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作 者:徐秋香[1] 郁红礼[1,2] 吴皓[1,3] 宫乐[1] 潘耀宗[1] 邱韵萦[1]
机构地区:[1]南京中医药大学药学院,南京210029 [2]江苏省中药炮制重点实验室,南京210019 [3]国家教育部中药炮制规范及标准工艺研究中心,南京210019
出 处:《中国实验方剂学杂志》2013年第3期62-65,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家中医药管理局中医药行业科研专项(201007010)
摘 要:目的:建立同时测定四君子汤中人参皂苷Rg1、人参皂苷Re、人参皂苷Rb1和甘草酸含量的方法。方法:采用HPLC测定,Thermo Hypersil BDS色谱柱(4.6 mm×250 mm,5μm),流动相为乙腈-0.03%甲酸梯度洗脱,流速0.9 mL.min-1,柱温30℃,检测波长202,250 nm。结果:人参皂苷Rg1在1.522~12.176μg线性关系良好,平均回收率为100.86%,RSD2.34%,人参皂苷Re在1.368~10.944μg线性关系良好,平均回收率为100.57%,RSD 2.95%;人参皂苷Rb1在3.198~15.990μg线性关系良好,平均回收率97.88%,RSD 2.86%;甘草酸在5.036~40.286μg线性关系良好,平均回收率99.25%,RSD 2.97%。结论:该方法简便、准确、实用性强,可用于四君子汤中4种指标性成分的含量测定。Objective: To establish the method for determining simultaneously four components in Sijunzi Tang, ginsenosid Rgl, ginsenosid Re, ginsenosid Rb1 and glycyrrhizic acid. Method: HPLC was carried out on the Hypersil BDS column (4.6 mm × 250 mm, 5μm) with acetonitrile-0.03% phosphoric acid, gradient elution, the volume of flow 0.9 mL -min-1 , column temperature 30℃ , detection wavelength 202 nm and 250 nm. Result : The correlation coefficients of the four components were higher than 0. 999 and the average recoveries were 100.86% , 100.57% , 97.88% , 99.25% , respectively; and RSD of the above four components were 2. 34% , 2.95%, 2.86%, 2.97%, respectively. Conclusion: The method is proved to be so easy and accurate and practical that it can be used to determine the four components in Sijunzi Tang.
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