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
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.