Vertox Laboratory, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002, M.P., India.
J Chromatogr A. 2010 Apr 23;1217(17):2887-94. doi: 10.1016/j.chroma.2010.02.071. Epub 2010 Mar 3.
The detection and identification of the degradation products of nitrogen mustard and nerve agent VX by high performance liquid chromatography coupled to on-line solid-phase extraction-nuclear magnetic resonance spectroscopy (HPLC-UV-SPE-NMR) were demonstrated. The analytes selected for the study were N,N-dimethylaminoethanol (DMAE), N,N-diethylaminoethanol (DEAE), N,N-diisopropylaminoethanol (DIAE) and triethanolamine (TEA). Offline solid-phase extraction (SPE) followed by derivatization was applied to eliminate the interferents and make the analytes amenable for UV detection. Thereafter, chromatographically separated derivatives were trapped on on-line SPE cartridges. They were subsequently eluted and 1H NMR and COSY spectra were obtained. The overall detection limits of the LC-UV-SPE-NMR method for the mentioned analytes were found to be 18, 23, 25, and 32 mg/L respectively. Applicability of the method to real samples was demonstrated by the analysis of samples provided during the 22nd OPCW official proficiency test. The method gave reproducible NMR spectra devoid of intense background signals.
采用高效液相色谱-在线固相萃取-核磁共振波谱联用(HPLC-UV-SPE-NMR)技术对氮芥和神经毒剂 VX 的降解产物进行了检测和鉴定。选择 N,N-二甲基氨基乙醇(DMAE)、N,N-二乙基氨基乙醇(DEAE)、N,N-二异丙基氨基乙醇(DIAE)和三乙醇胺(TEA)作为研究对象。离线固相萃取(SPE)结合衍生化技术用于消除干扰物,使分析物可进行 UV 检测。然后,色谱分离的衍生物被捕获在在线 SPE 小柱上。随后洗脱并获得 1H NMR 和 COSY 谱。对于上述分析物,LC-UV-SPE-NMR 方法的总检测限分别为 18、23、25 和 32mg/L。通过对第 22 届化武组织官方能力验证提供的样品进行分析,证明了该方法对实际样品的适用性。该方法得到了重现性良好的 NMR 谱,且无强烈的背景信号。