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基于介孔金属有机框架的肽分子印迹材料的制备与应用

Preparation and application of peptide molecularly imprinted material based on mesoporous metal-organic framework.

作者信息

Wang Min, Zhang Lingyi, Zhao Yameng, Zhang Weibing

机构信息

Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry & Molecular Engineering, East China University of Science and Technology, Shanghai, PR China.

Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry & Molecular Engineering, East China University of Science and Technology, Shanghai, PR China.

出版信息

Talanta. 2021 Mar 1;224:121765. doi: 10.1016/j.talanta.2020.121765. Epub 2020 Oct 10.

Abstract

In this study, a new molecularly imprinted material, MIP@UiO-66-NH, was synthesized with glutathione (GSH) as template and mesoporous metal organic framework (UiO-66-NH) as matrix. The molecularly imprinted polymer was modified on the surface and into the pores of the UiO-66-NH by surface molecular imprinting method with thin polymer layer. Based on high specific surface area (1091.93 m g) and appropriate pore size (35 nm) of the ordered mesoporous UiO-66-NH, the adsorption capacity for GSH reached 94.43 mg g, and the adsorption equilibrium could be achieved within 30 min. The adsorption isotherm data of MIP@UiO-66-NH could be described well by Freundlich model and the kinetic data complied well with pseudo-second-order model. In addition, the MIP@UiO-66-NH showed low adsorption capacity to GSH structural analogs (Q = 6.51 mg g), suggesting great selectivity for GSH recognition. Finally, the MIP@UiO-66-NH was successfully applied for selective separation of GSH from BSA, skim milk and egg white tryptic digest.

摘要

在本研究中,以谷胱甘肽(GSH)为模板、介孔金属有机框架(UiO-66-NH)为基质,合成了一种新型分子印迹材料MIP@UiO-66-NH。采用表面分子印迹法,通过薄聚合物层在UiO-66-NH的表面和孔内修饰分子印迹聚合物。基于有序介孔UiO-66-NH的高比表面积(1091.93 m²/g)和合适的孔径(35 nm),其对GSH的吸附容量达到94.43 mg/g,且在30分钟内可达到吸附平衡。MIP@UiO-66-NH的吸附等温线数据能很好地用Freundlich模型描述,动力学数据与伪二级模型吻合良好。此外,MIP@UiO-66-NH对GSH结构类似物的吸附容量较低(Q = 6.51 mg/g),表明其对GSH识别具有高度选择性。最后,MIP@UiO-66-NH成功应用于从牛血清白蛋白、脱脂牛奶和蛋清胰蛋白酶消化物中选择性分离GSH。

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