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Journal of Analytical Toxicology Article Abstracts

Journal of Analytical Toxicology Horizontal Line

Published: Journal of Analytical Toxicology, ISSN 0146-4760, Volume 26, Number 1, April 2002, pp. 113-118

CASE REPORT: Distribution Study of 3,4-Methylenedioxy-methamphetamine and 3,4-Methylenedioxy-amphetamine in a Fatal Overdose
Els A. De Letter[1], Karine M. Clauwaert[2], Willy E. Lambert[3], Jan F. Van Bocxlaer[2], André P. De Leenheer[2],[3], and Michel H.A. Piette[1]
1Ghent University, Department of Forensic Medicine, J. Kluyskensstraat 29, B-9000 Ghent, Belgium; 2Ghent University, Department of Medical Biochemistry and Clinical Analysis, Harelbekestraat 72, B-9000 Ghent, Belgium; and 3Ghent University, Department of Toxicology, Harelbekestraat 72, B-9000 Ghent, Belgium

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.

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