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Reference type: Journal
Authors: Jia M, Yang J, Sun YK, Bai X, Wu T, Liu ZS, Aisa HA
Article Title: Improvement of imprinting effect of ionic liquid molecularly imprinted polymers by use of a molecular crowding agent.
Publication date: 2018
Journal: Analytical and Bioanalytical Chemistry
Volume: 410
Issue: (2)
Page numbers: 595-604.
DOI: 10.1007/s00216-017-0760-5

Abstract: We aimed to improve the imprinting effect of ionic liquid molecularly imprinted polymers (MIPs) by use of a molecular crowding agent. The ionic liquid 1-vinyl-3-ethylimidazolium tetrafluoroborate ([VEIm][BF4]) was used as the functional monomer and aesculetin was used as the template molecule in a crowding environment, which was made up of a tetrahydrofuran solution of polystyrene. The ionic liquid MIPs that were prepared in the crowding environment displayed an enhanced imprinting effect. NMR peak shifts of active hydrogen of aesculetin suggested that interaction between the functional monomer and the template could be increased by the use of a crowding agent in the self-assembly process. The retention and selectivity of aesculetin were affected greatly by high molecular crowding, the amount of high molecular weight crowding agent, and the ratio of [VEIm][BF4] to aesculetin. The optimal MIPs were used as solid-phase extraction sorbents to extract aesculetin from Cichorium glandulosum. A calibration curve was obtained with aesculetin concentrations from 0.0005 to 0.05 mg mL-1 (correlation coefficient R2 of 0.9999, y = 1519x + 0.0923). The limit of quantification was 0.12 μg mL-1, and the limit of detection was 0.05 μg mL-1. The absolute recovery of aesculetin was (80 2)% (n = 3), and the purity of aesculetin was (92 0.5)% (n = 5). As a conclusion, molecular crowding is an effective approach to obtain ionic liquid MIPs with high selectivity even in a polar solvent environment
Template and target information: aesculetin
Author keywords: Molecular crowding agent, Ionic liquid monomer, Aesculetin, Solid-phase extraction, molecularly imprinted polymer


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