UHPLC-MS/MS analysis of cannabidiol metabolites in serum and urine samples. Application to an individual treated with medical cannabis.


Journal

Talanta
ISSN: 1873-3573
Titre abrégé: Talanta
Pays: Netherlands
ID NLM: 2984816R

Informations de publication

Date de publication:
01 Feb 2021
Historique:
received: 03 08 2020
revised: 08 10 2020
accepted: 11 10 2020
entrez: 10 12 2020
pubmed: 11 12 2020
medline: 15 5 2021
Statut: ppublish

Résumé

No analytical assay is currently available for the simultaneous determination of CBD major metabolites in serum or urine samples of individuals treated with medical cannabis or CBD-based pharmaceuticals. We developed and validated a method using ultra-high-performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS) for quantifying cannabidiol (CBD) and its metabolites, cannabidiol-7-oic acid (7-COOH-CBD), 7- hydroxycannabidiol (7-OH-CBD), 6-alpha-hydroxycannabidiol (6-α-OH-CBD) and 6-beta-hydroxycannabidiol (6-β-OH-CBD) in serum and urine samples of an individual treated with medical cannabis. The ionization was performed by electrospray in negative mode to reach the sensitivity required to detect trace amounts, with limits of quantification ranging from 0.05 to 0.1 ng/mL. The method is accurate (average inter/intra-day error, <15%), precise (inter/intra-day imprecision, <15%) and fast (8 min run time) and it is an essential tool to investigate CBD pharmacokinetics and pharmacodynamics in individuals treated with medical cannabis or with CBD-based medical preparations.

Identifiants

pubmed: 33298281
pii: S0039-9140(20)31063-8
doi: 10.1016/j.talanta.2020.121772
pii:
doi:

Substances chimiques

Medical Marijuana 0
Cannabidiol 19GBJ60SN5
Dronabinol 7J8897W37S

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

121772

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Simona Pichini (S)

National Centre on Addiction and Doping, Istituto Superiore di Sanità, Rome, Italy. Electronic address: simona.pichini@iss.it.

Sara Malaca (S)

Department of Excellence-Biomedical Sciences and Public Health, University Politecnica Delle Marche, Ancona, Italy.

Massimo Gottardi (M)

Comedical S.rL., Trento, Italy.

Ana Pilar Pérez-Acevedo (AP)

Clinical Pharmacology Unit, Hospital Universitari Germans Trias I Pujol (HUGTiP-IGTP), Badalona, Spain; Department of Pharmacology, Therapeutics and Toxicology, Universitat Autònoma de Barcelona, Cerdantola Del Vallés, Spain.

Esther Papaseit (E)

Clinical Pharmacology Unit, Hospital Universitari Germans Trias I Pujol (HUGTiP-IGTP), Badalona, Spain; Department of Pharmacology, Therapeutics and Toxicology, Universitat Autònoma de Barcelona, Cerdantola Del Vallés, Spain.

Clara Perez-Maña (C)

Clinical Pharmacology Unit, Hospital Universitari Germans Trias I Pujol (HUGTiP-IGTP), Badalona, Spain; Department of Pharmacology, Therapeutics and Toxicology, Universitat Autònoma de Barcelona, Cerdantola Del Vallés, Spain.

Magí Farré (M)

Clinical Pharmacology Unit, Hospital Universitari Germans Trias I Pujol (HUGTiP-IGTP), Badalona, Spain; Department of Pharmacology, Therapeutics and Toxicology, Universitat Autònoma de Barcelona, Cerdantola Del Vallés, Spain.

Roberta Pacifici (R)

National Centre on Addiction and Doping, Istituto Superiore di Sanità, Rome, Italy.

Adriano Tagliabracci (A)

Department of Excellence-Biomedical Sciences and Public Health, University Politecnica Delle Marche, Ancona, Italy.

Giulio Mannocchi (G)

University of Camerino, Camerino, Italy.

Francesco Paolo Busardò (FP)

Department of Excellence-Biomedical Sciences and Public Health, University Politecnica Delle Marche, Ancona, Italy.

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Classifications MeSH