Use of sulfated cyclofructan 6 and sulfated cyclodextrins for the chiral separation of four basic pharmaceuticals by capillary electrophoresis

Yi Jun Zhang, Ming Xian Huang, Yu Ping Zhang, Daniel Wayne Armstrong, Zachary S. Breitbach, Jae Jeong Ryoo

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

Sulfated cyclofructan 6 (S-CF6) and sulfated cyclodextrins (S-α-, β-, γ-CDs) are highly selective chiral selectors for the enantioseparation of basic solutes. In this study, S-CF6 was introduced for the enantiomeric separation of four basic pharmaceuticals (including tamsulosin, tiropramide, bupivacaine, and norephedrine) by capillary electrophoresis (CE), and the enantiomeric separation performance was compared with S-α-, β-, γ-CDs. The effects of the chiral selector type, chiral selector concentration, operating voltage, and column temperature were examined and optimized. Excellent resolutions were obtained for all solutes on these chiral selectors. Chirality 25:735-742, 2013.

Original languageEnglish
Pages (from-to)735-742
Number of pages8
JournalChirality
Volume25
Issue number11
DOIs
StatePublished - Nov 2013

Keywords

  • basic pharmaceuticals
  • capillary electrophoresis
  • chiral separations
  • sulfated cyclodextrins
  • sulfated cyclofructan 6

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