CHIRAL DETERMINATION OF AMPHETAMINE AND RELATED-COMPOUNDS USING CHLOROFORMATES FOR DERIVATIZATION AND HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY

Citation
R. Herraezhernandez et al., CHIRAL DETERMINATION OF AMPHETAMINE AND RELATED-COMPOUNDS USING CHLOROFORMATES FOR DERIVATIZATION AND HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Analyst (London. 1877. Print), 123(10), 1998, pp. 2131-2137
Citations number
23
Categorie Soggetti
Chemistry Analytical
ISSN journal
00032654
Volume
123
Issue
10
Year of publication
1998
Pages
2131 - 2137
Database
ISI
SICI code
0003-2654(1998)123:10<2131:CDOAAR>2.0.ZU;2-D
Abstract
The enantiomeric determination of amphetamine and various amphetamine- type compounds by liquid chromatography after chiral derivatization wi th 9-fluorenylmethyl chloroformate-L-proline (FMOC-L-Pro) is reported. The results obtained were compared with those achieved after achiral derivatization with 9-fluorenylmethyl chloroformate and subsequent sep aration of the derivatives on a beta-cyclodextrin chiral stationary ph ase. Conditions for the derivatization of amphetamines with FMOC-L-Pro were investigated, including the effect of the derivatization reagent concentration, pH and reaction time, using amphetamine, ephedrine and pseudoephedrine as model compounds. On the basis of these studies, po ssible conditions for the determination of each amphetamine are indica ted. To demonstrate the utility of the proposed procedures, data on li nearity, repeatability and sensitivity are given. Results of the deter mination of ephedrine enantiomers in different pharmaceutical samples are also presented.