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Original Articles

Separation of Dammarane‐Saponins from Notoginseng, Root of Panax notoginseng (Burk.) F. H. Chen, by HSCCC Coupled with Evaporative Light Scattering Detector

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Pages 1579-1591 | Received 21 Apr 2002, Accepted 07 Oct 2002, Published online: 06 Feb 2007
 

Abstract

High‐speed countercurrent chromatography (HSCCC) coupled with evaporative light scattering detection, was applied to the separation of saponins from notoginseng, the main root of Panax notoginseng (Burk.) F. H. Chen. Five individual dammarane saponins have been isolated with the solvent systems composed of CHCl3/MeOH/2‐BuOH/H2O (5:6:1:4, v/v/v/v) and EtOAc/1‐BuOH/H2O (1:1:2, v/v/v), successively. They were identified as ginsenoside‐Rg1, ginsenoside‐Rd, notoginsenoside‐R1, ginsenoside‐Re, and ginsenoside‐Rb1 by FAB‐MS and 13C NMR, together with HPLC and TLC analysis.

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