The sulfur-containing chemical warfare agents sulfur mustard HD and nerve agent VX are highly toxic and persistent in the environment. Therefore, their neutralisation requires harsh oxidation conditions, but also precise selectivity. Here we report the safe and effective detoxification of surrogates CEES and PhX by selective oxidation of the sulfur atom by generating peracetic acid from AcOEt and aq. HO assisted by the supported lipase CALB. Morever, it is possible to perform these neutralisations with safe 'on demand' generation of AcOOH in a flow system by using a packed bed reactor containing the supported biocatalyst.

Download full-text PDF

Source
http://dx.doi.org/10.1002/chem.202403701DOI Listing

Publication Analysis

Top Keywords

chemical warfare
8
warfare agents
8
oxidative neutralisation
4
neutralisation sulfur-based
4
sulfur-based chemical
4
agents mediated
4
mediated lipase
4
lipase batch
4
batch flow
4
flow reactor
4

Similar Publications

This publication explores the characteristics, threats, and challenges posed by fourth-generation chemical warfare agents - Novichoks. These highly toxic agents, recently introduced to the international security landscape, represent a significant risk not only to military forces, but also to civilian populations, especially in the context of potential terrorist attacks. The study examines the molecular structure, toxicity, and physiological effects of Novichoks, underscoring their resistance to conventional decontamination methods and their rapid, severe impact on human health.

View Article and Find Full Text PDF

Recent events involving nerve agents of the A-Series, a once elusive class of chemical warfare agents, have provoked a great concern in the international community. In this paper, continuing our research efforts in Medicinal Chemistry at the Brazilian Institute of Chemical, Biological, Radiological and Nuclear Defense (IDQBRN) (an OPCW-designated Laboratory for environmental samples), we explore ANMP, an A-230 surrogate, in the search for new treatment options for intoxications caused by these chemicals. Five isatin-pyridine oxime hybrids were evaluated as acetylcholinesterase (AChE) reactivators using a modified Ellman's assay.

View Article and Find Full Text PDF

Reexamining the acute toxicity of chloropicrin: Comprehensive estimation using in silico methods.

Toxicol In Vitro

May 2025

Department of Regulatory and Forensic Toxicology, Institute of Medical Expertises in Łódź, ul. Aleksandrowska 67/93, 91-205 Łódź, Poland; Laboratory of Innovative Toxicological Research and Analyzes, Institute of Medical Studies, Medical College, Rzeszów University, Al. mjr. W. Kopisto 2a, 35-959 Rzeszów, Poland. Electronic address:

Chloropicrin, historically infamous as a chemical warfare agent during World War I, has recently resurfaced in global conflicts, prompting a reevaluation of its acute toxicological significance. This study addresses the historical knowledge gap surrounding chloropicrin by employing in silico toxicology methods to estimate toxicophores and predict acute toxicity across various exposure routes. Allegations of its use in recent conflicts necessitate a deeper understanding of its toxicological profile, particularly in modern warfare scenarios.

View Article and Find Full Text PDF

The course and kinetics of the reactions of sulfur mustard, nitrogen mustard and their selected analogues with sodium ethoxide were studied using a gas chromatograph coupled with a mass spectrometer. 2-chloroethyl ethyl sulfide (CEES), a monofunctional analogue of sulfur mustard (HD), bis(2-chloroethyl) ether (BCEE), an oxygen analogue of sulfur mustard, and bis(2-chloroethyl)amine, an analogue of nitrogen mustard HN-3, in which one hydrogen atom remains unsubstituted with a chloroethyl group, were used as imitators of mustards. For the study, the last mentioned compound was given the acronym HN-0.

View Article and Find Full Text PDF

Structure-activity studies of bispyridinium antinicotinics to select candidates to treat soman intoxication as part of a combined therapy.

PLoS One

February 2025

Chemical, Biological and Radiological Sciences Division, Defence Science and Technology Laboratory (Dstl), Porton Down, Salisbury, Wiltshire, United Kingdom.

The standard treatment of atropine and oximes is insufficiently effective against all organophosphorus nerve agents. Bispyridinium non-oxime nicotinic antagonists are promising components to add to treatments. One of these, MB327, improves the survival of guinea-pigs after intoxication with tabun, sarin or soman.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!