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Collagen self-assembly on orthopedic magnesium biomaterials surface and subsequent bone cell attachment

机译:骨科镁生物材料表面的胶原蛋白自组装及随后的骨细胞附着

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Collagen monomer can form different structures on Mg biomaterial depending on the initial collagen monomer concentration. pH in the solution, assembly time, electrolytes, and the material surface roughness. The pH can change the electrostatic properties of collagen and final collagen structure. With the increase of collagen assembly time, small fibrils merge with adjacent fibrils forming thicker fibers. Materials with rough surface show stronger collagen adsorption ability. Initial cell attachment on RS of materials decreased independent of the composition of materials. AZ31 surface roughness and collagen structure did not affect cell proliferation for up to 7 days. Materials with high degradation rate may not change collagen assembly structure but can affect osteoblast cell proliferation. In the future study, the combined effect of those factors such as pH. material surface roughness, assembly time and electrolytes on collagen assembly, mineralization and bone cell interaction should be addressed.
机译:胶原蛋白单体可以根据初始胶原蛋白单体的浓度在镁生物材料上形成不同的结构。溶液中的pH值,组装时间,电解质和材料表面粗糙度。 pH可以改变胶原蛋白的静电特性和最终的胶原蛋白结构。随着胶原蛋白组装时间的增加,小的原纤维与相邻的原纤维合并形成较粗的纤维。具有粗糙表面的材料显示出较强的胶原蛋白吸附能力。材料在RS上的初始细胞附着减少,与材料的成分无关。 AZ31表面粗糙度和胶原蛋白结构在长达7天的时间内均未影响细胞增殖。具有高降解率的材料可能不会改变胶原蛋白的组装结构,但会影响成骨细胞的增殖。在将来的研究中,将综合考虑这些因素(例如pH)的影响。材料表面粗糙度,组装时间和电解质对胶原蛋白组装,矿化和骨细胞相互作用的影响。

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