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机构地区:[1]泸州医学院药学院药物研究所,泸州646000
出 处:《药物分析杂志》2008年第8期1316-1318,共3页Chinese Journal of Pharmaceutical Analysis
摘 要:目的:建立固相萃取-高效液相色谱法测定断血流胶囊中醉鱼草皂苷Ⅳb的含量。方法:色谱柱:Dikma Kromasil C_(18)柱(5 μm,250 mm×4.6 mm);流动相:甲醇-水(80:20);流速:0.8 mL·min^(-1);检测波长:250 nm;柱温:40℃。结果:醉鱼草皂苷Ⅳb在0.15~1.2μg范围内具有良好的线性关系(r=0.9999),总平均加样回收率为98.8%(n=9)。结论:该方法简便、快速、有效、灵敏、准确,具有良好的重复性和回收率,可作为该制剂的定量分析方法。Objective:To establish a method for the content determination of buddlejasaponins Ⅳ b in Duanxueliu capsules by SPE -HPLC. Methods:The separation was carried out on a Dikma Kromasil C18 column (5 μm,250 mm × 4. 6 mm). The mobile phase was methanol - water( 80: 20). The flow rate was 0. 8 mL ·min^ -1. The detective wavelength was set at 250 nm. The column temperature was 40 ℃. Results : The calibration curve showed good linearity over the range of 0. 15 - 1.2 μg( r = 0. 9999). The average recovery was 98.8% ( n = 9 ). Conclusion: This method is simple, rapid, efficient, sensitive, accurate and reproducible, it can be used as a quantitative analysis method for this preparation.
关 键 词:SPE HPLC 断血流胶囊 醉鱼草皂苷Ⅳb 含量测定
分 类 号:R917[医药卫生—药物分析学]
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