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作 者:戴杰 高云睿 梁中卫 赵宏云[2] 吴忱凯 Dai Jie;Gao Yunrui;Liang Zhongwei;Zhao Hongyun;Wu Chenkai(Jiangsu Food&Pharmaceutical Science College School of Pharmaceutical Engineering,Huai’an 223003,China;Jiangsu Tasly Diyi Pharmaceutical Co.,Ltd.,Huai’an 223003,China)
机构地区:[1]江苏食品药品职业技术学院制药工程学院,江苏淮安223003 [2]江苏天士力帝益药业有限公司,江苏淮安223003
出 处:《山东化工》2021年第20期103-104,共2页Shandong Chemical Industry
摘 要:建立HPLC法同时定量测定氟比洛芬酯注射液中的氟比洛芬酯和氟比洛芬。采用Venusil XBP C18色谱柱(4.6 mm×250 mm,5μm),以V(乙腈)∶V(水)∶V(冰醋酸)=1200∶800∶3为流动相,流速1.0 mL·min^(-1),进样量10μL,柱温40℃,检测波长254 nm。在所选色谱条件下,主药与该有关物质能较好分离,氟比洛芬在0.51~20.22 g·mL^(-1)(r^(2)=0.9999)、氟比洛芬酯在10.36~207.16 g·mL^(-1)(r^(2)=1.0000)范围内线性良好;平均加样回收率(n=9)分别为98.8%和99.3%。该方法简便、快速、灵敏,分离度好,适用于氟比洛芬酯注射液的质量监控。To establish a quantitative HPLC analytical method for simultaneous determination of flurbiprofen axetil and flurbiprofen in the flurbiprofen axetil injection.The separation was performed on a Venusil XBP C_(18) column(4.6 mm×250 mm,5μm)using an isocratic elution mobile phase system composed of acetonitrile–water–acetic acid(1200∶800∶3)at a flow rate of 1.0 mL·min^(-1),injection volume 10μL,column temperature 40℃and detection wavelengtH_(2)54 nm,respectively.Drug and its related substances were completely separated under selected chromatographic conditions,good linear relationships were observed in the range of flurbiprofen(0.51~20.22 g·mL^(-1);r^(2)=0.9999)and flurbiprofen axetil(10.36~207.16 g·mL^(-1);r^(2)=1.0000).The average recoveries(n=9)of flurbiprofen and flurbiprofen axetil were 98.8%and 99.3%,respectively.This method is simple,rapid,accurate,sensitive and reliable for quality control of the flurbiprofen axetil injection.
关 键 词:氟比洛芬酯注射液 氟比洛芬 氟比洛芬酯 含量测定 高效液相色谱法
分 类 号:R917[医药卫生—药物分析学]
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