Separation and purification of astaxanthin from Phaffia rhodozyma by preparative high-speed counter-current chromatography

J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Sep 1:1029-1030:191-197. doi: 10.1016/j.jchromb.2016.06.042. Epub 2016 Jun 25.

Abstract

An effective high-speed counter-current chromatography (HSCCC) method was established for the preparative isolation and purification of astaxanthin from Phaffia rhodozyma. With a two-phase solvent system composed of n-hexane-acetone-ethanol-water (1:1:1:1, v/v/v/v), 100mg crude extract of P. rhodozyma was separated to yield 20.6mg of astaxanthin at 92.0% purity. By further one step silica gel column chromatography, the purity reached 99.0%. The chemical structure of astaxanthin was confirmed by thin layer chromatography (TLC), UV spectroscopy scanning, high performance liquid chromatography with a ZORBAX SB-C18 column and a Waters Nova-pak C18 column, and ESI/MS/MS.

Keywords: Astaxanthin; High-speed counter-current chromatography; Phaffia rhodozyma; Separation and purification.

MeSH terms

  • Acetone / chemistry
  • Antioxidants / analysis
  • Antioxidants / isolation & purification*
  • Chromatography, High Pressure Liquid
  • Chromatography, Thin Layer
  • Countercurrent Distribution / instrumentation
  • Countercurrent Distribution / methods*
  • Equipment Design
  • Ethanol / chemistry
  • Hexanes / chemistry
  • Solvents / chemistry
  • Tandem Mass Spectrometry
  • Xanthophylls / analysis
  • Xanthophylls / isolation & purification
  • Yeasts / chemistry*

Substances

  • Antioxidants
  • Hexanes
  • Solvents
  • Xanthophylls
  • Acetone
  • n-hexane
  • Ethanol
  • astaxanthine