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HPLC法测定不同产地白花蛇舌草中2种蒽醌化合物的含量

Simultaneous HPLC determination of two anthraquinones in Hedyotis diffusa Willd.of different sources

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【作者】 李俊明于莉马临李燕郭兴杰

【Author】 LI Jun-ming~1 YU Li~1 Ma Lin~1 LI Yan~2 GUO Xing-jie~11.School of Pharmacy,Shenyang Pharmaceutical University,Shenyang 110016,China;2.National Institute of Genetics,Japan

【机构】 沈阳药科大学药学院日本国立遗传研究所

【摘要】 目的:建立同时测定白花蛇舌草中2-甲基-3-羟基-4-甲氧基蒽醌(Ⅰ)和2-甲基-3-羟基蒽醌(Ⅱ)含量的高效液相色谱方法。方法:采用 Diamonsil C18色谱柱(200 mm×4.6 mm,5μm),以甲醇-水(62:38,v/v)为流动相,流速1.0 mL·min-1,检测波长267 nm,柱温为室温。结果:Ⅰ和Ⅱ浓度分别在0.1~5.0μg·mL-1(r=0.9999)和0.2~10.0μg·mL-1(r=0.9999)范围内线性关系良好;加样回收率(n=6)分别为99.2%(RSD=1.9%)和99.8%(RSD=2.3%)。结论:本法准确可靠,重复性好,适用于白花蛇舌草中Ⅰ和Ⅱ的含量分析。

【Abstract】 Objective:To develop an HPLC method for quantitative determination of 2-methyl-3-hydroxy-4 -methoxyanthraquinone(Ⅰ)and 2-methyl-3-hydroxyanthraquinone(Ⅱ)in Hedyotis diffusa Willd.Methods: A Diamonsil C18 column(200 mm×4.6 mm,5 μm)was used with a mobile phase of methanol-water(62:38,v/ v)at the flow rate of 1.0 mL·min-1;The detection wavelength was set at 267 nm and the column temperature was room temperature.Results:The calibration curves were linear in the ranges of 0.1-5.0 μg·mL-1(r=0.9999) for Ⅰ and 0.2-10.0 μg·mL-1(r=0.9999)for Ⅱ.The average recoveries(n=6)of Ⅰ and Ⅱ were 99.2% and 99.8%,respectively.Conclusion:The method is accurate,reproducible for determination of Ⅰ and Ⅱ in Hedyotis diffusa Willd.

【基金】 2005年第二批教育部“春晖计划”科研合作项目(Z2005-2-11016)
  • 【文献出处】 药物分析杂志 ,Chinese Journal of Pharmaceutical Analysis , 编辑部邮箱 ,2008年09期
  • 【分类号】R284
  • 【被引频次】9
  • 【下载频次】245
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