Simultaneous determination of sixteen ginsenosides in Panax ginseng and its preparation by HPLC
Guo Chon
Abstract
Guo Chon
Abstract
Objective In order to evaluate the quality of Panax ginseng and its preparation, a simple and accurate HPLC method for determining the contents of 16 ginsenosides from P. ginseng was established. Methods The chromatographic separation was achieved on a C18 column(150 mm × 4.6 mm, 5 μm) using a mobile phase made up of acetonitrie and water at a flow rate of 1.0 mL/min. The detection wavelength and column temperature were set as 203 nm and 35 ℃, respectively. Results Sixteen ginsenosides(Rg1, Re, Rf, Rb1, Rg2, Rc, Rb2, Rb3, F1, Rd, F2, Rg3, protopanaxatriol, compound K, Rh2, and protopanaxadiol) were separated at baseline with good linearity(r ≥ 0.999 0). The recovery rates were 95%—102%(RSD 2%). Conclusion The method is simple, fast, accurate, and could be applied to the quality control of P. ginseng and its preparation.
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Objective In order to evaluate the quality of Panax ginseng and its preparation, a simple and accurate HPLC method for determining the contents of 16 ginsenosides from P. ginseng was established. Methods The chromatographic separation was achieved on a C18 column(150 mm × 4.6 mm, 5 μm) using a mobile phase made up of acetonitrie and water at a flow rate of 1.0 mL/min. The detection wavelength and column temperature were set as 203 nm and 35 ℃, respectively. Results Sixteen ginsenosides(Rg1, Re, Rf, Rb1, Rg2, Rc, Rb2, Rb3, F1, Rd, F2, Rg3, protopanaxatriol, compound K, Rh2, and protopanaxadiol) were separated at baseline with good linearity(r ≥ 0.999 0). The recovery rates were 95%—102%(RSD 2%). Conclusion The method is simple, fast, accurate, and could be applied to the quality control of P. ginseng and its preparation.
Key concepts: Ginseng, Chromatography, Protopanaxadiol, Chemistry, Ginsenoside, High-performance liquid chromatography, Araliaceae, Chromatographic separation