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头孢特仑新戊酯片溶出度测定方法研究

Study on the dissolution of Cefteram Pivoxil Tablets
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摘要 目的建立紫外-可见分光光度法测定头孢特仑新戊酯片的溶出度方法。方法本试验采用ZRS-6智能溶出试验仪,以0.1mol·L^-1的盐酸溶液900mL为溶出介质,选用紫外-可见分光光度法测定本品的溶出度。结果用此法测定本品的溶出度,头孢特仑在2.7-24.2μg·mL^-1浓度范围内,吸光度与浓度线性关系良好,线性方程为Y=0.0395X+0.0046,r=0.9999;溶液稳定;平均回收率为99.46%。结论该方法简便、快速、准确,能有效控制该制剂的质量。 OBJECTIVE To establish an ultraviolet spectrophotometry (UV) method for the determination of the dissolution of Cefteram Pivoxil tablets. METHODS Intellectual diffusion meter(ZRS-6)was used to determine the dissolution of Cefteram Pivoxil Tablets. 0. 1mol · L^-1 hydrochloric acid solution was used as dissolution medium and the sample was measured by UV speetrophotometry. RESULTS The calibration curve of Cefteram Pivoxil was linear( r =0. 9999) in the range of 2.7 24.2μg· mL^-1. The linear equation was Y = 0. 0395 X +0. 0046, the solution was stability. The recovery rate was 99. 46% CONCLUSION The method was simple.rapid and accurate for quality control of the preparation.
出处 《齐鲁药事》 2008年第3期154-156,共3页 qilu pharmaceutical affairs
关键词 头孢特仑新戊酯片 溶出度 紫外法 Cefteram Pivoxil Tablets dissolution rate UV spcctrophotometry
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