Journal
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
Volume 824, Issue 1-2, Pages 283-294Publisher
ELSEVIER
DOI: 10.1016/j.jchromb.2005.07.042
Keywords
acrylamide (AA); glycidamide (GA); biological monitoring; mercapturic acids; metabolites; N-Acetyl-S-(2-carbamoylethyl)-L-cysteine (AAMA); N-(R/S)-Acetyl-S-(2-carbamoyl-2-hydroxyethyl)-L-cysteine (GAMA)
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We developed a LC-MS/MS method for the quantitative determination of the mercapturic acid (MA) metabolites of acrylamide (AA) AAMA and of its oxidative metabolite glycidamide (GA) GAMA in urine samples from the general population. The method requires 4 mL of urine which is solid phase extracted prior to LC-MS/MS analysis. The metabolites are detected by ESI-tandem mass spectrometry in negative ionisation mode and quantified by isotope dilution. Detection limits ranged down to 1.5 mu g/L urine for both AAMA and GAMA. The imprecision expressed as R.S.D. lay between 2% and 6% for both analytes (intra- and inter-assay). First results on a small group of 29 persons out of the general population ranged from 5 to 338 mu g/L AAMA and
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