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Received on February 19, 2006
Accepted on June 8, 2006
Drug Monitoring and Toxicology |
1 Chemistry and Drug Metabolism, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, 5500 Nathan Shock Drive, Baltimore, MD
* To whom correspondence should be addressed. E-mail: mhuestis{at}intra.nida.nih.gov.
Background: A sensitive gas chromatography-mass spectrometry method was developed and validated for the simultaneous measurement of MDEA, MDMA, and its metabolites, HMA, MDA, and HMMA, in human urine.
Methods: We hydrolyzed 1 mL urine, fortified with MDMA-d5, MDA-d5, and MDEA-d6, with 100 µL of concentrated hydrochloric acid at 120 °C for 40 min. One hundred microliters 10 N sodium hydroxide and 3 mL phosphate buffer 0.1 N (pH 6.0) were added to hydrolyzed urine specimens before solid-phase extraction. After elution and evaporation, we derivatized extracts with heptafluorobutyric acid anhydride and analyzed with gas chromatography-mass spectrometry operated in EI-selected ion-monitoring mode.
Results: Limits of quantification were 25 µg/L for MDEA, MDMA, and its metabolites. Calibration curves were linear to 5000 µg/L for MDEA, MDMA, HMA, MDA, and HMMA, with a minimum r2 > 0.99. At 3 concentrations spanning the linear dynamic range of the assay, mean overall extraction efficiencies from urine were >85.5% for all compounds of interest. Intra- and inter-assay precision, produced as CV, were <15% for all drugs at 30, 300, and 3000 µg/L.
Conclusions: This gas chromatography-mass spectrometry assay provides adequate sensitivity and performance characteristics for the simultaneous quantification of MDEA, MDMA, and its metabolites HMMA, MDA, and HMA in human urine. The method meets and exceeds the requirements of the proposed Substance Abuse and Mental Health Administration's guidelines for federal workplace drug testing of MDEA and MDMA in urine.
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