Development of a Rapid and Sensitive Method for the Quantitation of Amphetamines in Human Plasma and Oral Fluid by LC-MS-MS
Author(s) -
Michelle Wood,
Gert De Boeck,
Nele Samyn,
Michael Morris,
Donald P. Cooper,
R. A. A. Maes,
E. A. de Bruijn
Publication year - 2003
Publication title -
journal of analytical toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.161
H-Index - 76
eISSN - 1945-2403
pISSN - 0146-4760
DOI - 10.1093/jat/27.2.78
Subject(s) - chromatography , chemistry , derivatization , mass spectrometry , ephedrine , sample preparation , protein precipitation , forensic toxicology , tandem mass spectrometry , human plasma , solid phase extraction , liquid chromatography–mass spectrometry , gas chromatography–mass spectrometry , quantitative analysis (chemistry) , bioanalysis , extraction (chemistry) , pharmacology , medicine
Target analysis of amphetamines in biological samples is of great importance for clinical and forensic toxicologists alike. At present, most laboratories analyze such samples by gas chromatography-mass spectrometry. However, this procedure is labor-intensive and time-consuming, particularly as a preliminary extraction and derivatization are usually unavoidable. Here we describe the development of an alternative method. Amphetamines were isolated from human plasma and oral fluid using a simple methanol precipitation step and subsequently analyzed using reversed-phase liquid chromatography-tandem mass spectrometry. Quantitation of the drugs was performed using multiple reaction monitoring. The developed method, which requires only 50 microL of biological sample, has a total analysis time of less than 20 min (including sample preparation) and enables the simultaneous quantitation of 3,4-methylenedioxymethamphetamine, 3,4-methylenedioxyamphetamine, 3,4-methylenedioxyethylamphetamine, amphetamine, methamphetamine, and ephedrine in a single chromatographic run. Limits of detection of 2 microg/L or better were obtained. The method has been validated and subsequently applied to the analysis of plasma and oral fluid samples collected from current drug users.
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