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机构地区:[1]山东省中医药研究院,山东济南250014 [2]山东大学,山东济南250100
出 处:《中华中医药学刊》2008年第12期2555-2556,共2页Chinese Archives of Traditional Chinese Medicine
摘 要:目的:建立桂枝茯苓微丸的质量标准。方法:采用薄层色谱法对丹皮、赤芍、茯苓进行了定性鉴别,采用高效液相色谱法测定了微丸中芍药苷的含量,采用Lichrospher C18柱(5μm,200mm×4.6mm);检测波长230nm;流动相:乙腈-水-磷酸(15:85:0.1);流速:1.0mL/min;柱温:室温。结果:此法线性范围1.506-2.550μg,Y=64.3537924X+145.99898,r=0.9996;芍药苷的平均回收率为97.04%,RSD为2.03%。结论:该方法稳定、可靠,可作为该制剂的质量控制方法。Objective: To establilsh the quality standard for Guizhi fuling micropill.Methods:TLC was performed to identify Cortex moutan,Paeoniae radix and Poria.HPLC was used to determine Peoniflorin.Lichrospher C18 column(5μm,200mm×4.6mm) was used.The detecting wave length was at 230 nm.The mobile phase consisted of acetonitrile-water-phosphoric acid(15∶85∶0.1).The flow rate was 1.0 mL/min and column temperature was at room temperature.Results:A good linearity was shown in the concentration range of 1.506~2.550μg,Y=64.3537924X+145.99898,r=0.9996.The average recovery of Peoniflorin was 97.04%,RSD was 2.03%.Conclusion:The method is convenient,reliable and accurate for the quality control of Guizhi fuling micropill
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