Determination of major metabolites of MAM-2201 and JWH-122 in in vitro and in vivo studies to distinguish their intake

Forensic Sci Int. 2014 Nov:244:85-91. doi: 10.1016/j.forsciint.2014.08.008. Epub 2014 Aug 20.

Abstract

Abuse of fluorinated synthetic cannabinoid analogs to avoid existing legal regulations has increased globally. The fluorinated JWH-122 analog, MAM-2201, was first reported in September 2012 as an ingredient in herbal mixtures in Korea. MAM-2201 is more potent than JWH-122 and a fatal intoxication case has been reported. In this study, we identified major MAM-2201 and JWH-122 metabolites from in vitro metabolism studies using human liver microsomes and compared the results with those of urine specimens from suspected MAM-2201 or JWH-122 users. MAM-2201 and JWH-122 produced common metabolites, N-5-hydroxylated, N-4-hydroxylated and carboxylated JWH-122 metabolites. Trace amounts of an N-4-hydroxylated MAM-2201 metabolite, a characteristic MAM-2201 metabolite, was detected in only a few urine specimens from MAM-2201 users. Both in vitro and in vivo studies demonstrated that N-5-hydroxylated JWH-122 metabolite was the primary metabolite of MAM-2201, whereas N-4-hydroxylated JWH-122 metabolite was predominant in JWH-122 metabolism. Based on these results, relative concentrations of N-5- and N-4-hydroxylated JWH-122 metabolites should be considered to verify MAM-2201 or JWH-122 users.

Keywords: In vitro metabolism; JWH-122; MAM-2201; Synthetic cannabinoid; Urine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Hydroxylation
  • Illicit Drugs / analysis*
  • Illicit Drugs / chemistry
  • In Vitro Techniques
  • Indoles / analysis*
  • Indoles / chemistry
  • Microsomes, Liver / chemistry*
  • Molecular Structure
  • Naphthalenes / analysis*
  • Naphthalenes / chemistry

Substances

  • 1-(5-fluoropentyl)-3-(4-methyl-1-naphthoyl)indole
  • Illicit Drugs
  • Indoles
  • Naphthalenes
  • (4-methyl-1-naphthyl)-(1-pentylindol-3-yl)methanone