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HPLC法测定灯盏花素脂质体中灯盏乙素的含量

HPLC Method for Assay of Breviscapine Liposome

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【作者】 高展黄罗生赵浩如

【Author】 GAO-Zhan~1,HUANG Luo-sheng~1,ZHAO Hao-ru~1(TCM School of China Pharmaceutical University,Nanjing 210038,China)

【机构】 中国药科大学中药研究所中药制剂研究室中国药科大学中药研究所中药制剂研究室 南京210038南京210038

【摘要】 目的建立HPLC测定灯盏花素脂质体中药物含量的定量方法。方法色谱柱:D IKM A D iam onsil(TM)C185μm 4.6×250 mm,流动相:甲醇-四氢呋喃-0.1%磷酸(14∶14∶72),检测波长:335nm;柱温:40℃。结果在此色谱条件下灯盏乙素与辅料及溶剂峰均得到良好的分离,灯盏乙素在5~100μg.mL-1范围内线性良好(r=0.9999),平均加样回收率为102.1%,RSD为1.26%。结论该方法简便准确,专属性强,能满足该制剂质量标准的要求。

【Abstract】 OBJECTIVE To establish an RP-HPLC method to determine the drug substance content of Breviscapine Liposomes.METHODS Using methanol-tetrahydrofuran-0.1% phosphoric acid(14∶14∶72) as mobile phase,the separation was performed on a DIKMA Diamonsil(TM) C18(5μm 4.6×250nm) column with a flow rate of 1.0mL·min-1.The detective wavelength was 335nm and the column temperature was 40℃.RESULTS Peaks for scutellarin,excipients or solvents were separated well in the chromatographic file with the RP-HPLC method.Regression analysis of the data of scutellarin concentration against its peak area showed good straight line over the range:5~100 μg·mL-1(r=0.9999).And the average recovery was 102.1%.CONCLUSION The method was simple,specific and accurate,and can effectively control quality of Dangguisini granules.

  • 【文献出处】 海峡药学 ,Strait Pharmaceutical Journal , 编辑部邮箱 ,2006年01期
  • 【分类号】R286.0
  • 【被引频次】2
  • 【下载频次】299
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