HPLC-ELSD测定盾叶薯蓣中伪原薯蓣皂苷的含量  

HPLC-ELSD Determination of Pseudoprodioscin in Dioscorea zingiberensis

作　　者：白雁[1] 左春芳[1] 谢彩侠[1] 雷敬卫[1] 李磊[1] 

机构地区：[1]河南中医学院,郑州450008

出　　处：《中国实验方剂学杂志》2012年第16期84-86,共3页Chinese Journal of Experimental Traditional Medical Formulae

基　　金：河南省高等学校青年骨干教师计划(2010GGJS-134);河南省教育厅自然科学研究项目(2011A360021)

摘　　要：目的:建立盾叶薯蓣中伪原薯蓣皂苷的含量测定方法。方法:采用高效液相色谱-蒸发光散射检测法(HPLC-ELSD),Dikma C18色谱柱(4.6 mm×250 mm,5μm),流动相乙腈-水(30∶70),流速1.0 mL.min-1;蒸发光散射检测器参数:漂移管温度60℃,气压4.5 kPa。结果:伪原薯蓣皂苷在10～40μg(r=0.999 8)线性关系良好,平均回收率98.7%(RSD 1.6%,n=6)。结论:该方法简便、快速、灵敏、准确,可作为盾叶薯蓣的质量控制方法。Objective： To establish a method for the determination of pseudoprodioscin in Dioscorea zingiberensis. Method： HPLC-ELSD was used in the quantitative analysis with Dikma C1s chromatography column （4.6 mm ×250 mm, 5 μm） and acetonitrile-water （30：70） as a mobile phase. The flow rate of mobile was 1.0 mL ·min^-l ; the drifting tube temperature of the detecor was set at 60 ℃. The pressure of pure air was 4.5 kPa. Result： The linear range for pseudoprodioscin was 10-40 μg （ r = 0. 999 8 ）. The average recovery was 98.7% （RSD 1.6% , n =6）. Conclusion： This method is simple, rapid, sentive, accurate, and can be regarded as the quality control method of D. zingiberensis.

关 键 词：盾叶薯蓣 高效液相色谱-蒸发光散射检测法 伪原薯蓣皂苷 

分 类 号：R284.1[医药卫生—中药学]