Literature DB >> 9832251

Chiral separation of pharmaceuticals possessing a carboxy moiety.

T Arai1.   

Abstract

The separation of carboxylic enantiomers in the pharmaceutical field using high-performance liquid chromatographic and capillary electrophoretic techniques is reviewed. The techniques used for chiral separation include diastereomer derivatization, a chiral mobile phase, a chiral stationary phase (high-performance liquid chromatography) and chiral additives (capillary electrophoresis). Practical and conventional separation systems for pharmaceutical applications, such as pharmacokinetics, optical purity testing and stability studies, are described. A comprehensive collection of applications to carboxylic drugs and other carboxylic compounds of pharmaceutical interest is listed in the tables. The characteristics of each enantioseparation method are also discussed briefly.

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Year:  1998        PMID: 9832251     DOI: 10.1016/s0378-4347(98)00246-1

Source DB:  PubMed          Journal:  J Chromatogr B Biomed Sci Appl        ISSN: 1387-2273


  1 in total

1.  Enantioselective analysis of ritalinic acids in biological samples by using a protein-based chiral stationary phase.

Authors:  Jianhua Zhang; Yulin Deng; Jim Fang; Gordon McKay
Journal:  Pharm Res       Date:  2003-11       Impact factor: 4.200

  1 in total

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