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Licensed Unlicensed Requires Authentication Published by De Gruyter September 27, 2014

Urinary prevalence, metabolite detection rates, temporal patterns and evaluation of suitable LC-MS/MS targets to document synthetic cannabinoid intake in US military urine specimens

  • Ariane Wohlfarth , Karl B. Scheidweiler , Marisol Castaneto , Adarsh S. Gandhi , Nathalie A. Desrosiers , Kevin L. Klette , Thomas M. Martin and Marilyn A. Huestis EMAIL logo

Abstract

Background: Identifying synthetic cannabinoid designer drug abuse challenges toxicologists and drug testing programs. The best analytical approach for reliably documenting intake of emerging synthetic cannabinoids is unknown. Primarily metabolites are found in urine, but optimal metabolite targets remain unknown, and definitive identification is complicated by converging metabolic pathways.

Methods: We screened 20,017 US military urine specimens collected from service members worldwide for synthetic cannabinoids between July 2011 and June 2012. We confirmed 1432 presumptive positive and 1069 presumptive negative specimens by qualitative liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis including 29 biomarkers for JWH-018, JWH-073, JWH-081, JWH-122, JWH-200, JWH-210, JWH-250, RCS-4, AM2201 and MAM2201. Specimen preparation included enzyme hydrolysis and acetonitrile precipitation prior to LC-MS/MS analysis. We evaluated individual synthetic cannabinoid metabolite detection rates, prevalence, temporal patterns and suitable targets for analytical procedures.

Results: Prevalence was 1.4% with 290 confirmed positive specimens, 92% JWH-018, 54% AM2201 and 39% JWH-122 metabolites. JWH-073, JWH-210 and JWH-250 also were identified in 37%, 4% and 8% of specimens, respectively. The United States Army Criminal Investigation Command seizure pattern for synthetic cannabinoid compounds matched our urine specimen results over the time frame of the study. Apart from one exception (AM2201), no parent compounds were observed.

Conclusions: Hydroxyalkyl metabolites accounted for most confirmed positive tests, and in many cases, two metabolites were identified, increasing confidence in the results, and improving detection rates. These data also emphasize the need for new designer drug metabolism studies to provide relevant targets for synthetic cannabinoid identification.


Corresponding author: Professor Dr. Dr. (h.c.) Marilyn A. Huestis, Chief, National Institute on Drug Abuse, National Institutes of Health, Chemistry and Drug Metabolism, IRP, 251 Bayview Boulevard Suite 200, Room 05A-721, Baltimore, MD 21224, USA, Phone: +1 443 740 2524, Fax: +1 443 740 2823, E-mail:
aPresent address: Department of Bioanalysis and Physiology, Lundbeck Research Inc., Paramus, NJ, USA

Acknowledgments

Assistance and support of the Forensic Toxicology Drug Testing Laboratory, Fort Meade, MD, are greatly appreciated.

Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

Financial support: This research was funded by the Intramural Research Program of the National Institute on Drug Abuse (NIDA-IRP) and by an Interagency Agreement (Y3-DA-1116-01) between Department of Defense Counter Narcotics Program and NIDA-IRP.

Employment or leadership: None declared.

Honorarium: None declared.

Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Supplemental Material

The online version of this article (DOI: 10.1515/cclm-2014-0612) offers supplementary material, available to authorized users.


Received: 2014-6-10
Accepted: 2014-8-24
Published Online: 2014-9-27
Published in Print: 2015-2-1

©2015 by De Gruyter

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