Determination of the enantiomeric purity of S-ropivacaine by capillary electrophoresis with methyl-beta-cyclodextrin as chiral selector using conventional and complete filling techniques

Eur J Pharm Sci. 1999 Oct;9(1):17-24. doi: 10.1016/s0928-0987(99)00035-4.

Abstract

Capillary electrophoresis (CE) methods based on the conventional and complete filling techniques for determination of the enantiomeric purity of S-ropivacaine are described. The complete filling technique is a separation method which can be used instead of the partial filling technique in order to reduce the total analysis time, when the chiral selector solution does not absorb UV light. In the complete filling technique the total length of the capillary is filled with the chiral selector solution, prior to application of the analyte. During the run both ends of the capillary are connected to the background electrolyte, i.e. without chiral agent. An interlaboratory study was performed to validate the method. The limit of detection and quantification for R-ropivacaine were found to be about 0.6 and 1.6 microg/ml, respectively, corresponding to 0. 1 and 0.25% enantiomeric purity of S-ropivacaine. Good performances were demonstrated for the repeatability and linearity. The consumption of the chiral selector was about 160 times lower with the complete filling technique compared with the conventional CE technique.

Publication types

  • Comparative Study

MeSH terms

  • Amides / isolation & purification*
  • Anesthetics, Local / isolation & purification*
  • Cyclodextrins / chemistry*
  • Electrophoresis, Capillary / methods*
  • Ropivacaine
  • Stereoisomerism
  • beta-Cyclodextrins*

Substances

  • Amides
  • Anesthetics, Local
  • Cyclodextrins
  • beta-Cyclodextrins
  • methyl-beta-cyclodextrin
  • Ropivacaine