Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9748894 | Journal of Chromatography A | 2005 | 6 Pages |
Abstract
Sample solubility in the mobile phase and enantioselectivity are key factors in chiral preparative chromatography. In the search for a high throughput process for production of pure enantiomers, the rational design of the mobile phase and the selection of a suitable chiral stationary phase (CSP) are essential. However, one may sometimes be faced with the incompatibility between the CSP and the preferential eluent for sample solubility. Such a limitation may be circumvented by using an immobilized CSP such as CHIRALPAK® IA. In this manuscript, the chiral separation of a Ca-sensitizing drug (EMD 53986) is optimized on CHIRALPAK® IA in terms of sample solubility, enantioselectivity and preparative productivity. The approaches for method optimization and the impact of sample solubility on productivity are discussed. The preparative potential of CHIRALPAK® IA is also demonstrated.
Related Topics
Physical Sciences and Engineering
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Analytical Chemistry
Authors
Tong Zhang, Mireille Schaeffer, Pilar Franco,