研究目的
To identify drugs purchased and commonly used by partygoers and music festivals attendants using a Raman-based portable instrument, as part of harm reduction efforts to provide information on circulating drugs and reduce risks.
研究成果
Portable Raman spectroscopy is effective for on-site identification of psychoactive drugs, including NPS, in harm reduction contexts. It provides rapid, non-destructive analysis but has limitations in sensitivity and fluorescence interference. The study revealed significant presence of NPS replacing traditional drugs, increasing overdose risks. Future work should focus on improving detection limits, expanding library coverage, and integrating drug checking with counseling services for comprehensive harm reduction.
研究不足
Limitations include the instrument's sensitivity issues with low-concentration substances, interference from fluorescence (especially for heroin and pigmented samples), inability to detect multiple active ingredients in mixtures (only the most abundant is reported), and the need for regular library updates to include new NPS. These factors can lead to inconclusive results and require complementary laboratory methods.
1:Experimental Design and Method Selection:
The study used a portable Raman spectroscopy device for on-site drug checking to identify psychoactive substances non-destructively through comparison with a spectral library. The design aimed for rapid analysis (less than 2 minutes per sample) without direct handling of substances.
2:Sample Selection and Data Sources:
472 alleged drug samples were voluntarily provided by users at 27 night events (e.g., electronic dance music festivals, rave parties) in Italy during 2016 and 2017. Samples included powders, crystals, and pills.
3:Samples included powders, crystals, and pills.
List of Experimental Equipment and Materials:
3. List of Experimental Equipment and Materials: Portable Raman analyser (ThermoScienti?c TruNarc?), plastic bags for sample containment, GC-MS and LC-MS/MS systems for laboratory confirmation (Agilent 6890 N GC, Agilent 5975 inert mass-selective detector, Agilent 1290 Infinity LC system, QTRAP? 4500 mass spectrometer), and various chemical standards and libraries.
4:Experimental Procedures and Operational Workflow:
Users placed a small amount of substance in a plastic bag; the bag was analyzed by the Raman instrument through the bag material. Results were categorized as alarm (controlled substance), warning (precursor), clear (non-controlled substance), or inconclusive. For inconclusive results, a small aliquot was collected for deferred GC-MS or LC-MS/MS analysis in the lab.
5:Data Analysis Methods:
Raman spectra were compared to a proprietary library. GC-MS and LC-MS/MS analyses used full scan spectra and selected reaction monitoring for identification, with comparisons to reference standards and libraries (e.g., PMWTox2, SWGDRUG).
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