Polysaccharide-based layer-by-layer nanoarchitectonics with sulfated chitosan for tuning anti-thrombogenic properties

壳聚糖 材料科学 粘附 表面改性 接触角 蛋白质吸附 血小板粘附 单层 纳米技术 聚合物 图层(电子) 吸附 化学工程 生物医学工程 化学 复合材料 有机化学 生物化学 医学 工程类
作者
João Batista Maia Rocha Neto,Francesco Copes,Pascale Chevallier,Rodrigo Silveira Vieira,Jorge Vicente Lopes da Silva,Diego Mantovani,Marisa Masumi Beppu
出处
期刊:Colloids and Surfaces B: Biointerfaces [Elsevier BV]
卷期号:213: 112359-112359 被引量:23
标识
DOI:10.1016/j.colsurfb.2022.112359
摘要

The development of blood-interacting surfaces is critical to fabricate biomaterials for medical use, such as prostheses, implants, biosensors, and membranes. For instance, thrombosis is one of the leading clinical problems when polymer-based materials interact with blood. To overcome this limitation is necessary to develop strategies that limit platelets adhesion and activation. In this work, hyaluronan (HA)/chitosan (Chi) based-films, recently reported in the literature as platforms for tumor cell capture, were developed and, subsequently, functionalized with sulfated chitosan (ChiS) using a layer-by-layer technique. ChiS, when compared to native Chi, presents the unique abilities to confer anti-thrombogenic properties, to reduce protein adsorption, and also to limit calcification. Film physicochemical characterization was carried out using FTIR and XPS for chemical composition assessment, AFM for the surface morphology, and contact angle for hydrophilicity evaluation. The deposition of ChiS monolayer promoted a decrease in both roughness and hydrophilicity of the HA/Chi films. In addition, the appearance of sulfur in the chemical composition of ChiS-functionalized films confirmed the film modification. Biological assay indicated that the incorporation of sulfated groups limited platelet adhesion, mainly because a significant reduction of platelets adhesion to ChiS-functionalized films was observed compared to HA/Chi films. On balance, this work provides a new insight for the development of novel antithrombogenic biomaterials, opening up new possibilities for devising blood-interaction surfaces.
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