Analytical profile of N-ethyl-N-cyclopropyl lysergamide (ECPLA), an isomer of lysergic acid 2,4-dimethylazetidide (LSZ).


Journal

Drug testing and analysis
ISSN: 1942-7611
Titre abrégé: Drug Test Anal
Pays: England
ID NLM: 101483449

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 15 07 2020
revised: 11 08 2020
accepted: 12 08 2020
pubmed: 18 8 2020
medline: 27 8 2021
entrez: 18 8 2020
Statut: ppublish

Résumé

Recent investigations have shown that N-ethyl-N-cyclopropyl lysergamide (ECPLA) produces LSD-like behavioral effects in mice, which suggests that it may act as a hallucinogen in humans. Although the use of ECPLA as a recreational drug has been limited, key analytical data that can be used to detect ECPLA are required for future forensic and clinical investigations. ECPLA is an isomer of (2'S,4'S)-lysergic acid 2,4-dimethylazetidide (LSZ), a lysergamide that emerged as a recreational drug in 2013. Several analytical approaches were examined, including single- and tandem mass spectrometry platforms at low and high resolution, gas- and liquid chromatography (GC, LC), nuclear magnetic resonance spectroscopy (NMR), and GC condensed-phase infrared spectroscopy (GC-sIR). ECPLA and LSZ could be differentiated by NMR, GC-sIR, GC, and LC-based methods. The electron ionization mass spectra of ECPLA and LSZ contained ion clusters typically observed with related lysergamides such as m/z 150-155, m/z 177-182, m/z 191-197, m/z 205-208, and m/z 219-224. One of the significant differences in abundance related to these clusters included ions at m/z 196 and m/z 207/208. The base peaks were detected at m/z 221 in both cases followed by the retro-Diels-Alder fragment at m/z 292. Minor but noticeable differences between the two isomers could also be seen in the relative abundance of m/z 98 and m/z 41. Electrospray ionization mass spectra included lysergamide-related ions at m/z 281, 251, 223, 208, 197, 180, and 140. LSZ (but not ECPLA) showed product ions at m/z 267 and m/z 98 under the conditions used.

Identifiants

pubmed: 32803833
doi: 10.1002/dta.2911
pmc: PMC9191644
mid: NIHMS1802270
doi:

Substances chimiques

Illicit Drugs 0
Lysergic Acid ITO20DAO7J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1514-1521

Subventions

Organisme : NIDA NIH HHS
ID : R01 DA041336
Pays : United States

Informations de copyright

© 2020 The Authors. Drug Testing and Analysis published by John Wiley & Sons Ltd.

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Auteurs

Simon D Brandt (SD)

School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, UK.

Pierce V Kavanagh (PV)

Department of Pharmacology and Therapeutics, School of Medicine, Trinity Centre for Health Sciences, St James Hospital, Dublin, Ireland.

Folker Westphal (F)

State Bureau of Criminal Investigation Schleswig-Holstein, Section Narcotics/Toxicology, Kiel, Germany.

Alexander Stratford (A)

Synex Synthetics BV, Maastricht, The Netherlands.

Simon P Elliott (SP)

Elliott Forensic Consulting, Birmingham, UK.

Geraldine Dowling (G)

Department of Pharmacology and Therapeutics, School of Medicine, Trinity Centre for Health Sciences, St James Hospital, Dublin, Ireland.
Department of Life Sciences, School of Science, Sligo Institute of Technology, Sligo, Ireland.

Adam L Halberstadt (AL)

Department of Psychiatry, University of California San Diego, La Jolla, CA, USA.
Research Service, VA San Diego Healthcare System, La Jolla, CA, USA.

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Classifications MeSH