Analysis of chemical warfare agents in organic liquid samples with magnetic dispersive solid phase extraction and gas chromatography mass spectrometry for verification of the chemical weapons convention

被引:16
作者
Singh, Varoon [1 ]
Purohit, Ajay Kumar [1 ]
Chinthakindi, Sridhar [1 ]
Raghavender, Goud D. [1 ]
Tak, Vijay [1 ]
Pardasani, Deepak [1 ]
Shrivastava, Anchal Roy [2 ]
Dubey, Devendra Kumar [1 ]
机构
[1] Def Res & Dev Estab, Vertox Lab, Jhansi Rd, Gwalior 474002, India
[2] Def Res & Dev Estab, Elect Microscopy Div, Jhansi Rd, Gwalior 474002, India
关键词
Chemical weapons convention; Chemical warfare agents; Magnetic dispersive solid phase extraction; GC-MS; Sample preparation; Magnetic nanoparticles; NERVE AGENTS; WATER; PHARMACEUTICALS; COMPOSITE; MARKERS;
D O I
10.1016/j.chroma.2016.04.058
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple, sensitive and low temperature sample preparation method is developed for detection and identification of Chemical Warfare Agents (CWAs) and scheduled esters in organic liquid using magnetic dispersive solid phase extraction (MDSPE) followed by gas chromatography-mass spectrometry analysis. The method utilizes Iron oxide@Poly(methacrylic acid-co-ethylene glycol dimethacrylate) resin (Fe2O3@Poly(MAA-co-EGDMA)) as sorbent. Variants of these sorbents were prepared by precipitation polymerization of methacrylic acid-co-ethylene glycol dimethacrylate (MAA-co-EGDMA) onto Fe2O3 nanoparticles. Fe2O3@poly(MAA-co-EGDMA) with 20% MM showed highest recovery of analytes. Extractions were performed with magnetic microspheres by MDSPE. Parameters affecting the extraction efficiency were studied and optimized. Under the optimized conditions, method showed linearity in the range of 0.1-3.0 mu g mL(-1) (r(2) = 0.9966-0.9987). The repeatability and reproducibility (relative standard deviations (RSDs) %) were in the range of 4.5-7.6% and 3.4-6.2% respectively for organophosphorous esters in dodecane. Limits of detection (S/N = 3/1) and limit of quantification (S/N = 10/1) were found to be in the range of 0.05-0.1 mu g mL(-1) and 0.1-0.12 mu g mL(-1) respectively in SIM mode for selected analytes. The method was successfully validated and applied to the extraction and identification of targeted analytes from three different organic liquids i.e. n-hexane, dodecane and silicon oil. Recoveries ranged from 58.7 to 97.3% and 53.8 to 95.5% at 3/kg mL(-1) and 1 mu g mL(-1) spiking concentrations. Detection of diethyl methylphosphonate (DEMP) and O-Ethyl S-2-diisopropylaminoethyl methylphosphonothiolate (VX) in samples provided by the Organization for Prohibition of Chemical Weapons Proficiency Test (OPCW-PT) proved the utility of the developed method for the off-site analysis of CWC relevant chemicals. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 41
页数:10
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