摘要
本文报道了HPLC内标法加校正因子测定法测定益泼丰原料药中益泼丰的含量。选ODS色谱柱,以醋酸曲安缩松为内标物,甲醇:水(72:28)为流动相。益泼丰对照品与内标物的量之比对其色谱峰面积比作图,线性关系良好,相关系数r=0.9998,平均回收率为99.8%。相对标准差RSD为0.4%(n=15).平均校正因子f=0.2764,RSD=06%(n=5).方法简便,快速,准确。
This report describes an HPLC method of internal standardization with correction factor for determining quantitatively the contents of Iprifiavone in its raw material.An ODS column and a mobile phase of methanol and water(72:28) were used and Triamcinoloni acetas was selected as the internal standard.The linear relationship between the quantitative ratio of the standard of Iprifiavone to the internal standard and the ratio of their peek area is quite good. The correlation coefficient is 0.9998,the average recovery is 99.8%,and RSD is 0.4%(n=15).This method is rapid and easy,the accuracy is quite good.It is a practical method for the assay of Iprifiavone raw material.
出处
《沈阳药科大学学报》
CAS
CSCD
1996年第2期117-120,共4页
Journal of Shenyang Pharmaceutical University
关键词
益泼丰
醋酸曲安缩松
高效液相色谱
Ipriflavone
Triamcinoloni acetas,HPLC,Interal standerdization