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Forensic Chemistry

ISSN 2468-1709

4 papers in the library · 48 citations · publishing 2021-2025

Papers

Electrochemical detection of MDMA and 2C-B in ecstasy tablets using a selectivity enhancement strategy by in-situ derivatization

Forensic Chemistry November 23, 2021 Robin van Echelpoel, Ruben F. Kranenburg, Arian van Asten et al. 24 citations

A two-step electrochemical sensor distinguishes between the drugs MDMA and 2C-B. In the first step, direct electrochemical analysis detects MDMA, but testing over 70 substances showed that 2C-B was the only common drug producing a false positive for MDMA. The second step uses formaldehyde to chemically modify 2C-B, creating a distinct electrochemical signal that differentiates it from MDMA. Testing on 71 ecstasy tablets seized by the Amsterdam Police, the sensor correctly identified all 39 MDMA-containing tablets and 10 of 11 tablets containing 2C-B. It also worked on dark-colored tablets where spectroscopic and colorimetric tests failed.

Combining FTIR-ATR and OPLS-DA methods for magic mushrooms discrimination

Forensic Chemistry April 8, 2022 Cátia Esteves, Elena M. M. de Redrojo, José Luis Manjón et al. 19 citations

A non-destructive method using FTIR-ATR spectroscopy combined with OPLS-DA chemometric analysis can distinguish hallucinogenic mushrooms from edible and toxic species, even though specific psilocybin or psilocin bands were not identified. The technique successfully separated hallucinogenic mushrooms from others, making it a promising initial screening tool for forensic identification of seized samples. The study analyzed 64 mushroom samples from various genera, including hallucinogenic, edible, and toxic species.

Testing human hair after magic mushrooms abuse by LC-MS/MS: Pitfalls and limitations

Forensic Chemistry September 20, 2021 P. Kintz, J. Raul, A. Ameline 4 citations

A method using liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed to detect psilocin, the active metabolite of psilocybin from magic mushrooms, in human hair. The technique involves incubating 10 mg of hair in acid methanol with a labeled internal standard, followed by chromatographic separation. The method was linear from 1 to 200 pg/mg, with a detection limit of 0.4 pg/mg and good precision. Analysis of hair from a regular magic mushroom user found psilocin levels of 2.5, 4.4, and 5.4 pg/mg in successive 1-cm segments. Cold conditions and protection from light are essential to prevent psilocin degradation during preparation.

A UHPLC-(ESI)MS/MS method for the determination of the psychedelic secondary metabolite mescaline in San Pedro (Trichocereus spp.) and its applicability for screening mescaline in other cacti varieties.

Forensic Chemistry March 25, 2025 Pragna Gaur, Liam Engel, Damian Robert Hall et al. 1 citation

Mescaline concentrations in ornamental San Pedro cacti vary widely, posing risks of unintended low or high doses if used illicitly. A new UHPLC-(ESI)MS/MS method rapidly and reliably quantifies mescaline in these cacti and screens others. Preliminary results suggest higher mescaline levels in the chlorenchyma than in the parenchyma of San Pedro. Screening revealed mescaline in two varieties of Echinopsis subdenudata for the first time, at concentrations from 36 μg/g to 2.45 mg/g, while six other cacti had none. This finding supports the chemotaxonomic argument that Trichocereus and Echinopsis genera may not be distinct and should be combined. The discovery of mescaline in a popular ornamental cactus highlights the need for routine forensic screening to keep pace with emerging psychedelic drug trends.