FAST CHIRAL SEPARATION OF AMINO-ACID DERIVATIVES AND ACIDIC DRUGS BY CO-ELECTROOSMOTIC FLOW CAPILLARY-ELECTROPHORESIS WITH VANCOMYCIN AS CHIRAL SELECTOR
Jw. Kang et al., FAST CHIRAL SEPARATION OF AMINO-ACID DERIVATIVES AND ACIDIC DRUGS BY CO-ELECTROOSMOTIC FLOW CAPILLARY-ELECTROPHORESIS WITH VANCOMYCIN AS CHIRAL SELECTOR, Journal of chromatography, 825(1), 1998, pp. 81-87
Citations number
30
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
A fast chiral separation method for acidic enantiomers, including 9-fl
uorenylmethyl chloroformate (FMOC) amino acid derivatives and ketoprof
en, with vancomycin as chiral selector is presented. In this method, h
exadimethrine bromide (HDB), a polycationic polymer, was added to the
run buffer as electroosmotic flow (EOF) modifier. The reversed EOF mig
rated in the same direction as the anionic analytes. Consequently, the
separation time was shortened. Another advantage of using HDB as buff
er additive is that the adsorption of vancomycin onto the capillary wa
ll was minimized, hence, the separation efficiency was improved. The e
ffects of buffer pH and vancomycin concentration on separation were in
vestigated. Base line chiral separation of 12 FMOC-amino acid derivati
ves, ketoprofen and drug intermediate 6,5'6'-bismethylenedioxybiphenyl
-2,2'-dicarboxylic acid were obtained. The separation time for each en
antiomers was not more than 4.5 min, and the average efficiency of 3.2
.10(5) plates/m was obtained. (C) 1998 Elsevier Science B.V. All right
s reserved.