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快速简便的茶皂素制备方法的开发及其与茶籽油皂素表面张力差异的研究。

Development of a Rapid and Simple Method for Preparing Tea-Leaf Saponins and Investigation on Their Surface Tension Differences Compared with Tea-Seed Saponins.

机构信息

College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310058, China.

出版信息

Molecules. 2018 Jul 20;23(7):1796. doi: 10.3390/molecules23071796.

DOI:10.3390/molecules23071796
PMID:30037015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6099727/
Abstract

The relative overcapacity in China's tea-leaf production and the potential application of tea-leaf saponins in soil remediation encouraged in-depth developments and comprehensive utilizations of tea-leaf resources. Through variables optimizations using Box⁻Behnken designs for ultrasonic power, temperature as well as ultrasonic treatment time in ultrasonic-assisted water extraction and single-variable experiments for acetone-extraction solution ratio in acetone precipitation, a rapid and simple method was developed for preparing tea-leaf saponins. Tea-leaf saponins with the concentration of 3.832 ± 0.055 mg/mL and the purity of 76.5% ± 1.13% were acquired under the optimal values of 78 w, 60 °C, 20 min and 0.1 ratio of acetone-extraction solution. Both Fourier transform-infrared (FT-IR) spectra and ultraviolet (UV) spectra revealed slight composition differences between tea-leaf saponins and tea-seed saponins, while these differences were not reflected in the critical micelle concentration (CMC) and the surface tension of tea-leaf saponins and tea-seed saponins, indicating there was no need to distinguish them at the CMC. Further research attention on where tea-leaf saponins were in low concentrations is deserved to discover whether they had differences in comparison with tea-seed saponins, which was beneficial to apply them in the phytoremediation of contaminated soils.

摘要

中国茶叶产量相对过剩,茶叶皂素在土壤修复中的潜在应用,促使人们对茶叶资源进行了深入的开发和综合利用。通过超声辅助水提法的超声功率、温度和超声处理时间的 Box⁻Behnken 设计变量优化,以及丙酮沉淀法中丙酮提取液比的单变量实验,建立了一种快速、简单的茶叶皂素制备方法。在超声功率 78 W、温度 60°C、超声处理时间 20 min 和丙酮提取液比 0.1 的最佳条件下,获得了浓度为 3.832 ± 0.055 mg/mL、纯度为 76.5% ± 1.13%的茶叶皂素。傅里叶变换红外(FT-IR)光谱和紫外(UV)光谱表明,茶叶皂素和茶籽皂素的组成存在细微差异,但这些差异并未反映在茶叶皂素和茶籽皂素的临界胶束浓度(CMC)和表面张力上,表明在 CMC 处无需对其进行区分。进一步研究茶叶皂素在低浓度下的存在情况,以发现其与茶籽皂素是否存在差异,这有利于将其应用于污染土壤的植物修复中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/46e021079ee3/molecules-23-01796-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/f3c677d0fb1e/molecules-23-01796-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/2fbc1bb2811a/molecules-23-01796-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/79056baec339/molecules-23-01796-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/30cd962bb0c4/molecules-23-01796-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/46e021079ee3/molecules-23-01796-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/f3c677d0fb1e/molecules-23-01796-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/2fbc1bb2811a/molecules-23-01796-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/79056baec339/molecules-23-01796-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/30cd962bb0c4/molecules-23-01796-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fb/6099727/46e021079ee3/molecules-23-01796-g005.jpg

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