Optimization of the chiral separation of a Ca-sensitizing drug on an immobilized polysaccharide-based chiral stationary phase - Case study with a preparative perspective

被引:65
作者
Zhang, T [1 ]
Schaeffer, M [1 ]
Franco, P [1 ]
机构
[1] Chiral Technol Europe, F-67404 Illkirch Graffenstaden, France
关键词
CHIRALPAK (R) IA; amylose 3,5-dimethylphenylcarbamate; immobilized chiral stationary phase; chiral drug; chiral separation; sample solubility; method development; productivity; SMB;
D O I
10.1016/j.chroma.2005.06.003
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
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 (R) IA. In this manuscript, the chiral separation of a Ca-sensitizing drug (EMD 53986) is optimized on CHIRALPAK (R) 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 (R) IA is also demonstrated. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:96 / 101
页数:6
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