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

[Image: see text] 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 effec...

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Autores principales: Behymer, Matthew M., Mo, Huaping, Fujii, Naoaki, Suresh, Vallabh, Chan, Adriano, Lee, Jangweon, Nath, Anjali K., Saha, Kusumika, Mahon, Sari B., Brenner, Matthew, MacRae, Calum A., Peterson, Randall, Boss, Gerry R., Knipp, Gregory T., Davisson, Vincent Jo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682522/
https://www.ncbi.nlm.nih.gov/pubmed/36201358
http://dx.doi.org/10.1021/acs.chemrestox.2c00157
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author Behymer, Matthew M.
Mo, Huaping
Fujii, Naoaki
Suresh, Vallabh
Chan, Adriano
Lee, Jangweon
Nath, Anjali K.
Saha, Kusumika
Mahon, Sari B.
Brenner, Matthew
MacRae, Calum A.
Peterson, Randall
Boss, Gerry R.
Knipp, Gregory T.
Davisson, Vincent Jo
author_facet Behymer, Matthew M.
Mo, Huaping
Fujii, Naoaki
Suresh, Vallabh
Chan, Adriano
Lee, Jangweon
Nath, Anjali K.
Saha, Kusumika
Mahon, Sari B.
Brenner, Matthew
MacRae, Calum A.
Peterson, Randall
Boss, Gerry R.
Knipp, Gregory T.
Davisson, Vincent Jo
author_sort Behymer, Matthew M.
collection PubMed
description [Image: see text] 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 in vivo 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(5)–DMSO and Na (NH(3))(2)PtCl–DMSO complexes in the absence of excess DMSO provided agents with enhanced reactivity toward cyanide in vitro and fully recapitulated in vivo 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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spelling pubmed-96825222022-11-24 Identification of Platinum(II) Sulfide Complexes Suitable as Intramuscular Cyanide Countermeasures Behymer, Matthew M. Mo, Huaping Fujii, Naoaki Suresh, Vallabh Chan, Adriano Lee, Jangweon Nath, Anjali K. Saha, Kusumika Mahon, Sari B. Brenner, Matthew MacRae, Calum A. Peterson, Randall Boss, Gerry R. Knipp, Gregory T. Davisson, Vincent Jo Chem Res Toxicol [Image: see text] 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 in vivo 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(5)–DMSO and Na (NH(3))(2)PtCl–DMSO complexes in the absence of excess DMSO provided agents with enhanced reactivity toward cyanide in vitro and fully recapitulated in vivo 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. American Chemical Society 2022-10-06 2022-11-21 /pmc/articles/PMC9682522/ /pubmed/36201358 http://dx.doi.org/10.1021/acs.chemrestox.2c00157 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Behymer, Matthew M.
Mo, Huaping
Fujii, Naoaki
Suresh, Vallabh
Chan, Adriano
Lee, Jangweon
Nath, Anjali K.
Saha, Kusumika
Mahon, Sari B.
Brenner, Matthew
MacRae, Calum A.
Peterson, Randall
Boss, Gerry R.
Knipp, Gregory T.
Davisson, Vincent Jo
Identification of Platinum(II) Sulfide Complexes Suitable as Intramuscular Cyanide Countermeasures
title Identification of Platinum(II) Sulfide Complexes Suitable as Intramuscular Cyanide Countermeasures
title_full Identification of Platinum(II) Sulfide Complexes Suitable as Intramuscular Cyanide Countermeasures
title_fullStr Identification of Platinum(II) Sulfide Complexes Suitable as Intramuscular Cyanide Countermeasures
title_full_unstemmed Identification of Platinum(II) Sulfide Complexes Suitable as Intramuscular Cyanide Countermeasures
title_short Identification of Platinum(II) Sulfide Complexes Suitable as Intramuscular Cyanide Countermeasures
title_sort identification of platinum(ii) sulfide complexes suitable as intramuscular cyanide countermeasures
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682522/
https://www.ncbi.nlm.nih.gov/pubmed/36201358
http://dx.doi.org/10.1021/acs.chemrestox.2c00157
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