D'Agostino P A, Hancock J R, Chenier C L, Lepage C R Jackson
DRDC Suffield, P.O. Box 4000 Station Main, Medicine Hat, Alta., Canada T1A 8K6.
J Chromatogr A. 2006 Mar 31;1110(1-2):86-94. doi: 10.1016/j.chroma.2006.01.083. Epub 2006 Feb 9.
Most prior analytical studies have dealt with the determination of chemical warfare agents in environmental or biological matrices that would typically be collected following battlefield use or in support of the Chemical Weapons Convention. These methods may be useful for some investigations, but may not be practical for indoor forensic investigations where chemical warfare agent use is suspected. There is a need for analytical methods for chemical warfare agent identification in office media, including flooring, wall surfaces, office fabrics and paper products, which would typically be collected in an office environment during forensic investigations. During this study, typical office environment media were spiked at the 4-20microg/g level with either a complex munitions grade sample of tabun (GA) or with a standard containing the three nerve agents, sarin (GB), cyclohexyl methylphosphonofluoridate (GF), soman (GD) and the nerve agent simulant, triethyl phosphate (TEP), to evaluate the potentials of liquid chromatography electrospray ionization mass spectrometry (LC-ESI-MS) and liquid chromatography electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) for forensic purposes. An emerging technique, desorption electrospray ionization (DESI-MS/MS), was also investigated for the direct determination of TEP, GB and GD sampled onto solid phase microextraction (SPME) fibers exposed to spiked office media. The spiked chemical warfare agents were recovered with varying efficiencies during this study, but in all cases sufficient chemical warfare agent was recovered for mass spectrometric identification purposes. Full high resolution mass spectra were acquired for all the chemical warfare agents in the continuum mode, which typically resulted in mass measurement errors of 0.001Da or less.
大多数先前的分析研究都涉及环境或生物基质中化学战剂的测定,这些基质通常是在战场使用后收集的,或用于支持《化学武器公约》。这些方法可能对某些调查有用,但对于怀疑使用化学战剂的室内法医调查可能并不实用。需要用于在办公介质中识别化学战剂的分析方法,这些介质包括地板、墙面、办公织物和纸制品,在法医调查期间通常会在办公环境中收集。在本研究中,典型的办公环境介质以4 - 20微克/克的水平添加了塔崩(GA)的复杂弹药级样品,或添加了含有三种神经性毒剂沙林(GB)、环己基甲基膦酰氟(GF)、梭曼(GD)以及神经性毒剂模拟物磷酸三乙酯(TEP)的标准品,以评估液相色谱电喷雾电离质谱(LC - ESI - MS)和液相色谱电喷雾电离串联质谱(LC - ESI - MS/MS)用于法医目的的潜力。还研究了一种新兴技术,解吸电喷雾电离(DESI - MS/MS),用于直接测定吸附在暴露于添加了化学战剂的办公介质的固相微萃取(SPME)纤维上的TEP、GB和GD。在本研究中,添加的化学战剂以不同效率被回收,但在所有情况下,回收的化学战剂足以用于质谱鉴定目的。以连续模式获取了所有化学战剂的全高分辨率质谱,其质量测量误差通常在0.001Da或更小。