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作 者:杨敏[1]
机构地区:[1]深圳市药品检验所,深圳518029
出 处:《中国药品标准》2002年第3期28-29,共2页Drug Standards of China
摘 要:目的:建立HPLC法测定盐酸西替利嗪片的含量。方法:色谱条件:C_(18)柱,甲醇-水-三乙胺-磷酸(700:300:5:6.5)(pH3.5)为流动相,咖啡因为内标物,检测波长为230nm。结果:平均回收率为99.85%,RSD=0.45%(n=6);线性范围:20.64~103.2μg/ml,r=0.9999。结论:该法准确,可靠,能满足质量控制的要求。Objective: To establish the method of the determination of cetirizine hydrochloride tablets. Method: The HPLC with C_(18)column,mobile phase of methanol-water-triethytamine-phospheric acid(700: 300:5:6.5)(pH3.5),detection wavelength of 230nm and caffeine as interal standard were used.Results: The average recovery rate of the method was 99.85%,RSD was 0.45%(n=6),The rang of linear corellation it was 20.64~103.2μg/ml,r=0.9999.Conolusion:The method was accurate and reliable,it can be used for the assay of cetirizine hydrochloride tablets.
关 键 词:HPLC 盐酸西替利嗪 含量测定 选择性组胺H1受体拮抗剂
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