Abstract

High-performance liquid chromatography with a chiral crown ether stationary phase and capillary electrophoresis (CE) with a chiral crown ether dissolved in the operating buffer were used for the separation of enantiomers of analogues of DOPA and tyrosine and some analogues of γ-aminobutyric acid (GABA). CE and HPLC yielded similar results for the DOPA and tyrosine analogues. However, for the analogues of GABA, three of the four compounds tested were well resolved by HPLC but only one was well resolved by CE. It was necessary to use an indirect detection scheme for the CE of GABA analogues. The influence of substituents on the different compounds on the resolution factors observed by the two methods is discussed, in addition to the advantages and disadvantages of the two methods in practical applications.

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