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Tentative identification of phase I metabolites of HU-210, a classical synthetic cannabinoid, by LC-MS/MS

Authors
Kim, UnyongJin, Ming JiLee, JaeickHan, Sang BeomIn, Moon KyoYoo, Hye Hyun
Issue Date
May-2012
Publisher
Elsevier BV
Keywords
HU-210; Synthetic cannabinoid; Metabolism; LC-MS/MS
Citation
Journal of Pharmaceutical and Biomedical Analysis, v.64-65, pp.26 - 34
Indexed
SCIE
SCOPUS
Journal Title
Journal of Pharmaceutical and Biomedical Analysis
Volume
64-65
Start Page
26
End Page
34
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/33051
DOI
10.1016/j.jpba.2012.02.007
ISSN
0731-7085
Abstract
(6aR,10aR)-9-(Hydroxymethyl)-6,6-dimethyl-3-(2-methyloctan-2-yl)-6a,7,10,10a-tetrahydrobenzo[c]chromen-1-ol (HU-210) is a synthetic cannabinoid, with a classical cannabinoid structure similar to Delta(9)-tetrahydrocannabinol (Delta(9)-THC). In this study, the in vitro metabolism of HU-210 was investigated in human liver microsomes to characterize associated phase I metabolites. HU-210 was incubated with human liver microsomes, and the reaction mixture was analyzed using LC-MS/MS. HU-210 was metabolized in human liver microsomes, yielding about 24 metabolites. These metabolites were structurally characterized on the basis of accurate mass analyses and MS/MS fragmentation patterns. The major metabolic route for HU-210 was oxygenation. Metabolites M1-M7 were identified as mono-oxygenated metabolites; MB-M15, mono-hydroxylated metabolites; M16-M20, di-oxygenated metabolites; and M21-M24, di-hydroxylated metabolites. These results provide evidence for in vivo HU-210 metabolism, and they may be applied to the analysis of HU-210 and its relevant metabolites in biological samples. (C) 2012 Elsevier B.V. All rights reserved.
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