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Biomimetic Mineralization of Woven Bone-Like Nanocomposites: Role of Collagen Cross-Links

机译:仿生的仿骨纳米复合材料的仿生矿化:胶原蛋白交联的作用。

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Ideal biomaterials for bone grafts must be biocompatible, osteoconductive, osteoinductive and have appropriate mechanical properties. For this, the development of synthetic bone substitutes mimicking natural bone is desirable, but this requires controllable mineralization of the collagen matrix. In this study, densified collagen films (up to 100 μm thick) were fabricated by a plastic compression technique and cross-linked using carbodiimide. Then, collagen-hydroxyapatite composites were prepared by using a polymer-induced liquid-precursor (PILP) mineralization proc-ess. Compared to traditional methods that produce only extrafibrillar hydroxyapatite (HA) clusters on the surface of collagen scaffolds, by using the PILP mineralization process, homogeneous intra- and extrafibrillar minerals were achieved on densified collagen films, leading to a similar nanostructure as bone, and a woven microstructure analogous to woven bone. The role of collagen cross-links on mineralization was examined and it was found that the cross-linked coEagen films stimulated the mineralization reaction, which in turn enhanced the mechanical properties (hardness and modulus). The highest value of hardness and elastic modulus was 0.7 ± 0.1 and 9.1 ± 1.4 GPa in the dry state, respectively, which is comparable to that of woven bone. In the wet state, the values were much lower (177 ±31 and 8 ± 3 MPa) due to inherent microporosity in the films, but still comparable to those of woven bone in the same conditions. Mineralization of collagen films with controllable mineral content and good mechanical properties provide a biomimetic route toward the development of bone substitutes for the next generation of biomaterials. This work also provides insight into understanding the role of collagen fibrils on mineralization.
机译:理想的骨移植生物材料必须具有生物相容性,骨传导性,骨诱导性并具有适当的机械性能。为此,需要开发模仿天然骨骼的合成骨骼替代物,但这需要胶原基质的可控矿化作用。在这项研究中,通过塑性压缩技术制备了致密化的胶原膜(厚达100μm),并使用碳二亚胺进行了交联。然后,通过使用聚合物诱导的液体前体(PILP)矿化过程制备了胶原-羟基磷灰石复合材料。与在胶原蛋白支架表面仅产生原纤维状羟基磷灰石(HA)簇的传统方法相比,通过使用PILP矿化工艺,可以在致密化的胶原蛋白膜上获得均匀的原纤维内和原纤维状矿物,从而产生与骨骼相似的纳米结构,并且编织的微观结构类似于编织的骨头。检查了胶原蛋白交联在矿化中的作用,发现交联的CoEagen膜刺激了矿化反应,从而增强了机械性能(硬度和模量)。在干燥状态下,硬度和弹性模量的最高值分别为0.7±0.1 GPa和9.1±1.4 GPa,与编织骨相当。在湿状态下,由于薄膜固有的微孔性,该值要低得多(177±31和8±3 MPa),但仍可与相同条件下的编织骨相媲美。具有可控制的矿物质含量和良好的机械性能的胶原蛋白膜的矿化作用为仿制下一代生物材料的骨替代物提供了一条仿生途径。这项工作还提供了了解胶原蛋白原纤维在矿化中作用的见解。

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