2005Yaowu fenxi zazhiRequires access

Simultaneous Determination of Notoginsenoside R_1 and Ginsenoside Rg_1 Contents in Shuxiong Tablets by HPLC

BI Kai-shun

Open publisher page 0 citations

Abstract

Objective:An RP-HPLC method was developed to determine the contents of notoginsenoside R_1 and ginsenoside Rg_1 simultaneously in Shuxiong tablets.Methods:Kromasil ODS(250 mm×4.6 mm,5 μm)was used,the mobile phase was acetonitrile-water-phospharic acid(21.5:78.5:0.02)at a flow rate of 1.0 mL· min~(-1) The UV detection wavelength was 203nm,and the column temperature was room temperature.Results:The linear range was 2.5-49.6 μg·mL~(-1)(r=0.9997,n=7)for notoginsenoside R_1 and 23.6-472.0 μg·mL~(-1)(r =0.9999,n=7)for ginsenoside Rg_1.The average recoveries of notoginsenoside R_1 and ginsenoside Rg_1 were 98.9% (n=9) and 99.1%(n=9)respectively.Conclusion:The method was found to be simple and accurate for simultaneous analysis of notoginsenoside R_1 and ginsenoside Rg_1 in Shuxiong tablets,and provided a reliable way for evaluating the quality of it.

About this research paper

What this paper is about

Objective:An RP-HPLC method was developed to determine the contents of notoginsenoside R_1 and ginsenoside Rg_1 simultaneously in Shuxiong tablets.Methods:Kromasil ODS(250 mm×4.6 mm,5 μm)was used,the mobile phase was acetonitrile-water-phospharic acid(21.5:78.5:0.02)at a flow rate of 1.0 mL· min~(-1) The UV detection wavelength was 203nm,and the column temperature was room temperature.Results:The linear range was 2.5-49.6 μg·mL~(-1)(r=0.9997,n=7)for notoginsenoside R_1 and 23.6-472.0 μg·mL~(-1)(r =0.9999,n=7)for ginsenoside Rg_1.The average recoveries of notoginsenoside R_1 and ginsenoside Rg_1 were 98.9% (n=9) and 99.1%(n=9)respectively.Conclusion:The method was found to be simple and accurate for simultaneous analysis of notoginsenoside R_1 and ginsenoside Rg_1 in Shuxiong tablets,and provided a reliable way for evaluating the quality of it.

Why it matters

A significance statement is not available in the OpenAlex record.

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:An RP-HPLC method was developed to determine the contents of notoginsenoside R_1 and ginsenoside Rg_1 simultaneously in Shuxiong tablets.Methods:Kromasil ODS(250 mm×4.6 mm,5 μm)was used,the mobile phase was acetonitrile-water-phospharic acid(21.5:78.5:0.02)at a flow rate of 1.0 mL· min~(-1) The UV detection wavelength was 203nm,and the column temperature was room temperature.Results:The linear range was 2.5-49.6 μg·mL~(-1)(r=0.9997,n=7)for notoginsenoside R_1 and 23.6-472.0 μg·mL~(-1)(r =0.9999,n=7)for ginsenoside Rg_1.The average recoveries of notoginsenoside R_1 and ginsenoside Rg_1 were 98.9% (n=9) and 99.1%(n=9)respectively.Conclusion:The method was found to be simple and accurate for simultaneous analysis of notoginsenoside R_1 and ginsenoside Rg_1 in Shuxiong tablets,and provided a reliable way for evaluating the quality of it.

Key concepts: Chemistry, Chromatography, Ginsenoside, High-performance liquid chromatography, Ginsenoside Rg1, Linear range, Detection limit, Ginseng

Related papers

Back to paper searchBrowse research topicsOriginal source
Simultaneous Determination of Notoginsenoside R_1 and Ginsenoside Rg_1 Contents in Shuxiong Tablets by HPLC — Research Paper | ScholarLens