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首页> 外文期刊>Molecules >Identification and Determination of Flavonoids in Astragali Radix by High Performance Liquid Chromatography Coupled with DAD and ESI-MS Detection
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Identification and Determination of Flavonoids in Astragali Radix by High Performance Liquid Chromatography Coupled with DAD and ESI-MS Detection

机译:高效液相色谱-DAD-ESI-MS联用法鉴定黄芪中的黄酮类成分

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A method for the analysis of flavonoids in Astragali Radix by high-performance liquid chromatography (HPLC) combined with photodiode-array detection (DAD) and an electrospray ionization (ESI) - mass spectrometry (MS) was developed. After the samples were extracted with ethanol, the optimum separation conditions for these analytes were achieved using a gradient elution system and a 2.0 × 150 mm Shimadzu VP-ODS column. Eight flavonoids were identified to exist in Astragali Radix based on their characteristic UV data and mass spectra. The concentrations of three major components in this herb-ononin, calycosin and formononetin-were determined by LC/ESI-MS in positive selective ion monitoring (SIM) mode. The calibration curves were linear in the range of 0.9~180.0 μg·mL~(-1) for ononin, 1.8~360.0 μg·mL~(-1) for calycosin and 1.4~280 μg·mL~(-1) for formononetin, respectively. The limits of quantification (LOQ) and detection (LOD) were 0.9 μg· mL~(-1) and 0.2 μg mL~(-1) for ononin, 1.8 μg mL~(-1) and 0.5 μg·m~(-1) for calycosin, 1.4 μg mL~(-1) and 0.5 μg·mL~(-1) for formononetin, respectively. The standard recoveries were between 95.4~104.7%. The developed method was proven to be useful for the quantitative and qualitative analysis of flavonoid constituents in various resources of Astragali Radix.
机译:建立了高效液相色谱(HPLC)结合光电二极管阵列检测(DAD)和电喷雾电离(ESI)-质谱(MS)分析黄芪中黄酮类化合物的方法。用乙醇萃取样品后,使用梯度洗脱系统和2.0×150 mm Shimadzu VP-ODS色谱柱可实现这些分析物的最佳分离条件。根据黄芪中特征性的紫外线数据和质谱,鉴定出八种黄酮存在于黄芪中。 LC / ESI-MS在正选择性离子监测(SIM)模式下测定了该药草紫红素,花胶苷和formononetin中三种主要成分的浓度。洋葱蛋白的校正曲线在0.9〜180.0μg·mL〜(-1),钙黄绿素为1.8〜360.0μg·mL〜(-1),莫诺涅汀为1.4〜280μg·mL〜(-1)范围内呈线性关系。 , 分别。 ononin的定量限(LOQ)和检测限(LOD)为0.9μg·mL〜(-1),0.2μgmL〜(-1),1.8μgmL〜(-1)和0.5μg·m〜(- 1)钙黄绿素分别为1.4μgmL〜(-1)和0.5μg·mL〜(-1)。标准回收率在95.4%至104.7%之间。实践证明,所开发的方法可用于黄芪中多种资源中黄酮类成分的定量和定性分析。

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