首页> 外文期刊>Bulletin of the Korean Chemical Society >Quantitative Evaluation of Radix Astragali through the Simultaneous Determination of Bioactive Isoflavonoids and Saponins by HPLC/UV and LC-ESI-MS/MS
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Quantitative Evaluation of Radix Astragali through the Simultaneous Determination of Bioactive Isoflavonoids and Saponins by HPLC/UV and LC-ESI-MS/MS

机译:通过HPLC / UV和LC-ESI-MS / MS同时测定生物活性异黄酮和皂苷的定量评价黄芪

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摘要

The three major active isoflavonoids (calycosin-7-O- -glucoside, isomucronulatol 7-O--glucoside, formononetin) and two main saponins (astragaloside I, astragaloside IV) in an extract of Radix Astragali were determined using rapid, sensitive, reliable HPLC/UV and LC-ESI-MS/MS methods. The separation conditions employed for HPLC/UV were optimized using a phenyl-hexyl column (4.6 】 150 mm, 5 レm) with the gradient elution of acetonitrile and water as the mobile phase at a flow rate of 1.0 mL/min and a detection wavelength of 230 nm. The specificity of the peaks was determined using a triple quadrupole tandem mass spectrometer equipped with an electrospray ionization (ESI) source that was operated in multiple reaction monitoring (MRM) in the positive mode. These methods were fully validated with respect to the linearity, accuracy, precision, recovery and robustness. The HPLC/UV method was applied successfully to the quantification of three major isoflavonoids in the extract of Radix Astragali. The results indicate that the established HPLC/UV and LC-ESI-MS/MS methods are suitable for the quantitative analysis and quality control of multi-components in Radix Astragali.
机译:三种主要的活性类黄酮(calycosin-7- O - mo -葡萄糖苷,异核糖醛7- O - mo 使用快速,灵敏,可靠的HPLC / UV和LC-ESI-MS / MS方法测定了黄芪提取物中的β-葡糖苷,formononetin)和两种主要皂苷(阿斯古拉糖苷I,黄芪甲苷IV)。 HPLC / UV的分离条件通过使用苯基己基色谱柱(4.6】150 mm,5μm)进行优化,以乙腈和水作为流动相的梯度洗脱以1.0 mL / min的流速进行检测波长为230 nm。使用配备有电喷雾电离(ESI)源的三重四极杆串联质谱仪确定峰的特异性,该质谱仪在正反应模式下的多反应监测(MRM)中运行。这些方法在线性,准确性,精密度,回收率和鲁棒性方面都得到了充分验证。 HPLC / UV方法已成功应用于黄芪提取物中三种主要异黄酮的定量分析。结果表明,建立的HPLC / UV和LC-ESI-MS / MS方法适用于黄芪中多组分的定量分析和质量控制。

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