H. Nishi et al., ENANTIOMERIC SEPARATION OF DRUGS BY AFFINITY ELECTROKINETIC CHROMATOGRAPHY USING DEXTRAN SULFATE, Electrophoresis, 15(10), 1994, pp. 1335-1340
Dextran sulfate (sodium salt), which is a mixture of a linear alpha-(1
,6)-linked D-glucose polymer having a sulfate group in the molecule, h
as been employed as a chiral selector in affinity electrokinetic chrom
atography (EKC) for the separation of enantiomers of drugs. Enantiomer
s of trimetoquinol hydrochloride and its positional isomer have been s
uccessfully separated by the method using a 3-5% dextran sulfate buffe
r solution of pH 5.5 within 20 min. The effects of buffer pH, concentr
ation of dextran sulfate, and additives (such as an organic solvent, u
rea and a surfactant) on the enantioselectivity were investigated. The
choice of pH and the concentration of dextran sulfate has been import
ant for the improvement in selectivity.