Separation of basic drugs by capillary electrophoresis using selectively modified cyclodextrins as chiral selectors
✍ Scribed by Gerald Weseloh; Holger Bartsch; Wilfried A. König
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 474 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1040-7685
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✦ Synopsis
Abstract
The influence of seven differently methylated β‐cyclodextrin derivatives and of pure β‐cyclodextrin (β‐CD) on the enantiomeric resolution by capillary electrophoresis of six basic chiral pharmaceuticals is investigated. The methyl substitution pattern affects enantioselectivity much more than other experimental parameters. The purity of the used cyclodextrin derivatives is analyzed by successive hydrolysis, reduction, acetylation, and GC/MS of each CD derivative and by MALDI‐TOF mass spectrometry. © 1995 John Wiley & Sons, Inc.
📜 SIMILAR VOLUMES
## Abstract High resolution could be achieved for the enantiomers of acidic drugs, namely, sulindac, fenoprofen, ketoprofen, warfarin, and hexobarbital, in a buffer of pH 3 by the simultaneous addition of uncharged and charged β‐cyclodextrin derivatives. The interaction of the analytes with the ani