Accelerated solvent extraction and pH-zone-refining counter-current chromatographic purification of yunaconitine and 8-deacetylyunaconitine from Aconitum vilmorinianum Kom

J Sep Sci. 2013 Aug;36(16):2680-5. doi: 10.1002/jssc.201300472. Epub 2013 Jul 19.

Abstract

This study aimed to seek an efficient method to extract and purify yunaconitine and 8-deacetylyunaconitine from Aconitum vilmorinianum Kom. by accelerated solvent extraction combined with pH-zone-refining counter-current chromatography. The major extraction parameters for accelerated solvent extraction were optimized by an orthogonal test design L9 (3)(4). Then a separation and purification method was established using pH-zone-refining counter-current chromatography with a two-phase solvent system composed of petroleum ether/ethyl acetate/methanol/water (5:5:2:8, v/v) with 10 mM triethylamine in the upper phase and 10 mM HCl in the lower phase. From 2 g crude extract, 224 mg of 8-deacetylyunaconitine (I) and 841 mg of yunaconitine (II) were obtained with a purity of over 98.0%. The chemical structures were identified by ESI-MS and (1)H and (13)C NMR spectroscopy.

Keywords: Accelerated solvent extraction; Aconitum vilmorinianum Kom.; Counter-current chromatography; Traditional Chinese medicines; Yunaconitine.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aconitine / analogs & derivatives*
  • Aconitine / chemistry
  • Aconitine / isolation & purification
  • Aconitum / chemistry*
  • Countercurrent Distribution / methods*
  • Molecular Structure
  • Plant Extracts / chemistry
  • Plant Extracts / isolation & purification*
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Plant Extracts
  • yunaconitine
  • Aconitine