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Number of results
2014 | 2 | 1 |

Article title

The isolation and characterisation of the synthetic
cannabinoid AM-2201 from commercial products
using purification by HPLC-DAD

Content

Title variants

Languages of publication

EN

Abstracts

EN
A total of six products containing legal highs
were purchased via the internet from the UK- based
retailers and screened for the presence of synthetic
cannabinoids using a fast GC-MS method and identified,
in the absence of reference materials, by comparing the
mass spectra with the Scientific Working Group for the
Analysis of Seized Drugs (SWGDRUG) mass spectral
library. Four synthetic cannabinoids were detected: RCS-4,
CP-47, 497, UR-144 and AM-2201. The active ingredient
(1-(5-fluoropentyl)-3-(1-naphthoyl) indole), with the street
name AM-2201, detected in the product named Doob was
isolated and purified from the methanolic extract of the
product using preparative HPLC with analytical column
(column overloading method). The structure of the
substance was confirmed using NMR. This approach used
common analytical equipment found in forensic and other
analytical laboratories (except for the NMR), therefore can
be useful for the identification of unknown psychoactive
substances in drugs of abuse.

Publisher

Year

Volume

2

Issue

1

Physical description

Dates

online
15 - 6 - 2015
received
19 - 11 - 2014
accepted
6 - 5 - 2015

Contributors

  • School of Chemistry,
    University of Lincoln, Lincoln, United Kingdom LN6 7TS
author
  • School of Chemistry,
    University of Lincoln, Lincoln, United Kingdom LN6 7TS
author
  • School of Chemistry,
    University of Lincoln, Lincoln, United Kingdom LN6 7TS

References

  • Choi H., Heo S., Kim E., Hwang B.Y, Lee C., Lee J., Identification of (1-pentylindol-3-yl)-(2,2,3,3-tetramethylcyclopropyl)methanone and its 5-pentyl fluorinated analog in herbal incense seized for drug trafficking, Forensic Toxicology, 2013, 31 (1), 86-92.[WoS][Crossref]
  • Dargan P.I., Hudson S., Ramsey J., Wood D. M., The impact of changes in UK classification of the synthetic cannabinoid receptor agonists in “Spice”, The International Journal on Drug Policy, 2011, 22(4), 274–7. [WoS]
  • Denooz R., Vanheugen J. C., Frederich M., de Tullio P., Charlier C., Identification and structural elucidation of four cannabimimetic compounds (RCS-4, AM-2201, JWH-203 and JWH-210) in seized products, Journal of Analytical Toxicology, 2013, 37(2), 56–63. [WoS]
  • Elie M.P., Elie L.E., Baron M.G., Keeping pace with NPS releases: fast GC-MS screening of legal high products, Drug Testing and Analysis, 2012, 5(5), 281-290.
  • Ernst L., Schiebel H. M., Theuring C., Lindigkeit R., Beuerle T., Identification and characterization of JWH-122 used as new ingredient in “Spice-like” herbal incenses, Forensic Science International, 2011, 208(1-3), e31–5.[WoS]
  • Ernst L., Kruger K., Lindigkeit R., Schiebel H. M., Beuerle T., Synthetic cannabinoids in “spice-like” herbal blends: first appearance of JWH-307 and recurrence of JWH-018 on the German market, Forensic Science International, 2012, 222(1-3), 216–22[WoS]
  • European Monitoring Centre for Drugs and Drug Addiction-EMCDDA. European Drug Report. Trends and developments 2013. [pdf] Available at http://www.emcdda.europa.eu/publications/edr/trends-developments/2013 , Acessed on 30.06.2013. doi:10.2810/88175[Crossref]
  • Fattore L., Fratta W., Beyond THC: The New Generation of Cannabinoid Designer Drugs, Frontiers in Behavioral Neuroscience, 2011, 5, article number 60. [WoS]
  • Huber U., Majors R.E., Principles in Preparative HPLC: A Primer, Agilent Technologies, 2007
  • Hudson S., Ramsey J., The emergence and analysis of synthetic cannabinoids, Drug Testing and Analysis, 2011, 3(7-8), 466–78.
  • Jankovics P.,Varadi A., Tolgyesi L., Lohner S., Nemeth-Palotas J., Balla J., Detection and identification of the new potential synthetic cannabinoids 1-pentyl-3-(2-iodobenzoyl)indole and 1-pentyl-3-(1-adamantoyl)indole in seized bulk powders in Hungary, Forensic Science International, 2012, 214(1-3), 27–32.[WoS]
  • Logan B.K., Reinhold L. E., Xu A., Diamond F. X., 2012. Identification of synthetic cannabinoids in herbal incense blends in the United States, Journal of Forensic Sciences, 2012, 57(5), 1168–80. [Crossref][WoS]
  • Makriyannis A., Deng H., 2007, Cannabimimetic Indole Derivates, US Patent No. 2080090871A10 2007
  • Moosmann B., Kneisel S., Girreser U., Brecht V., Separation and structural characterization of the synthetic cannabinoids JWH-412 using GC – MS , NMR analysis and a flash chromatography system, Forensic Science International, 2012, 220, 17–22.[WoS]
  • SWGDRUG (2013) SWGDRUG Mass Spectral Library Available online at http://www.swgdrug.org/ms.htm , Accessed on 28.03.2013.
  • Vardakou I., Pistos C., Spiliopoulou C., Spice drugs as a new trend: mode of action, identification and legislation, Toxicology Letters, 2010, 197(3), 157–62. [WoS]
  • Zuba D., Byrska B., Maciow M., Comparison of “herbal highs” composition, Analytical and bioanalytical chemistry, 2011, 400(1), 119–26.

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_1515_sampre-2015-0004
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