Tentative Identification of Etazene (Etodesnitazene) Metabolites in Rat Serum and Urine by Gas Chromatography-Mass Spectrometry and Accurate Mass Liquid Chromatography-Mass Spectrometry.


Journal

Journal of analytical toxicology
ISSN: 1945-2403
Titre abrégé: J Anal Toxicol
Pays: England
ID NLM: 7705085

Informations de publication

Date de publication:
24 Jan 2023
Historique:
received: 13 10 2021
revised: 20 12 2021
accepted: 05 01 2022
pubmed: 8 1 2022
medline: 26 1 2023
entrez: 7 1 2022
Statut: ppublish

Résumé

2-Benzylbenzimidazole derivatives comprise a small but forensically significant group of synthetic opioids. In humans, the metabolism of some members of this group is extensive, with little or none of the parent compound remaining. The recent detection of the 2-benzylbenzimidazole derivative, etazene (etodesnitazene), in products seized in Russia required the detection of its metabolites in biofluids for forensic toxicology purposes. Using gas chromatography--mass spectrometry (GC-MS) and high resolution accurate mass (HRAM) liquid chromatography-mass spectrometry (LC-MS), eight etazene metabolites were found in the urine and serum of rats. These were tentatively identified as products of N-deethylation, O-deethylation, hydroxylation or N-oxidation of benzimidazole moiety and combinations of these processes. The parent substance and its O-deethylated metabolite prevailed in rat serum, while in urine, the level of etazene was low compared to N,O-deethylated and N-deethylated with hydroxylation metabolites. Glucuronidated, sulfonated and glutathionated forms were not found. Taking into account reports on the study of the metabolism of other 2-benzylbenzimidazole derivatives in humans, it may be concluded that the mono-deethylated and mono-hydroxylated metabolites are suitable as target analytes in urine.

Identifiants

pubmed: 34994784
pii: 6498217
doi: 10.1093/jat/bkac001
doi:

Substances chimiques

etazene 0
bendazole 26601THN1D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1032-1037

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Andrej Grigoryev (A)

Forensic-Chemical Division, Bureau of Forensic-Medical Expertise's, 1th Vladimirskaya Str. 33, Build. 1, Moscow 111401, Russia.

Pierce Kavanagh (P)

Department of Pharmacology and Therapeutics, School of Medicine, Trinity Centre for Health Sciences, Saint James's Hospital, Dublin D08 W9RT, Ireland.

Geraldine Dowling (G)

Department of Pharmacology and Therapeutics, School of Medicine, Trinity Centre for Health Sciences, Saint James's Hospital, Dublin D08 W9RT, Ireland.
School of Science, Institute of Technology Sligo, Ash Lane, Sligo F91 YW50, Ireland.

Igor Rodin (I)

Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1, Moscow 119991, Russia.
Department of Epidemiology and Evidence-Based Medicine, Sechenov First Moscow State Medical University, Trubeckaya Str. 8, Buld. 2, Moscow 119435, Russia.

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Classifications MeSH