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作 者:计耀成[1] 王玲[1] 曲京红[2] 李志浩[2]
机构地区:[1]湖北丹江口市第一医院药学部,丹江口442700 [2]湖北郧阳医学院附属东风医院药剂部,十堰442008
出 处:《中国医药导刊》2010年第10期1818-1819,1766,共3页Chinese Journal of Medicinal Guide
摘 要:目的:建立同时测定当归养血丸中芍药苷、白术内酯Ⅰ和白术内酯Ⅲ含量的方法。方法:采用HPLC法,ZORBAX-C18柱(4.6mm×250mm,5μm),流动相为乙腈(A)∶0.2%磷酸溶液(B),进行梯度洗脱(0-40min,A18%-62%,B82%-38%),流速为0.8ml·min^(-1),柱温:30℃,检测波长为222nm。结果:芍药苷、白术内酯Ⅰ和白术内酯Ⅲ分别在(0.014~0.276)mg·ml^(-1)(r=0.9996),(0.6~12.0)μg·ml^(-1)(r=0.9995)和(1.3~26.0)μg·ml^(-1)(r=0.9998)浓度范围内均有良好的线性关系,平均加样回收率分别为99.0%,98.0%,97.9%;RSD均小于2.0%。结论:本方法简便,准确,重复性好,可用于该制剂的质量控制。Objective:To establish a method for the determination of buddleoside, atractylenolide Ⅰ and atractylenolide III in Danggui Yangxue Wan.Methods:The HPLC system consisting the ZORBAX-C18(4.6mm×250mm,5μm)column,the mobile phase consisted of Acetonitrile(A)-0.2%H3PO4(B)with the gradient elution(0-40min,A18%-62%,B82%-38%),the flow rate was 0.8ml.min^-1,the column temperature was 30℃,The UV detector was set at 222nm.Results:The linear response range was (0.014-0.276)ml.min^-1(r=0.9996),(0.6-12:0)μg.ml^-1(r=0.9995)and (1.3-26.0)μg·ml^-1(r=0.9998),respectively.The average recovery of buddleoside, atractylenolide Ⅰ and atractylenolide Ⅲ were 99.0%,98.0%,97.9%,respectively.Conclusion:The assay demonstrated that the method is simple, accurate and repeatable, it can be applied in quality control of Danggui Yangxue Wan.
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