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

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dc.contributor.authorJang, Moonhee-
dc.contributor.authorShin, Ilchung-
dc.contributor.authorYang, Wonkyung-
dc.contributor.authorChang, Hyejin-
dc.contributor.authorYoo, Hye Hyun-
dc.contributor.authorLee, Jaesin-
dc.contributor.authorKim, Eunmi-
dc.date.accessioned2021-06-22T22:23:06Z-
dc.date.available2021-06-22T22:23:06Z-
dc.date.created2021-01-21-
dc.date.issued2014-11-
dc.identifier.issn0379-0738-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/21503-
dc.description.abstractAbuse 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. (C) 2014 Elsevier Ireland Ltd. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherElsevier BV-
dc.titleDetermination of major metabolites of MAM-2201 and JWH-122 in in vitro and in vivo studies to distinguish their intake-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoo, Hye Hyun-
dc.identifier.doi10.1016/j.forsciint.2014.08.008-
dc.identifier.scopusid2-s2.0-84907735372-
dc.identifier.wosid000345017000025-
dc.identifier.bibliographicCitationForensic Science International, v.244, pp.85 - 91-
dc.relation.isPartOfForensic Science International-
dc.citation.titleForensic Science International-
dc.citation.volume244-
dc.citation.startPage85-
dc.citation.endPage91-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaLegal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, Legal-
dc.subject.keywordPlusSYNTHETIC CANNABINOIDS-
dc.subject.keywordPlusURINARY METABOLITES-
dc.subject.keywordPlusJWH-018-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusAM-2201-
dc.subject.keywordAuthorSynthetic cannabinoid-
dc.subject.keywordAuthorJWH-122-
dc.subject.keywordAuthorMAM-2201-
dc.subject.keywordAuthorIn vitro metabolism-
dc.subject.keywordAuthorUrine-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0379073814003223?via%3Dihub-
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