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作 者:石莉[1] 张晶[2] 李乐[1] 沙延淳[1] 邓波[1] 杨祝仁[1] 杨红玉[1]
机构地区:[1]辽宁省药物研究院,沈阳110015 [2]沈阳药科大学,沈阳110016
出 处:《实用药物与临床》2014年第10期1302-1305,共4页Practical Pharmacy and Clinical Remedies
摘 要:目的建立酮洛芬凝胶中药物含量测定的方法,并明确光照对含量测定的影响。方法采用Diamonsil ODS柱(4.6 mm×200 mm,5μm);流动相为0.01 mol/L磷酸二氢钾溶液(用磷酸调pH值至3.0)-乙腈(50∶50),流速1.0 mL/min,检测波长为255 nm,柱温为室温。结果在本试验条件下,酮洛芬凝胶中与辅料及有关物质分离度均符合要求,酮洛芬进样量在0.525-1.575μg范围内线性关系良好(r=0.999 9,n=5),平均回收率为98.41%,RSD为1.35%(n=3)。经光照,酮洛芬含量明显降低,杂质A明显增加,杂质A为酮洛芬的光照降解产物。结论本方法简单、快捷,可用于酮洛芬凝胶中药物含量的测定。Objective To establish a RP-HPLC method for the determination of ketoprofen in ketoprofen gel.Methods The separation was performed with a Diamonsil C18column(4. 6 mm × 200 mm,5 μm) at room temperature,with the mobile phase of 0. 01 mol /L potassium phosphate(adjust with phosphoric acid to pH value of 3. 0)-acetonitrile(50∶ 50). The flow rate was 1 mL /min. Ketoprofen was detected at 255 nm. Results There was a good linear relationship between A and concentration over the range of 0. 525 -1. 575 μg(r = 0. 999 9,n = 5). The average recovery was 98. 41%,RSD was 1. 35%. After light irradiation,the content of ketoprofen decreased obviously and the impurity A ketoprofen increased significantly. Conclusion This method is applicable for the determination of ketoprofen in ketoprofen gel.
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