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Study on the chiral separation of anisodamine by high performance capillary electrophoresis

  • Hong Wang*
  • , Junling Gu
  • , Rongji Dai
  • , Ruonong Fu
  • , Hanfang Hu
  • , Tianhui Ding
  • *Corresponding author for this work
  • Beijing Institute of Technology
  • Hebei University

Research output: Contribution to journalArticlepeer-review

Abstract

Aim: To study the enantiomeric separation of anisodamine. Methods: The factors influencing complexation and resolution were investigated using ß-cyclodextrin (ß-CD) and 2, 6-di-O-carboxymethyl-ß- cyclodextrin (CM-ß-CD) as the chiral selectors by high performance capillary electrophoresis (HPCE). Results: The optimum chiral separation system for anisodamine was established. Conclusion: CM-ß-CD can give a baseline chiral separation for anisodamine and no resolution is found for scopolamine or atropine.

Original languageEnglish
Pages (from-to)380-384
Number of pages5
JournalBeijing Ligong Daxue Xuebao/Transaction of Beijing Institute of Technology
Volume18
Issue number3
Publication statusPublished - 1998

Keywords

  • Anisodamine
  • Chiral separation
  • High performance capillary electrophoresis
  • ß-CDs

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