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出 处:《中国药品标准》2011年第1期64-67,共4页Drug Standards of China
摘 要:目的:建立异福片溶出度测定方法。方法:采用转篮法,以盐酸溶液(9→1 000)为溶剂,转速为100 r.min-1,30 min时取样。以高效液相色谱法,C18柱(3.8 mm×300 mm,10μm)为固定相,以水-磷酸盐缓冲液-甲醇(850∶100∶50)为流动相,测定异烟肼的溶出度,检测波长为254 nm,流速为1.5 mL.min-1。结果:异烟肼在0.3245~1.333 5 mg.L-1的浓度范围内,线性关系良好。线性方程为:A=56 475C+149.7(r=1.000 0);测定异烟肼平均回收率为99.7%(RSD%=0.51%,n=12)。结论:增加异烟肼溶出度检查项极为必要。本方法操作简便,结果正确,为完善异福片的质量标准提供有效手段。Objective : To establish the method for determination of dissolution of Rifampin and Isoniazid Tablets. Method : The apparatus was used with hydrochloric acid (9→1000) as dissolution medium at a rotate speed of 100 r·min^-1. According to the HPLC method for determined the easd of isoniazid which was dissolved from its tablets in 30 minutes. The dissolution relation were taken and analyzed by HPLC method. A C ls (3.9 mm × 300 mm, 10 t^m) colum was used with a mobile phase consisted of a mixture of water, phosphate buffer solution and methanol (850: 100: 50). The wavelength used for detection was 254 nm. The flow rate was about 1.5 mL per minute. Results: The linear range of isoniazid 0. 324 5 - 1. 333 5 mg·L^-1 , A =56 475C + 149.7( r = 1. 000 0). The satisfactory recoveries were obtained: isoniazid was 99. 7% (RSD% =0. 51% ,n = 12). Conclusion: It is necessary to set up the method of dissolution of Rifampin and Isoniazid Tablets. The method is rapid, convenient, accurate and reliable. It can be used as a reliable method of quality control for Rifampin and Isoniazid Tablets.
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