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Preventing Mislabeling: A Comparative Chromatographic Analysis for Classifying Medical and Industrial Cannabis

Gas chromatography (GC) techniques for analyzing and determining the cannabinoid profile in cannabis (Cannabis sativa L.) are widely used in standard laboratories; however, these methods may mislabel the profile when used under rapid conditions. Our study aimed to highlight this problem and optimize...

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Autores principales: Salazar-Bermeo, Julio, Moreno-Chamba, Bryan, Martínez-Madrid, María Concepción, Valero, Manuel, Rodrigo-García, Joaquín, Hosseinian, Farah, Martín-Bermudo, Francisco, Aguado, Manuel, de la Torre, Rosa, Martí, Nuria, Saura, Domingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143857/
https://www.ncbi.nlm.nih.gov/pubmed/37110787
http://dx.doi.org/10.3390/molecules28083552
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author Salazar-Bermeo, Julio
Moreno-Chamba, Bryan
Martínez-Madrid, María Concepción
Valero, Manuel
Rodrigo-García, Joaquín
Hosseinian, Farah
Martín-Bermudo, Francisco
Aguado, Manuel
de la Torre, Rosa
Martí, Nuria
Saura, Domingo
author_facet Salazar-Bermeo, Julio
Moreno-Chamba, Bryan
Martínez-Madrid, María Concepción
Valero, Manuel
Rodrigo-García, Joaquín
Hosseinian, Farah
Martín-Bermudo, Francisco
Aguado, Manuel
de la Torre, Rosa
Martí, Nuria
Saura, Domingo
author_sort Salazar-Bermeo, Julio
collection PubMed
description Gas chromatography (GC) techniques for analyzing and determining the cannabinoid profile in cannabis (Cannabis sativa L.) are widely used in standard laboratories; however, these methods may mislabel the profile when used under rapid conditions. Our study aimed to highlight this problem and optimize GC column conditions and mass spectrometry (MS) parameters to accurately identify cannabinoids in both standards and forensic samples. The method was validated for linearity, selectivity, and precision. It was observed that when tetrahydrocannabinol (Δ9-THC) and cannabidiolic acid (CBD-A) were examined using rapid GC conditions, the resulting derivatives generated identical retention times. Wider chromatographic conditions were applied. The linear range for each compound ranged from 0.02 μg/mL to 37.50 μg/mL. The R(2) values ranged from 0.996 to 0.999. The LOQ values ranged from 0.33 μg/mL to 5.83 μg/mL, and the LOD values ranged from 0.11 μg/mL to 1.92 μg/mL. The precision values ranged from 0.20% to 8.10% RSD. In addition, forensic samples were analyzed using liquid chromatography (HPLC-DAD) in an interlaboratory comparison test, with higher CBD and THC content than GC–MS determination (p < 0.05) in samples. Overall, this study highlights the importance of optimizing GC techniques to avoid mislabeling cannabinoids in cannabis samples.
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spelling pubmed-101438572023-04-29 Preventing Mislabeling: A Comparative Chromatographic Analysis for Classifying Medical and Industrial Cannabis Salazar-Bermeo, Julio Moreno-Chamba, Bryan Martínez-Madrid, María Concepción Valero, Manuel Rodrigo-García, Joaquín Hosseinian, Farah Martín-Bermudo, Francisco Aguado, Manuel de la Torre, Rosa Martí, Nuria Saura, Domingo Molecules Article Gas chromatography (GC) techniques for analyzing and determining the cannabinoid profile in cannabis (Cannabis sativa L.) are widely used in standard laboratories; however, these methods may mislabel the profile when used under rapid conditions. Our study aimed to highlight this problem and optimize GC column conditions and mass spectrometry (MS) parameters to accurately identify cannabinoids in both standards and forensic samples. The method was validated for linearity, selectivity, and precision. It was observed that when tetrahydrocannabinol (Δ9-THC) and cannabidiolic acid (CBD-A) were examined using rapid GC conditions, the resulting derivatives generated identical retention times. Wider chromatographic conditions were applied. The linear range for each compound ranged from 0.02 μg/mL to 37.50 μg/mL. The R(2) values ranged from 0.996 to 0.999. The LOQ values ranged from 0.33 μg/mL to 5.83 μg/mL, and the LOD values ranged from 0.11 μg/mL to 1.92 μg/mL. The precision values ranged from 0.20% to 8.10% RSD. In addition, forensic samples were analyzed using liquid chromatography (HPLC-DAD) in an interlaboratory comparison test, with higher CBD and THC content than GC–MS determination (p < 0.05) in samples. Overall, this study highlights the importance of optimizing GC techniques to avoid mislabeling cannabinoids in cannabis samples. MDPI 2023-04-18 /pmc/articles/PMC10143857/ /pubmed/37110787 http://dx.doi.org/10.3390/molecules28083552 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Salazar-Bermeo, Julio
Moreno-Chamba, Bryan
Martínez-Madrid, María Concepción
Valero, Manuel
Rodrigo-García, Joaquín
Hosseinian, Farah
Martín-Bermudo, Francisco
Aguado, Manuel
de la Torre, Rosa
Martí, Nuria
Saura, Domingo
Preventing Mislabeling: A Comparative Chromatographic Analysis for Classifying Medical and Industrial Cannabis
title Preventing Mislabeling: A Comparative Chromatographic Analysis for Classifying Medical and Industrial Cannabis
title_full Preventing Mislabeling: A Comparative Chromatographic Analysis for Classifying Medical and Industrial Cannabis
title_fullStr Preventing Mislabeling: A Comparative Chromatographic Analysis for Classifying Medical and Industrial Cannabis
title_full_unstemmed Preventing Mislabeling: A Comparative Chromatographic Analysis for Classifying Medical and Industrial Cannabis
title_short Preventing Mislabeling: A Comparative Chromatographic Analysis for Classifying Medical and Industrial Cannabis
title_sort preventing mislabeling: a comparative chromatographic analysis for classifying medical and industrial cannabis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143857/
https://www.ncbi.nlm.nih.gov/pubmed/37110787
http://dx.doi.org/10.3390/molecules28083552
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