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机构地区:[1]广州医学院羊城医院,广州510140 [2]广州中医药大学第一附属医院,广州510405
出 处:《中药新药与临床药理》2009年第2期158-160,共3页Traditional Chinese Drug Research and Clinical Pharmacology
摘 要:目的建立高效液相色谱法测定益视颗粒中大黄素的含量。方法采用高效液相色谱法,色谱柱为AlltechC18柱(250mm×4.6mm,5μm);流动相:甲醇-0.1%磷酸(80:20);流速:1mL·min-1;检测波长:254nm;柱温:30℃。结果大黄素分离良好,在32.8~131.2μg范围内与峰面积线性关系良好,r=0.9999,平均回收率为100.2%,RSD=1.52%(n=6)。结论该测定方法简便可行、重复性好,可用于该制剂中有效成分大黄素的含量测定。Objective To establish a method of HPLC assay for determining emodin in Yishi Granules. Methods The effeetive components in Yishi Granules were determined by HPLC. The chromatographic conditions were as follows: Alhech C18 eolumn (250 mm ×4.60 mm, 5 μm), mobile phase consisting of methanol -0. 1% phosphoric acid (80 : 20), flow rate at 1 mL · min- 1, detecting wavelength being 254 nm, and the column temperature being 30 ℃. Results The separation and the linearity were good in the range of 32.8 - 131.2 μg, r =0. 999 9. The average reeovery of emodin was 100.20 % , and RSD = 1.52 % ( n = 6). Conclusion The quantitative method for determining the active eomponents of Yishi Granules is simple, feasible and reprodueible, and is beneficial for the quality control of Yishi Granules.
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