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使用碳酸羟基磷灰石多孔支架重建大鼠股骨临界尺寸节段性缺损。

Reconstruction of critical-size segmental defects in rat femurs using carbonate apatite honeycomb scaffolds.

机构信息

Department of Orthopedic Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Department of Biomaterials, Faculty of Dental Science, Kyushu University, Fukuoka, Japan.

出版信息

J Biomed Mater Res A. 2021 Sep;109(9):1613-1622. doi: 10.1002/jbm.a.37157. Epub 2021 Feb 28.

Abstract

Critical-size segmental defects are formidable challenges in orthopedic surgery. Various scaffolds have been developed to facilitate bone reconstruction within such defects. Many previously studied scaffolds achieved effective outcomes with a combination of high cost, high-risk growth factors or stem cells. Herein, we developed honeycomb scaffolds (HCSs) comprising carbonate apatite (CO Ap) containing 8% carbonate, identical to human bone composition. The CO Ap HCSs were white-columned blocks harboring regularly arranged macropore channels of a size and wall thickness of 156 ± 5 μm and 102 ± 10 μm, respectively. The compressive strengths of the HCSs parallel and perpendicular to the macropore channel direction were 51.0 ± 11.8 and 15.6 ± 2.2 MPa, respectively. The HCSs were grafted into critical-sized segmental defects in rat femurs. The HCSs bore high-load stresses without any observed breakage. Two-weeks post-implantation, calluses formed around the HCSs and immature bone formed in the HCS interior. The calluses and immature bone matured until 8 weeks via endochondral ossification. At 12 weeks post-implantation, large parts of the HCSs were gradually replaced by newly formed bone. The bone reconstruction efficacy of the CO Ap HCSs alone was comparable to that of protein and cell scaffolds, while achieving a lower cost and increased safety.

摘要

临界尺寸节段性缺损是骨科手术中的一大难题。为了促进此类缺损内的骨重建,已经开发出各种支架。许多先前研究的支架通过结合高成本、高风险的生长因子或干细胞实现了有效的结果。在此,我们开发了包含 8%碳酸盐的碳酸磷灰石(CO Ap)的蜂窝状支架(HCS),其组成与人体骨骼相同。CO Ap HCS 是白色柱状块,其中含有规则排列的大孔通道,其大小和壁厚分别为 156±5μm 和 102±10μm。HCS 平行于和垂直于大孔通道方向的抗压强度分别为 51.0±11.8 和 15.6±2.2 MPa。将 HCS 移植到大鼠股骨的临界尺寸节段性缺损中。HCS 承受高负荷的压力而没有观察到任何断裂。植入后 2 周,HCS 周围形成骨痂,HCS 内部形成不成熟的骨。骨痂和不成熟的骨通过软骨内成骨成熟至 8 周。植入后 12 周,HCS 的大部分逐渐被新形成的骨取代。CO Ap HCS 的单独骨重建效果可与蛋白质和细胞支架相媲美,同时降低成本并提高安全性。

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