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作 者:吴国清[1] 张家建[1] 孙萍萍[1] 吴燕燕[1] 张玲[2]
机构地区:[1]浙江省立同德医院,浙江杭州310012 [2]浙江中医药大学,浙江杭州310053
出 处:《中华中医药学刊》2014年第2期402-404,共3页Chinese Archives of Traditional Chinese Medicine
摘 要:目的:建立止痛化瘀搽剂中欧前胡素和细辛脂素的含量测定方法,为其质量标准制定奠定基础。方法:Kromasil C18柱(4.6mm×250mm,5μm),欧前胡素含量测定流动相为:甲醇-水(65:35),流速为1.0mL/min,检测波长为300nm;细辛脂素含量测定流动相为:乙腈-水,梯度洗脱,流速为1.0mL/min,检测波长为287nm.结果:欧前胡素在25.0—375ng范围内呈良好的线性(r=0.9997),加样回收率为98.96%(n=6),RSD为2.28%;细辛脂素在74.0—1110ng范围内呈良好的线性(r=0.9996),加样回收率为96.12%(n=6),RSD为2.20%。结论:该法操作简便,专属性强,重现性好,可为止痛化瘀搽剂质量标准的制定提供科学依据。Objective:To establish a determination method for imperatorin and asarinin in Eliminating Pain and Stasis Liniment, so as to lay a foundation for its quality standards. Methods : The column was Kromasil C18 (4. 6 mm × 250 mm, 5 μm). The mobile phase for determination of imperatorin was methanol - water (65 : 35 ), the flow rate was 1.0 mL/ min, and the detective wavelength was 300 nm. The mobile phase for determination of asarinin was acetonitrile -water, gradient elution, the flow rate was 1.0 mL/min, and the detective wavelength was 287 nm. Results : The linear range of imperatorin and asarinin were 25.0 - 375 ng and 74.0 - 1110 ng respectively. The average recoveries were 98.96% ( n = 6) and 96.12% (n =6),with RSI)=2.28% and RSD =2.20%. Conclusion:The method is simple operation,highly specific with good reproducibility. This method can provide scientific basis for the quality standards formulating of Eliminating Pain and Stasis Liniment.
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