Bundeswehr Institute of Pharmacology and Toxicology, Neuherbergstrasse 11, 80937 Munich, Germany.
J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Sep 15;879(26):2704-13. doi: 10.1016/j.jchromb.2011.07.031. Epub 2011 Jul 30.
The present study was initiated to develop a sensitive and highly selective method for the simultaneous quantification of the nerve agent VX (O-ethyl S-[2(diisopropylamino)ethyl] methylphosphonothioate) and its toxic metabolite (EA-2192) in blood and plasma samples in vivo and in vitro. For the quantitative detection of VX and EA-2192 the resolution was realized on a HYPERCARB HPLC phase. A specific procedure was developed to isolate both toxic analytes from blood and plasma samples. The limit of detection was 0.1 pg/ml and the absolute recovery of the overall sample preparation procedure was 74% for VX and 69% for EA-2192. After intravenous and percutaneous administration of a supralethal doses of VX in anaesthetised swine both VX and EA-2192 could be quantified over 540 min following exposure. This study is the first to verify the in vivo formation of the toxic metabolite EA-2192 after poisoning with the nerve agent VX. Further toxicokinetic and therapeutic studies are required in order to determine the impact of EA-2192 on the treatment of acute VX poisoning.
本研究旨在开发一种灵敏且高度选择性的方法,用于同时定量检测体内和体外血液和血浆样品中的神经毒剂 VX(O-乙基 S-[2(二异丙基氨基)乙基]甲基膦酸硫酯)及其有毒代谢物(EA-2192)。为了定量检测 VX 和 EA-2192,在 HYPERCARB HPLC 相上实现了分辨率。开发了一种特定的程序来从血液和血浆样品中分离这两种有毒分析物。检测限为 0.1 pg/ml,整个样品制备过程的绝对回收率为 VX 的 74%和 EA-2192 的 69%。在麻醉猪中静脉内和经皮给予超致死剂量的 VX 后,暴露后可在 540 分钟内定量检测到 VX 和 EA-2192。这项研究首次验证了在神经毒剂 VX 中毒后有毒代谢物 EA-2192 的体内形成。需要进一步进行毒代动力学和治疗研究,以确定 EA-2192 对急性 VX 中毒治疗的影响。