| Literature DB >> 24657413 |
Veniero Gambaro1, Sebastiano Arnoldi1, Stefania Bellucci1, Eleonora Casagni1, Lucia Dell'Acqua1, Laura Fumagalli1, Marco Pallavicini1, Gabriella Roda2, Chiara Rusconi1, Ermanno Valoti1.
Abstract
In vitro incubation with human liver microsomes of JWH-018, JWH-073, JWH-122 and for the first time 1-butyl-3-(1-(4-methyl)naphthoyl)indole (the 4-methylnaphthoyl analogue of JWH-073) was investigated to identify the principal metabolites of alkylindole synthetic cannabinoids, thus helping the discovering of synthetic cannabinoids abusers. The results obtained showed that the most abundant metabolites were mono-hydroxylated derivatives either on the alkyl chain (ω or ω-1 position) or on the indole (presumably in position 5 or 6) and naphthalene moieties. Moreover the extraction conditions of these derivatives from biological fluids, mainly plasma and urine spiked with commercially available metabolite standards, and the incubation procedure were investigated to obtain a fast, reliable and suitable extraction protocol to detect either the parent drugs or their metabolites by means of GC/MS.Entities:
Keywords: Alkylindole metabolites; GC/FID; GC/MS; JWH-018; JWH-073; JWH-122 ;1-Butyl-3-(1-(4-methyl)naphthoyl)indole
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Year: 2014 PMID: 24657413 DOI: 10.1016/j.jchromb.2014.03.001
Source DB: PubMed Journal: J Chromatogr B Analyt Technol Biomed Life Sci ISSN: 1570-0232 Impact factor: 3.205