Published: Journal of Analytical Toxicology, Volume 20, Number 6, October 1996, pp. 432-440.
Analysis of 3,4-Methylenedioxymethamphetamine (MDMA) and
its Metabolites in Plasma and Urine by HPLC–DAD and GC–MS
Hans-Jörg Helmlin, Katrin Bracher, Daniel Bourquin, David Vonlanthen,
Rudolf Brenneisen, and Juraj Styk
In Europe, the compound 3,4-methylenedioxymethamphetamine (MDMA, Ecstasy, Adam), in addition to cannabis, is the most abused illicit drug at all-night “techno” parties. Methods for the determination of MDMA and its metabolites, 4-hydroxy-3-methoxymethamphetamine (HMMA), 3,4-dihydroxy- methamphetamine (HHMA), 3,4-methylenedioxyamphetamine (MDA), 4-hydroxy-3-methoxyamphetamine (HMA), and 3,4-dihydroxyamphetamine (HHA), in biological fluids were established. Plasma and urine samples were collected from two patients in a controlled clinical study over periods of 9 and 22 h, respectively. MDMA and MDA were determined in plasma and urine by reversed-phase high-performance liquid chromatography with diode array detection (HPLC–DAD) after solid-phase extraction on cation-exchange columns. Acidic or enzymatic hydrolysis was necessary to detect HMMA, HMA, HHMA, and HHA, which are mainly excreted as glucuronides. Gas chromatography–mass spectrometry (GC–MS) was used for confirmation. Sample extraction and on-disc derivatization with heptafluorobutyric anhydride (HFBA) were performed on Toxi-Lab SPEC solid-phase extraction concentrators. After administration of a single oral dose of 1.5 mg/kg body weight MDMA, peak plasma levels of 331 ng/mL MDMA and 15 ng/mL MDA were measured after 2 h and 6.3 h, respectively. Peak concentrations of 28.1 µg/mL MDMA in urine appeared after 21.5 h. Up to 2.3 µg/mL MDA, 35.1 µg/mL HMMA, and 2.1 µg/mL HMA were measured within 16–21.5 h. Conjugated HMMA and HHMA are the main urinary metabolites of MDMA.
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