HPLC法测定复方皂矾丸中西洋参的含量 |
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引用本文: | 文永盛,彭善贵,罗霄.HPLC法测定复方皂矾丸中西洋参的含量[J].中国药品标准,2011,12(2):94-98. |
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作者姓名: | 文永盛 彭善贵 罗霄 |
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作者单位: | 成都市食品药品检测中心,成都,610045 |
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摘 要: | 目的:建立复方皂矾丸中西洋含量测定测方法.方法:采用高效液相色谱法同时测定西洋参中人参皂苷Rg1、人参皂苷Re和人参皂苷Rb1的含量.结果:高效液相色谱人参皂苷Rg1的线性范围是0.63~5.06 μg(r=0.999 9),平均加样回收率101.12%(RSD=2.14%),人参皂苷Re的线性范围是1.05~8.4 μg(r=0.999 8),平均加样回收率100.71%(RSD=1.57%),人参皂苷Rb1的线性范围是2.468~19.744μg(r=0.999 7),平均加样回收率97.22%(RSD=1.92%).结论:该方法操作简便、结果准确、重现性好,可用于复方皂矾丸中西洋参的含量测定.
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关 键 词: | 复方皂矾丸 西洋参 人参皂苷Rg1 人参皂苷Re 人参皂苷Rb1 |
Determination of American Ginseng in Compound Zaofan Pills |
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Authors: | Wen Yong-sheng Peng Shan-gui Luo Xiao |
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Institution: | Wen Yong-sheng,Peng Shan-gui Luo Xiao(Chengdu Institute for Food and Drug Control,Chengdu 610045) |
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Abstract: | Objecitve: To establish a method to determine the content of American ginseng in Compound Zaofan Pills. Methods: HPLC was used to determine the content of ginsenoside Rg1 , Re and Rb1 of the American ginseng. Results : This method had good lin earity in the range of 0. 63 - 5.06 μg( r = 0. 999 9 ), and the average recovery was 101.12% with RSD of 2. 14% for ginsenoside Rg1. It had good linearity in the range of 1.05 N 8.4μg( r = 0. 999 8) , and the average recovery was 100. 71% with RSD of 1.57% for ginsenoside Re. It had good linearity in the range of 2.47 - 19. 74μg( r=0.9997), and the average recovery was 97.22% with RSD of 1.92% for ginsenoside Rbl. Conclusion: The method was shown to be convenient, accurate with good repeatability, so it was suitable to determine the content of American ginseng in Compound Zaofan Pills. |
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Keywords: | HPLC |
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