Enantioseparations of basic and bifunctional pharmaceuticals by capillary electrochromatography using polysaccharide stationary phases
β Scribed by Debby Mangelings; Nancy Hardies; Mohamed Maftouh; Christina Suteu; D. Luc Massart; Yvan Vander Heyden
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 135 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0173-0835
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β¦ Synopsis
Abstract
A fast screening strategy was developed in capillary electrochromatography (CEC) for the chiral separation of basic and bifunctional compounds. The screening conditions were determined on polysaccharide chiral stationary phases using 15 pharmaceutical compounds. The content and type of organic modifier, as well as the pH of the mobile phase appeared to have the largest influence on the chiral resolution. ItΒ was seen that for acidic compounds, our approach was not suitable. A generic mobile phase for basic and bifunctional compounds was determined. The testing on 20 additional compounds showed that the proposed mobile phase performed well since enantioselectivity was observed for 86% of the investigated compounds. A comparison of CEC andΒ reversedβphase liquid chromatography (RPLC) results wasΒ attempted to demonstrate the potential of the used technique for chiral method development.
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## Abstract The influence of using normalβphase and reversedβphase versions of four commercial polysaccharide stationary phases on chiral separations was investigated with capillary electrochromatography (CEC). Both versions of the stationary phases, Chiralcel OD, OJ, and Chiralpak AD, AS were test
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