AI Article Synopsis

  • The development of fast-acting cyanide countermeasures through intramuscular injection addresses a critical need for treating cyanide exposure in emergency situations.
  • Previous research has shown that certain platinum-based compounds, particularly when mixed with dimethyl sulfoxide (DMSO), can effectively reduce cyanide toxicity in animal models.
  • New platinum(II) complexes, especially those with sulfide and amine ligands, have been found to have improved effectiveness against cyanide when administered intramuscularly, showing no acute toxicity and a significant safety margin in preliminary tests.

Article 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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682522PMC
http://dx.doi.org/10.1021/acs.chemrestox.2c00157DOI Listing

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