摘要
目的:建立牛黄上清片中栀子苷的含量测定方法。方法:采用高效液相色谱法测定牛黄上清片中栀子苷的含量。色谱柱:Dikma Kromasil C18柱(250×4.6mm,5μm);流动相:乙腈-水(15:85);检测波长:238nm;柱温:25℃;流速:1.0ml/min;进样量:10.0μl。结果:栀子苷在0.4204~4.204μg范围内有良好的线性关系(r=0.9998),平均回收率为98.03%,相对标准差(RSD)为1.15%(n=6)。测得牛黄上清片中栀子苷的平均含量为2.3848mg/g。结论:该方法简便易行、快速准确,具有良好的重复性和回收率,可作为牛黄上清片中栀子苷的定量分析方法。
Objective :To establish a method for the content determination of geniposide in Niuhuang Shangqing Tablets.Methods: The content of geniposide was detected by HPLC.The separation was carried out on a Dikma Kromasil C18 column (5 μm,250×4.6 mm). The mobile phase was acetontrile-water(15:85);the flow rate was 1.0ml/min ;the detective wavelength was set at 238 nm;the column temperature was 25℃ and the sample size was 10.0 μl.Results:The calibration curve showed good linearity over the range of 0.4204-4.204 μg (r=0.9998).The average recovery rate was 98.03% with RSD 1.15%(n=6).The sample contained geniposide 2.3848 mg/g. Conclusion: This method was simple,rapid,accurate with good repeatability and recovery,it can be used as a quantitative analysis method for the content determination of geniposide in Niuhuang Shangqing Tablets.
出处
《现代医药卫生》
2009年第10期1444-1445,共2页
Journal of Modern Medicine & Health
关键词
高效液相
牛黄上清片
栀子苷
含量测定
HPLC
Niuhuang Shangqing Tablets
Geniposide
Content determination