4.8 Article

Structure Defect Tuning of Metal-Organic Frameworks as a Nanozyme Regulatory Strategy for Selective Online Electrochemical Analysis of Uric Acid

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 44, 页码 52987-52997

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c17974

关键词

structure defects; metal-organic frameworks; oxidase-like activity; nanozyme microreactor; UA; in vivo online electrochemical detection

资金

  1. National Natural Science Foundation [22074095]
  2. High-level Teachers in Beijing Municipal Universities in the Period of 13th Five year Plan [CITTCD20190330]
  3. Yanjing Young Scholar Program of Capital Normal University

向作者/读者索取更多资源

Nanozymes have been designed to overcome the limitations of natural enzymes in analytical applications. This study demonstrates the use of structure defects in metal-organic frameworks to enhance the catalytic efficiency of artificial nanozymes, specifically for oxidase-like MOFs. By introducing defects into the ZIF-L-Co MOF, the catalytic activities were significantly improved, offering a promising platform for investigating brain function and diseases related to uric acid.
Nanozymes have been designed to address the limitations of high cost and poor stability involving natural enzymes in analytical applications. However, the catalytic efficiency of the nanozyme still needs to be improved so that it can meet the selectivity and stability requirements of accurate biomolecule analysis. Here, we presented structure defects of metal-organic frameworks (MOFs) as a tuning strategy to regulate the catalytic efficiency of artificial nanozymes and investigated the roles of defects on the catalytic activity of oxidase-like MOFs. Structural defects were introduced into a novel Co-containing zeolitic imidazolate framework with gradually loosened morphology (ZIF-L-Co) by doping cysteine (Cys). It was found that with the increase in defect degree, the properties of materials such as ascorbate oxidase-like, glutathione oxidase-like, and laccase-like were obviously enhanced by over 5, 2, and 3 times, respectively. In-depth structural investigations indicate that the doping of sulfur inducing structural defects which may destroy the equilibrium state between cobalt and nitrogen in 2-methylimidazole and distort the crystal lattice, thereby enhancing the adsorption of oxygen and thus promoting the oxidase-like activity. The ZIF-L-Co-10 mg with enhanced ascorbate oxidase- and laccase-like activity was loaded into a microreactor and integrated into an online electrochemical system (OECS) in the upstream of the detector. This nanozyme-based microreactor can completely remove ascorbic acid, dopamine, and 3,4-dihydroxyphenylacetic acid which are the main interference toward uric acid (UA) electrochemical measurement, and the ZIF-L-Co-10 mg Cys-based OECS system is capable of continuously capturing UA change in rat brain following ischemia-reperfusion injury. Structure defect tuning of ZIF-L-Co not only provides a new regulatory strategy for artificial nanozyme activity but also provides a critical chemical platform for the investigation of UA-related brain function and brain diseases.

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