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机构地区:[1]辽宁省药物研究院,沈阳110015 [2]济宁医学院药学院,山东日照276826
出 处:《实用药物与临床》2013年第6期517-519,共3页Practical Pharmacy and Clinical Remedies
摘 要:目的建立内标法测定奥扎格雷钠颗粒含量。方法采用C18柱,以0.02 mol/L乙酸铵溶液-甲醇(75∶25)为流动相,流速:1.0 mL/min,柱温:25℃,检测波长:276 nm。结果浓度在0.028~0.066 mg/mL范围内具有良好的线性关系(r=0.999 9),平均回收率为99.37%,RSD为0.92%(n=9),精密度RSD为1.07%(n=6)。结论该方法简便、快速、专属性强,能满足制剂质量标准的要求。Objective To establish a method to determine ozagrel sodium granules by internal standard method.Methods The analysis w as conducted w ith C18 column,and the column temperature w as 25 ℃,the mobile phase consisted of 0.02 mol / L ammonium acetate solution-methanol(75∶ 25) w ith the flow rate of 1.0 mL / min,the detection w avelength w as at 276 nm.Results A good linear relationship existed in 0.028 ~ 0.066 mg / mL(r = 0.999 9),the average recovery rate w as 99.73%,RSD = 0.92%(n = 9),the RSD of precision w as 1.07%(n = 6).Conclusion The method is simple,rapid,highly specific and can meet the requirements of the standard of quality of the preparations.
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