生物活性玻璃可以潜在地加固较大的骨缺损

N. V. Gestel, J. Arts, D. Hulsen, J. Geurts, Keita Ito, B. Rietbergen
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Materials and Methods Four different BAG/bone graft mixtures were impacted in a cylindrical holder, mechanically tested in confined compression and scanned with micro-CT. From these images, bone graft material and glass were segmented using two different threshold values. The interface between bone and BAG was modelled separately by dilating the glass phase. Micro-Finite-Element (FE) models of the composites were made using a Young9s modulus of 2.5 GPa for bone and 35 GPa for BAG. The Young9s modulus for the interface region was determined by fitting experimental and micro-FE results for the same specimens. (82 μm resolution) CT scans of a 9 mm region of the distal tibia of 3 subjects were used. Micro-FE models of this region were made to determine its stiffness in the original state, with a simulated cortical defect and after a mixture of BAG/bone was modelled in the defect. 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引用次数: 1

摘要

生物活性玻璃(BAG)具有良好的骨导电性、抗菌性和血管生成性,是一种很有前途的骨移植替代品。潜在地,它也可以机械地加固缺陷,从而使其适用于承重缺陷。然而,由BAG/同种异体骨移植混合物组成的重建层的力学性能尚不清楚。因此,本研究的目的是,首先测量不同BAG/骨移植混合物的力学性能,其次,通过显微有限元分析和高分辨率CT扫描,研究这种混合物在多大程度上可以强化胫骨远端缺陷。材料与方法将4种不同的BAG/bone graft混合物嵌塞在一个圆柱形支架中,进行有限压缩力学测试,并用micro-CT扫描。从这些图像中,使用两种不同的阈值对骨移植材料和玻璃进行分割。通过扩展玻璃相分别模拟骨与BAG之间的界面。采用杨氏模量(young - 9s)建立复合材料的有限元模型,骨模量为2.5 GPa,袋模量为35 GPa。通过拟合相同试样的实验和微观有限元结果,确定了界面区域的杨氏模量。(82 μm分辨率)对3例受试者胫骨远端9mm区域进行CT扫描。制作该区域的微观有限元模型,以确定其在原始状态,模拟皮质缺损以及在缺损中模拟BAG/bone混合物后的刚度。结果封闭压缩试验表明,BAG/bone复合材料的模量与BAG的用量有较强的相关性,在116.7±18.2 ~ 654.2±35.2 MPa之间。当界面层刚度为25 MPa时,微观有限元结果可以很好地再现这些测量模量。骨皮质缺损的微观有限元分析表明,骨皮质缺损使胫骨节段刚度降低13±3%。经BAG/bone复合材料处理后,关节刚度恢复到原来的101±6%。实验表明,BAG/bone混合物具有成分相关的刚度,在小梁骨的刚度范围内,可以从微观有限元分析中很好地估计。此外,胫骨微有限元分析表明,这些混合物有可能恢复该部位大骨缺损的刚度。该模型的未来发展可能会具体预测BAG/bone混合物患者的力学行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BIOACTIVE GLASS CAN POTENTIALLY REINFORCE LARGE BONE DEFECTS
Background Bio-Active Glass (BAG) is a promising bone graft substitute for large bone defect reconstruction because of its favourable osteoconductive, antibacterial and angiogenic properties. Potentially, it could also mechanically reinforce the defect, thus making it suitable for load-bearing defects. However, the mechanical properties of the reconstructive layer consisting of BAG/bone allograft mixtures are unknown. The goals of this study therefore were, first, to measure the mechanical properties of different BAG/bone graft mixtures and, second, to investigate to what extent such mixtures could reinforce distal tibial defects using micro-FE analysis and high-resolution CT scans. Materials and Methods Four different BAG/bone graft mixtures were impacted in a cylindrical holder, mechanically tested in confined compression and scanned with micro-CT. From these images, bone graft material and glass were segmented using two different threshold values. The interface between bone and BAG was modelled separately by dilating the glass phase. Micro-Finite-Element (FE) models of the composites were made using a Young9s modulus of 2.5 GPa for bone and 35 GPa for BAG. The Young9s modulus for the interface region was determined by fitting experimental and micro-FE results for the same specimens. (82 μm resolution) CT scans of a 9 mm region of the distal tibia of 3 subjects were used. Micro-FE models of this region were made to determine its stiffness in the original state, with a simulated cortical defect and after a mixture of BAG/bone was modelled in the defect. Results The confined compression tests showed a strong dependence of the modulus of the BAG/bone composite on the amount of BAG, ranging from 116.7 ± 18.2 to 654.2 ± 35.2 MPa. The micro-FE results could well reproduce these measured moduli, when using a stiffness of 25 MPa for the interface layer. The micro-FE analyses of the cortical defect demonstrated that the stiffness of the tibial segment would be reduced by 13 ± 3 % with the defect. Treatment with the BAG/bone composite could restore the stiffness to 101 ± 6 % of its original value. Discussion The experiments demonstrate that BAG/bone mixtures have a composition-dependent stiffness, in the range of that of trabecular bone, which can be well estimated from micro-FE analyses. Furthermore, the tibial micro-FE analyses demonstrate that these mixtures potentially can restore the stiffness of large bone defects at this site. Future development of the model may predict mechanical behaviour of BAG/bone mixtures patient specifically.
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