Abstract
Maltodextrins, i.e., mixtures of linear α-(1–4)-linked d-glucose polymers, were found to be effective as chiral electrolyte modifiers to perform direct, rapid separations by capillary electrophoresis of racemic mixtures of 2-arylpropionic acid non-steroidal anti-inflammatory compounds and coumarinic anticoagulant drugs, and also diastereomeric cefalosporin antibiotics. Enantioselectivity seemed to be dependent on an as yet unidentified combination of variables.
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