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Mass-Spectrometry-Based Identification of Synthetic Drug Isomers Using Infrared Ion Spectroscopy
[Image: see text] Infrared ion spectroscopy (IRIS), a mass-spectrometry-based technique exploiting resonant infrared multiple photon dissociation (IRMPD), has been applied for the identification of novel psychoactive substances (NPS). Identification of the precise isomeric forms of NPS is of signifi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240807/ https://www.ncbi.nlm.nih.gov/pubmed/32286052 http://dx.doi.org/10.1021/acs.analchem.0c00915 |
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author | Kranenburg, Ruben F. van Geenen, Fred A. M. G. Berden, Giel Oomens, Jos Martens, Jonathan van Asten, Arian C. |
author_facet | Kranenburg, Ruben F. van Geenen, Fred A. M. G. Berden, Giel Oomens, Jos Martens, Jonathan van Asten, Arian C. |
author_sort | Kranenburg, Ruben F. |
collection | PubMed |
description | [Image: see text] Infrared ion spectroscopy (IRIS), a mass-spectrometry-based technique exploiting resonant infrared multiple photon dissociation (IRMPD), has been applied for the identification of novel psychoactive substances (NPS). Identification of the precise isomeric forms of NPS is of significant forensic relevance since legal controls are dependent on even minor molecular differences such as a single ring-substituent position. Using three isomers of fluoroamphetamine and two ring-isomers of both MDA and MDMA, we demonstrate the ability of IRIS to distinguish closely related NPS. Computationally predicted infrared (IR) spectra are shown to correspond with experimental spectra and could explain the molecular origins of their distinctive IR absorption bands. IRIS was then used to investigate a confiscated street sample containing two unknown substances. One substance could easily be identified by comparison to the IR spectra of reference standards. For the other substance, however, this approach proved inconclusive due to incomplete mass spectral databases as well as a lack of available reference compounds, two common analytical limitations resulting from the rapid development of NPS. Most excitingly, the second unknown substance could nevertheless be identified by using computationally predicted IR spectra of several potential candidate structures instead of their experimental reference spectra. |
format | Online Article Text |
id | pubmed-7240807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-72408072020-05-21 Mass-Spectrometry-Based Identification of Synthetic Drug Isomers Using Infrared Ion Spectroscopy Kranenburg, Ruben F. van Geenen, Fred A. M. G. Berden, Giel Oomens, Jos Martens, Jonathan van Asten, Arian C. Anal Chem [Image: see text] Infrared ion spectroscopy (IRIS), a mass-spectrometry-based technique exploiting resonant infrared multiple photon dissociation (IRMPD), has been applied for the identification of novel psychoactive substances (NPS). Identification of the precise isomeric forms of NPS is of significant forensic relevance since legal controls are dependent on even minor molecular differences such as a single ring-substituent position. Using three isomers of fluoroamphetamine and two ring-isomers of both MDA and MDMA, we demonstrate the ability of IRIS to distinguish closely related NPS. Computationally predicted infrared (IR) spectra are shown to correspond with experimental spectra and could explain the molecular origins of their distinctive IR absorption bands. IRIS was then used to investigate a confiscated street sample containing two unknown substances. One substance could easily be identified by comparison to the IR spectra of reference standards. For the other substance, however, this approach proved inconclusive due to incomplete mass spectral databases as well as a lack of available reference compounds, two common analytical limitations resulting from the rapid development of NPS. Most excitingly, the second unknown substance could nevertheless be identified by using computationally predicted IR spectra of several potential candidate structures instead of their experimental reference spectra. American Chemical Society 2020-04-14 2020-05-19 /pmc/articles/PMC7240807/ /pubmed/32286052 http://dx.doi.org/10.1021/acs.analchem.0c00915 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Kranenburg, Ruben F. van Geenen, Fred A. M. G. Berden, Giel Oomens, Jos Martens, Jonathan van Asten, Arian C. Mass-Spectrometry-Based Identification of Synthetic Drug Isomers Using Infrared Ion Spectroscopy |
title | Mass-Spectrometry-Based Identification of Synthetic
Drug Isomers Using Infrared Ion Spectroscopy |
title_full | Mass-Spectrometry-Based Identification of Synthetic
Drug Isomers Using Infrared Ion Spectroscopy |
title_fullStr | Mass-Spectrometry-Based Identification of Synthetic
Drug Isomers Using Infrared Ion Spectroscopy |
title_full_unstemmed | Mass-Spectrometry-Based Identification of Synthetic
Drug Isomers Using Infrared Ion Spectroscopy |
title_short | Mass-Spectrometry-Based Identification of Synthetic
Drug Isomers Using Infrared Ion Spectroscopy |
title_sort | mass-spectrometry-based identification of synthetic
drug isomers using infrared ion spectroscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240807/ https://www.ncbi.nlm.nih.gov/pubmed/32286052 http://dx.doi.org/10.1021/acs.analchem.0c00915 |
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