A method for the analysis of reducing sugar enantiomers in beverages using
capillary zone electrophoresis is presented. Based on previous results, a r
esolution of all aldo-hexoses, -pentoses, -tetroses and trioses is achieved
. Additional separation of uronic acids, deoxy and amino sugars in differen
t buffer systems is demonstrated. Derivatives of sugar enantiomers change t
heir migration order if derivatized with the phenylethylamine enantiomer. T
hus. the use of a chiral derivatizing agent leads to simpler peak validatio
n and opens new opportunities for the development of new applications. Scre
ening of pharmaceutical drugs or food for rare sugar enantiomers with a det
ection limit of 25 fmol (5 mu M) is feasible. Adaptation of the general met
hod to wine. juice and instant coffee is demonstrated. The aldose, uronic a
cid and deoxy aldose enantiomer composition of the presented beverages is o
btained in a single run.