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Determination of the active compounds of Panax notoginseng and Panax ginseng in Kangerxin capsules

Haiyan Luo

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Abstract

Objective:To develop a method for the determination of active compounds of Panax notoginseng and Panax ginseng in Kangerxin capsules.Methods: The diamonsil C18 column(250 mm×4.6 mm,5 μm)was used with acetonitrile as the mobile phase A and water as the mobile phase B.The linear grade is 0~9.5min,A27%;9.5~15 min,A 27%~45%;15~22 min,A45%;22~23min,A45%~27%;23~30 min,A 27%.The flow rate was 1.0 mL·min-1.The temperature of column is 35℃.Results: The linear ranges of ginsenoside Rg1,Rb1,notoginsenoside R1 in Kangerxin capsules were 0.0396~0.1584μg,0.04076~0.16304μg,0.0412~0.1648 μg respectively.The average recoveris were 100.20%、 100.13%、 99.68% respectively.RSD were 0.38%,0.39%、0.36%respectively.Conclusion: This method is convenient,reliable and stable for the determination of the quality control of Kangerxin capsules.

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What this paper is about

Objective:To develop a method for the determination of active compounds of Panax notoginseng and Panax ginseng in Kangerxin capsules.Methods: The diamonsil C18 column(250 mm×4.6 mm,5 μm)was used with acetonitrile as the mobile phase A and water as the mobile phase B.The linear grade is 0~9.5min,A27%;9.5~15 min,A 27%~45%;15~22 min,A45%;22~23min,A45%~27%;23~30 min,A 27%.The flow rate was 1.0 mL·min-1.The temperature of column is 35℃.Results: The linear ranges of ginsenoside Rg1,Rb1,notoginsenoside R1 in Kangerxin capsules were 0.0396~0.1584μg,0.04076~0.16304μg,0.0412~0.1648 μg respectively.The average recoveris were 100.20%、 100.13%、 99.68% respectively.RSD were 0.38%,0.39%、0.36%respectively.Conclusion: This method is convenient,reliable and stable for the determination of the quality control of Kangerxin capsules.

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Available abstract

Objective:To develop a method for the determination of active compounds of Panax notoginseng and Panax ginseng in Kangerxin capsules.Methods: The diamonsil C18 column(250 mm×4.6 mm,5 μm)was used with acetonitrile as the mobile phase A and water as the mobile phase B.The linear grade is 0~9.5min,A27%;9.5~15 min,A 27%~45%;15~22 min,A45%;22~23min,A45%~27%;23~30 min,A 27%.The flow rate was 1.0 mL·min-1.The temperature of column is 35℃.Results: The linear ranges of ginsenoside Rg1,Rb1,notoginsenoside R1 in Kangerxin capsules were 0.0396~0.1584μg,0.04076~0.16304μg,0.0412~0.1648 μg respectively.The average recoveris were 100.20%、 100.13%、 99.68% respectively.RSD were 0.38%,0.39%、0.36%respectively.Conclusion: This method is convenient,reliable and stable for the determination of the quality control of Kangerxin capsules.

Key concepts: Panax notoginseng, Ginseng, Ginsenoside Rg1, Chromatography, Ginsenoside, Chemistry, Araliaceae, High-performance liquid chromatography

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