Identification of three unexpected new psychoactive substances at an Australian drug checking service.
Jess L Algar, Douglas J Lawes, Adam J Carroll, David Caldicott, Malcolm D. Mcleod
Drug Testing and Analysis October 1, 2024 DOI: 10.1002/dta.3637 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Case study Case report Peer reviewed |
|---|---|
| Sample size | 3 |
| Population | Drug samples presented to a fixed-site drug checking service |
| Keywords | Drug checking Drugs Harm reduction New psychoactive substances Pill testing |
| Citations | 14 |
| Key findings | Three samples expected to be known substances were identified as three novel new psychoactive substances not previously described in the literature. |
Abstract
Drug checking is a harm reduction measure that provides people with the opportunity to confirm the identity and purity of substances before consumption. The CanTEST Health and Drug Checking Service is Australia's first fixed-site drug checking service, where clients can learn about the contents of the samples they provide while receiving tailored harm reduction and health advice. Three samples were recently presented to the service with the expectation of 4-fluoromethylphenidate (4F-MPH) 1, methoxetamine (MXE) 2 and 3-methylmethcathinone (3-MMC) 3. The identity of all three samples did not meet these expectations and remained unknown on-site, as no high confidence identifications were obtained. However, further analysis by nuclear magnetic resonance spectroscopy, high resolution gas chromatography-electron ionisation-mass spectrometry and liquid chromatography-electrospray ionisation-mass spectrometry at the nearby Australian National University allowed for the structure elucidation of the three samples as 4-fluoro-α-pyrrolidinoisohexanophenone (4F-α-PiHP) 4, 1-(4-fluorobenzyl)-4-methylpiperazine (4F-MBZP) 5 and N-propyl-1,2-diphenylethylamine (propylphenidine) 6, respectively. Given all three samples were not of the expected identity and have not yet been described as new psychoactive substances in the literature, this study presents a full characterisation of each compound. As exemplified by this rapid identification of three unexpected new psychoactive substances, drug checking can be used as an effective method to monitor the unregulated drug market.
Citations in the library
Cited by 2
- Adulteration and substitution of drugs purchased in Australia from cryptomarkets: An analysis of Test4Pay Drug and Alcohol Review March 4, 2024
- Global emergence and γ-aminobutyric acid type A (GABAA) receptor activity of the new designer benzodiazepine ethylbromazolam Archives of Toxicology May 20, 2026
Cites 7
- Pharmacological Investigations of the Dissociative ‘Legal Highs’ Diphenidine, Methoxphenidine and Analogues PLoS One June 17, 2016
- Para-Halogenation Affects Monoamine Transporter Inhibition Properties and Hepatocellular Toxicity of Amphetamines and Methcathinones Frontiers in Pharmacology April 24, 2019
- Para-Halogenation of Amphetamine and Methcathinone Increases the Mitochondrial Toxicity in Undifferentiated and Differentiated SH-SY5Y Cells International Journal of Molecular Sciences April 18, 2020
- Ephenidine, diphenidine, and methoxphenidine complications reported to the French Addictovigilance Network. Fundamental and Clinical Pharmacology December 1, 2018
- Drug testing in Europe: monitoring results of the Trans European Drug Information (TEDI) project. Drug Testing and Analysis February 2017
and 2 more in the library