Molecules · 2016 · 18 citations · 15 references
PharmacyMedicinal ChemistryPharmaceutical AnalysisAnalytical ChemistryChromatographic AnalysisSeparation ScienceChiral ChromatographyChiral Impurity AnalysisChiral SeparationChromatographyChromatography CouplingLiquid ChromatographyAnalytical Chiral SeparationChiral High-performance Liquid ChromatographyChiral Impurity SeparationChromatographic Chiral SeparationChromatographic SelectivityDirect Chiral SeparationHigh-performance Liquid ChromatographySensitivity
The chromatographic resolution of pregabalin enantiomers has been often achieved by derivatization of the molecule, in order to reach enough sensitivity at low concentrations of the minor enantiomer present in the active principle. In the present article, the development and optimization of two liquid chromatographic methods are presented for the direct resolution of pregabalin enantiomers on a chiral stationary phase (CSP) containing a zwitterionic selector derived from cinchona alkaloid and sulfonic acid (CHIRALPAK ZWIX). The key parameters for the separation as well as the compatibility of chromatographic conditions with different detection modes (ultraviolet and mass spectrometry) were investigated. The resulting methods were found to be selective, of high performance and low limits of detection (2 µg/mL by UV and 1 ng/mL by MS, respectively) and quantification (6 µg/mL by UV and 5 ng/mL by MS, respectively) for the minor enantiomer which is considered as a chiral impurity.
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