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经等离子体处理的 3D 挤出 PCL 支架表面提高了成骨细胞的亲和性。

Improved osteoblast cell affinity on plasma-modified 3-D extruded PCL scaffolds.

机构信息

Centre for Rapid and Sustainable Product Development, Polytechnic Institute of Leiria, Portugal.

出版信息

Acta Biomater. 2013 Apr;9(4):5997-6005. doi: 10.1016/j.actbio.2012.12.031. Epub 2013 Jan 8.

Abstract

Cellular adhesion and proliferation inside three-dimensional synthetic scaffolds represent a major challenge in tissue engineering. Besides the surface chemistry of the polymers, it is well recognized that scaffold internal architecture, namely pore size/shape and interconnectivity, has a strong effect on the biological response of cells. This study reports for the first time how polycaprolactone (PCL) scaffolds with controlled micro-architecture can be effectively produced via bioextrusion and used to enhance the penetration of plasma deposited species. Low-pressure nitrogen-based coatings were employed to augment cell adhesion and proliferation without altering the mechanical properties of the structures. X-ray photoelectron spectroscopy carried out on different sections of the scaffolds indicates a uniform distribution of nitrogen-containing groups throughout the entire porous structure. In vitro biological assays confirm that plasma deposition sensitively promotes the activity of Saos-2 osteoblast cells, leading to a homogeneous colonization of the PCL scaffolds.

摘要

细胞黏附和增殖在三维合成支架内是组织工程的一大挑战。除了聚合物的表面化学性质外,人们已经认识到支架的内部结构,即孔径/形状和连通性,对细胞的生物学反应有很强的影响。本研究首次报道了如何通过生物挤出有效地生产具有受控微观结构的聚己内酯(PCL)支架,并将其用于增强等离子体沉积物质的渗透。低压基于氮气的涂层被用来提高细胞黏附和增殖,而不改变结构的机械性能。在支架的不同部位进行的 X 射线光电子能谱分析表明,含氮基团在整个多孔结构中均匀分布。体外生物学检测证实,等离子体沉积能灵敏地促进 Saos-2 成骨细胞的活性,从而使 PCL 支架得到均匀的定植。

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