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Enzyme Immunoassay for Measuring Aflatoxin B1 in Legal Cannabis

The diffusion of the legalization of cannabis for recreational, medicinal and nutraceutical uses requires the development of adequate analytical methods to assure the safety and security of such products. In particular, aflatoxins are considered to pose a major risk for the health of cannabis consum...

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Autores principales: Di Nardo, Fabio, Cavalera, Simone, Baggiani, Claudio, Chiarello, Matteo, Pazzi, Marco, Anfossi, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232199/
https://www.ncbi.nlm.nih.gov/pubmed/32326118
http://dx.doi.org/10.3390/toxins12040265
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author Di Nardo, Fabio
Cavalera, Simone
Baggiani, Claudio
Chiarello, Matteo
Pazzi, Marco
Anfossi, Laura
author_facet Di Nardo, Fabio
Cavalera, Simone
Baggiani, Claudio
Chiarello, Matteo
Pazzi, Marco
Anfossi, Laura
author_sort Di Nardo, Fabio
collection PubMed
description The diffusion of the legalization of cannabis for recreational, medicinal and nutraceutical uses requires the development of adequate analytical methods to assure the safety and security of such products. In particular, aflatoxins are considered to pose a major risk for the health of cannabis consumers. Among analytical methods that allows for adequate monitoring of food safety, immunoassays play a major role thanks to their cost-effectiveness, high-throughput capacity, simplicity and limited requirement for equipment and skilled operators. Therefore, a rapid and sensitive enzyme immunoassay has been adapted to measure the most hazardous aflatoxin B1 in cannabis products. The assay was acceptably accurate (recovery rate: 78–136%), reproducible (intra- and inter-assay means coefficients of variation 11.8% and 13.8%, respectively), and sensitive (limit of detection and range of quantification: 0.35 ng mL(−1) and 0.4–2 ng mL(−1), respectively corresponding to 7 ng g(−1) and 8–40 ng g(−1) ng g(−1) in the plant) and provided results which agreed with a HPLC-MS/MS method for the direct analysis of aflatoxin B1 in cannabis inflorescence and leaves. In addition, the carcinogenic aflatoxin B1 was detected in 50% of the cannabis products analyzed (14 samples collected from small retails) at levels exceeding those admitted by the European Union in commodities intended for direct human consumption, thus envisaging the need for effective surveillance of aflatoxin contamination in legal cannabis.
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spelling pubmed-72321992020-05-22 Enzyme Immunoassay for Measuring Aflatoxin B1 in Legal Cannabis Di Nardo, Fabio Cavalera, Simone Baggiani, Claudio Chiarello, Matteo Pazzi, Marco Anfossi, Laura Toxins (Basel) Article The diffusion of the legalization of cannabis for recreational, medicinal and nutraceutical uses requires the development of adequate analytical methods to assure the safety and security of such products. In particular, aflatoxins are considered to pose a major risk for the health of cannabis consumers. Among analytical methods that allows for adequate monitoring of food safety, immunoassays play a major role thanks to their cost-effectiveness, high-throughput capacity, simplicity and limited requirement for equipment and skilled operators. Therefore, a rapid and sensitive enzyme immunoassay has been adapted to measure the most hazardous aflatoxin B1 in cannabis products. The assay was acceptably accurate (recovery rate: 78–136%), reproducible (intra- and inter-assay means coefficients of variation 11.8% and 13.8%, respectively), and sensitive (limit of detection and range of quantification: 0.35 ng mL(−1) and 0.4–2 ng mL(−1), respectively corresponding to 7 ng g(−1) and 8–40 ng g(−1) ng g(−1) in the plant) and provided results which agreed with a HPLC-MS/MS method for the direct analysis of aflatoxin B1 in cannabis inflorescence and leaves. In addition, the carcinogenic aflatoxin B1 was detected in 50% of the cannabis products analyzed (14 samples collected from small retails) at levels exceeding those admitted by the European Union in commodities intended for direct human consumption, thus envisaging the need for effective surveillance of aflatoxin contamination in legal cannabis. MDPI 2020-04-20 /pmc/articles/PMC7232199/ /pubmed/32326118 http://dx.doi.org/10.3390/toxins12040265 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Di Nardo, Fabio
Cavalera, Simone
Baggiani, Claudio
Chiarello, Matteo
Pazzi, Marco
Anfossi, Laura
Enzyme Immunoassay for Measuring Aflatoxin B1 in Legal Cannabis
title Enzyme Immunoassay for Measuring Aflatoxin B1 in Legal Cannabis
title_full Enzyme Immunoassay for Measuring Aflatoxin B1 in Legal Cannabis
title_fullStr Enzyme Immunoassay for Measuring Aflatoxin B1 in Legal Cannabis
title_full_unstemmed Enzyme Immunoassay for Measuring Aflatoxin B1 in Legal Cannabis
title_short Enzyme Immunoassay for Measuring Aflatoxin B1 in Legal Cannabis
title_sort enzyme immunoassay for measuring aflatoxin b1 in legal cannabis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232199/
https://www.ncbi.nlm.nih.gov/pubmed/32326118
http://dx.doi.org/10.3390/toxins12040265
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