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Evaluation of BMP-2 and VEGF loaded 3D printed hydroxyapatite composite scaffolds with enhanced osteogenic capacity in vitro and in vivo

机译:BMP-2和VEGF负载3D印花羟基磷灰石复合支架的评价,具有增强的成骨容量和体内

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摘要

Large-sized bone defect repair is a challenging task in orthopedic surgery. Porous scaffolds with controlled release of growth factors have been investigated for many years. In this study, a hydroxyapatite composite scaffold was prepared by 3D printing at low temperature and coating with layer-by-layer (LBL) assembly. Bone morphogenic protein-2 (BMP-2) and vascular endothelial growth factors (VEGF) were loaded into the composite scaffolds. The release of dual growth factors was analyzed in vitro. The cell growth and osteogenic differentiation were assessed by culturing MC3T3-E1 cells onto the scaffolds. In an established rabbit model of critical-sized calvarial defect (15 mm in diameter), the osteogenic and angiogenic properties after implantation of scaffolds were evaluated by micro-computed tomography (micro-CT) and stained sections. Our results showed that the scaffolds possessed well-designed porous structure and could release two growth factors in a sustained way. The micro-CT analysis showed that the scaffolds with BMP-2/VEGF could accelerate new bone formation. Findings of immunochemical staining of collagen type I and lectin indicated that better osteogenic and angiogenic properties induced by BMP-2 and VEGF. These results suggested that the novel composite scaffolds combined with BMP-2/VEGF had both osteogenic and angiogenic abilities which could enhance new bone formation with good quality. Thus, the combination of 3D printed scaffolds loaded with BMP-2/VEGF might provide a potential solution for bone repair and regeneration in clinical applications.
机译:大型骨缺损修复是骨科手术中有挑战性的任务。多年来已经研究了具有受控生长因子的多孔支架。在该研究中,通过在低温下在低温和涂覆层(LBL)组件的涂覆时制备羟基磷灰石复合支架。将骨形态发生蛋白-2(BMP-2)和血管内皮生长因子(VEGF)加载到复合支架中。在体外分析了双生长因子的释放。通过将MC3T3-E1细胞培养到支架上来评估细胞生长和成骨分化。在临界大小的颅脑缺损(直径为15mm)的建立的兔模型中,通过微计算机断层扫描(微型CT)和染色部分评估支架后植入支架后的成骨和血管生成性能。我们的研究结果表明,支架具有精心设计的多孔结构,可以以持续的方式释放两种生长因子。微型CT分析表明,具有BMP-2 / VEGF的支架可以加速新的骨形成。胶原I型和凝集素的免疫化素染色的结果表明,BMP-2和VEGF诱导的更好的骨质骨质和血管生成特性。这些结果表明,新型复合支架与BMP-2 / VEGF结合的血管发生和血管生成能力既可以提高质量良好的新骨形成。因此,加载的BMP-2 / VEGF的3D印刷支架的组合可以在临床应用中提供骨修复和再生的潜在解决方案。

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