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评估用于生物传感器设计的酶和氧化还原反应的可调谐范围。

Assessing the range of enzymatic and oxidative tunability for biosensor design.

机构信息

Department of Biomedical Engineering, University of Texas at Austin, Austin, TX 78712, USA.

出版信息

J Mater Chem B. 2020 Apr 29;8(16):3460-3487. doi: 10.1039/c9tb02666e.

Abstract

Development of multi-functional materials and biosensors that can achieve an in situ response designed by the user is a current need in the biomaterials field, especially in complex biological environments, such as inflammation, where multiple enzymatic and oxidative signals are present. In the past decade, there has been extensive research and development of materials chemistries for detecting and monitoring enzymatic activity, as well as for releasing therapeutic and diagnostic agents in regions undergoing oxidative stress. However, there has been limited development of materials in the context of enzymatic and oxidative triggers together, despite their closely tied and overlapping mechanisms. With research focusing on enzymatically and oxidatively triggered materials separately, these systems may be inadequate in monitoring the complexity of inflammatory environments, thus limiting in vivo translatability and diagnostic accuracy. The intention of this review is to highlight a variety of enzymatically and oxidatively triggered materials chemistries to draw attention to the range of synthetic tunability available for the construction of novel biosensors with a spectrum of programmed responses. We focus our discussion on several types of macromolecular sensors, generally classified by the causative material response driving ultimate signal detection. This includes sensing based on degradative processes, conformational changes, supramolecular assembly/disassembly, and nanomaterial interactions, among others. We see each of these classes providing valuable tools toward coalescing current gaps in the biosensing field regarding specificity, selectivity, sensitivity, and flexibility in application. Additionally, by considering the materials chemistry of enzymatically and oxidatively triggered biomaterials in tandem, we hope to encourage synthesis of new biosensors that capitalize on their synergistic roles and overlapping mechanisms in inflammatory environments for applications in disease diagnosis and monitoring.

摘要

开发多功能材料和生物传感器,使其能够实现用户设计的原位响应,是生物材料领域的当前需求,特别是在复杂的生物环境中,如炎症,其中存在多种酶和氧化信号。在过去的十年中,人们广泛研究和开发了用于检测和监测酶活性的材料化学,并在经历氧化应激的区域中释放治疗和诊断剂。然而,尽管它们的机制紧密相关且重叠,但在酶和氧化触发物的共同背景下,材料的开发仍然有限。由于研究重点是分别针对酶和氧化触发的材料,因此这些系统可能不足以监测炎症环境的复杂性,从而限制了体内的可转化性和诊断准确性。本综述的目的是强调各种酶和氧化触发材料化学,以引起人们对构建具有一系列程序化响应的新型生物传感器的合成可调性范围的关注。我们将讨论重点放在几种类型的高分子传感器上,这些传感器通常根据引起最终信号检测的材料响应进行分类。这包括基于降解过程、构象变化、超分子组装/解组装以及纳米材料相互作用等的传感。我们认为这些类别中的每一种都为弥合生物传感领域在特异性、选择性、灵敏度和应用灵活性方面的当前差距提供了有价值的工具。此外,通过同时考虑酶和氧化触发生物材料的材料化学,我们希望鼓励合成新的生物传感器,以利用它们在炎症环境中的协同作用和重叠机制,应用于疾病诊断和监测。

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Enzyme responsive materials: design strategies and future developments.酶响应性材料:设计策略与未来发展
Biomater Sci. 2013 Jan 30;1(1):11-39. doi: 10.1039/c2bm00041e. Epub 2012 Sep 21.

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