Supramolecular peptidic dopants for inducing photoconductivity and mechanical tunability in digital light processable hydrogels†

IF 3.1 3区 化学 Q2 Chemistry
Harrison C. Jeong, Yuyao Kuang, Ze-Fan Yao and Herdeline Ann M. Ardona
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引用次数: 0

Abstract

This work presents a strategy for generating composite hydrogels bearing photoconductive conduits held by supramolecular interactions that are compatible with digital light processing (DLP) printing. Conductive polymers are typically processed with organic solvents as the film, yet if used as biomaterials, excitable cells often require matching with the mechanical and structural properties of their native, aqueous three-dimensional (3-D) microenvironment. Here, we utilize peptide-functionalized porphyrin units capable of self-assembling into photoconductive nanostructures with defined nanomorphologies under aqueous conditions. In addition to the DXXD peptide arms (X = V, F), the sequence variants studied here include a peptidic moiety bearing allyloxycarbonyl (alloc) groups that can serve as crosslinking sites of the acrylate-based monomers that ultimately form the base 3-D covalent network for the hydrogels. We investigate the impact of pre-templating polymeric gelators with supramolecular assemblies vs. printing a dispersed peptide–porphyrin in a polymer composite, specifically, the potential impact of the morphologies of the supramolecular additives or “dopants” on the resulting mechanical property, conductivity, and printability of the hydrogels, comprised of a hybrid between acrylated polymers and supramolecular peptide–porphyrin assemblies. Lastly, we demonstrate the role of photophysical properties that emerge from peptide-tuned porphyrin assemblies as a photoabsorber additive that influences the printing outcomes of the composite hydrogel. Overall, we present a covalent-supramolecular composite hydrogelator system where the self-assembled networks offer a pathway for energy transport and mechanical reinforcement/dissipation at the same time, leading to the formation of a hydrogel with optoelectronic, mechanical, and printable behavior that can be influenced by self-assembled dopants.

Abstract Image

数字光处理水凝胶中用于诱导光导性和机械可调性的超分子肽掺杂剂。
这项工作提出了一种生成复合水凝胶的策略,该复合水凝胶承载了与数字光处理(DLP)印刷兼容的超分子相互作用所保持的光导导管。导电聚合物通常用有机溶剂作为薄膜进行加工,但如果用作生物材料,可兴奋细胞通常需要与其原生水性三维微环境的机械和结构特性相匹配。在这里,我们利用肽功能化的卟啉单元,能够在水条件下自组装成具有明确纳米形态的光导纳米结构。除了DXXD肽臂(X = V, F),这里研究的序列变异包括一个带有烯丙氧羰基(alloc)基团的肽段,它可以作为丙烯酸酯基单体的交联位点,最终形成水凝胶的碱性3-D共价网络。我们研究了带超分子组件的预模板聚合物凝胶与在聚合物复合材料中打印分散的肽-卟啉的影响,特别是,超分子添加剂或“掺杂剂”的形态对由丙烯酸化聚合物和超分子肽-卟啉组件组成的水凝胶的机械性能、电导率和可打印性的潜在影响。最后,我们证明了肽调卟啉组合作为光吸收剂添加剂所产生的光物理性质对复合水凝胶打印结果的影响。总的来说,我们提出了一种共价-超分子复合水凝胶体系,其中自组装网络同时为能量传输和机械强化/耗散提供了途径,从而形成了具有光电、机械和可打印行为的水凝胶,这些行为可以受到自组装掺杂剂的影响。
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
Faraday Discussions
Faraday Discussions CHEMISTRY, PHYSICAL-
CiteScore
4.90
自引率
0.00%
发文量
259
审稿时长
2.8 months
期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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