Study of the enantiomeric separation of the anticholinergic drugs on two immobilized polysaccharide-based chiral stationary phases by HPLC and the possible chiral recognition mechanisms

Electrophoresis. 2018 Jun;39(11):1361-1369. doi: 10.1002/elps.201800039. Epub 2018 Mar 30.

Abstract

In this work, the enantiomeric separation of ten anticholinergic drugs was first examined on two derivative polysaccharide chiral stationary phases (CSPs), i.e., Chiralpak ID and Chiralpak IA in the normal phase mode. Except for scopolamine hydrobromide, the remaining nine analytes could be completely separated with good resolutions using both columns under the optimized mobile phase conditions. And the enantiomeric discrimination ability of the studied CSPs towards nine analytes was in the order of Chiralpak ID > Chiralpak IA. The influences of organic modifier types, alcohol content, and base/acid additives on the enantiomeric separation were evaluated and optimized. According to the experimental results, the effect of the structures of analytes on enantiomeric separation was discussed. Additionally, the chiral recognition mechanisms were proposed based on the thermodynamic analysis of the experimental data.

Keywords: Anticholinergic drugs; Chiral stationary phase; Enantiomeric separation; Thermodynamic analysis.

MeSH terms

  • Cholinergic Antagonists / chemistry
  • Cholinergic Antagonists / isolation & purification*
  • Chromatography, High Pressure Liquid / methods*
  • Polysaccharides
  • Stereoisomerism
  • Thermodynamics

Substances

  • Cholinergic Antagonists
  • Polysaccharides