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作 者:王姿婧[1] 刘青[1] 戴学文[1] 房志仲[1]
机构地区:[1]天津医科大学药学院药剂学教研室,天津市临床药物关键技术重点实验室,天津300070
出 处:《天津医科大学学报》2013年第6期502-506,共5页Journal of Tianjin Medical University
摘 要:目的:建立硝苯地平分散片中硝苯地平的质量控制方法,保证该制剂质量.方法:采用高效液相色谱法测定硝苯地平的含量,色谱柱为Kromasil-C1s柱(200 mm×4.6 mm,5 μm),甲醇-水(65:35)为流动相,检测波长为237 nm,流速为0.8 mL/min,进样量为20μL,柱温为室温.结果:硝苯地平的含量为标示量的100.09%;在5.0~35.0 μg/mL的浓度范围内与峰面积线性关系良好;平均回收率为100.07%.制剂有关物质检测合格.结论:高效液相色谱法专属性好,操作方便,结果准确,重现性好,能有效地控制硝苯地平分散片的质量.Objective:To establish a method for the quality control of the nifedipine in the nifedipine dispersible tablet and maintain the quality of the test tablets.Methods:The concentration of nifedipine were determined by HPLC; column was represented by Kromasil-C18 (200 mm×4.6 mm,5 μm) while mobile phase,methanol-water (65:35) ; the examine wavelength was 237 nm,velocity of flow 0.8 mL/ min; the injection volume was 20 μL at room temperature.Results:The content of nifedipine was 100.09% of labeled amount.At the concentration of nifedipine between 5.0~35.0 μg/mL,it indicated a fine linear relationship with peak aera,with the average recovery rate of 100.07%.The substances of the test tablets were qualified to standard.Conclusion:The method is efficient,simple,accurate and replicable.It can be used for quality control of the nifedipine dispersible tablet.
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