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高效液相色谱法测定依达拉奉注射液的含量及其有关物质 被引量:2

Determination of the content and the related substances of edaravone by HPLC
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摘要 目的建立测定依达拉奉注射液含量及有关物质的高效液相色谱法。方法采用Shimadzu ODS-C18柱(4.6mm×150mm,5μm);流动相:甲醇-0.015mol·L^-1磷酸二氢钠-三乙胺(35∶65∶0.1)混合后,用磷酸调pH为6.0±0.5;检测波长239nm;流速为1.0mL·min^-1;柱温:35℃。结果在建立的色谱条件下,依达拉奉与样品中杂质分离完全;在0.14-1.11 mg·mL^-1范围内,峰面积与其浓度线性关系良好(r=0.9999);平均回收率为100.36%(RSD=0.41%,n=9);最低检出量为0.024ng。结论本法简便快速,准确可靠,可用于依达拉奉注射液的质量控制。 OBJECTIVE To establish an HPLC method for the determination of edaravone injection and its related substance.METHODS A Shimadzu ODS-C18 column(4.6mm×150mm,5μm) was adopted.The mobile phase were methanol-0.015mol·L^-1 sodium dihydrogen phosphate-triethylamine(35∶65∶0.1,adjusted to pH 6.0±0.5 with phosphoric acid) at a flow rate of 1.0mL·min^-1,detection was done at 239nm.RESULTS Under the described chromatographic condition,edaravone was completely separated from its impurities.Edaravone had a good linear relation in the range of 0.14~1.11 mg·mL^-1(r=0.9999).The average recovery was 100.36%(RSD=0.41%,n=9),and the lowest detectable amount was 0.024ng.CONCLUSION The method can be used for quality control of edaravone injection and its related substance,it is accurate,simple and convenient.
出处 《海峡药学》 2010年第5期77-78,共2页 Strait Pharmaceutical Journal
关键词 依达拉奉 HPLC 有关物质 含量测定 HPLC Edaravone Related substance Assay
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  • 1Watanabe K,Morinaka Y,Iseki K,et al.Structure-activity relationship of 3-methyl-1-pheny1-2-pyrazolin-5-one (edaravone)[J].Redox Rep.2003,8(3):151-5.

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