摘要
目的 建立酸枣仁颗粒中酸枣仁皂苷A与酸枣仁皂苷B的含量测定方法。方法反相高效液相色谱法,采用Hy.persilC18柱为分析柱,使用以乙腈和水为流动相的二元梯度洗脱方法,检测波长为201nm,流速为1ml·min^-1。结果酸枣仁皂苷A在50.01—198.2μg·ml^-1与峰面积呈良好的线性关系(r=0,9998,n=5),平均回收率为99.41%;酸枣仁皂苷B在66.25—209.0μg·ml^-1与峰面积呈良好的线性关系(r=0.9998,n=5),平均回收率为99.34%。结论该法简便、快速、重现性好,适用于酸枣仁颗粒中酸枣仁皂苷A与酸枣仁皂苷B的定量分析。
Objective To develop a method for the determination of Jujubaside A and Jujubaside B in Ziziphus jujuba Mill(ZJM) Granules. Methods An RP - HPLC method was set up with Hypersil 18 column. The mobile phase consisted of acetonitrile and water, and a gradient elution program was applied. The DAD detector was set at 201 nm. Results The calibration curve of Jujubaside A was linear in the range of 50.01 - 198.2μg · ml^ - 1, the average recovery was 99.41% ; the calibration curve of Jujubaside B was linear in the range of 66, 25 - 209, 0μg · ml^-1 ,the average recovery was 99.34%, Conclusion The method is appropriate for the determination of Jujubaside A and Jujubaside B.
出处
《时珍国医国药》
CAS
CSCD
北大核心
2008年第3期718-719,共2页
Lishizhen Medicine and Materia Medica Research