How to realize the linear scale-up process for rapid purification using high-performance counter-current chromatography

J Chromatogr A. 2008 Jun 20;1194(2):192-8. doi: 10.1016/j.chroma.2008.04.049. Epub 2008 Apr 24.

Abstract

This study used the isolation of six constituents from Selaginella tamariscina as an example to demonstrate how to achieve rapid and predictable linear scale-up processes in both normal- and reversed-phase high-performance counter-current chromatography. After systematic optimization of solvent systems, sample concentration, sample loading volume, rotation speed and flow rate on the analytical Mini-DE centrifuge, the optimized parameters obtained were directly transferred to the preparative Midi-DE centrifuge, with nearly the same purities, resolutions and elution times but with 50 times the throughput. Amentoflavone (446.7 mg, 97.8%), robustaflavone (21.6 mg, 89.4%), bilobetin (80.7 mg, 92.7%), hinokiflavone (15.1 mg, 85.5%), isocryptomerin (34.8 mg, 89.6%) and an apigenin-diglucoside (46.3mg, 96.4%) were obtained with amounts and purities shown in parentheses as analysed by HPLC. The process, therefore, offers an efficient and rapid method of obtaining sufficient quantities of target compounds with significantly increased throughput after a linear scale-up.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biflavonoids / chemistry
  • Biflavonoids / isolation & purification
  • Chromatography, High Pressure Liquid / methods*
  • Countercurrent Distribution / methods*
  • Molecular Structure
  • Reproducibility of Results
  • Selaginellaceae / chemistry

Substances

  • Biflavonoids
  • amentoflavone