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作 者:翟丽[1] 段漓童[1] 郭瑞华[1] 吴来娣[1]
出 处:《时珍国医国药》2008年第11期2708-2709,共2页Lishizhen Medicine and Materia Medica Research
基 金:河北省科研与发展第二批指导计划项目(No.05276460)
摘 要:目的建立以高效液相色谱(HPLC)法测定双黄连注射剂中组分含量的方法。方法以甲醇-水(10%的磷酸溶液调节pH至2.7)为流动相,流速为1.0ml/min,检测波长为326nm,在Diamonsil(钻石)C18(5μm,4.6mm×150mm)色谱柱上洗脱,外标法定量,黄芩苷含量可测定。结果黄芩苷在5.1~81.6μg/ml范围内呈良好的线性关系,r=0.9998,平均加样回收率为100.34%,RSD=0.82%(n=5)。结论该方法简便,灵敏,重复性好,结果准确,精密度较高,线性关系良好,回收率也较高,测定结果显示12h内黄芩苷稳定,适合于双黄连注射剂的质量控制。Objective To develop an HPLC method for the determination of the components in Shuanghuanglian. Methods The HPLC column was Diamonsil C18 (5 μm, 150 mm ×4.6 mm). A gradient methanolwater (pH2.7, adjusted by 10% phosphate solution) solvent was used as mobile phase, with a flow rate of 1.0ml/min, and the detection wavelength was 326 nm. Results - Baicalin had a good linear relationship within the range of 5.1 - 81.6μg/ml ,r = 0.9998, and the average recovery was 100.34 % , with the RSD = 0.82 % ( n = 5 ). Conclusion The method is simple, accurate, highly sensitive, and reproducible, with a high recovery and good linear within the measure limitation. Under the measure condition, baiealin is stable within 12 h, which makes it suitable for the quality control of Shuanghuanglian injection.
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