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首页> 外文期刊>Pharmacognosy magazine >Simultaneous quantification of six main active constituents in Chinese Angelica by high-performance liquid chromatography with photodiode array detector
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Simultaneous quantification of six main active constituents in Chinese Angelica by high-performance liquid chromatography with photodiode array detector

机译:高效液相色谱-光电二极管阵列检测仪同时定量当归中的六种主要活性成分

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Background:Angelica sinensis is a famous traditional Chinese medicinalherb, which is predominantly used in the treatment of gynecological conditions. It is the first report for the simultaneous determination of six major active components in Chinese Angelica, which is important for quality control.Objective:A validated HPLC-PAD method was first developed to evaluate the quality of crude and processed Radix Angelica through simultaneous determination of six bioactive compounds, namely ferulic acid, senkyunolide I, senkyunolide H, coniferyl ferulate, Z/E-ligustilide and Z/E-butylidenephthalide.Materials and Methods:Samples were separated on a Xtimate?C18 column (250 × 4.6 mm, 5 μm) and detected by PAD. Mobile phase was composed of (A) aqueous phosphoric acid (0.02%, v/v) and (B) acetonitrile (MeCN) (including 10% tetrahydrofuran, v/v) using a gradient elution. Analytes were performed at 30°C with a flow rate of 1.0 mL/min.Results:All calibration curves showed good linear regression (r2 ≥ 0.9963) within the tested ranges, and the recovery of the method was in the range of 91.927–105.859%.Conclusion:The results demonstrate that the developed method is accurate and reproducible and could be readily utilized as a suitable quality control method for the quantification of Radix Angelica.
机译:背景:当归是一种著名的中草药,主要用于妇科疾病的治疗。这是同时测定中药材中六种主要有效成分的第一份报告,对质量控制具有重要意义。目的:首先建立一种经过验证的HPLC-PAD方法,通过同时测定当归中的粗制和加工后的当归质量来进行评估。六种生物活性化合物,分别是阿魏酸,千古内酯I,千古内酯H,针叶树阿魏酸酯,Z / E-ligustilide和Z / E-亚丁基萘。材料和方法:在Xtimate?C18柱上分离样品(250×4.6 mm,5μm ),并由PAD检测到。流动相由(A)磷酸水溶液(0.02%,v / v)和(B)乙腈(MeCN)(包括10%四氢呋喃,v / v)组成,采用梯度洗脱。在30°C下以1.0 mL / min的流速进行分析。结果:所有校准曲线在测试范围内均表现出良好的线性回归(r2≥0.9963),方法的回收率在91.927-105.859之间。结论:结果表明所建立的方法准确,可重复,可作为当归定量的合适质量控制方法。

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