|
Title
|
|
|
|
Forensic analysis of synthetic cathinones on nanomaterials-based platforms : chemometric-assisted voltametric and UPLC-MS/MS investigation
| |
|
Author
|
|
|
|
| |
|
Abstract
|
|
|
|
| Synthetic cathinones (SCs) are a group of new psychoactive substances often referred to as "legal highs" or "bath salts", being characterized by a dynamic change, new compounds continuously emerging on the market. This creates a lack of fast screening tests, making SCs a constant concern for law enforcement agencies. Herein, we present a fast and simple method for the detection of four SCs (alpha-pyrrolidinovalerophenone, N-ethylhexedrone, 4-chloroethcathinone, and 3-chloromethcathinone) based on their electrochemical profiles in a decentralized manner. In this regard, the voltametric characterization of the SCs was performed by cyclic and square wave voltammetry. The elucidation of the SCs redox pathways was successfully achieved using liquid chromatography coupled to (tandem) mass spectrometry. For the rational identification of the ideal experimental conditions, chemometric data processing was employed, considering two critical qualitative and quantitative variables: the type of the electrochemical platform and the pH of the electrolyte. The analytical figures of merit were determined on standard working solutions using the optimized method, which exhibited wide linear ranges and LODs suitable for confiscated sample screening. Finally, the performance of the method was evaluated on real confiscated samples, the resulting validation parameters being similar to those obtained with another portable device (i.e., Raman spectrometer). |
| |
|
Language
|
|
|
|
English
| |
|
Source (journal)
|
|
|
|
Nanomaterials
| |
|
Publication
|
|
|
|
2023
| |
|
ISSN
|
|
|
|
2079-4991
| |
|
DOI
|
|
|
|
10.3390/NANO13172393
| |
|
Volume/pages
|
|
|
|
13
:17
(2023)
, p. 1-19
| |
|
Article Reference
|
|
|
|
2393
| |
|
ISI
|
|
|
|
001061205100001
| |
|
Pubmed ID
|
|
|
|
37686901
| |
|
Medium
|
|
|
|
E-only publicatie
| |
|
Full text (Publisher's DOI)
|
|
|
|
| |
|
Full text (open access)
|
|
|
|
| |
|