:14:59Z
dc.date.issued2009
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/50993
dc.description.abstractTaurine is an amino acid which is not incorporated into proteins but found in the cytosol of many mammalian cells, in high concentrations (2-30 mM). Increase in plasma taurine concentration has already been reported after surgical trauma, X-radiation, muscle necrosis, carbon tetrachloride-induced liver damage, and paracetamol overdose. Plasma taurine concentration was measured using LC with fluorescence detection following derivatization by o-phtalaldehyde plus 3-mercapto-propionic acid and alpha-aminobutyric acid as internal standard. Under these conditions the retention time of taurine was 10 min. This method was sensitive enough, to quantify 150 pg mL(-1) and detect 50 pg mL(-1) of taurine ranging normally between 65 and 179 mmol L(-1) (8-22 mu g mL(-1)). The validated method allowed simple determination of human plasma taurine in pharmacokinetic and biomarker studies.
dc.language.isoEnglish
dc.relation.ispartofCHROMATOGRAPHIA
dc.subjectColumn liquid chromatography
dc.subjectTaurine
dc.subjectalpha-Aminobutyric acid, o-phtalaldehyde, and 3-mercapto-propionic acid
dc.titleA Rapid Determination of Taurine in Human Plasma by LC
dc.typeArticle
dc.citation.volume69
dc.citation.issue12
dc.citation.spage1427
dc.citation.epage1430
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1365/s10337-009-1055-6


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