HPLC法测定姜状三七根茎中的人参皂苷Rg1、人参皂苷Rb1和三七皂苷R1

Determination of notoginsenoside R1、ginsenoside Rg1 andginsenoside Rb1 in Panax zingiberensis by HPLC

  • 摘要: 建立人参属植物姜状三七根茎中人参皂苷Rg1、人参皂苷Rb1和三七皂苷R1的含量测定方法.采用HPLC法,色谱柱为Phenomenex C18(250 mm× 4.6 mm,5 μm);流速为1.0 mL/min;检测波长203 mm;柱温30 ℃;流动相为乙腈-水(梯度洗脱).三七皂苷R1的线性范围为0.315~1.575 μg(r= 0.999 1),平均回收率为三七皂苷R1101.4%,RSD=1.79%;人参皂苷Rg1的线性范围为1.203~6.015 μg(r=0.999 8),平均回收率为人参皂苷Rg198.54%,RSD=1.90%;人参皂苷Rb1的线性范围为0.276~1.38 μg(r=0.999 6),平均回收率人参皂苷Rb1102.10%,RSD=1.53%.所建方法简便、准确、重复性好,可同时测定姜状三七根茎中人参皂苷Rg1、人参皂苷Rb1和三七皂苷R1的含量.

     

    Abstract: A method is established for the determination of notoginsenoside R1,ginsenoside Rg1 and ginsenoside Rb1 in Panax zingiberensis.A HPLC method was adopted.The analysis was carried out on all analytical column C18(50 mm×4.6 mm,luna 5 μm).The flow rate was 1.0 mL·min-1 and the detective wavelength was set at 203 mm with column temperature of 30 ℃.The mobile phase consisted of acetonitrile-water(gradient elution).The linear range was 0.315—1.575 μg(r=0.999 1)and the average recovery was 101.4%with the RSD of 1.79% for notoginsenoside R1.The linear range was 1.203—6.015 μg(r=0.999 8)and the average recovery was 98.54%with the RSD of 1.9% for ginsenoside Rg1.The linear range was 0.276—1.38 μg(r= 0.999 6)and the average recovery was 102.1%with the RSD of 1.53% for ginsenoside Rb1.The method is simple,reproducible and suitable for determination of notoginsenoside R1,ginsenoside Rg1 and ginsenoside Rb1 in Panax zingiberensis.

     

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