Enantiomeric separation of a series of β-lactams using capillary zone electrophoresis

C. Jiang, D. W. Armstrong, A. Péter, F. Fülöp

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Twelve racemic substituted β-lactam compounds were examined via capillary zone electrophoresis using three chiral selectors: sulfated α-cyclodextrin (SAC), sulfated β-cyclodextrin (SBC), and carboxymethyl β-cyclodextrin (CMBC). Ten of the twelve β-lactams are separated and each of the ten compounds is baseline separated by at least one of the chiral run buffer additives under optimized conditions. SAC was found to be the most effective chiral selector, baseline separating seven of the analytes and partially separating another two. The concentration of the chiral selector had a prominent effect on the resolution, generally higher concentrations gave longer migration times and better resolutions. Addition of organic modifier also increased analyses time but gave lower resolution. Decreasing the pH of the run buffer generally decreased analyses times as well as resolution. Decreasing the applied voltage generally improved resolution.

Original languageEnglish
Pages (from-to)1709-1721
Number of pages13
JournalJournal of Liquid Chromatography and Related Technologies
Volume30
Issue number12
DOIs
Publication statusPublished - Jan 1 2007

Keywords

  • Capillary electrophoresis (CE)
  • Carboxymethyl β-cyclodextrin (CMBC)
  • Pseudophase separations
  • Sulfated α-Cyclodextrin (SAC)
  • Sulfated β-cyclodextrin (SBC)
  • β-Lactam

ASJC Scopus subject areas

  • Analytical Chemistry
  • Biochemistry
  • Pharmaceutical Science
  • Clinical Biochemistry

Fingerprint Dive into the research topics of 'Enantiomeric separation of a series of β-lactams using capillary zone electrophoresis'. Together they form a unique fingerprint.

  • Cite this