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机构地区:[1]河北医科大学药学院,石家庄050017 [2]百药集团中诺药业(百家庄)有限公司产品开发部,石家庄050051
出 处:《药物分析杂志》2008年第6期870-872,共3页Chinese Journal of Pharmaceutical Analysis
基 金:河北省自然科学基金资助项目(C2004000562)
摘 要:目的:建立简便、快速分析唑来膦酸及与其有关物质的毛细管区带电泳方法。方法:采用非涂渍石英毛细管(50cm×50 μm)为分离通道,3 mmol·L^(-1)磷酸盐缓冲液(pH 7.9)为运行缓冲体系;工作电压25 kV;进样电压2 kV,进样时间5 s;紫外检测波长为210nm。结果:唑来膦酸在31.2~998μg·mL^(-1)的范围内线性关系良好(r=0.9997);注射用唑来膦酸的平均回收率(n=9)为100.2%,RSD 为1.1%;唑来膦酸注射剂的平均回收率(n=9)为100.7%,RSD 为1.0%;最低检测限为10.4μg·mL^(-1),该条件下唑来膦酸与其有关物质分离良好。结论:本方法简便、快速、灵敏,为唑来膦酸生产合成中的质量控制提供了一种新的可靠的分析手段。Objective:To estebalish a simple and rapid capillary zone electrophoresis method for the analysis of zoledronic acid and its related substance. Methods :An uncoated fused - silica capillary column of 50 cm×50 μm was used. The method was developed by utilizing a eleetrokinetic injection(2 kV,5 s) , a running voltage of 25 kV and a 3 mmol·L^-1 phosphate electrolyte solution at pH 7.9. The detection wavelength was 210 nm. Results:The calibration curve was linear in the range of 31.2 -998μg ·mL^-3(r =0. 9997) ,the average recovery of zoledronie acid for injection was 100.2% with RSD of 1.1% ;for zoledronic acid injection the average recovery was 100.7% with RSD of 1.0% ;the LOD was 10. 4μg·mL^-1 ,the active ingredient - zoledronic acid was successfully separated from its related substance. Conclusion: The method is simple, rapid and accurate ; it provides a new reliable means for the quality control of zoledronic acid.
分 类 号:R917[医药卫生—药物分析学]
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