Molecular Network-Based Identification of Tramadol Metabolites in a Fatal Tramadol Poisoning.

clinical toxicology high-resolution tandem mass spectrometry molecular network tramadol untargeted metabolomics

Journal

Metabolites
ISSN: 2218-1989
Titre abrégé: Metabolites
Pays: Switzerland
ID NLM: 101578790

Informations de publication

Date de publication:
19 Jul 2022
Historique:
received: 24 06 2022
revised: 13 07 2022
accepted: 14 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

Identification of xenobiotics and their phase I/II metabolites in poisoned patients remains challenging. Systematic approaches using bioinformatic tools are needed to detect all compounds as exhaustively as possible. Here, we aimed to assess an analytical workflow using liquid chromatography coupled to high-resolution mass spectrometry with data processing based on a molecular network to identify tramadol metabolites in urine and plasma in poisoned patients. The generated molecular network from liquid chromatography coupled to high-resolution tandem mass spectrometry data acquired in both positive and negative ion modes allowed for the identification of 25 tramadol metabolites in urine and plasma, including four methylated metabolites that have not been previously reported in humans or in vitro models. While positive ion mode is reliable for generating a network of tramadol metabolites displaying a dimethylamino radical in their structure, negative ion mode was useful to cluster phase II metabolites. In conclusion, the combined use of molecular networks in positive and negative ion modes is a suitable and robust tool to identify a broad range of metabolites in poisoned patients, as shown in a fatal tramadol-poisoned patient.

Identifiants

pubmed: 35888789
pii: metabo12070665
doi: 10.3390/metabo12070665
pmc: PMC9323855
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Romain Magny (R)

Laboratoire de Toxicologie, Fédération de Toxicologie, AP-HP, Hôpital Lariboisière, 75006 Paris, France.
Université Paris Cité, CNRS, CiTCoM, 75006 Paris, France.

Nicolas Auzeil (N)

Université Paris Cité, CNRS, CiTCoM, 75006 Paris, France.

Bertrand Lefrère (B)

Laboratoire de Toxicologie, Fédération de Toxicologie, AP-HP, Hôpital Lariboisière, 75006 Paris, France.

Bruno Mégarbane (B)

Réanimation Médicale et Toxicologique, Fédération de Toxicologie, AP-HP, Hôpital Lariboisière, 75010 Paris, France.
Inserm, UMRS-1144, Université Paris Cité, 75006 Paris, France.

Pascal Houzé (P)

Laboratoire de Toxicologie, Fédération de Toxicologie, AP-HP, Hôpital Lariboisière, 75006 Paris, France.
Université Paris Cité, CNRS, INSERM, Unité des Technologies Chimiques Et Biologiques Pour La Santé (UTCBS), 75006 Paris, France.

Laurence Labat (L)

Laboratoire de Toxicologie, Fédération de Toxicologie, AP-HP, Hôpital Lariboisière, 75006 Paris, France.
Inserm, UMRS-1144, Université Paris Cité, 75006 Paris, France.

Classifications MeSH