Enantioselective HPLC analysis of escitalopram oxalate and its impurities using a cellulose-based chiral stationary phase under normal- and green reversed-phase conditions

J Sep Sci. 2022 Mar;45(5):1059-1066. doi: 10.1002/jssc.202100913. Epub 2022 Jan 12.

Abstract

Normal-phase and reversed-phase high-performance liquid chromatography methods for the separation of the active pharmaceutical ingredient escitalopram from its (R)-enantiomer impurity have been developed on the cellulose-based Chiralcel OJ-H chiral stationary phase. Both methods share two features: they use ethanol as a cosolvent and are able to give a complete enantioseparation without interference from other associated chiral impurities. With the green eluent mixture ethanol-water-diethylammine 70:30:0.1 (v/v/v), the resolution between escitalopram and (R)-enantiomer was 2.09 at 30°C. The limits of quantification for the (S) and (R) enantiomers were 4.5 and 3.8 μg mL-1 , respectively.

Keywords: absolute configuration; cellulose tris(4-methylbenzoate); citalopram; escitalopram; green high-performance liquid chromatography.

MeSH terms

  • Cellulose* / chemistry
  • Chromatography, High Pressure Liquid / methods
  • Escitalopram*
  • Oxalates
  • Stereoisomerism

Substances

  • Oxalates
  • Escitalopram
  • Cellulose