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机构地区:[1]吉林省食品药品检验所,长春130033 [2]长春卫尔赛生物药业有限公司,长春130033 [3]吉林敖东药业集团延吉股份有限公司,延吉133000 [4]长春经开药业有限公司,长春130033
出 处:《中国药品标准》2014年第3期202-205,共4页Drug Standards of China
摘 要:目的:采用HPLC法测定活力源口服液中人参茎叶总皂苷的含量。方法:色谱柱为C18(4.6 mm ×250 mm,5μm);流动相为乙腈-0.05%磷酸(20∶80);检测波长为203 nm。结果:人参皂苷Rg1在0.1813~1.816μg范围内与峰面积线性关系良好( r=0.9999),平均回收率为96.2%, RSD为1.9%;人参皂苷Re在0.496~4.96μg范围内与峰面积线性关系良好( r=0.9999),平均回收率为95.6%,RSD为1.5%。结论:该方法重复性好、操作简便,可用于活力源口服液中人参茎叶总皂苷的质量控制。Objective:To establish an HPLC method for determination of ginsenoside of stems and leaves in Huoliyuan Koufuye.Methods:The analysis was performed on a C18 (4.6 mm ×250 mm,5 μm) column, the mobile phase was acetonitrile-0.05% phosphonic acid solution(20∶80) and the detection wavelength was at 203 nm.Results:The calibration curve of ginsenoside Rg1 was linear in the range of 0.1813-1.816 μg( r=0.9999 ) , the average recovery was 96.2%and RSD was 1.9%.The linear range of ginsenoside Re was 0.496-4.96 μg ( r=0.9999 ) , the average recovery was 95.6%and RSD was 1.5%.Conclusion:The method is reproducible ,simple and can be used to control the quality of ginsenoside of stems and leaves in Huoliyuan Koufuye .
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