超细纤维
自愈水凝胶
材料科学
脚手架
聚己内酯
静电纺丝
角膜
细胞外基质
组织工程
生物医学工程
再生(生物学)
纳米纤维
纳米技术
复合材料
化学
聚合物
高分子化学
细胞生物学
光学
物理
生物
医学
生物化学
作者
Sina Sharifi,Hannah Sharifi
标识
DOI:10.1021/acsabm.2c00751
摘要
Despite rigorous investigations, the hydrogels currently available to replace damaged tissues, such as the cornea, cannot fulfill mechanical and structural requirements and, more importantly, cannot be sutured into host tissues due to the lack of hierarchical structures to dissipate exerted stress. In this report, solution electrospinning of polycaprolactone (PCL), protein-based hydrogel perfusion, and layer-by-layer stacking are used to generate a hydrogel–microfiber composite with varying PCL fiber diameters and hydrogel concentrations. Integrating PCL microfibers into the hydrogel synergistically improves the mechanical properties and suturability of the construct up to 10-fold and 50-fold, respectively, compared to the hydrogel and microfiber scaffolds alone, approaching those of the corneal tissue. Human corneal cells cultured on composites are viable and can spread, proliferate, and retain phenotypic characteristics. Moreover, corneal stromal cells migrate into the scaffold, degrade it, and regenerate the extracellular matrix. The current hydrogel reinforcing system paves the way for producing suturable and, therefore, transplantable tissue constructs with desired mechanical properties.
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