Free Content CASE REPORT: Distribution Study of 3,4-Methylenedioxymethamphetamine and 3,4-Methylenedioxy-amphetamine in a Fatal Overdose

Authors: De Letter E.A.1; Clauwaert K.M.2; Lambert W.E.3; Van Bocxlaer J.F.2; De Leenheer A.P.4; Piette M.H.A.5

Source: Journal of Analytical Toxicology, Volume 26, Number 2, March 2002 , pp. 113-118(6)

Publisher: Preston Publications

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Abstract:

In this study, regional tissue distributions of the amphetamine analogue 3,4-methylenedioxymethamphetamine (MDMA, “ecstasy”) and its metabolite 3,4-methylenedioxyamphetamine (MDA) in a fatal overdose are presented. Quantitation of MDMA and MDA levels occurred in blood samples taken centrally (right and left heart and main adjacent great vessels) and peripherally (subclavian and femoral blood). In addition, MDMA and MDA concentrations were determined in cardiac and iliopsoas muscle, both lungs, liver, both kidneys, spleen, the four brain lobes, cerebellum and brainstem, and adipose tissue. Finally, MDMA and MDA levels were determined in serum, vitreous humor, urine, and bile. For all samples, a fully validated high-pressure liquid chromatography procedure with fluorescence detection was used. The found substances were also identified with liquid chromatography–tandem mass spectrometry. Our data confirm that blood sampling from an isolated peripheral vein is recommended for MDMA and MDA. In addition, the vitreous humor MDMA level indicates that this fluid can be an interesting alternative when a suitable blood sample is missing. Considering the substantial differences in concentrations in blood samples taken from various sites in the body and the high levels in some tissues (e.g., in liver), we concluded that the influence of postmortem redistribution should be taken into account in the interpretation of toxicological data when an appropriate peripheral sample cannot be obtained or when blood samples are not available because of putrefaction.

Language: English

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Affiliations: 1: Ghent University, Department of Forensic Medicine, J. Kluyskensstraat 29, B-9000 Ghent, Belgium 2: Ghent University, Department of Medical Biochemistry and Clinical Analysis, Harelbekestraat 72, B-9000 Ghent, Belgium 3: Ghent University, Department of Toxicology, Harelbekestraat 72, B-9000 Ghent, Belgium 4: Ghent University, Department of Medical Biochemistry and Clinical Analysis, Harelbekestraat 72, B-9000 Ghent, Belgium; Ghent University, Department of Toxicology, Harelbekestraat 72, B-9000 Ghent, Belgium 5: Ghent University, Department of Forensic Medicine, J. Kluyskensstraat 29, B-9000 Ghent, Belgium, E-mail: Michel.Piette@rug.ac.be

Publication date: 2002-03-01

More about this publication?
  • The Journal of Analytical Toxicology (JAT), established in 1977 and published 9 times a year, is the international source covering a broad range of clinical, forensic, and industrial laboratory topics regarding the isolation, identification, and quantitation of potentially toxic substances.

    With an emphasis on practical application, JAT articles provide improved and novel techniques for use in clinical, forensic, workplace, sports testing (doping), and other toxicology laboratories. Articles describe newly developed methods in immunoassay testing, gas chromatography, liquid chromatography, mass spectrometry, atomic absorption spectrometry, solid and liquid phase extraction techniques, and other analytical approaches. Worldwide readership includes toxicologists, pathologists, chemists, clinicians, researchers, and educators working in medical examiner and law enforcement laboratories, hospitals, university and independent analytical laboratories, as well as the drug manufacturing industry.

    Each year in October, we publish a special issue from the Society of Forensic Toxicologists.

    JAT, as determined by ISI Citation Index, is one of the two most referenced international journals in forensic science.

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