Liquid Chromatography
Development of a rapid and convenient method to separate eight ginsenosides from Panax ginseng by high-speed counter-current chromatography coupled with evaporative light scattering detection
Article first published online: 13 APR 2011
DOI: 10.1002/jssc.201000932
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Shehzad, O., Jin Ha, I., Park, Y., Wan Ha, Y. and Shik Kim, Y. (2011), Development of a rapid and convenient method to separate eight ginsenosides from Panax ginseng by high-speed counter-current chromatography coupled with evaporative light scattering detection. Journal of Separation Science, 34: 1116–1122. doi: 10.1002/jssc.201000932
Publication History
- Issue published online: 5 MAY 2011
- Article first published online: 13 APR 2011
- Manuscript Accepted: 25 FEB 2011
- Manuscript Revised: 15 FEB 2011
- Manuscript Received: 30 DEC 2010
Funded by
- National Research Foundation of Korea
- Basic Research Promotion Fund. Grant Number: 2010-0008384
- Korean government (MEST). Grant Number: 20090083533
Keywords:
- Ginsenosides;
- High-speed counter-current chromatography;
- Panax ginseng;
- Protopanaxadiol;
- Protopanaxatriol
Abstract
Ginsenosides exhibit diverse biological activities and are major well-known components isolated from the radix of Panax ginseng C.A. Meyer. In the present work, a rapid and facile method for the separation and purification of eight ginsenosides from P. ginseng by high-speed counter-current chromatography coupled with evaporative light scattering detector (HSCCC-ELSD) was successfully developed. The crude samples for HSCCC separation were first purified from ginseng extract using a macroporous resin; the extract was loaded onto a Diaion-HP20 column and fractionated by methanol and water gradient elution. The ginsenosides-protopanaxadiol (PPD) and protopanaxatriol (PPT) fractions were subsequently eluted with 65 and 80% methanol and water gradient elution, respectively. Furthermore, these two fractions were separated by HSCCC-ELSD. The two-phase solvent system used for separation was composed of chloroform/methanol/water/isopropanol at a volume ratio of 4:3:2:1. Each fraction obtained was collected and dried, yielding the following eight ginsenosides: Rg1, Re, Rf, Rh1, Rb1, Rc Rb2 and Rd. The purity of these ginsenosides was greater than 97% as assessed by HPLC-ELSD, and their structures were characterized by electrospray-ionization mass spectrometry (ESI-MS) and nuclear magnetic resonance spectroscopy. This is the first report regarding the separation of the ginsenosides Rh1, Rb2 and Rc from P. ginseng by HSCCC.

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