2014•ZhongcaoyaoRequires access

Simultaneous determination of sixteen ginsenosides in Panax ginseng and its preparation by HPLC

Guo Chon

Open publisher page 6 citations

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.

About this research paper

What this paper is about

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.

Why it matters

OpenAlex reports 6 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available 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.

Key concepts: Ginseng, Chromatography, Protopanaxadiol, Chemistry, Ginsenoside, High-performance liquid chromatography, Araliaceae, Chromatographic separation

Related papers

Back to paper searchBrowse research topicsOriginal source
Simultaneous determination of sixteen ginsenosides in Panax ginseng and its preparation by HPLC — Research Paper | ScholarLens