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机构地区:[1]安徽省铜陵市人民医院,铜陵244000 [2]安徽省合肥信风科技开发有限公司,合肥230022
出 处:《江苏药学与临床研究》2006年第4期236-238,共3页Jiangsu Pharmacertical and Clinical Research
摘 要:目的建立依达拉丰氯化钠注射液含量测定的HPLC方法。方法采用Hypersil C18柱(250mm×4.6mm,5μm),以甲醇-乙腈-0.1mol·L^-1 醋酸钠(40:15:55,冰醋酸调pH=4.5)为流动相,流量:1.0ml·min^-1,检测波长:245nm,进样体积:10出。结果线性范围为8.9—53.4μg·ml^-1(r=0.9998,n=6);高、中、低3种不同浓度的平均回收率为99.50%(RSD%:0.35%);精密度为0.220%(n=5)。结论本法快速、准确、专属性高,适于依达拉丰氯化钠注射液的含量测定。AIM To develop a HPLC method for the determination of edaravone sodium chloride Injection. METHOD The determination was performed on a Hypersil C18 column(250 mm × 4.6 mm,5μm)with the mobile phase consisting of methanol-acetonitrile-0.1 mol·L^-1 sodium acetate buffer(40:15:55,regulate pH to4.5 with acetic acid) and detected at 245 nm. The flow rate was 1.0 ml·min^-1 The injection volume was 10/11. RESULTS The method offered good linearity from 8.9 to 53.4μg·ml^-1( r = 0.9998, n =6). The average recovery was 99.50% ( RSD % = 0.35 % ) for three different levels of the added amount of edaravone. The precision of the method was 0.22% ( n = 5). CONCLUSION The developed HPLE method was,accurate and specific,and could be used for the detennination of edaravone in injection.
关 键 词:依达拉丰氯化钠注射液 HPLC法 含量测定
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