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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.


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Enantiomeric separation of acidic drugs
✍ Fillet, Marianne ;Bechet, Isabelle ;Schomburg, Gerhard ;Hubert, Philippe ;Cromme 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 472 KB 👁 1 views

## 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