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机构地区:[1]辽宁省食品药品检验所,辽宁沈阳110023 [2]葫芦岛市药品检验所,辽宁葫芦岛125000
出 处:《沈阳药科大学学报》2008年第5期376-380,共5页Journal of Shenyang Pharmaceutical University
摘 要:目的 用高效液相色谱-蒸发光散射(HPLC-ELSD)法测定红药片中三七皂苷R1及人参皂苷Rg1、Re、Rb1的含量。方法 色谱柱填料为氨基键合硅胶(4.6mm×250mm,5μm),流动相为乙腈-水(体积比为80:20),漂移管温度为90℃,载气流速为2.IL·min^-1。结果 三七皂苷R.及人参皂苷Rg1、Re、Rb1质量分别在0.214~2.14μg、0.808~8.08μg、0.3084~3.04μg及0.996~9.96μg内的对数值与相应峰面积的对数值呈良好线性关系;制剂中4种成分的平均回收率(n=6)分别为96.7%(RSD=2.1%)、96.0%(RSD=1.2%)、96.8%(RSD=2.4%)和96.6%(RSD=2.5%)。结论 该方法准确、分离效果好、无干扰,可用于红药片的质量控制。Objective To establish the quantitative method of notoginsenoside R1, ginsenoside Rg1, Re and Rb1 in Hongyao tablets (traditional Chinese medicine)by HPLC-ELSD. Methods The column used was a Lichrospher NH2(4.6 mm ×250 mm) packed with a 5 μm stationary phase. The mobile phase consisted of acetonitrile-water( V: V = 80:20). The temperature of drift tube was 90 ℃ and the nebulizer nitrogen flow rate was 2.1 L·min^-1. Results The linear relationship were obtained within the range of 0.214 - 2.14 μg, 0. 808 - 8.08 μg, 0. 308 4 - 3.04 μg and 0. 996 - 9.96 μg for the four components respectively. The average recoveries of the four components( n = 6) were 96.7 % (RSD = 2.1% ), 96.0 % (RSD = 1.2 % ), 96.8 % (RSD = 2.4 % ) and 96.6 % ( RSD = 2.5 % ), respectively. Conclusions It is proved that the HPLC-ELSD method is reliable, well separated, and precise; it can be used in quantitative analysis of Hongyao tablets.
关 键 词:红药片 三七皂苷R1 人参皂苷RG1 人参皂苷Re人参皂苷Rb1 高效液相色谱-蒸发光散射检测法
分 类 号:R917[医药卫生—药物分析学]
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