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基于离子液体的真空微波辅助萃取,随后用大孔树脂富集,用于从杨树皮中分离水杨苷、金丝桃苷和芦丁这三种糖苷。

Ionic liquid-based vacuum microwave-assisted extraction followed by macroporous resin enrichment for the separation of the three glycosides salicin, hyperin and rutin from Populus bark.

作者信息

Chen Fengli, Mo Kailin, Liu Zhaizhi, Yang Fengjian, Hou Kexin, Li Shuangyang, Zu Yuangang, Yang Lei

机构信息

Key Laboratory of Forest Plant Ecology, Ministry of Education, Northeast Forestry University, Harbin 150040, China.

Sichuan Academy of Forestry, Chengdu 610081, China.

出版信息

Molecules. 2014 Jul 7;19(7):9689-711. doi: 10.3390/molecules19079689.

DOI:10.3390/molecules19079689
PMID:25004075
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6271344/
Abstract

An effective ionic liquid vacuum microwave-assisted method was developed for extraction of the thermo- and oxygen-sensitive glycosides salicin, hyperin and rutin from Populus bark due to the strong solvating effects of ionic liquids on plant cell walls. In this study, [C4mim]BF4 solution was selected as the extracting solution for extraction of the target analytes. After optimization by single factor experiments and response surface methodology, the optimum condition parameters were achieved, which included 1.0 M [C4mim]BF4, 2 h soaking time, -0.08 MPa vacuum, 20 min microwave irradiation time, 400 W microwave irradiation power and 25 mL/g liquid/solid ratio. Under the optimum conditions, higher extraction yields of salicin (35.53 mg/g), hyperin (1.32 mg/g) and rutin (2.40 mg/g) were obtained. Compared with other extraction methods, the developed method provided higher yields of the three target components after a relatively shorter extraction time (20 min). No obvious degradation of the target analytes was observed under the optimum conditions in performed stability studies and the proposed method had a high reproducibility. Meanwhile, after adsorption and desorption on macroporous D101 resin, the target analytes can be effectively separated from the [C4mim]BF4 ionic liquid extraction solution and the yields of salicin, hyperin and rutin were 89%, 82% and 84%, respectively. The recovered [C4mim]BF4 ionic liquid presented a good extraction effect on the three analytes after recycling five times.

摘要

由于离子液体对植物细胞壁具有较强的溶剂化作用,因此开发了一种有效的离子液体真空微波辅助方法,用于从杨树皮中提取对热和氧敏感的糖苷水杨苷、金丝桃苷和芦丁。在本研究中,选择[C4mim]BF4溶液作为提取目标分析物的提取液。通过单因素实验和响应面法进行优化后,获得了最佳条件参数,包括1.0 M [C4mim]BF4、2 h浸泡时间、-0.08 MPa真空度、20 min微波辐照时间、400 W微波辐照功率和25 mL/g液固比。在最佳条件下,水杨苷(35.53 mg/g)、金丝桃苷(1.32 mg/g)和芦丁(2.40 mg/g)的提取率较高。与其他提取方法相比,所开发的方法在相对较短的提取时间(20 min)后,三种目标成分的产率更高。在进行的稳定性研究中,在最佳条件下未观察到目标分析物有明显降解,且该方法具有较高的重现性。同时,在大孔D101树脂上进行吸附和解吸后,目标分析物可从[C4mim]BF4离子液体提取液中有效分离出来,水杨苷、金丝桃苷和芦丁的产率分别为89%、82%和84%。回收的[C4mim]BF4离子液体在循环使用五次后,对三种分析物仍具有良好的提取效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/56765c2fceae/molecules-19-09689-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/6c6067bd659f/molecules-19-09689-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/e540504bf8a8/molecules-19-09689-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/51fcb27f3211/molecules-19-09689-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/b2af4d914600/molecules-19-09689-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/e1f02d47dc91/molecules-19-09689-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/8fe8cf3b1504/molecules-19-09689-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/ab6d3bd747a9/molecules-19-09689-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/56765c2fceae/molecules-19-09689-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/6c6067bd659f/molecules-19-09689-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/e540504bf8a8/molecules-19-09689-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/51fcb27f3211/molecules-19-09689-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/b2af4d914600/molecules-19-09689-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/e1f02d47dc91/molecules-19-09689-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/8fe8cf3b1504/molecules-19-09689-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/ab6d3bd747a9/molecules-19-09689-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdc0/6271344/56765c2fceae/molecules-19-09689-g008.jpg

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