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 language | English |
|---|---|
| Pages (from-to) | 380-384 |
| Number of pages | 5 |
| Journal | Beijing Ligong Daxue Xuebao/Transaction of Beijing Institute of Technology |
| Volume | 18 |
| Issue number | 3 |
| Publication status | Published - 1998 |
Keywords
- Anisodamine
- Chiral separation
- High performance capillary electrophoresis
- ß-CDs
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