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鉴定适合作为肌肉内氰化物解毒剂的二价铂硫化物配合物。

Identification of Platinum(II) Sulfide Complexes Suitable as Intramuscular Cyanide Countermeasures.

机构信息

Department of Industrial and Physical Pharmacy, Purdue University, 575 Stadium Mall Drive, West Lafayette, Indiana47907, United States.

Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, 575 Stadium Mall Drive, West Lafayette, Indiana47907, United States.

出版信息

Chem Res Toxicol. 2022 Nov 21;35(11):1983-1996. doi: 10.1021/acs.chemrestox.2c00157. Epub 2022 Oct 6.

Abstract

The development of rapidly acting cyanide countermeasures using intramuscular injection (IM) represents an unmet medical need to mitigate toxicant exposures in mass casualty settings. Previous work established that cisplatin and other platinum(II) or platinum(IV)-based agents effectively mitigate cyanide toxicity in zebrafish. Cyanide's reaction with platinum-containing materials was proposed to reduce the risk of acute toxicities. However, cyanide antidote activity depended on a formulation of platinum-chloride salts with dimethyl sulfoxide (DMSO) followed by dilution in phosphate-buffered saline (PBS). A working hypothesis to explain the DMSO requirement is that the formation of platinum-sulfoxide complexes activates the cyanide scavenging properties of platinum. Preparations of isolated NaPtCl-DMSO and Na (NH)PtCl-DMSO complexes in the absence of excess DMSO provided agents with enhanced reactivity toward cyanide and fully recapitulated cyanide rescue in zebrafish and mouse models. The enhancement of the cyanide scavenging effects of the DMSO ligand could be attributed to the activation of platinum(IV) and (II) with a sulfur ligand. Unfortunately, the efficacy of DMSO complexes was not robust when administered IM. Alternative Pt(II) materials containing sulfide and amine ligands in bidentate complexes show enhanced reactivity toward cyanide addition. The cyanide addition products yielded tetracyanoplatinate(II), translating to a stoichiometry of 1:4 Pt to each cyanide scavenger. These new agents demonstrate a robust and enhanced potency over the DMSO-containing complexes using IM administration in mouse and rabbit models of cyanide toxicity. Using the zebrafish model with these Pt(II) complexes, no acute cardiotoxicity was detected, and dose levels required to reach lethality exceeded 100 times the effective dose. Data are presented to support a general chemical design approach that can expand a new lead candidate series for developing next-generation cyanide countermeasures.

摘要

肌内注射(IM)快速作用氰化物解毒剂的开发代表了缓解大规模伤亡情况下毒物暴露的未满足的医疗需求。以前的工作表明,顺铂和其他铂(II)或铂(IV)基试剂可有效减轻斑马鱼中的氰化物毒性。氰化物与含铂材料的反应被认为可降低急性毒性的风险。然而,氰化物解毒剂的活性取决于铂-氯化物盐与二甲基亚砜(DMSO)的配方,然后在磷酸盐缓冲盐水(PBS)中稀释。解释 DMSO 需求的工作假设是,铂-亚砜配合物的形成激活了铂的氰化物清除特性。在不存在过量 DMSO 的情况下制备的分离的 NaPtCl-DMSO 和 Na(NH)PtCl-DMSO 配合物提供了对氰化物具有增强反应性的试剂,并完全重现了斑马鱼和小鼠模型中的氰化物解救。DMSO 配体对氰化物清除作用的增强可以归因于硫配体对铂(IV)和(II)的激活。不幸的是,当通过 IM 给药时,DMSO 配合物的功效并不强。含有二齿配合物中的硫代和胺配体的替代 Pt(II)材料对氰化物加成具有增强的反应性。氰化物加成产物生成四氰合铂(II),转化为 1:4 Pt 到每个氰化物清除剂的化学计量比。这些新试剂在使用 IM 给药的小鼠和兔氰化物毒性模型中显示出比含 DMSO 配合物更强的稳健性和增强的效力。在使用这些 Pt(II)配合物的斑马鱼模型中,未检测到急性心脏毒性,达到致死所需的剂量水平超过有效剂量的 100 倍。提供的数据支持了一种通用的化学设计方法,该方法可以扩展用于开发下一代氰化物解毒剂的新候选物系列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8688/9682522/34cd003d83b1/tx2c00157_0002.jpg

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