Article de Périodique
Emergence of counterfeit oxycodone tablets containing Nitazenes in France: First national alert and analytical characterization (2025)
Auteur(s) :
DUGUES, P. ;
RABAI, A. ;
CHENORHOKIAN, S. ;
PFAU, G. ;
CHERKI, S. ;
BELLOUARD, M. ;
ALVAREZ, J. C. ;
LARABI, I. A.
Dans :
Toxicologie Analytique et Clinique (Toxicologie Analytique et Clinique Vol.37, n°4, Décembre 2025)
Année
2025
Page(s) :
529-539
Langue(s) :
Anglais
Refs biblio. :
39
Domaine :
Drogues illicites / Illicit drugs
Discipline :
MAR (Marchés / Markets)
Thésaurus géographique
FRANCE
;
VILLE DE PARIS
Thésaurus mots-clés
OPIOIDES
;
DROGUES DE SYNTHESE
;
CONTREFACON
;
PHENOMENE EMERGENT
;
NITAZENES
;
ANALYSE CHIMIQUE
;
MARCHE DE LA DROGUE
;
ETUDE DE CAS
Autres mots-clés
Résumé :
Background: Nitazenes, a class of synthetic opioids more potent than fentanyl, have been increasingly detected in the global illicit drug market, particularly within counterfeit medicines, causing intoxication and death. They represent a significant public health concern due to their high toxicity and their invisibility to conventional toxicological screening methods.
Methods: Five counterfeit oxycodone tablets were collected in Paris by a drug-checking service between February and May 2025. Visual inspection indicated the tablets mimicked authentic oxycodone "M30" formulations. Two tablets were received intact and three in powder form (ground beforehand). Analytical testing was conducted using LC-DAD, GC-MS, LC-MS/MS, and LC-HRMS. Quantification was performed by LC-MS/MS for 340 substances, including 163 new psychoactive substances (NPS).
Results: No oxycodone was detected in any of the samples; instead, all contained the synthetic opioids metonitazene and protonitazene. Quantification showed that tablets contained between 3.2% and 6.0% metonitazene, with protonitazene present in smaller amounts (less than 0.2%). The estimated metonitazene content in intact tablets (n=2) ranged from 3.7 to 4.0mg, approximately equivalent to 23mg of fentanyl, far exceeding lethal thresholds.
Conclusion: These findings confirm the circulation of synthetic opioids in counterfeit tablets sold as oxycodone in Paris and its suburbs. The presence of multiple nitazenes underscores the complexity and risk of the current illicit market. Drug-checking services and toxicological analyses are essential for early detection and public health response. Enhanced surveillance, harm reduction, and regulatory coordination are urgently required to mitigate the growing threat of nitazene-related poisonings worldwide. [Author's abstract]
Methods: Five counterfeit oxycodone tablets were collected in Paris by a drug-checking service between February and May 2025. Visual inspection indicated the tablets mimicked authentic oxycodone "M30" formulations. Two tablets were received intact and three in powder form (ground beforehand). Analytical testing was conducted using LC-DAD, GC-MS, LC-MS/MS, and LC-HRMS. Quantification was performed by LC-MS/MS for 340 substances, including 163 new psychoactive substances (NPS).
Results: No oxycodone was detected in any of the samples; instead, all contained the synthetic opioids metonitazene and protonitazene. Quantification showed that tablets contained between 3.2% and 6.0% metonitazene, with protonitazene present in smaller amounts (less than 0.2%). The estimated metonitazene content in intact tablets (n=2) ranged from 3.7 to 4.0mg, approximately equivalent to 23mg of fentanyl, far exceeding lethal thresholds.
Conclusion: These findings confirm the circulation of synthetic opioids in counterfeit tablets sold as oxycodone in Paris and its suburbs. The presence of multiple nitazenes underscores the complexity and risk of the current illicit market. Drug-checking services and toxicological analyses are essential for early detection and public health response. Enhanced surveillance, harm reduction, and regulatory coordination are urgently required to mitigate the growing threat of nitazene-related poisonings worldwide. [Author's abstract]
Affiliation :
Pharmacology and Toxicology Laboratory, Raymond-Poincaré University Hospital, AP-HP, Garches, France
UVSQ - Université Paris Saclay, Inserm U1018, CESP (Center for Research in Epidemiology and Population Health), MOODS team (mental health), Montigny-le-Bretonneux, France
Analyse Ton Prod-IDF, Paris, France
National Toxic and Substance Identification System (SINTES), French Monitoring Centre for Drugs and Drug Addiction (OFDT), Paris, France
UVSQ - Université Paris Saclay, Inserm U1018, CESP (Center for Research in Epidemiology and Population Health), MOODS team (mental health), Montigny-le-Bretonneux, France
Analyse Ton Prod-IDF, Paris, France
National Toxic and Substance Identification System (SINTES), French Monitoring Centre for Drugs and Drug Addiction (OFDT), Paris, France
Cote :
Abonnement
Historique