首页|UPLC法测定水红花子中花旗松素及槲皮素的含量

UPLC法测定水红花子中花旗松素及槲皮素的含量

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目的 应用超高效液相色谱法(UPLC)建立同时测定水红花子药材中花旗松素和槲皮素含量的方法.方法 采用Agilent ZORBAX SB-C18色谱柱,以乙腈-0.1%磷酸水为流动相梯度洗脱,柱温25 ℃,检测波长290 nm,流速0.2 mL·min-1,进样量1 μL.结果 建立的分析方法方法学考察良好.花旗松素、槲皮素进样浓度分别在 3.258~104.272 μg·mL-1、2.983~95.452 μg·mL-1内呈良好的线性关系(r2=0.999 9),平均加样回收率为 98.8%、98.8%,RSD值为1.9%、2.2%.结论 本方法简便、快速,可在同一波长下快速测定水红花子中花旗松素及槲皮素的含量,为水红花子药材质量控制提供参考依据.
Determination of Taxifolin and Quercetin in Polygoni Orientalis Fructus by UPLC
Objective To apply ultra performance liquid chromatography(UPLC)to establish a method for the simultaneous determination of taxifolin and quercetin in Polygoni Orientalis Fructus.Methods The separation was performed on an Agilent ZORBAX SB-C18 column with the gradient elution of acetonitrile-0.1%phosphoric acid in water as the mobile phase,the column temperature was 25 ℃,the detection wavelength was 290 nm,the flow rate was 0.2 mL·min-1,and the injection volume was 1 μL.Results The.established analytical method has been examined and found to be satisfactory.Taxifolin and quercetin exhibited a good linear relationship within the concentration range of 3.258 to 104.272 µg·mL-1 and 2.983 to 95.452 μg·mL-1,respectively,with a correlation coefficient(r2=0.9999).The average recovery rates of the spiked samples were 98.8%and 98.8%,with relative standard deviation(RSD)values of 1.9%and 2.2%,respectively.Conclusion The method is simple,rapid,and can determine the contents of taxifolin and quercetin at the same wavelength,which can provide a reference basis for the quality control of Polygoni Orientalis Fructus.

Polygoni Orientalis FructusUPLCtaxifolinquercetin

刘玉甜、黎冠兰、韩丽娟、钱正明、李宁

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康美华大基因技术有限公司,广东深圳 518128

康美药业股份有限公司,广东揭阳 515300

湘南学院医学影像检验与康复学院,湖南郴州 423000

云南中医药大学中药学院,云南昆明 650500

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水红花子 UPLC 花旗松素 槲皮素

广东省药品监督管理局科技创新项目

2021ZDB05

2024

云南中医学院学报
云南中医学院

云南中医学院学报

影响因子:0.933
ISSN:1000-2723
年,卷(期):2024.47(2)
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