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Identification and quantification of both isomers of hexahydrocannabinol, (9R)-hexahydrocannabinol and (9S)-hexahydrocannabinol, in three different matrices by mass spectrometry.
Bottinelli, Charline; Baradian, Pauline; Poly, Amélie; Hoizey, Guillaume; Chatenay, Camille.
Afiliação
  • Bottinelli C; LATLUMTOX Laboratory, Bron, France.
  • Baradian P; LATLUMTOX Laboratory, Bron, France.
  • Poly A; LATLUMTOX Laboratory, Bron, France.
  • Hoizey G; LATLUMTOX Laboratory, Bron, France.
  • Chatenay C; LATLUMTOX Laboratory, Bron, France.
Rapid Commun Mass Spectrom ; 38(7): e9711, 2024 Apr 15.
Article em En | MEDLINE | ID: mdl-38342829
ABSTRACT
CONTEXT Hexahydrocannabinol (HHC), a compound derived from synthetic production using cannabidiol (CBD) or delta-9-tetrahydrocannabinol (Δ9 -THC), has gained recent attention due to its presence in seized materials across Europe. Sold legally in various forms, HHC poses potential health risks, particularly as a legal alternative to THC in some countries. Despite its historical description in the 1940s, limited toxicology data, pharmacological understanding, and analytical methods for HHC exist.

METHOD:

This study proposes analytical techniques using mass spectrometry to detect, identify, and quantify (9R)-HHC and (9S)-HHC, concurrently with THC and CBD in various matrices, including oral fluid, whole blood, and seized material. Three distinct methods were employed for different matrices GC/MS for seized material, GC/MS/MS for whole blood, and UHPLC/MS/MS for oral fluid. Methods were validated qualitatively for oral fluid with a FLOQSwab® device and quantitatively in whole blood and seized material according to Peters et al's recommendations and ICH guidelines.

RESULTS:

Validated methods were considered reliable in detecting and quantifying HHC isomers in terms of repeatability, reproducibility, and linearity with r2 systematically >0.992. These methods were applied to authentic cases, including seized materials and biological samples from traffic control (whole blood and oral fluid). In seized materials, (9R)-HHC levels ranged from 2.09% to 8.85% and (9R)-HHC/(9S)-HHC ratios varied from 1.36 to 2.68. In whole blood sample, (9R)-HHC and (9S)-HHC concentrations were, respectively, 2.38 and 1.39 ng/mL. For all analyzed samples, cannabinoids such as THC and CBD were also detected.

CONCLUSION:

This research contributes analytical insights into differentiating and simultaneously analyzing (9R)-HHC and (9S)-HHC, using widely applicable mass spectrometric methods. The study emphasizes the need for vigilance among toxicologists, as new semisynthetic cannabinoids continue to emerge in Europe, with potential health implications. The findings underscore the importance of reliable analytical methods for monitoring these compounds in forensic and clinical settings.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canabidiol / Canabinoides Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Idioma: En Revista: Rapid Commun Mass Spectrom Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canabidiol / Canabinoides Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Idioma: En Revista: Rapid Commun Mass Spectrom Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França