首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Mixture design and Doehlert matrix for optimization of the ultrasonic assisted extraction of caffeic acid, rutin, catechin and trans-cinnamic acid in Physalis angulata L. and determination by HPLC DAD
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Mixture design and Doehlert matrix for optimization of the ultrasonic assisted extraction of caffeic acid, rutin, catechin and trans-cinnamic acid in Physalis angulata L. and determination by HPLC DAD

机译:用于优化超声波辅助提取咖啡酸,芦丁,儿茶素和体肉桂酸中的优化的混合物设计和道德利基金。HPLC爸爸的测定

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The present article describes the development of an ultrasonic assisted extraction of phenolic compounds in Physalis angulata and determination of caffeic acid, rutin, catechin and trans-cinnamic acid by HPLC DAD. The mixtures were composed of extractor solvent and its ratio optimized using a mixture design. Doehlert matrix was used to optimize the extractor solvent volume and sonication time while using total phenolics as analytical response. The optimized conditions for the extractor solvent were the ratio of: 57% water, 35% ethanol and 8% methanol. The best experimental conditions for ultrasound were a sonication time of 10 min and extractor volume of 15 mL. The limit of detection varied from 5.0 to 30 mu g L-1. The methods precision was expressed as relative standard deviation (RSD) and presented values lower than 3.0% for all analytes. The accuracy was evaluated using spike test with recoveries between 91% and 107%. The method was applied for the determination of caffeic acid, rutin, catechin and trans-cinnamic in four samples of Physalis angulata aerial parts and the concentration varied from 15.5 to 22.5 mu g g(-1) for catechin, from 25.0 to 32.5 mu g g(-1) for caffeic acid, 75.6 to 88.2 mu g g(-1) for rutin and varied from 23.5 to 110.7 mu g g(-1) for trans-cinnamic acid.
机译:本文介绍了通过HPLC达克测定酸痛,芦丁,儿茶素和反肉桂酸的超声辅助萃取酚类化合物的显影。混合物由提取物溶剂组成及其使用混合物设计优化的比例。使用总酚类作为分析反应的同时,使用道德基质优化提取物溶剂体积和超声时间。提取物溶剂的优化条件为:57%水,35%乙醇和8%甲醇的比例。超声波的最佳实验条件是10分钟的超声处理时间,萃取体积为15毫升。检测限度范围从5.0到30μgl-1不同。该方法精度表示为相对标准偏差(RSD),并且对所有分析物的呈现值低于3.0%。使用峰值试验评价的准确度,回收率在91%和107%之间。该方法用于测定咖啡酸,芦丁,儿茶素和反式肉桂酸的四种样品中的甘露酸,芦丁,儿茶素和反式肉桂酸,其浓度从15.5〜22.5μg(-1)变化为儿茶素,从25.0至32.5μggg( -1)对于咖啡酸,芦丁的75.6至88.2μg(-1),可从23.5-110.7μg(-1)变化,用于反式肉桂酸。

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