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一种取代β-环糊精对神经毒剂的解毒作用:改良生物测定法的应用

Detoxification of nerve agents by a substituted beta-cyclodextrin: application of a modified biological assay.

作者信息

Wille T, Tenberken O, Reiter G, Müller S, Le Provost R, Lafont O, Estour F, Thiermann H, Worek F

机构信息

Bundeswehr Institute of Pharmacology and Toxicology, Neuherbergstrasse 11, 80937 Munich, Germany.

出版信息

Toxicology. 2009 Nov 30;265(3):96-100. doi: 10.1016/j.tox.2009.09.018. Epub 2009 Oct 1.

Abstract

Chemical warfare agents (nerve agents) are still available and present a real threat to the population. Numerous in vitro and in vivo studies showed that various nerve agents, e.g. tabun and cyclosarin, are resistant towards standard therapy with atropine and oxime. Based on these facts we applied a modified biological assay for the easy, semi-quantitative testing of the detoxifying properties of the beta-cyclodextrin derivative CD-IBA. Cyclosarin, sarin, tabun and VX were incubated with CD-IBA for 1-50 min at 37 degrees C, then an aliquot was added to erythrocyte acetylcholinesterase (AChE) and the percentage of AChE inhibition was determined. The validity of the assay was confirmed by concomitant quantification of tabun by GC-MS. Different concentrations of cyclosarin were detoxified by CD-IBA in a concentration-dependent velocity. The ability to detoxify various nerve agents decreased in the order cyclosarin>sarin>tabun>>VX. Hereby, no detoxification of VX could be detected. Sarin was detoxified in a biphasic reaction with a fast reduction of inhibitory potential in the first phase and a slower detoxification in the second phase. CD-IBA detoxified tabun in a one phase decay and, compared to cyclosarin and sarin, a longer half-life was determined with tabun. The modified biological assay is appropriate for the initial semi-quantitative screening of candidate compounds for the detoxification of nerve agents. The beta-cyclodextrin derivative CD-IBA demonstrated its ability to detoxify different nerve agents.

摘要

化学战剂(神经毒剂)仍然存在,对民众构成实际威胁。大量的体外和体内研究表明,各种神经毒剂,如塔崩和环沙林,对阿托品和肟的标准治疗具有抗性。基于这些事实,我们应用了一种改良的生物测定法,用于简便、半定量地测试β-环糊精衍生物CD-IBA的解毒特性。将环沙林、沙林、塔崩和VX与CD-IBA在37℃下孵育1至50分钟,然后取一份加入红细胞乙酰胆碱酯酶(AChE)中,测定AChE抑制百分比。通过气相色谱-质谱联用(GC-MS)同时定量塔崩来确认该测定法的有效性。不同浓度的环沙林被CD-IBA以浓度依赖的速度解毒。解毒各种神经毒剂的能力按环沙林>沙林>塔崩>>VX的顺序降低。据此,未检测到VX的解毒情况。沙林以双相反应解毒,第一阶段抑制电位快速降低,第二阶段解毒较慢。CD-IBA以单相衰减方式解毒塔崩,与环沙林和沙林相比,塔崩的半衰期更长。这种改良的生物测定法适用于对神经毒剂解毒候选化合物进行初步半定量筛选。β-环糊精衍生物CD-IBA展示了其解毒不同神经毒剂的能力。

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