超疏水性介导的增强酶动力学和高性能生物测定

Droplet Pub Date : 2023-02-22 DOI:10.1002/dro2.51
Dandan Wang, Liping Chen, Xinjian Feng
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引用次数: 4

摘要

作为一种典型的超润湿性行为,超疏水性可以提供一种适当的策略来增强多相化学反应中的质量传输。在基于氧化酶的酶促反应中,对反应物氧的精细调节对于开发基于氧化酶的高性能生物传感器至关重要。然而,在固液两相条件下,氧化酶催化反应的动力学受到延迟的质量传输和较差的氧溶解度的抑制。为了解决这一限制,根据超疏水性和亲水性的二元协同作用,提出了固体-液体-空气三相界面的设计。在三相接头界面上,氧化酶催化反应所需的氧可以通过微/纳米结构的超疏水基底从空气相直接扩散到反应中心,从而改善氧化酶催化反应的动力学。在这篇小型综述中,我们总结了用于氧化酶生物传感器的基于不同超疏水底物的三相反应体系的制备的最新进展。常见的基底包括纤维网络、纳米线阵列、3D多孔框架和空心球结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Superhydrophobicity-mediated enhanced enzymatic kinetics and high-performance bioassays

Superhydrophobicity-mediated enhanced enzymatic kinetics and high-performance bioassays

As a typical superwettability behavior, superhydrophobicity can provide an appropriate strategy to enhance the mass transport in multiphase chemical reactions. In the oxidase-based enzymatic reactions, the elaborately regulating of reactant oxygen are critical to the development of an oxidase-based high-performance biosensor. In solid–liquid diphase condition, however, the kinetics of oxidase-catalyzed reactions is inhibited by delayed mass transport and poor solubility of oxygen. To address this limitation, the design of the solid–liquid–air triphase interface is proposed according to the binary cooperation of superhydrophobicity and hydrophilicity. On the triphase joint interface, oxygen required for the oxidase-catalyzed reactions can diffuse directly to the reaction center from the air phase through the micro/nanostructured superhydrophobic substrate, thus improving the kinetics of the oxidase-catalyzed reactions. In this minireview, we summarize recent advances in the fabrication of triphase reaction system based on different superhydrophobic substrate for oxidase-based biosensors. Common substrates including fibrous network, nanowire arrays, 3D porous framework, and hollow sphere structures are outlined in categories.

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CiteScore
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