摘要
目的建立人参固本口服液中人参皂苷Rg1和Re含量测定的方法。方法色谱柱为C18柱;流动相为乙腈-水(22:78,调甲酸pH至2.4);流速1.0 ml.min-1;ELSD参数:漂移管温度110℃,空气流速3.0 L.min-1。结果人参皂苷Rg1在0.4~2.4μg范围内呈良好的线性关系(r=0.997 0),平均回收率为98.9%,RSD=0.32%;Re在0.2~1.2μg的浓度范围内呈良好的线性关系(r=0.998 6),平均回收率为97.7%,RSD=0.25%。结论用此法分析结果准确可靠,适用于此制剂的质量控制。
Objective To establish the method for determination of ginsenoside Rg1 and Re in renshenguben oral liquid. Method The C18 column was used .The mobile phase consisted of acetonitrile-water (22:78,adjusted to pH=2.4 with formic acid), at a flow rate of 1.0 ml·min^-1 and the ELSD was used. Results The calibration curves were liner for ginsenoside Rg1 within 0.4 - 2.4 μg (r=0.99 0) and for ginsenoside Re within 0.2 - 1.2 μg (r=0.9986):The average recoveries were 98.9%(RSD=0.32%) for ginsenoside Rg1 and 97.7%(RSD=0.25%) for ginsenoside Re, respectively. Conclusion The method is suitable for oral liquid. the determination of ginsenoside Rg1 and Re in renshenguben oral liquid.
出处
《食品与药品》
CAS
2005年第10A期50-52,共3页
Food and Drug
关键词
人参固本口服液
人参皂苷
高效液相色谱-蒸发光散射检测法
Renshenguben oral liquid
ginsenoside
high performance liquid chromatography-evaporative light scattering detector