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Journal Article

Citation

Weissberg A, Madmon M, Elgarisi M, Dagan S. J. Chromatogr. A 2018; 1577: 24-30.

Affiliation

Department of Analytical Chemistry, Israel Institute for Biological Research (IIBR), P.O. Box 19, Ness Ziona, Israel.

Copyright

(Copyright © 2018, Elsevier Publishing)

DOI

10.1016/j.chroma.2018.09.052

PMID

30297234

Abstract

A highly sensitive method for the detection and identification of sarin (GB), soman (GD) and cyclosarin (GF) chemical warfare agents (CWAs) in environmental outdoor and indoor matrices such as soil, asphalt, linoleum, formica, concrete and cloth was developed. The method incorporates derivatization of the G-type nerve agent extracts with 2-[(dimethylamino)methyl]phenol (2-DMAMP), followed by LC-ESI(+)-MS/MS analysis. Four LC-amenable extraction solvents were explored in terms of their extraction efficiency and the reaction rate of the derivatizing agent. The reaction time, temperature and derivatization reagent amount were optimized. The optimal procedure was found to be extraction with water by agitation (2 min), followed by the addition of 2-DMAMP directly into the injection vial and stirring for 5 min prior to LC-ESI(+)-MS/MS analysis, without any other pretreatment. The method was applied to real-world samples and exhibited very low detection limits (LODs) of 0.8-20 pg/cm2 in asphalt, linoleum, cloth, formica and concrete and 4 pg/g in soil. The newly developed method demonstrated significantly superior sensitivity compared to conventional GC-MS- and LC-MS-based methods for the identification of G-nerve agents and allowed the determination of both G-nerve agents and their hydrolysis products within a single LC-MS/MS run. The proposed methodology may be practical for verifying contaminated matrices collected in the battlefield or terror scenes in forensic investigations where trace level analysis is required.

Copyright © 2018 Elsevier B.V. All rights reserved.


Language: en

Keywords

Aqueous extraction; Derivatization; Environmental matrices; G-type nerve agents; LC–MS/MS

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