Advanced Polymer Materials Group, Faculty of Applied Chemistry and Materials Science, University POLITEHNICA of Bucharest, 1-7 Gheorghe Polizu Street, Sector 1, 011061, Bucharest, Romania.
Faculty of Medical Engineering, University POLITEHNICA of Bucharest, 1-7 Gheorghe Polizu Street, Sector 1, 011061, Bucharest, Romania.
J Mater Sci Mater Med. 2017 Aug 31;28(10):153. doi: 10.1007/s10856-017-5966-8.
Nano-apatite and gelatin-alginate hydrogel microparticles have been prepared by a one-step synthesis combined with electrostatic bead generation, for the reconstruction of bone defects. Based on the analysis of bone composition, architecture and embryonic intramembranous ossification, a bio-inspired fabrication has been developed. Accordingly, the mineral phase has been in situ synthesized, calcifying the hydrogel matrix while the latter was crosslinked, finally generating microparticles that can assemble into a bone defect to ensure interconnected pores. Although nano-apatite-biopolymer composites have been widely investigated, microstructural optimization to provide improved distribution and stability of the mineral is rarely achieved. The optimization of the developed method progressively resulted in two types of formulations (15P and 7.5P), with 15 and 7.5 (wt%) phosphate content in the initial precursor. The osteolytic potential was investigated using differentiated macrophages. A commercially available calcium phosphate bone graft substitute (Eurocer 400) was incorporated into the hydrogel, and the obtained composites were in vitro tested for comparison. The cytocompatibility of the microparticles was studied with mouse osteoblast-like cell line MC3T3-E1. Results indicated the best in vitro performance have been obtained for the sample loaded with 7.5P. Preliminary evaluation of biocompatibility into a critical size (3 mm) defect in rabbits showed that 7.5P nanocomposite is associated with newly formed bone in the proximity of the microparticles, after 28 days.
纳米磷灰石和明胶-海藻酸钠水凝胶微球已通过一步合成与静电珠生成相结合制备,用于重建骨缺损。基于对骨组成、结构和胚胎膜内成骨的分析,开发了一种仿生制造方法。相应地,在水凝胶基质交联的同时原位合成了矿物相,最终生成可以组装成骨缺损以确保相互连通的孔的微球。尽管已经广泛研究了纳米磷灰石-生物聚合物复合材料,但很少实现微观结构的优化以提供改善的矿物质分布和稳定性。开发方法的优化逐渐产生了两种配方(15P 和 7.5P),初始前体中的磷酸盐含量分别为 15 和 7.5(wt%)。使用分化的巨噬细胞研究了溶骨性潜力。将市售的钙磷酸盐骨移植替代物(Eurocer 400)掺入水凝胶中,并对获得的复合材料进行体外测试进行比较。用小鼠成骨样细胞系 MC3T3-E1 研究了微球的细胞相容性。结果表明,负载 7.5P 的样品表现出最佳的体外性能。在兔子的临界尺寸(3mm)缺陷中进行的初步生物相容性评估表明,在 28 天后,7.5P 纳米复合材料与微球附近的新形成的骨相关。