Chiral Separation of Calcium (−)-2(S)-2-Benzyl-4-oxo-4-(cis-hexahydro-2-isoindolinyl)butyrate Enantiomers by High-performance Liquid Chromatography

2009 ◽  
Vol 27 (1) ◽  
pp. 29-32
Author(s):  
Zhefeng ZHANG ◽  
Gengliang YANG ◽  
Wenhui GAO ◽  
Yi CHEN
2020 ◽  
Vol 16 (5) ◽  
pp. 456-473
Author(s):  
Prachi Raikar ◽  
Gurupadayya Bannimath

Chiral separation plays a very important role in the modern pharmaceutical analysis and will continue in upcoming years. Separation and identification of chiral impurities are indispensable. According to ICH guidelines, only the active enantiomer of the drug has to be marketed, so there is a focus on separation of the inactive enantiomer which acts as a chiral impurity. The impurities present in the enantiomers also pose various toxic adverse effects on bioavailability and efficacy, hence the need to separate these impurities will forever be trending. This review primarily focuses on the separation techniques like Capillary Electrophoresis (CE), High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Supercritical Fluid Chromatography (SFC) followed by the year-wise trend in the separation of selected chiral impurities. In the coming years, researchers should work on using ultra-fast, selective, and sensitive methods for the effective separation of chiral impurities.


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