Decarbonylation: A metabolic pathway of cannabidiol in humans.


Journal

Drug testing and analysis
ISSN: 1942-7611
Titre abrégé: Drug Test Anal
Pays: England
ID NLM: 101483449

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 03 12 2018
revised: 24 01 2019
accepted: 24 01 2019
pubmed: 31 1 2019
medline: 22 1 2020
entrez: 31 1 2019
Statut: ppublish

Résumé

Cannabidiol (CBD) is a non-psychoactive cannabinoid, which is of growing medical interest. Previous studies on the metabolism of CBD showed mainly the formation of hydroxylated or oxidized derivatives, the formation of carboxylic acids or modifications of the aliphatic side chain. Using incubation of CBD with hepatic microsomes of mice, the formation of carbon monoxide was reported. We investigated the phase I metabolism of CBD and cannabidivarin (CBDV) using in vitro experiments with human liver microsomes in order to discover so far not considered metabolites. Identification of metabolites was done by liquid chromatography coupled with quadrupole time of flight mass spectrometry (LC-QToF-MS). Within these experiments, we came across decarbonylation of CBD and CBDV. Further investigations were focused on observed decarbonylated CBD (DCBD). To confirm this metabolite in humans in vivo, plasma samples containing large amounts of cannabinoids as well as serum and urine samples, collected after a voluntary intake of a CBD-containing food supplement, were analyzed by LC coupled to triple quadrupole mass spectrometry (LC-QQQ-MS). DCBD was detected in in vitro incubation mixtures, serum samples, and urine samples (after alkaline or enzymatic hydrolysis) collected after the voluntary intake, as well as in plasma samples of cannabis users. DCBD appears to be an important supplementary human metabolite that might be helpful for the analytical confirmation of a CBD uptake and might improve the interpretation of the consumption of CBD-containing products. Results of this study indicate a prolonged detectability of DCBD (in serum) in comparison to CBD after oral CBD ingestion.

Identifiants

pubmed: 30698361
doi: 10.1002/dta.2572
doi:

Substances chimiques

Cannabinoids 0
Carboxylic Acids 0
Cannabidiol 19GBJ60SN5
cannabidivarin I198VBV98I

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

957-967

Informations de copyright

© 2019 John Wiley & Sons, Ltd.

Auteurs

Michael Kraemer (M)

Institute of Forensic Medicine, Forensic Toxicology, University Bonn, Stiftsplatz 12, 53111, Bonn, Germany.

Sebastian Broecker (S)

Broeckers Solutions, Dyrotzer Straße 8, 13583, Berlin, Germany.

Burkhard Madea (B)

Institute of Forensic Medicine, Forensic Toxicology, University Bonn, Stiftsplatz 12, 53111, Bonn, Germany.

Cornelius Hess (C)

Institute of Forensic Medicine, Forensic Toxicology, University Bonn, Stiftsplatz 12, 53111, Bonn, Germany.
Institute of Forensic Medicine, Forensic Toxicology, University Mainz, Am Pulverturm 3, 55131, Mainz, Germany.

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Classifications MeSH