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作 者:王羽凝[1] 穆丽华[2] 王石 魏沛沛 王茹[5] 刘屏[2]
机构地区:[1]解放军总医院外科临床部,北京100853 [2]解放军总医院临床药理研究室,北京100853 [3]解放军医学院,北京100853 [4]蚌埠医学院,安徽蚌埠233003 [5]解放军总医院门诊药房,北京100853
出 处:《中国药物应用与监测》2016年第2期77-79,84,共4页Chinese Journal of Drug Application and Monitoring
基 金:军队"十二五"中医药推广研发项目(10ZYZ141)
摘 要:目的:建立同时测定芍枣胶囊中3种主要成分的RP-HPLC方法。方法:采用RP-HPLC法,选用Kromasil C18色谱柱(4.6 mm×250 mm,5μm),流动相:乙腈(A)和水(B);洗脱梯度:0~10 min 10%~19%A,10~16 min 19%~20%A,16~22 min20%~90%A,22~25 min 90%A,25~25.1 min 90%~10%A,25.1~35 min 10%A;流速:0.8 m L·min-1。Alltech 2000ES ELSD检测器,漂移管温度:115℃,空气流速3.3 L·min-1。结果:结果表明芍药苷,斯皮诺素,3,6'-二芥子酰基蔗糖的检测分别在0.975~5.850μg,0.060~0.660μg,0.100~0.600μg范围内线性关系良好。上述3种成分的平均回收率(n=9)分别为99.5%(RSD 0.69%),100.2%(RSD 1.03%),99.9%(RSD 1.20%)。结论:该方法操作简单、结果准确,具有较好的重复性和稳定性,为芍枣胶囊的质量控制提供理论参考。Objective: To establish the quantitative method of three main constituents in Shaozao capsules by RPHPLCmethod. Methods: The separation was performed on Kromasil C18 column (4.6 mm × 250 mm, 5 μm) by RP-HPLCmethod. The mobile phase consisted of acetonitrile (A) and water (B), elution gradient was as follows: 0 –10 min 10% –19% A; 10 – 16 min 19% – 20% A; 16 – 22 min 20% – 90% A; 22 – 25 min 90% A; 25 – 25.1 min 90% – 10% A; 25.1 –35 min 10% A. The flow rate was 0.8 mL·min-1. The detector was Alltech 2000ES ELSD. The temperature of drift tube was115 ℃ and the air flow rate was 3.3 L·min-1. Results: The linear ranges of the three components were 0.975 – 5.850 μg(paeoniflorin), 0.060 – 0.660 μg (spinosin) and 0.100 – 0.600 μg (3,6'-disinapoyl sucrose) respectively. The average recoveriesof the above three components in Shaozao capsules were 99.5% (RSD 0.69%), 100.2% (RSD 1.03%), 99.9% (RSD 1.20%)respectively. Conclusion: The method was reliable, simple, and precise, which was suitable for quality control of Shaozao capsules.
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