Chromatographic separation of R-(-)/S-(+)-enantiomers of amphetamine and methamphetamine: differentiation between single methamphetamine consumption and co-consumption with amphetamine using enantioselective quantitative LC-MS/MS analysis.


Journal

International journal of legal medicine
ISSN: 1437-1596
Titre abrégé: Int J Legal Med
Pays: Germany
ID NLM: 9101456

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 15 08 2018
accepted: 04 12 2018
pubmed: 20 12 2018
medline: 4 4 2019
entrez: 20 12 2018
Statut: ppublish

Résumé

The differentiation between single methamphetamine consumption and co-consumption with amphetamine is difficult, however possible by enantioselective analysis due to different preferred synthesis pathways of both substances. We quantified (R)-(-) and (S)-(+)-enantiomers of methamphetamine and amphetamine by a fast liquid chromatographic tandem-mass spectrometric method using a Lux® 3-μm AMP 150 × 3.0 mm analytical column after simple protein precipitation with methanol. Method validation for quantitative detection showed limits of quantification < 5 ng/mL, linearity in a range between 5 and 300 ng/mL and bias and imprecision data < 15%. Overall, 134 plasma samples of police cases from the German regions of Franconia and Northrhine-Westphalia were analyzed for the enantiomers of methamphetamine and amphetamine. In 28 cases, the intake of racemic illicit amphetamine could be demonstrated; (R)-(-) / (S)-(+)-amphetamine concentration ratios in these cases were between 1.38 and 4.50 with most of the ratios being < 2.0. These ratios were compared to a subgroup of 25 consumers with a co-consumption of (S)-(+)-methamphetamine and racemic amphetamine detected by the qualitative proof of (R)-(-)-amphetamine but also by (R)-(-) / (S)-(+)-amphetamine concentration ratios (< 1 in 11 of 25 cases). Within our collective of 106 plasma samples after methamphetamine use, 25 samples showed co-consumption with amphetamine which shows that co-consumption of both stimulants is not a rare scenario. Furthermore, we could show that if non-stereoselective methods are used and the concentration ratio of total methamphetamine/total amphetamine is determined, a reliable estimation of co-consumption is not possible.

Identifiants

pubmed: 30564915
doi: 10.1007/s00414-018-1979-1
pii: 10.1007/s00414-018-1979-1
doi:

Substances chimiques

Central Nervous System Stimulants 0
Methamphetamine 44RAL3456C
Amphetamine CK833KGX7E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

467-473

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Auteurs

Cornelius Hess (C)

Institute of Forensic Medicine, University of Bonn, Forensic Toxicology, Stiftsplatz 12, 53111, Bonn, Germany. hess@uni-mainz.de.
Institute of Forensic Medicine, University of Mainz, Forensic Toxicology, Am Pulverturm 3, 55131, Mainz, Germany. hess@uni-mainz.de.

Moritz Losacker (M)

Institute of Forensic Medicine, University of Bonn, Forensic Toxicology, Stiftsplatz 12, 53111, Bonn, Germany.

Alexandra Maas (A)

Institute of Forensic Medicine, University of Bonn, Forensic Toxicology, Stiftsplatz 12, 53111, Bonn, Germany.

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Classifications MeSH