Unlocking the biological potential of emulsion-templated matrices through surface engineering for biomedical applications

IF 4.1 2区 化学 Q2 POLYMER SCIENCE
Emircan Sert , Ece Ozmen , Robert Owen , Betül Aldemir Dikici
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引用次数: 0

Abstract

Emulsion templating is a highly advantageous route for the fabrication of porous materials, enabling the development of matrices with high porosity, high interconnectivity, and precise morphological control. Synthetic polymers are most widely used in the fabrication of emulsion-templated tissue engineering scaffolds due to their superior mechanical strength, ease of fabrication, control over polymer properties, and batch-to-batch stability. The biological response is strongly associated with the surface properties of the biomaterials; however, scaffolds constructed from synthetic polymers often lack cell recognition sites and exhibit limited bioactivity. Thus, synthetic polymer-based porous matrices commonly require surface post-modification to improve cell adhesion, proliferation, migration, gene expression, and differentiation processes. To date, extensive work has been carried out investigating surface modification of scaffolds fabricated via traditional scaffold fabrication techniques. Still, studies addressing the post-modification of emulsion-templated matrices are comparatively limited despite an exponential increase in the number of publications on emulsion templating for tissue engineering in recent years. This review will first examine the fundamentals of emulsion templating, then describe cell adhesion and the characteristics of scaffolds that influence cell-material interactions. It will then provide a comprehensive analysis of surface modification techniques and recent advancements in surface-modified emulsion-templated matrices for tissue engineering applications. Finally, we address the challenges and future directions in this rapidly evolving field. We anticipate that this comprehensive literature review will present the current state-of-the-art and serve as a valuable roadmap for researchers seeking to enhance the biological performance of their emulsion-templated scaffolds through surface modifications. Such scaffold optimisation strategies not only improve cell-material interactions but also hold translational potential for advancing human healthcare through more effective regenerative therapies.

Abstract Image

通过生物医学应用的表面工程解锁乳剂模板基质的生物学潜力
乳液模板是制备多孔材料的一种非常有利的途径,可以开发出具有高孔隙率、高连通性和精确形态控制的基质。合成聚合物由于其优越的机械强度、易于制造、对聚合物性能的控制以及批次间的稳定性,在乳液模板组织工程支架的制造中得到了更广泛的应用。生物反应与生物材料的表面特性密切相关;然而,由合成聚合物构建的支架通常缺乏细胞识别位点并且表现出有限的生物活性。因此,合成聚合物基多孔基质通常需要表面后修饰来改善细胞粘附、增殖、迁移、基因表达和分化过程。迄今为止,已经开展了大量的工作来研究通过传统支架制造技术制造的支架的表面改性。尽管近年来关于组织工程中乳液模板的出版物数量呈指数级增长,但针对乳液模板基质后修饰的研究相对有限。本综述将首先研究乳液模板的基本原理,然后描述细胞粘附和影响细胞-材料相互作用的支架的特性。然后,它将全面分析表面改性技术和组织工程应用中表面改性乳液模板基质的最新进展。最后,我们讨论了这一快速发展领域的挑战和未来方向。我们期望这篇全面的文献综述将展示当前最先进的技术,并为研究人员寻求通过表面修饰来提高其乳液模板支架的生物性能提供有价值的路线图。这种支架优化策略不仅可以改善细胞-物质相互作用,而且还具有通过更有效的再生疗法推进人类医疗保健的转化潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Polymer
Polymer 化学-高分子科学
CiteScore
7.90
自引率
8.70%
发文量
959
审稿时长
32 days
期刊介绍: Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics. The main scope is covered but not limited to the following core areas: Polymer Materials Nanocomposites and hybrid nanomaterials Polymer blends, films, fibres, networks and porous materials Physical Characterization Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films Polymer Engineering Advanced multiscale processing methods Polymer Synthesis, Modification and Self-assembly Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization Technological Applications Polymers for energy generation and storage Polymer membranes for separation technology Polymers for opto- and microelectronics.
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