Micellar electrokinetic capillary chromatography in a mixture of taurodeoxycholic acid and β-cyclodextrin
- 1 January 1992
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 17,p. 1189-1192
- https://doi.org/10.1039/c39920001189
Abstract
A mixture of taurodeoxycholic acid and β-cyclodextrin is found to form a ‘pseudo-stationary’ phase, which is very effective for the separation of the enantiomers of a variety of chiral compounds using micellar electrokinetic capillary chromatography (MECC); resolution is considerably superior to that obtained by using either taurodeoxycholic acid or β-cyclodextrin alone.Keywords
This publication has 7 references indexed in Scilit:
- Chiral separation of naphthalene-2,3-dicarboxaldehyde-labeled amino acid enantiomers by cyclodextrin-modified micellar electrokinetic chromatography with laser-induced fluorescence detectionAnalytical Chemistry, 1991
- Bile salt surfactants in micellar electrokinetic capillary chromatographyJournal of Chromatography A, 1991
- Application of micellar electrokinetic chromatography to pharmaceutical analysisElectrophoresis, 1990
- Sodium glyco- and taurodeoxycholate: possible helical models for conjugated bile salt micellesThe Journal of Physical Chemistry, 1989
- chiral separation by electronkinetic chromatography while bile salt micellesJournal of Chromatography A, 1989
- Determination of the critical micelle concentration of surfactants using the fluorescent probe N-phenyl-1-naphthylamineAnalytical Biochemistry, 1986
- Solvent Effects on Amphiphilic AggregationPublished by Springer Nature ,1979