A Strategy for Simultaneous Isolation of Less Polar Ginsenosides, Including a Pair of New 20-Methoxyl Isomers, from Flower Buds of Panax ginseng

Molecules. 2017 Mar 10;22(3):442. doi: 10.3390/molecules22030442.

Abstract

The present study was designed to simultaneously isolate the less polar ginsenosides from the flower buds of Panax ginseng (FBPG). Five ginsenosides, including a pair of new 20-methoxyl isomers, were extracted from FBPG and purified through a five-step integrated strategy, by combining ultrasonic extraction, Diaion Hp-20 macroporous resin column enrichment, solid phase extraction (SPE), reversed-phase high-performance liquid chromatography (RP-HPLC) analysis and preparation, and nuclear magnetic resonance (NMR) analysis. The quantification of the five ginsenosides was also discussed by a developed method with validations within acceptable limits. Ginsenoside Rg5 showed content of about 1% in FBPG. The results indicated that FBPG might have many different ginsenosides with diverse chemical structures, and the less polar ginsenosides were also important to the quality control and standardization of FBPG.

Keywords: 20(R)-methoxyl-ginsenoside Rg3; 20(S)-methoxyl-ginsenoside Rg3; flower buds of Panax ginseng; isomer; quantification.

MeSH terms

  • Chromatography, High Pressure Liquid
  • Flowers / chemistry*
  • Ginsenosides / chemistry*
  • Ginsenosides / isolation & purification*
  • Isomerism
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Panax / chemistry*
  • Plant Extracts / chemistry
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Solid Phase Extraction

Substances

  • Ginsenosides
  • Plant Extracts