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HPLC法测定齐多夫定及其注射液的含量及有关物质
引用本文:华莲,郝桂明,唐素芳.HPLC法测定齐多夫定及其注射液的含量及有关物质[J].天津药学,2014(4):1-4.
作者姓名:华莲  郝桂明  唐素芳
作者单位:天津市药品检验所,天津300070
基金项目:2012年全球基金项目国家药品标准提高品种(No.GF2012-08/09)
摘    要:目的:建立HPLC梯度洗脱法测定齐多夫定及其注射液的含量及有关物质.方法:采用岛津Shim-packCLC-ODS色谱柱(150 mm ×6.0 mm,5μm),流动相A为甲醇,流动相B为水,按照时间程序进行梯度洗脱,流速为1.0ml/min,检测波长为215 nm,柱温为40℃.结果:杂质A和杂质C在0.2~50.0 μg/ml浓度范围内均与其峰面积呈良好的线性关系(r =0.999 9),杂质A平均回收率为99.3%,RSD为1.4%(n=9);杂质C平均回收率为98.2%,RSD为1.9%(n=9);杂质B在0.4 ~ 50.0 μg/ml浓度范围内与其峰面积呈良好的线性关系(r=0.999 9),平均回收率为95.8%,RSD为1.0%(n=9);杂质D在0.2 ~ 25.0μg/ml浓度范围内与其峰面积呈良好的线性关系(r=0.9998),平均回收率为106.8%,RSD为0.8%(n=9);齐多夫定在0.4~ 50.0 μg/ml浓度范围内与其峰面积呈良好的线性关系(r=0.999 9).结论:该方法在一个色谱系统中同时检出杂质A、B、C、D,重复性好,结果准确,可用于齐多夫定及其注射液的含量及有关物质测定.

关 键 词:齐多夫定  注射液  杂质  质量控制  标准提高  高效液相色谱法

HPLC determination of content and related substances in zidovudine and injection
Hua Lian,Hao Guiming,Tang Sufang.HPLC determination of content and related substances in zidovudine and injection[J].Tianjin Pharmacy,2014(4):1-4.
Authors:Hua Lian  Hao Guiming  Tang Sufang
Institution:(Tianjin Institute for Drug Control, Tianjin 300070)
Abstract:Objective: To establish a HPLC gradient elutioned method for evaluating the content and the related substances of zidovudine and injection. Methods : Used Shim - pack CLC - ODS column ( 150 mm × 4.6 mm, 5 μm) , and the mobile phaseA was methanol, mobile phaseB was water, gradient elutioned, the flow rate was 1.0 ml/min with column temperature at 40 ℃. The detection wavelength was 215 nm. Results :The assay displayed a good linearity of impurity A and C over the concentration range of 0.2 50.0 μg/ml( r = 0. 999 9 ) , the average recoveries were 99.3% ( RSD was 1.4% , n = 9 ) and 98.2% ( RSD was 1.9% , n = 9 ). A good linearity of impurity B over the concentration range of 0.4 - 50.0 μg/ml ( r = 0. 999 9 ) , the average recoveries were 95.8% ( RSD was 1.0%, n = 9 ). A good linearity of impurity D over the concentration range of 0. 2 - 25.0 μg/ml ( r = 0. 999 8) ,the average recoveries was 106.8% (RSD was 0.8% , n = 9 ). A good linearity of zidovudine over the concentration range of 0.4 -50.0 μg/ml( r = 0. 999 9). Conclusion: The method is simple, accurate and can be used to the determination of the content and impurity A、B、C and D in the same chromatographic system.
Keywords:zidovudine  injection  impurity  quality control  standard improvement  HPLC
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