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New Method for Simultaneous Quantification of 12 Ginsenosides in Red Ginseng Powder and Extract: In-house Method Validation

  • In, Gyo (Analysis Research Team, R&D Headquarters, Korea Ginseng Corporation) ;
  • Ahn, Nam-Geun (Analysis Research Team, R&D Headquarters, Korea Ginseng Corporation) ;
  • Bae, Bong-Seok (Analysis Research Team, R&D Headquarters, Korea Ginseng Corporation) ;
  • Han, Sung-Tai (Analysis Research Team, R&D Headquarters, Korea Ginseng Corporation) ;
  • Noh, Kil-Bong (Analysis Research Team, R&D Headquarters, Korea Ginseng Corporation) ;
  • Kim, Cheon-Suk (Analysis Research Team, R&D Headquarters, Korea Ginseng Corporation)
  • Received : 2011.01.24
  • Accepted : 2012.02.27
  • Published : 2012.04.15

Abstract

For quality control of components in Korean red ginseng powder and extract, a new method for simultaneous quantification of 12 ginsenosides ($Rg_1$, Re, Rf, $Rh_1$, $Rg_2$[S], $Rg_2$[R], $Rb_1$, Rc, $Rb_2$, Rd, $Rg_3$[S], and $Rg_3$[R]) was studied. Compared to the official method for quantification of marker substances (ginsenosides $Rg_1$ and $Rb_1$), the proposed methods were guaranteed by in-house method validation. Several criteria such as linearity, specificity, precision and accuracy were evaluated. For red ginseng powder, recovery (averaging 95% to 105%) was calculated, and analysis of variance was carried out to estimate the relative standard deviation (0.20% to 2.12%). For red ginseng extract, the average recovery rate was 90% to 99% and the relative standard deviation was 0.39% to 2.40%. These results indicate that the proposed method could be used in the laboratory for determination of 12 ginsenosides in red ginseng powder and extract. In addition, this method was found to be suitable for quality control of ginseng products and potentially offer time and cost benefits.

Keywords

References

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