Baseline separation of the enantiomers of a number of negatively charged am
ino and mandelic acid derivatives was achieved in less than 10 min by capil
lary electrophoresis in a polyacrylamide coated capillary using the "partia
l filling method" (PFM) with submillimolar concentration of Teicoplanin (TE
) as the chiral selector. The influence of the charge and concentration of
TE, electrolyte solution composition and pH, on the enantioresolution was e
xamined. Further proofs were brought to corroborate the hypothesis that the
enantio-recognition takes place at the D-Ala-D-Ala binding site, whose blo
ckade is responsible for the antibacterial activity of glycopeptide antibio
tics. While the dependence of the chiral recognition capabilities of TE on
electrolyte solution composition and pH could limit its applicability, impr
oved sensitivity, reduction of TE wall adsorption, resulting in a good effi
ciency, and high cost reduction, due to the very small amount of chiral sel
ector required, were shown as advantages of the PFM adopted in this study.