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Advances in new psychoactive substances identification: the U.R.I.To.N. Consortium
Identification of new psychoactive substances (NPS) in biological and non-biological samples represents a hard challenge for forensic toxicologists. Their great chemical variety and the speed with which new NPS are synthesised and spread make stringent the need of advanced tools for their detection...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445230/ https://www.ncbi.nlm.nih.gov/pubmed/28629236 http://dx.doi.org/10.1080/14756366.2017.1333987 |
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author | Bertol, Elisabetta Vaiano, Fabio Mari, Francesco Di Milia, Maria Grazia Bua, Silvia Supuran, Claudiu T. Carta, Fabrizio |
author_facet | Bertol, Elisabetta Vaiano, Fabio Mari, Francesco Di Milia, Maria Grazia Bua, Silvia Supuran, Claudiu T. Carta, Fabrizio |
author_sort | Bertol, Elisabetta |
collection | PubMed |
description | Identification of new psychoactive substances (NPS) in biological and non-biological samples represents a hard challenge for forensic toxicologists. Their great chemical variety and the speed with which new NPS are synthesised and spread make stringent the need of advanced tools for their detection based on multidisciplinary approaches. For this reason, in August 2016, the “Unit of Research and Innovation in Forensic Toxicology and Neuroscience of Addiction” (U.R.I.To.N.) was founded by the Forensic Toxicology Division of the University of Florence. In this Research Unit, various professionals (i.e. forensic toxicologists, chemists, physicians) collaborate to study all the aspects of drugs of abuse, especially NPS. Herein, we describe the multidisciplinary approach comprising liquid chromatography coupled to tandem mass spectrometry (LC–MS/MS), gas chromatography hyphenated to mass spectrometry (GC–MS) and solution nuclear magnetic resonance analysis that allowed the identification of three NPS such as 1-(benzofuran-5-yl)-N-methylpropan-2-amine, 2-amino-1-(4-bromo-2,5-dimethoxyphenyl)ethan-1-one (bk-2C-B), and 3-(2-aminopropyl)indole (α-methyltryptamine) in seized materials. |
format | Online Article Text |
id | pubmed-6445230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-64452302019-04-09 Advances in new psychoactive substances identification: the U.R.I.To.N. Consortium Bertol, Elisabetta Vaiano, Fabio Mari, Francesco Di Milia, Maria Grazia Bua, Silvia Supuran, Claudiu T. Carta, Fabrizio J Enzyme Inhib Med Chem Research Paper Identification of new psychoactive substances (NPS) in biological and non-biological samples represents a hard challenge for forensic toxicologists. Their great chemical variety and the speed with which new NPS are synthesised and spread make stringent the need of advanced tools for their detection based on multidisciplinary approaches. For this reason, in August 2016, the “Unit of Research and Innovation in Forensic Toxicology and Neuroscience of Addiction” (U.R.I.To.N.) was founded by the Forensic Toxicology Division of the University of Florence. In this Research Unit, various professionals (i.e. forensic toxicologists, chemists, physicians) collaborate to study all the aspects of drugs of abuse, especially NPS. Herein, we describe the multidisciplinary approach comprising liquid chromatography coupled to tandem mass spectrometry (LC–MS/MS), gas chromatography hyphenated to mass spectrometry (GC–MS) and solution nuclear magnetic resonance analysis that allowed the identification of three NPS such as 1-(benzofuran-5-yl)-N-methylpropan-2-amine, 2-amino-1-(4-bromo-2,5-dimethoxyphenyl)ethan-1-one (bk-2C-B), and 3-(2-aminopropyl)indole (α-methyltryptamine) in seized materials. Taylor & Francis 2017-06-20 /pmc/articles/PMC6445230/ /pubmed/28629236 http://dx.doi.org/10.1080/14756366.2017.1333987 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Bertol, Elisabetta Vaiano, Fabio Mari, Francesco Di Milia, Maria Grazia Bua, Silvia Supuran, Claudiu T. Carta, Fabrizio Advances in new psychoactive substances identification: the U.R.I.To.N. Consortium |
title | Advances in new psychoactive substances identification: the U.R.I.To.N. Consortium |
title_full | Advances in new psychoactive substances identification: the U.R.I.To.N. Consortium |
title_fullStr | Advances in new psychoactive substances identification: the U.R.I.To.N. Consortium |
title_full_unstemmed | Advances in new psychoactive substances identification: the U.R.I.To.N. Consortium |
title_short | Advances in new psychoactive substances identification: the U.R.I.To.N. Consortium |
title_sort | advances in new psychoactive substances identification: the u.r.i.to.n. consortium |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445230/ https://www.ncbi.nlm.nih.gov/pubmed/28629236 http://dx.doi.org/10.1080/14756366.2017.1333987 |
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