Literature DB >> 34994784

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

Andrej Grigoryev1, Pierce Kavanagh2, Geraldine Dowling2,3, Igor Rodin4,5.   

Abstract

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 GC-MS and HRAM 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.
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Entities:  

Keywords:  Etazene; GC–MS; LC–QTOF; Metabolites; Rat serum; Rat urine; Synthetic opioids

Year:  2022        PMID: 34994784     DOI: 10.1093/jat/bkac001

Source DB:  PubMed          Journal:  J Anal Toxicol        ISSN: 0146-4760            Impact factor:   3.367


  1 in total

1.  First identification, chemical analysis and pharmacological characterization of N-piperidinyl etonitazene (etonitazepipne), a recent addition to the 2-benzylbenzimidazole opioid subclass.

Authors:  Marthe M Vandeputte; Nick Verougstraete; Donna Walther; Grant C Glatfelter; Jeroen Malfliet; Michael H Baumann; Alain G Verstraete; Christophe P Stove
Journal:  Arch Toxicol       Date:  2022-04-21       Impact factor: 6.168

  1 in total

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