Direct separation of pregabalin enantiomers using a zwitterionic chiral selector by high performance liquid chromatography coupled to mass spectrometry and ultraviolet detection

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Abstract

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.

Figures

  • Figure 1. Chemical structures of PRG (a), its (R)-enantiomer (b), and the chiral selectors in ZWIX columns (c).
  • Table 1. Effects of additive concentration, column temperature and water percentage on chromatographic parameters.
  • Figure 2. LC-MS chromatograms of: (a) PRG and (b) PRG spiked with 0.15% (R)-enantiomer. Conditions: (5 mM ammonium formate + 5 mM formic acid) in MeOH/water (96/4, v/v), 25 °C, CHIRALPAK ZWIX(+) (150 × 3.0 mm i.d.), MS detection on positive ion mode, SIM acquisition, m/z 160.
  • Figure 3. LC-MS chromatograms for LOD/LOQ determination with the racemic mixture: (a) blank chromatogram, (b) LOD chromatogram at 1 ng/mL, (c) LOQ chromatogram at 5 ng/mL. Chromatographic conditions are the same as in Figure 2.
  • Table 2. Resolution and S/N ratio values of (R)-enantiomer for different sample concentrations and injection volumes (API spiked with 0.15% of (R)-enantiomer).
  • Figure 4. Chromatograms with optimized UV conditions: 5 mM ammonium hydrogen orthophosphate in MeOH/water (90/10, v/v), 10 ◦C, CHIRALPAK ZWIX(+) (250 × 4.0 mm i.d.), 0.5 mL/min, UV at 212 nm. (a) PRG spiked with 0.15% (R)-enantiomer, (b) blank chromatogram.

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APA

Chennuru, L. N., Choppari, T., Nandula, R. P., Zhang, T., & Franco, P. (2016). Direct separation of pregabalin enantiomers using a zwitterionic chiral selector by high performance liquid chromatography coupled to mass spectrometry and ultraviolet detection. Molecules, 21(11). https://doi.org/10.3390/molecules21111578

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