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dc.contributor.authorCarlier, J.
dc.contributor.authorDiao, X.
dc.contributor.authorSempio, C.
dc.date.accessioned2019-07-15T16:12:09Z
dc.date.available2019-07-15T16:12:09Z
dc.date.issued2017
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85008698302&doi=10.1208%2fs12248-016-0037-5&partnerID=40&md5=6d3d7f9b6decd5eb35a1abb127c48731
dc.identifier.urihttp://hdl.handle.net/10713/9911
dc.description.abstractDB-CHMINACA (MAB-CHMINACA) is a new synthetic cannabinoid with high potency and many reported adverse events and fatalities. The drug is currently scheduled in several countries in Europe and the USA. Analytical methods need to be developed to confirm ADB-CHMINACA intake for clinical and forensic programs. For many synthetic cannabinoids, parent compound is not detectable in biological samples after intake, making the detection of metabolites the only way to prove consumption. Therefore, detection of ADB-CHMINACA metabolites in biological specimens is critical. Since there are currently no published data on ADB-CHMINACA metabolism, we aimed to identify its major metabolites. Cryopreserved human hepatocytes were incubated with 10 μmol/L ADB-CHMINACA for 3 h. Incubations were analyzed with liquid chromatography on a biphenyl column, high resolution tandem mass spectrometry (orbitrap), and metabolite identification software. A reference standard of six commercially available potential metabolites was simultaneously analyzed under the same conditions to allow correct assignment of isomers. We detected ten major metabolites. Biotransformations mainly occurred at the cyclohexylmethyl tail of the compound, as also observed with structural analogs’ metabolism. Minor reactions also occurred at the tert-butyl chain. Only two analytical standards of potential metabolites matched an actual metabolite detected in hepatocyte incubations. We recommend A9 (ADB-CHMINACA hydroxycyclohexylmethyl), A4 (ADB-CHMINACA 4″-hydroxycyclohexyl), and A6 (ADB-CHMINACA hydroxycyclohexylmethyl) as metabolite targets to document ADB-CHMINACA intake in clinical and forensic cases. Additionally, these results will guide analytical standard manufacturers to better provide suitable references for further studies on ADB-CHMINACA metabolism. Copyright 2017, The Author(s).en_US
dc.description.urihttps://www.doi.org/10.1208/s12248-016-0037-5en_US
dc.language.isoen_USen_US
dc.publisherSpringer New York LLCen_US
dc.relation.ispartofAAPS Journal
dc.subjectADB-CHMINACAen_US
dc.subjecthepatocyte metabolismen_US
dc.subjecthigh resolution mass spectrometryen_US
dc.subjectMAB-CHMINACAen_US
dc.subjectsynthetic cannabinoiden_US
dc.titleIdentification of New Synthetic Cannabinoid ADB-CHMINACA (MAB-CHMINACA) Metabolites in Human Hepatocytesen_US
dc.typeArticleen_US
dc.identifier.doi10.1208/s12248-016-0037-5
dc.identifier.pmid28070717


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