Efficiency and selectivity of ionic liquids in microwave-assisted extraction of major lichen phenolic compounds: a scalable process with recycling of ionic liquids.
dc.contributor.author | Komaty, Sarah | |
dc.contributor.author | Sauvager, Aurélie | |
dc.contributor.author | Bazureau, Jean-Pierre | |
dc.contributor.author | Tomasi, Sophie | |
dc.contributor.author | Paquin, Ludovic | |
dc.date.accessioned | 2020-11-09T06:40:37Z | |
dc.date.available | 2020-11-09T06:40:37Z | |
dc.date.issued | 2020-11-04 | |
dc.date.submitted | 2020-07-03 | |
dc.identifier.citation | Komaty, S., Sauvager, A., Bazureau, J., Tomasi, S., & Paquin, L. (2020). Efficiency and selectivity of ionic liquids in microwave-assisted extraction of major lichen phenolic compounds: a scalable process with recycling of ionic liquids. Phytochemical Analysis. doi:10.1002/pca.3008 | |
dc.identifier.issn | 0958-0344 | |
dc.identifier.pmid | 33150689 | |
dc.identifier.doi | 10.1002/pca.3008 | |
dc.identifier.uri | http://hdl.handle.net/10754/665865 | |
dc.description.abstract | INTRODUCTION:Pseudevernia furfuracea, a lichen used classically for cosmetic applications, contains interesting metabolites possessing antimicrobial and anti-inflammatory or antioxidant properties. OBJECTIVES:Ionic liquid combined to microwave-assisted extraction (IL-MAE) was successfully applied for metabolites extraction from Pseudevernia furfuracea. MATERIALS AND METHODS:Three imidazolium and pyridinium-based ionic liquids (ILs): 1,3-dimethylimidazolium methylsulphate [C1 C1 Im][MeSO4 ], 1-ethyl-3-methylimidazolium ethylsulphate [C2 C1 Im][EtSO4 ], and N-ethylpyridinium ethylsulphate [C2 Py][EtSO4 ] were assessed for this process. The efficiency of the extraction method was evaluated using thin-layer chromatography (TLC) coupled to a Camag® spectrophotodensitometer and using high-performance liquid chromatography (HPLC) analysis. RESULTS:ILs under MAE showed extraction time efficiency (15 min vs. 24 h for conventional heating) and high selectivity in extracting the targeted metabolites: atranorin (AT), methyl-β-orcinol carboxylate (MOC), fumarprotocetraric acid (Fum. Ac.), and physodic acid (Phys. Ac.) despite the increased degradation of AT under MAE. We showed a tunable selectivity of ILs towards extracting metabolites by changing anion or cation due to the modification of the interaction between the IL and the metabolites. While [C2 Py][EtSO4 ] was the most efficient IL and could extract all the targeted metabolites, [C2 C1 Im][EtSO4 ] was the most selective. It fully extracted AT and partially Fum. Ac. Moreover, the lichen prepared by mixing procedure provided AT and Fum. Ac. more than the milled one. A 100 times scale-up extraction was successfully performed on mixed samples with full IL recycling after back extraction. CONCLUSION:IL-MAE is reliable for lichen metabolites extraction. The method is reproducible, scalable, with possible IL recycling, opening the door for potential industrial applications. | |
dc.description.sponsorship | This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors. | |
dc.description.sponsorship | Special thanks to J. M Bessiere, PNSM, Montpellier for providing thelichen specimen. | |
dc.publisher | Wiley | |
dc.relation.url | https://onlinelibrary.wiley.com/doi/10.1002/pca.3008 | |
dc.rights | Archived with thanks to Phytochemical analysis : PCA | |
dc.title | Efficiency and selectivity of ionic liquids in microwave-assisted extraction of major lichen phenolic compounds: a scalable process with recycling of ionic liquids. | |
dc.type | Article | |
dc.contributor.department | KAUST Catalysis Center (KCC) King Abdullah University of Science and Technology Thuwal Saudi Arabia | |
dc.identifier.journal | Phytochemical Analysis | |
dc.rights.embargodate | 2021-11-05 | |
dc.eprint.version | Post-print | |
dc.contributor.institution | CNRS, ISCR UMR 6226 University of Rennes Rennes France | |
kaust.person | Komaty, Sarah | |
dc.date.accepted | 2020-09-26 | |
refterms.dateFOA | 2020-11-11T12:04:51Z | |
dc.date.published-online | 2020-11-04 | |
dc.date.published-print | 2021-07 |