2014•China Modern MedicineRequires access

Determination of ginsenoside Rg_1 and notoginsenoside R_1 in Jiuweigantai capsule by UPLC

Wen Pin

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Abstract

Objective To establish an UPLC method for the content determination of ginsenoside Rg1 and notoginsenoside R1 in Jiuweigantai capsule. Methods ACQUITY BEH C18 analytical column(2.1 mm×50 mm,1.7 μm) was used with the mobile phase consisting of acetonitrile-water in gradient elution at a flow rate of 0.4 ml/min.The detection wavelength was 203 nm,column temperature was 35℃,and injection volume was 1 μl. Results Ginsenoside Rg1and notoginsenoside R1 in Jiuweigantai capsule had good linearity within the range of 0.1-1.5 mg/ml and 0.04-0.6 mg/ml respectively,and their recoveries were 99.4%,101.8%,with RSD of 0.5%,1.3% respectively. Conclusion The method is convenient,quick,correct for determination of ginsenoside Rg1 and notoginsenoside R1 in Jiuweigantai capsule,and can be used for the quality control for Jiuweigantai capsule.

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Objective To establish an UPLC method for the content determination of ginsenoside Rg1 and notoginsenoside R1 in Jiuweigantai capsule. Methods ACQUITY BEH C18 analytical column(2.1 mm×50 mm,1.7 μm) was used with the mobile phase consisting of acetonitrile-water in gradient elution at a flow rate of 0.4 ml/min.The detection wavelength was 203 nm,column temperature was 35℃,and injection volume was 1 μl. Results Ginsenoside Rg1and notoginsenoside R1 in Jiuweigantai capsule had good linearity within the range of 0.1-1.5 mg/ml and 0.04-0.6 mg/ml respectively,and their recoveries were 99.4%,101.8%,with RSD of 0.5%,1.3% respectively. Conclusion The method is convenient,quick,correct for determination of ginsenoside Rg1 and notoginsenoside R1 in Jiuweigantai capsule,and can be used for the quality control for Jiuweigantai capsule.

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Available abstract

Objective To establish an UPLC method for the content determination of ginsenoside Rg1 and notoginsenoside R1 in Jiuweigantai capsule. Methods ACQUITY BEH C18 analytical column(2.1 mm×50 mm,1.7 μm) was used with the mobile phase consisting of acetonitrile-water in gradient elution at a flow rate of 0.4 ml/min.The detection wavelength was 203 nm,column temperature was 35℃,and injection volume was 1 μl. Results Ginsenoside Rg1and notoginsenoside R1 in Jiuweigantai capsule had good linearity within the range of 0.1-1.5 mg/ml and 0.04-0.6 mg/ml respectively,and their recoveries were 99.4%,101.8%,with RSD of 0.5%,1.3% respectively. Conclusion The method is convenient,quick,correct for determination of ginsenoside Rg1 and notoginsenoside R1 in Jiuweigantai capsule,and can be used for the quality control for Jiuweigantai capsule.

Key concepts: Ginsenoside Rg1, Capsule, Medicine, Chromatography, High-performance liquid chromatography, Ginsenoside, Gradient elution, Chemistry

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