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Dermination of 4-Alkyl 2,5 dimethoxy-amphetamine derivatives by Capillary Electrophoresis with mass spectrometry detection from urine samples

Academic Article
Publication Date:
2007
Short description:
Dermination of 4-Alkyl 2,5 dimethoxy-amphetamine derivatives by Capillary Electrophoresis with mass spectrometry detection from urine samples / Nieddu, M., Boatto, G., Dessi', G.. - In: JOURNAL OF CHROMATOGRAPHY. B. - ISSN 1570-0232. - 852:1 - 2(2007), pp. 578-581. [10.1016/j.jchromb.2007.02.029]
abstract:
The methylenedioxy-derivatives of amphetamine represent the largest group of designer drugs. The 4-methyl (DOM), -ethyl (DOET) and -propyl
(DOPR) derivatives of 2,5-dimethoxy-amphetamine (2,5-DMA) were found to possess quite similar serotonin receptor affinities [R.A. Glennon,
D.L. Doot, R. Young, Pharmacol. Biochem. Behav. 14 (1981) 287.]. This paper describes a method to screen for and quantify DOM, DOET
and DOPR in urine samples, using capillary electrophoresis coupled to electrospray ionisation-mass spectrometry (CE-ESI-MS). Prior to CE-MS
analysis, a simple solid-phase extraction (SPE) was used for sample cleanup. The method was validated according to international guidelines.
Data for accuracy and precision were within required limits. Calibration curves were generated ranging from 10 to 1000 ng/mL and correlation
coefficients always exceeded 0.996.
Iris type:
1.1 Articolo in rivista
Keywords:
Urine; 2,5-Dimethoxy-4-methylamphetamine (DOM); 2,5-Dimethoxy-4-ethylamphetamine (DOET); 2,5-Dimethoxy-4-propylamphetamine (DOPR); Capillary electrophoresis-mass spectrometry (CE-MS)
List of contributors:
Nieddu, M.; Boatto, Gianpiero; Dessi', G.
Authors of the University:
NIEDDU Maria
Handle:
https://iris.uniss.it/handle/11388/58513
Published in:
JOURNAL OF CHROMATOGRAPHY. B
Journal
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