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作 者:宗艳平 王晓 张彤[4] 卢静华[2] 山广志[1]
机构地区:[1]中国医学科学院医药生物技术研究所,北京100050 [2]辽宁医学院药学院,锦州121000 [3]烟台东诚药业集团股份有限公司,烟台264006 [4]北京市药品检验所,北京100035
出 处:《药物分析杂志》2015年第2期333-337,共5页Chinese Journal of Pharmaceutical Analysis
基 金:科技部新药创制重大专项平台(2012ZX09301002-001-019)
摘 要:目的:建立用于三磷酸胞苷二钠注射液含量测定及有关物质检测的离子色谱方法。方法:采用Ion PacAS11-HC(4mm×250 mm)色谱柱,以氢氧化钾为淋洗液,采用梯度洗脱,流速为1.0 mL·min^-1,进样量10μL,以带DIONEX AERS5004-mm抑制器的电导检测器进行检测,三磷酸胞苷二钠注射液的含量按峰面积以外标法计算,主要降解杂质(二磷酸胞苷二钠、单磷酸胞苷二钠)按加校正因子的主成分自身对照法计算。结果:三磷酸胞苷二钠在0.000 164~1.60 mg·mL^-1范围内线性关系良好(r=0.999 8,n=6);平均加样回收率(n=9)为100.1%;三磷酸胞苷二钠对照品溶液在24 h内的稳定性良好(RSD=1.3%);三磷酸胞苷二钠(CTP-Na2)及主要降解杂质二磷酸胞苷二钠(CDP-Na2)、单磷酸胞苷二钠(CMP-Na2)的方法定量限分别为1.6、4.57、6.0 ng,检出限分别为0.50、1.48、1.88 ng。结论:本方法适用于三磷酸胞苷二钠注射液的质量控制。Objective: To establish a new method for determination and assay of cytidine disodium triphosphate( CTP-Na2) injection and related substances by ion chromatography. Methods: The Ion Pac AS11-HC column( 4 mm × 250 mm) was adopted with KOH solution of gradient elution at the flow rate of 1. 0 mL·min^-1. The injection volume was 10 μL,and the substances were detected conductively with the DIONEX AERS 500 4-mm suppressor. The content computation was performed with the peak area external reference method. The main degradation impurities( cytidine disodium diphosphate( CDP-Na2) and cytidine disodium monophosphate( CMP-Na2)) were determined with the correction factor comparison method to calculate principal components. Results: The linear range of cytidine disodium triphosphate was 0. 000 164-1. 60 mg·mL^-1( r = 0. 999 8,n = 6). The average recovery( n = 9) was 100. 1%. The solution of CTP-Na2 reference substance was stable within 24 hours( RSD = 1. 3%),the limits of quantitation of CTP-Na2 and the main degradation impurities CDP-Na2,CMP-Na2 were 1. 6 ng,4. 57 ng,6. 0 ng; the limits of detection were 0. 50 ng,1. 48 ng,1. 88 ng. Conclusion: The developed method can be applied to quality control of cytidine disodium triphosphate.
关 键 词:三磷酸胞苷二钠(CTP-Na2) 二磷酸胞苷二钠(CDP-Na2) 单磷酸胞苷二钠(CMP-Na2) 含量测定 离子色谱法 电导检测器
分 类 号:R917[医药卫生—药物分析学]
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