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Characterization of in vitro metabolites of methylenedioxypyrovalerone (MDPV): An N-oxide metabolite formation mediated by flavin monooxygenase

Authors
Kim, In SookRehman, Shaheed UrChoi, Min SunJang, MoonheeYang, WonkyungKim, EunmiYoo, Hye Hyun
Issue Date
Nov-2016
Publisher
Elsevier BV
Keywords
Methylenedioxypyrovalerone; Metabolite; N-oxide; FMO; Human liver microsomes
Citation
Journal of Pharmaceutical and Biomedical Analysis, v.131, pp.160 - 166
Indexed
SCIE
SCOPUS
Journal Title
Journal of Pharmaceutical and Biomedical Analysis
Volume
131
Start Page
160
End Page
166
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/12195
DOI
10.1016/j.jpba.2016.08.025
ISSN
0731-7085
Abstract
Methylenedioxypyrovalerone (MDPV) has emerged in recent years as a-recreational substance with psychostimulant properties. In this study, in vitro metabolites of MDPV were characterized based on liquid chromatography/quadrupole-time-of-flight mass spectrometry(LC/QTOF MS). MDPV was incubated with human liver microsomes, human recombinant cDNA-expressed cytochrome P450 enzymes and flavin monooxygenase (FMO). MDPV was metabolized to yield eight metabolites (M1-M8)with major metabolic reactions such as demethylenation and oxidation. Among them, M6 was assigned as an N-oxide metabolite. FMO was found to be a principal enzyme responsible for the formation of M6; FMO1 and FMO3 were the main enzymes involved in N-oxidation of MDPV. (C) 2016 Elsevier B.V. All rights reserved.
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