An overview on the use of mixtures of neutral and charged cyclodextrins as
chiral additives for the enantioseparation of drugs by capillary electropho
resis is presented. These so called dual cyclodextrin systems can often pro
vide unique selectivities. A brief theoretical background illustrating the
influence of the chiral discrimination ability and the effective mobility o
f the two cyclodextrins on the overall selectivity of the enantiomeric sepa
ration is given. Typical examples of applications in the pharmaceutical fie
ld, based on the simultaneous use of a charged (cationic or anionic) and ne
utral cyclodextrins, are described. (C) 2000 Elsevier Science BN. All right
s reserved.