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J Chromatogr B Analyt Technol Biomed Life Sci. 2010 May 15;878(17-18):1320-5. doi: 10.1016/j.jchromb.2010.02.019. Epub 2010 Feb 21.
Recently, several methods have been developed to verify exposure to nerve agents. Most of these methods, such as the fluoride reactivation technique and the analysis of inhibited phosphonylated butyrylcholinesterase (BuChE), are based on mass spectrometry. The high specificity of the mass spectrometer might also imply a disadvantage, because the acquisition mass, i.e. the identity of the analyte must be known beforehand in order to direct the MS analysis in the most sensitive mode. In real cases, the identity of the nerve agent is not always known beforehand and the mass spectrometer should be operated in a scanning mode, with the consequence that sensitivity of the method will be lower. Comprehensive GC, or GC x GC, is a technique which offers enhanced separation. The implied larger selectivity of the GC separation allows mass spectrometry to be conducted in a less specific, scanning, mode. By the use of this configuration, the identity of the nerve agent does not have to be known beforehand but can be traced. In order to be able to detect lower concentrations and assess lower exposure levels, a large volume injection technique was developed allowing sample sizes up to 100 microL. The technique was tested with plasma samples that had been inhibited with various nerve agents. Subsequently, the cholinesterase-bound nerve agent was regenerated by the fluoride reactivation technique. Using the newly developed comprehensive GC-MS method it was possible to detect nerve agent at an exposure level of 1% BuChE inhibition, which is approximately 70 pg nerve agent/mL. These low exposure levels cannot be verified with a cholinesterase (ChE) activity assay. Moreover, the identity of the regenerated nerve agent was verified by the mass spectrum that was generated by the TOF mass spectrometer. This paper presents a technique able to deliver full-scan data on the analysis of nerve agents in biomedical samples at relevant exposure levels (1% BuChE inhibition). This full-scan data meets for a large part the forensic requirements that are in place for the analysis of biomedical samples in the context of alleged use of Chemical Warfare Agents.
最近,已经开发出几种验证接触神经毒剂的方法。这些方法中的大多数,如氟化物再活化技术和抑制的膦酰化丁酰胆碱酯酶(BuChE)的分析,都是基于质谱法。质谱仪的高特异性也可能意味着一个缺点,因为为了以最敏感的模式引导 MS 分析,必须事先知道质量采集,即分析物的身份。在实际情况下,神经毒剂的身份并不总是事先知道的,质谱仪应该以扫描模式运行,因此方法的灵敏度会较低。综合气相色谱(GC)或 GC x GC 是一种提供增强分离的技术。GC 分离所隐含的更大选择性允许质谱以较低特异性、扫描模式进行。通过使用这种配置,不必事先知道神经毒剂的身份,但可以追踪。为了能够检测更低的浓度并评估更低的暴露水平,开发了一种大体积进样技术,允许进样量高达 100 微升。该技术已在受各种神经毒剂抑制的血浆样品上进行了测试。随后,通过氟化物再活化技术使胆碱酯酶结合的神经毒剂再生。使用新开发的综合 GC-MS 方法,可以在 1%BuChE 抑制的暴露水平下检测到神经毒剂,这大约是 70pg 神经毒剂/mL。这些低暴露水平不能用胆碱酯酶(ChE)活性测定来验证。此外,通过 TOF 质谱仪生成的质谱可以验证再生的神经毒剂的身份。本文提出了一种能够在相关暴露水平(1%BuChE 抑制)下对生物医学样品中的神经毒剂进行全扫描数据分析的技术。这种全扫描数据在很大程度上满足了在涉嫌使用化学战剂的情况下对生物医学样品进行分析的法医要求。