ENANTIOMERIC SEPARATION OF DRUGS BY AFFINITY ELECTROKINETIC CHROMATOGRAPHY USING DEXTRAN SULFATE

Citation
H. Nishi et al., ENANTIOMERIC SEPARATION OF DRUGS BY AFFINITY ELECTROKINETIC CHROMATOGRAPHY USING DEXTRAN SULFATE, Electrophoresis, 15(10), 1994, pp. 1335-1340
Citations number
24
Categorie Soggetti
Biochemical Research Methods
Journal title
ISSN journal
01730835
Volume
15
Issue
10
Year of publication
1994
Pages
1335 - 1340
Database
ISI
SICI code
0173-0835(1994)15:10<1335:ESODBA>2.0.ZU;2-1
Abstract
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.