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3D-printed scaffold combined to 2D osteoinductive coatings to repair a critical-size mandibular bone defect

机译:3D印刷的支架组合到2D骨诱导涂层修复临界颌骨骨缺损

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摘要

The reconstruction of large bone defects (12 cm3) remains a challenge for clinicians. We developed a new critical-size mandibular bone defect model on a minipig, close to human clinical issues. We analyzed the bone reconstruction obtained by a 3D-printed scaffold made of clinical-grade polylactic acid (PLA), coated with a polyelectrolyte film delivering an osteogenic bioactive molecule (BMP-2). We compared the results (computed tomography scans, microcomputed tomography scans, histology) to the gold standard solution, bone autograft. We demonstrated that the dose of BMP-2 delivered from the scaffold significantly influenced the amount of regenerated bone and the repair kinetics, with a clear BMP-2 dose-dependence. Bone was homogeneously formed inside the scaffold without ectopic bone formation. The bone repair was as good as for the bone autograft. The BMP-2 doses applied in our study were reduced 20- to 75-fold compared to the commercial collagen sponges used in the current clinical applications, without any adverse effects. Three-dimensional printed PLA scaffolds loaded with reduced doses of BMP-2 may be a safe and simple solution for large bone defects faced in the clinic.
机译:大骨缺陷的重建(12cm3)对临床医生来说仍然是挑战。我们在Minipig上开发了一种新的临界下颌骨缺损模型,接近人类临床问题。我们分析了由由临床级聚乳酸(PLA)制成的3D印刷支架获得的骨重建,涂覆有递送骨质发生的生物活性分子(BMP-2)的聚电解质膜。将结果(计算机断层扫描扫描,微锁定断层扫描扫描,组织学)进行了比较到金标准溶液,骨自体移植物。我们证明,从支架中递送的BMP-2剂量显着影响再生骨和修复动力学的量,透明BMP-2剂量依赖性。在没有异位骨形成的支架内均匀地形成骨骼。骨骼修复与骨自体移植一样好。与目前临床应用中使用的商业胶原海绵相比,我们研究中施用的BMP-2剂量减少了20至75倍,而没有任何不良影响。装载有减少剂量的BMP-2的三维印刷PLA支架可能是临床中面临的大骨缺陷的安全和简单的解决方案。

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