‘Dilute-and-Shoot’ RSLC–MS-MS Method for Fast Detection of Nerve and Vesicant Chemical Warfare Agent Metabolites in Urine
Author(s) -
И. А. Родин,
А. V. Braun,
А. Н. Ставрианиди,
Т. М. Baygildiev,
О. А. Шпигун,
Д. В. Орешкин,
И. В. Рыбальченко
Publication year - 2014
Publication title -
journal of analytical toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.161
H-Index - 76
eISSN - 1945-2403
pISSN - 0146-4760
DOI - 10.1093/jat/bku119
Subject(s) - chemistry , chromatography , formic acid , nerve agent , electrospray ionization , sulfur mustard , selected reaction monitoring , sarin , mass spectrometry , tandem mass spectrometry , urine , solid phase extraction , detection limit , metabolite , analyte , organic chemistry , biochemistry , toxicity , acetylcholinesterase , enzyme
A sensitive screening method based on fast liquid chromatography tandem mass-spectrometry (RSLC-MS-MS) has shown the feasibility of separation and detection of low concentration β-lyase metabolites of sulfur mustard and of nerve agent phosphonic acids in urine. The analysis of these compounds is of interest because they are specific metabolites of the chemical warfare agents (CWAs), sulfur mustard (HD), sarin (GB), soman (GD), VX and Russian VX (RVX). The 'dilute-and-shoot' RSLC-MS-MS method provides a sensitive and direct approach for determining CWA exposure in non-extracted non-derivatized samples from urine. Chromatographic separation of the metabolites was achieved using a reverse phase column with gradient mobile phases consisting of 0.5% formic acid in water and acetonitrile. Identification and quantification of species were achieved using electrospray ionization-tandem mass-spectrometry monitoring two precursor-to-product ion transitions for each compound. The method demonstrates linearity over at least two orders of magnitude and had detection limits of 0.5 ng/mL in urine.
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