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作 者:刘常青[1] 何百寅[1] 赖小平[1,2] 谢友良[1,2] 刘方艺[1]
机构地区:[1]广州中医药大学新药开发研究中心 [2]东莞广州中医药大学中医药数理工程研究院,广东东莞523808
出 处:《广东药学院学报》2010年第6期590-593,共4页Academic Journal of Guangdong College of Pharmacy
基 金:省部产学研结合示范基地项目(2008B090200004)
摘 要:目的建立经络贴巴布剂中三种皂苷成分的含量测定方法。方法采用高效液相色谱法,色谱柱为kromasil-C18(250 mm×4.6 mm,5μm)柱,乙腈-水(梯度洗脱)为流动相,检测波长203 nm,流速1 mL.min-1,柱温40℃。结果人参皂苷Rg1在0.82~8.2μg范围内与峰面积具有良好的线性关系(r=0.999 6),平均回收率为98.33%,RSD=2.723%(n=6);人参皂苷Rb1在0.3256~3.256μg范围内与峰面积具有良好的线性关系(r=0.999 9),平均回收率为99.30%,RSD=0.918%(n=6);三七皂苷R1在0.201~2.01μg范围内与峰面积具有良好的线性关系(r=0.999 8),平均回收率为97.90%,RSD=0.695%(n=6)。结论本方法准确、灵敏、重现性好,阴性无干扰,可用于经络贴中3种皂苷类成分的质量控制。Objective To establish a HPLC method for the determination of ginsenoside Rg1,ginsenoside Rb1 and notoginsenoside R1 in Jingluo cataplasm.Methods Kromasil-C18 column(250 mm×4.6 mm,5 μm) was used at 40 ℃,with the mobile phase consisted of acetonitrile-water(gradient elution) at a flow rate of 1 mL·min-1,and 203 nm as detected wavelength.Results The ginsenoside Rg1 showed good linearity in the range of 0.82-8.2 μg(r=0.999 6) and the average recovery was 98.33%(RSD=2.723%).The ginsenoside Rb1 showed good linearity in the range of 0.325 6-3.256 μg(r=0.999 9) and the average recovery was 99.30%(RSD=0.918%).The notoginsenoside R1 showed good linearity in the range of 0.201-2.01 μg(r=0.999 8) and the average recovery was 97.90%(RSD=0.695%).Conclusion The method is accurate,sensitive,reproducible and is suitable for the quality control of ginsenoside Rg1,ginsenoside Rb1 and notoginsenoside R1 in Jingluo cataplasm.
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