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HPLC测定贵州产知母药材中菝葜皂苷元的含量 被引量:3

Determination of Sarsasapogenin in Anemarrhenaasphodeloides Bge from Guizhou by high-performance liquid chromatography
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摘要 实验采用乙醇超声提取样品,HPLC梯度洗脱.菝葜皂苷的理论塔板数为5628,分离度为1.42,拖尾因子为1.01.回归方程为Y= 5×10^6X+610 06,r=0.999 0.在0.4~2.0mg/mL之间的线性关系良好.日内和日间精密度的RSD均小于2.0%,重复性试验的RSD为0.6% (n= 5),最低检测限为1.0μg/mL,加样回收率为96.5%、94.3%、97.2%,RSD(n=5)分别为2.7%、3.1%、2.6%. The medicinal plant was extracted with ethanol and the extraction was repeated for three times.The theoretical plate number of astragaloside Ⅳ was 5628,the resolution 1.42 and the tailing factor 1.01.The calibration curve was linear in the range of 0.4~2.0mg/mL,Y= 5×10^6X +61006,R = 0.9990.The intra-day and inter-day precisions(RSD) were all less than 2.0%,the RSD of recurrence was 0.6%(n=5).The limit of detection was 1.0 μg/ml,the recovery 96.5%,94.3%,97.2%,and RSD 2.7%,3.1%,2.6%(n=5) respectively for Sarsasapogenin.
出处 《贵州师范大学学报(自然科学版)》 CAS 2007年第3期98-101,共4页 Journal of Guizhou Normal University:Natural Sciences
关键词 HPLC-ELSD 菝葜皂苷 知母药材 high-performance liquid chromatography with evaporative light-scattering detection Sarsasapogenin Anemarrhenaasphodeloides Bge
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