Chiral pharmacokinetics of tetramisole stereoisomers : enantioselective quantification of levamisole and dexamisole in serum samples from users of adulterated cocaine

dc.contributor.authorLosacker, Moritz
dc.contributor.authorHundertmark, Marica
dc.contributor.authorZörntlein, Siegfried
dc.contributor.authorRöhrich, Jörg
dc.contributor.authorHess, Cornelius
dc.date.accessioned2023-01-24T09:27:15Z
dc.date.available2023-01-24T09:27:15Z
dc.date.issued2022
dc.description.abstractPhenyltetrahydroimidazothiazole (PTHIT, tetramisole) is the most frequently used adulterant of cocaine and exists in the two enantiomeric forms levamsiole (S) and dexamisole (R). Existing studies show diverse fractions of samples containing enantiopure levamsiole, levamisole-enriched mixtures, and racemic tetramisole as adulterant. However, blood samples have never been enantioselectively tested for PTHIT. Because enantiomers are usually metabolized stereoselectively, chiral analysis of blood samples can help estimate the time of drug use, provided that a racemic substance is ingested. Therefore, an enantioselective liquid chromatography–tandem mass spectrometry (LC–MS/MS) method was developed using a chiral column. Validation of the method was carried out for methanolic substance samples as well as serum samples and showed satisfactory selectivity, sensitivity, linearity (0.05–100 ng/mL), precision, and accuracy; 151 cocaine samples seized in Germany between 2018 and 2021 were analyzed. Most (94%, n = 48) of the 51 PTHIT-positive samples contained racemic tetramsiole, whereas there were two samples containing levamisole-enriched mixtures and one sample containing nearly enantiopure levamisole. Furthermore, 157 cocaine and/or benzoylecgonine-positive forensic serum samples were tested with cocaine-positive samples showing the highest frequency of PTHIT detection (43%). All positive samples contained either dexamisole alone or (R)/(S)-concentration ratios >1 (1.05–70.6). Finally, a self-administration study was conducted with three subjects taking 10 mg of racemic tetramisole each. Although peak concentrations and corresponding times did not differ significantly between the enantiomers, dexamisole showed significantly longer apparent elimination half-lives (7.02–10.0 h) than levamisole (2.87–4.77 h). The resulting steadily increasing (R)/(S)-ratios can therefore be helpful in estimating the time of cocaine consumption.en_GB
dc.description.sponsorshipGefördert durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491381577
dc.identifier.doihttp://doi.org/10.25358/openscience-8630
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/8646
dc.language.isoger
dc.rightsCC-BY-4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleChiral pharmacokinetics of tetramisole stereoisomers : enantioselective quantification of levamisole and dexamisole in serum samples from users of adulterated cocaineen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.pricePAR-Fee
jgu.apc.transformationcontractWiley (DEAL)
jgu.dfg.year2022
jgu.journal.issue6
jgu.journal.titleDrug testing and analysis
jgu.journal.volume14
jgu.organisation.departmentFB 04 Medizinde_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.end1064
jgu.pages.start1053
jgu.publisher.doi10.1002/dta.3227
jgu.publisher.issn1942-7611
jgu.publisher.nameWiley
jgu.publisher.placeHoboken, NJ
jgu.publisher.year2022
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode610
jgu.subject.dfgLebenswissenschaftende_DE
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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