Optimization of preparative electrophoretic chiral separation of ritalin enantiomers

J Pharm Biomed Anal. 2002 Jan 15;27(3-4):639-50. doi: 10.1016/s0731-7085(01)00572-6.

Abstract

Continuous free flow electrophoresis (CFFE) was applied to the preparative chiral separation of ritalin enantiomers. Sulfated beta-cyclodextrin (sbeta-CD) was used as the chiral additive. Liquid chromatography-mass spectrometry (LC-MS) experiments were applied to study the time averaged concentration of sbeta-CD in the separation chamber. The distribution of sbeta-CD in the separation chamber greatly influenced resolution and the angle of deflection. To optimize the separation, several parameters (methanol, concentration of sbeta-CD in the cathodic wash and in the separation buffer, and the introduction of a low conductivity zone) were investigated. The dependence of the resolution and deflection angles of ritalin enantiomers on the concentration of sbeta-CD in both the separation buffer and in the cathode wash solution appeared to be non-linear. Under close to optimal conditions, resolution of ritalin enantiomers was about 0.8 with an average processing rate of 0.5 mg/h. Overall, the enantiomeric purity of the individual isomers was approximately 83%; however, of the 20 vials containing ritalin, the presence of both enantiomers was only detected in three vials.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Central Nervous System Stimulants / analysis*
  • Electrophoresis / instrumentation
  • Electrophoresis / methods
  • Methylphenidate / analysis*
  • Stereoisomerism

Substances

  • Central Nervous System Stimulants
  • Methylphenidate