Literature DB >> 30193661

Extraction and isolation of cannabinoids from marijuana seizures and characterization by 1H NMR allied to chemometric tools.

Júlia de A Leite1, Marcos V L de Oliveira1, Raphael Conti1, Warley de S Borges1, Thalles R Rosa1, Paulo R Filgueiras2, Valdemar Lacerda1, Wanderson Romão3, Álvaro C Neto4.   

Abstract

Marijuana, a drug derived from the Cannabis sativa L. plant, is the world's most consumed illicit drug. In this paper, a total of 156 marijuana samples seized in the state of Espírito Santo (ES), Brazil were studied and analysed by proton nuclear magnetic resonance (1H NMR) spectroscopy to identify the major cannabinoids present. A crude extract of all samples was purified using high performance liquid chromatography so that these compounds could serve as reference substances. Nine fractions were obtained and analysed by 1H NMR and gas chromatography-mass spectrometry (GC-MS), with five presented cannabinoids. ∆9-THC (Δ9-trans-tetrahydrocannabinol), ∆9-THCA (∆9-tetrahydrocannabinolic acid), ∆8-THC (∆8-tetrahydrocannabinol), 11-hydroxycannabinol, CBV (cannabivarin), and CBN (cannabinol) were found, and their chemical structures were confirmed by GC-MS. The latter compound was obtained with high purity (≈100%), while the others were obtained as less complex mixtures with purity higher than 75% (except for Δ8-THC). Principal component analysis (PCA) was used on the 1H NMR spectra of the 156 samples, and it was found that the samples were grouped according to the months, differentiating into two groups (from July 2014 to January 2015 and from February 2015 to July 2015), where non-grouping was observed from four macro-regions of the ES state (North, Central, Metropolitan, and South). The chemical profile of the seized samples was correlated to the 1H NMR spectrum of an isolated CBN sub-fraction, in which the group formed by samples seized in the year 2015 presented lower CBN content in the chemical composition. From the PCA score plot, two groups of samples were confirmed using the partial least squares discriminant analysis and orthogonal projections to latent structures classification methods.
Copyright © 2018 The Chartered Society of Forensic Sciences. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  (1)H NMR; GC–MS; HPLC; Marijuana; PCA

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Year:  2018        PMID: 30193661     DOI: 10.1016/j.scijus.2018.06.005

Source DB:  PubMed          Journal:  Sci Justice        ISSN: 1355-0306            Impact factor:   2.124


  2 in total

Review 1.  Interpol review of controlled substances 2016-2019.

Authors:  Nicole S Jones; Jeffrey H Comparin
Journal:  Forensic Sci Int Synerg       Date:  2020-05-24

2.  Cannabidiol as the Substrate in Acid-Catalyzed Intramolecular Cyclization.

Authors:  Paola Marzullo; Francesca Foschi; Davide Andrea Coppini; Fabiola Fanchini; Lucia Magnani; Selina Rusconi; Marcello Luzzani; Daniele Passarella
Journal:  J Nat Prod       Date:  2020-09-29       Impact factor: 4.050

  2 in total

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