Simultaneous determination of eleven bioactive constituents in honey-processed licorice by high-performance liquid chromatography-diode array detector and its application from the perspective of processing influence under orthogonal design

IF 4.3 3区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE
Li-hong Chen, Yuanpeng Sun, H. Cai, Shuang Guo, Xiachang Wang, Wei-Dong Li, Chunqin Mao, Xun-hong Liu, Lin Yan, Heng-li Jiang, Tu-lin Lu
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引用次数: 2

Abstract

Objective: The aim of this study was to develop a reliable approach to simultaneously quantify 11 markers and explore the quality variation in honey-processed licorice. Materials and Methods: A high-performance liquid chromatography-diode array detector method was developed for the simultaneous determination of 11 markers (nine flavonoids and two triterpenoid saponins) in honey-processed licorice. The changes to the 11 markers in honey-processed licorice were investigated using an orthogonal design with three input factors. Results: The established method was precise, accurate, and sensitive enough for the simultaneous quantitative evaluation of 11 markers in honey-processed licorice. Intuitive analysis and variance analysis revealed that (1) the soaking time of crude licorice, stir-frying temperature, and stir-frying time remarkably influenced the content of liquiritin apioside, signifying the decomposition of liquiritin apioside to liquiritin or transformation of liquiritin apioside to isoliquiritin apioside, (2) stir-frying temperature significantly influenced licorice-saponin G2, (3) stir-frying temperature was the most important factor of the three input factors, (4) in terms of composition, honey fried licorice had significant effects on two components, namely liquiritin apioside and licorice-saponin G2. Conclusions: Honey processing influenced the content of the 11 licorice analytes differently. This paper highlights the first report on how the quality of honey-processed licorice varies under different processing conditions and suggests the optimal levels of the investigated three factors as A2B2C3 according to the degrees of influence of these factors on the 11 components. Specifically, the soaking time of crude licorice with honey solution, stir-frying temperature, and stir-frying time were 40 min, 100°C, and 20 min, respectively.
正交设计条件下高效液相色谱-二极管阵列检测器同时测定蜂蜜甘草中11种生物活性成分及其应用
目的:本研究旨在开发一种可靠的方法来同时定量11个标志物,并探索蜂蜜加工甘草的质量变化。材料与方法:采用高效液相色谱-二极管阵列检测器法同时测定蜂蜜甘草中的11种标志物(9种黄酮类化合物和2种三萜皂苷)。采用三因素正交设计,研究了蜂蜜甘草中11个标志物的变化。结果:建立的方法准确、准确、灵敏,可同时定量评价蜂蜜甘草中的11个标志物。直观分析和方差分析表明:(1)粗甘草浸泡时间、翻炒温度和翻炒时间对甘草苷含量有显著影响,表明甘草苷分解为甘草苷或由甘草苷转化为异甘草苷,(2)翻炒温度对甘草皂苷G2有显著影响,(3)在三个输入因素中,翻炒温度是最重要的因素。结论:蜂蜜加工对11种甘草分析物含量的影响不同。本文重点介绍了第一份关于蜂蜜加工甘草在不同加工条件下质量如何变化的报告,并根据这些因素对11种成分的影响程度,提出了所研究的三个因素A2B2C3的最佳水平。具体而言,粗甘草与蜂蜜溶液的浸泡时间、翻炒温度和翻炒时间分别为40分钟、100°C和20分钟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
World Journal of Traditional Chinese Medicine
World Journal of Traditional Chinese Medicine Medicine-Complementary and Alternative Medicine
CiteScore
5.40
自引率
2.30%
发文量
259
审稿时长
24 weeks
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