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普卢利沙星片含量和有关物质检测方法的研究

Study on Determination and Related Substances of Prulifloxacin Tablets
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摘要 目的:完善普卢利沙星片含量及有关物质的检测方法。方法:采用C18色谱柱,以0.1%磷酸溶液(三乙胺调节pH值至4.0)为流动相A,乙腈为流动相B,含量测定采用等度洗脱流动相A-流动相B(55∶45),有关物质采用梯度洗脱,检测波长为278nm。结果:主峰和杂质峰能得到良好的分离,普卢利沙星在12.9~413.8μg·mL^-1浓度范围内,杂质NM394在1.23~39.36μg·mL^-1浓度范围内呈良好线性关系;含量测定平均回收率为101.3%,RSD为1.46%(n=9)。结论:该法专属性强,灵敏、准确,可作为普卢利沙星片的质量控制方法。 Objective:To perfect the HPLC method for determination and related substances of prulifloxacin tablets.Methods: The separation was performed on a C18 column with a mixture of 0.1%phosphoric acid solution ( three triethylamine adjusted to pH4) as mobile phase A, acetonitrile as mobile phase B, isocratic elution A:B (55∶45) for determination and gradient elution for related sub-stances.The UV detection wavelength was 278 nm.Results:Prulifloxacin was well separated from other impurities.The calibration curve of prulifloxacin was linear in the range of 12.9-413.8 μg· mL^-1.The calibration curve of impurity NM 394 was linear in the range of 1.23-39.36 μg · mL^-1.The average recoveries ( n=9 ) was 101.3% ( RSD =1.46%).Conclusion: The method is proved to be specific , sensitive and accurate and could be used to control the quality of prulifloxacin tablets .
出处 《中国药品标准》 CAS 2014年第2期94-98,共5页 Drug Standards of China
关键词 普卢利沙星片 有关物质 含量测定 高效液相色谱法 prulifloxacin tablets related substances determination HPLC
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