Department of Materials Science and Engineering, McMaster University, Hamilton, ON, Canada.
Department of Materials Science and Engineering, McMaster University, Hamilton, ON, Canada.
Adv Colloid Interface Sci. 2020 Oct;284:102272. doi: 10.1016/j.cis.2020.102272. Epub 2020 Sep 19.
This review is focused on new electrophoretic deposition (EPD) mechanisms for deposition biomacromolecules, such as biopolymers, proteins and enzymes. Among the rich literature sources of EPD of biopolymers, proteins and enzymes for biomedical applications we selected papers describing new fundamental deposition mechanisms. Such deposition mechanisms are of critical importance for further development of EPD method and its emerging biomedical applications. Our goal is to emphasize innovative ideas which have enriched colloid and interface science of EPD during recent years. We describe various mechanisms of cathodic and anodic EPD of charged biopolymers. Special attention is focused on in-situ chemical modification of biopolymers and crosslinking techniques. Recent innovations in the development of natural and biocompatible charged surfactants and film forming agents are outlined. Among the important advances in this area are the applications of bile acids and salts for EPD of neutral polymers. Such innovations allowed for the successful EPD of various electrically neutral functional polymers for biomedical applications. Particularly important are biosurfactant-polymer interactions, which facilitate dissolution, dispersion, charging, electrophoretic transport and deposit formation. Recent advances in EPD mechanisms addressed the problem of EPD of proteins and enzymes related to their charge reversal at the electrode surface. Conceptually new methods are described, which are based on the use of biopolymer complexes with metal ions, proteins, enzymes and other biomolecules. This review describes new developments in co-deposition of biomacromolecules and future trends in the development of new EPD mechanisms and strategies for biomedical applications.
这篇综述专注于新的电泳沉积(EPD)机制,用于沉积生物大分子,如生物聚合物、蛋白质和酶。在生物聚合物、蛋白质和酶的 EPD 的丰富文献来源中,我们选择了描述新的基本沉积机制的论文。这些沉积机制对于进一步发展 EPD 方法及其新兴的生物医学应用至关重要。我们的目标是强调近年来丰富胶体和界面科学的 EPD 的创新思想。我们描述了带电荷的生物聚合物阴极和阳极 EPD 的各种机制。特别关注生物聚合物的原位化学改性和交联技术。概述了天然和生物相容带电表面活性剂和成膜剂的最新发展创新。在这一领域的重要进展中,胆酸及其盐类在中性聚合物的 EPD 中的应用尤为重要。这些创新使得各种用于生物医学应用的电中性功能聚合物的成功 EPD 成为可能。特别重要的是生物表面活性剂-聚合物相互作用,这有助于溶解、分散、带电、电泳传输和沉积物形成。最近关于 EPD 机制的进展解决了与蛋白质和酶在电极表面电荷反转相关的 EPD 问题。描述了基于使用与金属离子、蛋白质、酶和其他生物分子结合的生物聚合物复合物的新概念方法。这篇综述描述了生物大分子共沉积的新发展以及生物医学应用中新型 EPD 机制和策略的未来趋势。