Monitoring of herbal mixtures potentially containing synthetic cannabinoids as psychoactive compounds

Journal of Mass Spectrometry - Tập 45 Số 10 - Trang 1186-1194 - 2010
Sebastian Dresen1,2,3, Nerea Ferreirós4,1,3, Michael Pütz5, Folker Westphal6, Ralf Zimmermann7,2, Volker Auwärter1
1Institute of Forensic Medicine, Forensic Toxicology, University Medical Center Freiburg, Freiburg, Germany
2Joint Mass Spectrometric Centre, Institute of Chemistry, University of Rostock, Rostock, Germany
3These authors have contributed equally to this manuscript.
4Institute of Clinical Pharmacology, Goethe-University Frankfurt, Frankfurt, Germany
5Forensic Science Institute, Federal Criminal Police Office, Wiesbaden, Germany
6State Bureau of Criminal Investigation Schleswig-Holstein, Kiel, Germany
7Cooperation Group Analysis of Complex Molecular Systems—Joint Mass Spectrometric Centre, Institute for Ecological Chemistry, Helmholtz Zentrum München, Germany

Tóm tắt

AbstractHerbal mixtures like ‘Spice’ with potentially bioactive ingredients were available in many European countries since 2004 and are still widely used as a substitute for cannabis, although merchandized as ‘herbal incense’. After gaining a high degree of popularity in 2008, big quantities of these drugs were sold. In December 2008, synthetic cannabinoids were identified in the mixtures which were not declared as ingredients: the C8 homolog of the non‐classical cannabinoid CP‐47,497 (CP‐47,497‐C8) and a cannabimimetic aminoalkylindole called JWH‐018. In February 2009, a few weeks after the German legislation put these compounds and further pharmacologically active homologs of CP‐47,497 under control, another cannabinoid appeared in ‘incense’ products: the aminoalkylindole JWH‐073.In this paper, the results of monitoring of commercially available ‘incense’ products from June 2008 to September 2009 are presented. In this period of time, more than 140 samples of herbal mixtures were analyzed for bioactive ingredients and synthetic cannabimimetic substances in particular. The results show that the composition of many products changed repeatedly over time as a reaction to prohibition and prosecution of resellers. Therefore neither the reseller nor the consumer of these mixtures can predict the actual content of the ‘incense’ products. As long as there is no possibility of generic definitions in the controlled substances legislation, further designer cannabinoids will appear on the market as soon as the next legal step has been taken. This is affirmed by the recent identification of the aminoalkylindoles JWH‐250 and JWH‐398. As further cannabinoids can be expected to occur in the near future, a continuous monitoring of these herbal mixtures is required.The identification of the synthetic opioid O‐desmethyltramadol in a herbal mixture declared to contain ‘kratom’ proves that the concept of selling apparently natural products spiked with potentially dangerous synthetic chemicals/pharmaceuticals is a continuing trend on the market of ‘legal highs’. Copyright © 2010 John Wiley & Sons, Ltd.

Từ khóa


Tài liệu tham khảo

10.1002/jms.1558

10.1248/cpb.57.439

News item dpa 15.12.2008 THC Pharm Frankfurt Germany.

European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) Thematic Paper Understanding the ‘Spice’ phenomenon 2009.

V.Auwärter N.Ferreirós S.Dresen M.Müller W.Weinmann M.Pütz.“Spice” and other herbal blends: harmless incense or cannabinoid designer drugs?XVI. GTFCh Symposium Mosbach (Germany) 2009.

10.1016/j.forsciint.2009.06.008

Westphal F., 2010, Ein neuer Wirkstoff in SPICE‐artigen Kräutermischungen: Charakterisierung von JWH‐250, seinen Methyl‐ und Trimethylsilylderivaten (A new compound in herbal mixtures: characterisation of JWH‐250, its methyl‐ and trimethylsilyl‐derivatives), Toxichem. Krimtech., 77, 8

Weissman A., 1982, Cannabimimetic activity from CP‐47,497, a derivative of 3‐phenylcyclohexanol, J. Pharmacol. Exp. Ther., 223, 516

Compton D. R., 1992, Pharmacological profile of a series of bicyclic cannabinoid analogs: classification as cannabimimetic agents, J. Pharmacol. Exp. Ther., 260, 201

10.1016/j.bmcl.2005.06.008

10.1016/S0376-8716(99)00152-0

Wiley J. L., 1998, Structure–activity relationships of indole‐ and pyrrole‐derived cannabinoids, J. Pharmacol. Exp. Ther., 285, 995

Advisory Council on the Misuse of Drugs Consideration of the major cannabinoid agonists 2009.

Zimmermann U. S., 2009, Withdrawal phenomena and dependence syndrome after the consumption of “spice gold”, Dtsch. Arztebl. Int., 106, 464

10.2165/00003495-199346020-00008

Maurer H. H., 2007, Mass Spectral and GC Data on Drugs, Poisons, Pesticides, Pollutants and Their Metabolites

10.1093/jat/34.5.252

Fedorova I., 2001, Behavioral evidence for the interaction of oleamide with multiple neurotransmitter systems, J. Pharmacol. Exp. Ther., 299, 332

10.1016/j.pnpbp.2009.07.021