首页> 外文期刊>Journal of separation science. >Simultaneous determination of iridoids, phenolic acids, flavonoids, and saponins in Flos Lonicerae and Flos Lonicerae Japonicae by HPLC-DAD-ELSD coupled with principal component analysis.
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Simultaneous determination of iridoids, phenolic acids, flavonoids, and saponins in Flos Lonicerae and Flos Lonicerae Japonicae by HPLC-DAD-ELSD coupled with principal component analysis.

机译:HPLC-DAD-ELSD结合主成分分析法同时测定金银花和金银花中的鸢尾酮,酚酸,类黄酮和皂苷。

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摘要

A method, HPLC coupled with diode-array and evaporative light scattering detectors (HPLC-DAD-ELSD), was newly developed to evaluate the quality of Flos Lonicerae (FL) and Flos Lonicerae Japonicae (FLJ), through a simultaneous determination of multiple types of bioactive components. By employing DAD, the detection wavelengths were set at 240 nm for the determination of iridoids, 330 nm for phenolic acids, and 360 nm for flavonoids, respectively. While ELSD, connected in series after DAD, was applied to the determination of saponins. This assay was fully validated with respect to precision, repeatability, and accuracy. Moreover, principal component analysis (PCA) was used for the similarity evaluation of different samples, and it was proven straightforward and reliable to differentiate FL and FLJ samples from different origins. For PCA, two principal components have been extracted. Principal component 1 (PC1) influences the separation between different sample sets, capturing 54.598% variance, while principal component 2 (PC2) affects differentiation within sample sets, capturing 12.579% variance. In conclusion, simultaneous quantification of bioactive components by HPLC-DAD-ELSD coupled with PCA would be a well-acceptable strategy to differentiate the sources and to comprehensively control the quality of the medicinal plants FL and FLJ.
机译:新开发了一种结合二极管阵列和蒸发光散射检测器(HPLC-DAD-ELSD)的HPLC方法,通过同时测定多种类型的金银花(FL)和金银花(FLJ)来评估其质量。生物活性成分。通过使用DAD,检测波长分别设置为240纳米(用于测定虹吸素),330纳米(对于酚酸)和360纳米(对于黄酮)。在DAD之后串联连接的ELSD用于皂苷的测定。该测定法在准确性,可重复性和准确性方面得到了充分验证。此外,将主成分分析(PCA)用于不同样品的相似性评估,并且已证明将不同来源的FL和FLJ样品区分开来是直接且可靠的。对于PCA,已提取了两个主要成分。主成分1(PC1)影响不同样本集之间的分离,捕获54.598%的方差,而主成分2(PC2)影响样本集内的差异,捕获12.579%的方差。总之,通过HPLC-DAD-ELSD与PCA结合同时定量生物活性成分是一种很好的策略,可以区分来源并全面控制药用植物FL和FLJ的质量。

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