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作 者:袁利杰[1] 陈杰[1] 杨本霞[1] 郑子栋[1]
出 处:《中国药品标准》2014年第2期99-103,共5页Drug Standards of China
摘 要:目的:建立测定长春西汀葡萄糖注射液中有关物质及含量方法。方法:采用RP-HPLC法,色谱柱C18(4.6 mm ×250 mm,5μm),以乙腈-0.2 mol· L^-1醋酸铵溶液(60∶40)为流动相,流量1.0 mL· min^-1,检测波长280 nm,柱温30℃,进样量20μL。结果:在选定的色谱条件下,主成分及其有关物质能完全分离,已知杂质与长春西汀的相对响应因子均在0.9~1.1之间;长春西汀在0.0107~0.0305 mg· mL^-1范围内浓度与峰面积的线性关系良好(r=0.9997),平均回收率为99.7%,RSD为0.6%(n=9),检测限为0.071μg· mL^-1。结论:该法专属性强,准确度高,可用于长春西汀葡萄糖注射液中有关物质及含量的测定。Objective:To develop a RP-HPLC method for the determination of related substances and content of vinpocetine and glucose injection.Methods:A C18 column (4.6 mm ×250 mm,5 μm) was used with a mobile phase of acetonitrile -0.2 mol· L^-1 ammonium acetate solution (60∶40).The flow rate was 1.0 mL· min^-1 , the detection wavelength was 280 nm, the column temperature was 30 ℃and the volume of injection was 20 μL.Results:Related substances were completely separated from the main constituent.Relative response factors were in the range of 0.9-1.1 between the known impurities and vinpocetine.A good linear relation of vinpocetine was observed within the range of 0.0107-0.0305 mg· mL^-1 ( r=0.9997 ).The average recovery was 99.7%with RSD of 0.6%( n=9).The detection limit of vinpocetine was 0.071 μg· mL^-1.Conclusion:The method of precision and specificity can satisfy the requirements.It can be used for the control of related substances and content of vinpocetine for Vinpocetine and Glucose Injection .
关 键 词:长春西汀葡萄糖注射液 反相高效液相色谱 有关物质 含量
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