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通过可调谐分子相互作用设计仿生湿粘合剂。

Designing Bio-Inspired Wet Adhesives through Tunable Molecular Interactions.

机构信息

Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Alberta, T6G 1H9, Canada.

Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Alberta, T6G 1H9, Canada.

出版信息

J Colloid Interface Sci. 2023 Sep;645:591-606. doi: 10.1016/j.jcis.2023.04.150. Epub 2023 May 2.

Abstract

Marine organisms, such as mussels and sandcastle worms, can master rapid and robust adhesion in turbulent seawater, becoming leading archetypes for the design of underwater adhesives. The adhesive proteins secreted by the organisms are rich in catecholic amino acids along with ionic and amphiphilic moieties, which mediate the adaptive adhesion mainly through catechol chemistry and coacervation process. Catechol allows a broad range of molecular interactions both at the adhesive-substrate interface and within the adhesive matrix, while coacervation promotes the delivery and surface spreading of the adhesive proteins. These natural design principles have been translated to synthetic systems toward the development of biomimetic adhesives with water-resist adhesion and cohesion. This review provides an overview of the recent progress in bio-inspired wet adhesives, focusing on two aspects: (1) the elucidation of the versatile molecular interactions (e.g., electrostatic interactions, metal coordination, hydrogen bonding, and cation-π/anion-π interactions) used by natural adhesives, mainly through nanomechanical characterizations; and (2) the rational designs of wet adhesives based on these biomimetic strategies, which involve catechol-functionalized, coacervation-induced, and hydrogen bond-based approaches. The emerging applications (e.g., tissue glues, surgical implants, electrode binders) of the developed biomimetic adhesives in biomedical, energy, and environmental fields are also discussed, with future research directions proposed.

摘要

海洋生物,如贻贝和沙堡蠕虫,能够在湍急的海水中迅速而牢固地附着,成为水下粘合剂设计的主要原型。生物分泌的粘合蛋白富含儿茶酚氨基酸以及离子和两亲性部分,主要通过儿茶酚化学和共凝聚过程来调节适应性粘合。儿茶酚允许在粘合-基底界面和粘合基质内进行广泛的分子相互作用,而共凝聚则促进粘合蛋白的输送和表面扩散。这些自然设计原则已被转化为合成系统,用于开发具有耐水附着和内聚性的仿生粘合剂。本文综述了仿生湿粘合剂的最新进展,重点关注两个方面:(1)阐明天然粘合剂所使用的多种分子相互作用(例如静电相互作用、金属配位、氢键和阳离子-π/阴离子-π 相互作用),主要通过纳米力学特性来阐明;(2)基于这些仿生策略的湿粘合剂的合理设计,涉及儿茶酚功能化、共凝聚诱导和氢键基方法。还讨论了开发的仿生粘合剂在生物医学、能源和环境领域的新兴应用(例如组织胶、手术植入物、电极粘合剂),并提出了未来的研究方向。

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