Reference : Resolution Improvement by Use of Carboxymethyl-Beta-Cyclodextrin as Chiral Additive for ...

	Document type :	Scientific journals : Article
	Discipline(s) :	Human health sciences : Pharmacy, pharmacology & toxicology
	To cite this reference:	http://hdl.handle.net/2268/40778

Title :	Resolution Improvement by Use of Carboxymethyl-Beta-Cyclodextrin as Chiral Additive for the Enantiomeric Separation of Basic Drugs by Capillary Electrophoresis
Language :	English
Author, co-author :	Fillet, Marianne [Université de Liège - ULg > Département de pharmacie > Analyse des médicaments >]
	Bechet, I. [> > > >]
	Hubert, Philippe [Université de Liège - ULg > > Chimie analytique >]
	Crommen, Jacques [Université de Liège - ULg > Département de pharmacie > Analyse des médicaments >]
Publication date :	Jun-1996
Journal title :	Journal of Pharmaceutical & Biomedical Analysis
Volume :	14
Issue/season :	8-10
Pages :	1107-14
Audience :	International
ISSN :	0731-7085
Abstract :	[en] Three beta-cyclodextrin derivatives--carboxymethyl-, dimethyl- and hydroxypropyl-beta-cyclodextrin--were tested as chiral selectors for the enantioseparation of seven basic drugs in free solution capillary electrophoresis, using buffers made of 100 mM phosphoric acid adjusted to pH 3.0 with triethanolamine in fused silica capillaries thermostatted at 15 degrees C. The best results with respect to chiral resolution were obtained with carboxymethyl-beta-cyclodextrin (CMCD): the enantiomers of all compounds examined were completely resolved with this beta-cyclodextrin derivative. The influence of the CMCD concentration on the migration times, the apparent electrophoretic mobility difference and the resolution of the drug enantiomers was investigated thoroughly. Particularly impressive resolution values, up to 23.7, were obtained for several compounds in these capillary electrophoretic systems, using CMCD in the 5-15 mM concentration range.
Permalink :	http://hdl.handle.net/2268/40778
	also: http://hdl.handle.net/2268/22542

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