Electron activated dissociation - a complementary fragmentation technique to collision-induced dissociation for metabolite identification of synthetic cathinone positional isomers.

Collision-induced dissociation Electron activated dissociation Liquid chromatography Mass spectrometry Phase I metabolite identification Positional isomers Synthetic cathinones

Journal

Analytica chimica acta
ISSN: 1873-4324
Titre abrégé: Anal Chim Acta
Pays: Netherlands
ID NLM: 0370534

Informations de publication

Date de publication:
01 Dec 2023
Historique:
received: 07 07 2023
revised: 18 09 2023
accepted: 25 10 2023
medline: 20 11 2023
pubmed: 18 11 2023
entrez: 17 11 2023
Statut: ppublish

Résumé

Over the last decade, a remarkable number of new psychoactive substances (NPS) have emerged onto the drug market, resulting in serious threats to both public health and society. Despite their abundance and potential toxicity, there is little information available on their metabolism, a crucial piece of information for clinical and forensic purposes. NPS metabolism can be studied using in vitro models, such as liver microsomes, cytosol, hepatocytes, etc. The tentative structural elucidation of metabolites of NPS formed using in vitro models is typically carried out using liquid chromatography combined with high-resolution tandem mass spectrometry (LC-HRMS

Identifiants

pubmed: 37977786
pii: S0003-2670(23)01183-2
doi: 10.1016/j.aca.2023.341962
pii:
doi:

Substances chimiques

Synthetic Cathinone 0
Ions 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

341962

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Peng Che (P)

Vrije Universiteit Amsterdam, Department of Chemistry and Pharmaceutical Sciences, Amsterdam Institute of Molecular and Life Sciences (AIMMS), Division of BioAnalytical Chemistry, Amsterdam, the Netherlands; Center for Analytical Sciences Amsterdam (CASA), Amsterdam, the Netherlands.

J Tyler Davidson (JT)

Sam Houston State University, Department of Forensic Science, Huntsville, TX, USA.

Jeroen Kool (J)

Vrije Universiteit Amsterdam, Department of Chemistry and Pharmaceutical Sciences, Amsterdam Institute of Molecular and Life Sciences (AIMMS), Division of BioAnalytical Chemistry, Amsterdam, the Netherlands; Center for Analytical Sciences Amsterdam (CASA), Amsterdam, the Netherlands.

Isabelle Kohler (I)

Vrije Universiteit Amsterdam, Department of Chemistry and Pharmaceutical Sciences, Amsterdam Institute of Molecular and Life Sciences (AIMMS), Division of BioAnalytical Chemistry, Amsterdam, the Netherlands; Center for Analytical Sciences Amsterdam (CASA), Amsterdam, the Netherlands; Co van Ledden Hulsebosch Center (CLHC), Amsterdam Center for Forensic Science and Medicine, Amsterdam, the Netherlands. Electronic address: i.kohler@vu.nl.

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Classifications MeSH