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Separation of basic central nervous system drugs by capillary electrochromatography

โœ Scribed by Jan Jiskra; Henk A. Claessens; Carel A. Cramers


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
301 KB
Volume
26
Category
Article
ISSN
1615-9306

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โœฆ Synopsis


Abstract

This article describes the sample preparation and separation of three strongly basic central nervous system (CNS) drugs by capillary electrochromatography. The separation was developed on Hypersil C8 MOS and Hypersil Phenyl stationary phases using acetonitrile (ACN) as organic modifier together with mobile phase additives, ammonia, ethylenediamine, or 1,3โ€diaminopropane. A successful, fast separation after a simple derivatization procedure of the compound was achieved on the Hypersil Phenyl stationary phase using ethylenediamine as mobile phase additive. The general approach to method development for complex mixtures is discussed.


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## Abstract The influence of seven differently methylated ฮฒโ€cyclodextrin derivatives and of pure ฮฒโ€cyclodextrin (ฮฒโ€CD) on the enantiomeric resolution by capillary electrophoresis of six basic chiral pharmaceuticals is investigated. The methyl substitution pattern affects enantioselectivity much mor

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The influence of the choice of type and/or concentration of cyclodextrin, other additives, the temperature surrounding the capillary, and buffer pH on the separation of some chiral basic drug substances in capillary zone electrophoresis has been evaluated. It was found that pH of the buffer and type