CAPILLARY ELECTROPHORETIC SEPARATION OF BASIC DRUGS USING SURFACE-MODIFIED C-8 CAPILLARIES AND DERIVATIZED CYCLODEXTRINS AS STRUCTURAL CHIRAL SELECTORS

Citation
O. Stalberg et al., CAPILLARY ELECTROPHORETIC SEPARATION OF BASIC DRUGS USING SURFACE-MODIFIED C-8 CAPILLARIES AND DERIVATIZED CYCLODEXTRINS AS STRUCTURAL CHIRAL SELECTORS, Chromatographia, 40(11-12), 1995, pp. 697-704
Citations number
50
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
Journal title
ISSN journal
00095893
Volume
40
Issue
11-12
Year of publication
1995
Pages
697 - 704
Database
ISI
SICI code
0009-5893(1995)40:11-12<697:CESOBD>2.0.ZU;2-2
Abstract
Dynamic coating of bonded Cs fused silica capillaries with cationic am phiphiles is shown to minimize adsorption of basic drug molecules but also to facilitate control/reversal of electroosmotic flow. Optimizati on of the peak shapes was achieved by addition of cationic amphiphiles with a suitable mobility and adsorption to the capillary surface. The surface modification described, combined with the addition of cyclode xtrins as selectors into the background electrolyte, resulted in uniqu e CE systems showing excellent resolution for structural analogues. Th e separation of rotamers and enantiomers is demonstrated. Applications to the antipsychotic compound remoxipride and its related substances and to the chiral separation of asthma- and local anaesthetic drug ena ntiomers are given.