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硼酸功能化 FeO@CeO/Tb-MOF 作为发光纳米酶用于荧光检测和咖啡酸的降解。

Boric acid functionalized FeO@CeO/Tb-MOF as a luminescent nanozyme for fluorescence detection and degradation of caffeic acid.

机构信息

State Key Laboratory of Digital Medical Engineering, School of Biological Science and Medical Engineering, Southeast University, Nanjing, 210096, PR China.

State Key Laboratory of Digital Medical Engineering, School of Biological Science and Medical Engineering, Southeast University, Nanjing, 210096, PR China.

出版信息

Biosens Bioelectron. 2024 Nov 15;264:116637. doi: 10.1016/j.bios.2024.116637. Epub 2024 Aug 8.

Abstract

Caffeic acid (CA) is a natural polyphenol that can have various positive effects on human health. However, its extraction and processing can cause significant ecological issues. Therefore, it is crucial to detect and degrade CA effectively in the environment. In this study, we have developed a multifunctional magnetic luminescent nanozyme, FeO@CeO/Tb-MOF, which combines peroxidase activity to detect and degrade CA. The fluorescence of the nanozyme was significantly attenuated due to the specific nucleophilic reaction between its boronic acid moiety and the o-diphenol hydroxyl group of CA, energy competition absorption and photo-induced electron transfer (PET) effect. This nanozyme demonstrates a linear detection range from 50 nM to 500 μM and an exceptionally low detection limit of 18.9 nM, along with remarkable selectivity and stability. Moreover, the synergistic catalysis of FeO and CeO within FeO@CeO/Tb-MOF fosters peroxidase activity, leading to the generation of substantial free radicals catalyzed by HO, which ensures the efficient degradation of CA (∼95%). The superparamagnetic property of FeO further enables the efficient reuse and recycling of the nanozyme. This research provides a novel approach for the concurrent detection and remediation of environmental contaminants.

摘要

没食子酸(CA)是一种天然多酚,对人体健康有多种积极影响。然而,其提取和加工会对生态环境造成重大影响。因此,有效检测和降解环境中的 CA 至关重要。在本研究中,我们开发了一种多功能磁性发光纳米酶 FeO@CeO/Tb-MOF,它结合了过氧化物酶活性来检测和降解 CA。纳米酶的荧光由于其硼酸部分与 CA 的邻二酚羟基之间的特定亲核反应、能量竞争吸收和光诱导电子转移(PET)效应而显著减弱。该纳米酶的检测范围从 50 nM 到 500 μM,检测限低至 18.9 nM,具有显著的选择性和稳定性。此外,FeO@CeO/Tb-MOF 内的 FeO 和 CeO 的协同催化作用促进了过氧化物酶的活性,导致大量由 HO 产生的自由基的生成,从而确保 CA 的有效降解(约 95%)。FeO 的超顺磁性进一步实现了纳米酶的高效重复使用和回收。该研究为同时检测和修复环境污染物提供了一种新方法。

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