Journal of Separation Science · 2005 · 16 citations · 19 references
PharmacyMedicinal ChemistryPharmaceutical AnalysisChromatographic AnalysisDrug DiscoveryMass Spectrometric AnalysisChiral ChromatographyChromatographic Analysis Of PharmaceuticalsChromatographyInstrumental AnalysisLiquid ChromatographyStationary Phase ChemistryAnalytical Chiral ChromatographyAnalytical Liquid ChromatographyAnalytical Methods DevelopmentChiral Liquid ChromatographyChromatographic Chiral SeparationPolysaccharide-based Chiral Stationary PhasesRecovery Of Pharmaceutical CompoundsSeparation Factor
Novel HPLC methods were developed for the analytical and semipreparative resolution of new antianginal drug ranolazine enantiomers. Good baseline enantioseparation was achieved using cellulose tris (3,5-dimethylphenylcarbamate) (CDMPC) chiral stationary phases (CSPs) under both normal-phase and polar organic modes. The validation of the analytical methods including linearity, LODs, recovery, and precision, and the semipreparative resolution of ranolazine racemate were carried out using methanol as mobile phase without any basic and acidic additives under polar organic mode, using CDMPC CSPs. At analytical scale, the elution times of both enantiomers were less than 7.5 min at 20 degrees C and 1.0 mL/min, with the separation factor (a) 1.88 and the resolution factor (R(s)) 2.95. At semipreparative scale, about 14.3 mg/h enantiomers could be isolated and elution times of both enantiomers were less than 13 min at 2.0 mL/min. To increase the throughput, the technique of overlapping injections was used. The first eluted enantiomer was isolated with a purity of 99.6% enantiomer excess (e.e.) and > 99.0% yield. The second enantiomer was isolated with a purity of 98.8% e.e. and > 99.0% yield. In addition, optical rotation and circular dichroism spectroscopy of both ranolazine enantiomers isolated were also investigated.
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Yoshio Okamoto, Mitsunobu Kawashima, Koichi Hatada · Journal of Chromatography A · 1986 · 669 citations