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生物功能化且自支撑的聚吡咯框架作为类似细胞外基质的纳米结构生物界面。

Biofunctionalized and self-supported polypyrrole frameworks as nanostructured ECM-like biointerfaces.

作者信息

Lefèvre Damien, Louvegny Juliette, Naudin Mathieu, Ferain Etienne, Dupont-Gillain Christine, Demoustier-Champagne Sophie

机构信息

Institute of Condensed Matter and Nanosciences (Bio & Soft Matter) Croix du Sud 1 B-1348 Louvain-la-Neuve Belgium

It4ip S.A. Avenue J.-E. Lenoir B-1348 Louvain-la-Neuve Belgium.

出版信息

RSC Adv. 2018 Jun 22;8(41):22932-22943. doi: 10.1039/c8ra00325d. eCollection 2018 Jun 21.

Abstract

Hybrid nanobiointerfaces were designed as an original contribution to the challenge of synthesizing nanostructured biomaterials integrating a set of cell fate-determining cues, originally provided to cells by the extracellular matrix (ECM). The produced biointerfaces consist of a stiff framework of intersected polypyrrole (PPy) nanotubes supporting a soft multilayer composed of ECM-derived biomacromolecules: collagen (Col) and hyaluronic acid (HA). PPy frameworks with highly tunable characteristics were synthesized through chemical oxidative polymerization of pyrrole monomers, templated within track-etched polycarbonate (PC) membranes featuring a network of intersected nanopores. PPy interfaces with a porosity of 80%, composed of nanotubes with an average diameter ranging from 40 to 300 nm, intersecting at an angle of 90°, were shown to be self-supported. These rigid PPy nanostructured interfaces were functionalized with a self-assembling (HA/Col) multilayer deposited a layer-by-layer process. Biofunctionalized and unmodified PPy frameworks were both shown to promote sustained cell adhesion, therefore demonstrating the cytocompatibility of the engineered matrices. Such nanobiointerfaces, combining a mechanically-stable framework of tunable dimensions with a soft biopolymeric multilayer of highly versatile nature, pave the way towards cell-instructive biomaterials able to gather a wide range of cues guiding cell behavior. The developed self-supported structures could be used as a coating or as membranes bridging different tissues.

摘要

混合纳米生物界面的设计是对合成纳米结构生物材料这一挑战的原创贡献,该材料整合了一系列原本由细胞外基质(ECM)提供给细胞的细胞命运决定线索。所制备的生物界面由相互交叉的聚吡咯(PPy)纳米管的刚性框架组成,该框架支撑着由ECM衍生的生物大分子(胶原蛋白(Col)和透明质酸(HA))构成的柔软多层结构。通过吡咯单体的化学氧化聚合反应,在具有交叉纳米孔网络的径迹蚀刻聚碳酸酯(PC)膜内进行模板化,合成了具有高度可调特性的PPy框架。孔隙率为80%的PPy界面由平均直径在40至300纳米之间的纳米管组成,这些纳米管以90°角交叉,显示为自支撑结构。这些刚性的PPy纳米结构界面通过逐层沉积的自组装(HA/Col)多层结构进行功能化。生物功能化和未修饰的PPy框架均显示出能促进细胞持续粘附,因此证明了工程化基质的细胞相容性。这种纳米生物界面将具有可调尺寸的机械稳定框架与具有高度通用性的柔软生物聚合物多层结构相结合,为能够收集广泛引导细胞行为线索的细胞指导性生物材料铺平了道路。所开发的自支撑结构可用于涂层或作为连接不同组织的膜。

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