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首页> 外文期刊>The Journal of craniofacial surgery >Evaluation of 45S5 bioactive glass combined as a bone substitute in the reconstruction of critical size calvarial defects in rabbits.
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Evaluation of 45S5 bioactive glass combined as a bone substitute in the reconstruction of critical size calvarial defects in rabbits.

机译:评价45S5生物活性玻璃作为骨替代品在兔临界大小颅盖缺损的重建中的作用。

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摘要

Biomaterial research and tissue engineering have guided new developments in bone replacement. In this study, the osteoconductive and osteoinductive properties of 45S5 Bioglass (Novabone-C/M, Porex Surg., Newnan, GA), granules as a bone replacement material for large calvarial defects were evaluated. Rabbit periosteal cells were expanded in culture and used in vivo. Alkaline-phosphatase assay, collagen type I, and calcium expression were applied to confirm osteoblast phenotype. In the in vivo phase, a 15-mm diameter critical size calvarial defect was created in rabbits (n = 14). The defect was reconstructed according to four treatment groups: autogenous bone (n = 2), Bioglass alone (n = 2), Bioglass + bone (n = 5), Bioglass + periosteal cells (n = 5). The animals were killed 12 weeks after surgery, and the samples were analyzed. Periosteal cells grew successfully in vitro. Because of their fast proliferation and potential to differentiate into osteoblasts, they were an excellent source of cells for bonetissue engineering. The best ossification was seen when autogenous bone was used (79.4% ossified), whereas only 8.2% of the defect in the Bioglass group showed ossification. Addition of bone or cells to the Bioglass increased the area of ossification to 42.7% and 30.2%, respectively. Defects replaced with Bioglass showed varying degrees of inflammatory reaction because of the intense cell-mediated biodegradation process. Based on these findings, the use of Bioglass granules to repair large craniofacial defects cannot be advised.
机译:生物材料研究和组织工程指导了骨替代的新发展。在这项研究中,评估了45S5生物玻璃(Novabone-C / M,Porex Surg。,Newnan,GA)作为大颅盖骨缺损的骨替代材料的骨传导和骨诱导特性。兔骨膜细胞在培养中扩增并用于体内。应用碱性磷酸酶测定,I型胶原和钙表达来确认成骨细胞表型。在体内阶段,兔体内出现了直径为15毫米的临界尺寸颅盖缺损(n = 14)。根据四个治疗组重建缺损:自体骨(n = 2),仅生物玻璃(n = 2),生物玻璃+骨(n = 5),生物玻璃+骨膜细胞(n = 5)。手术后12周将动物处死,并分析样品。骨膜细胞在体外成功生长。由于它们的快速增殖和分化为成骨细胞的潜力,它们是用于骨组织工程的细胞的极好来源。当使用自体骨时,骨化效果最好(79.4%骨化),而Bioglass组中只有8.2%的骨化显示出骨化。向生物玻璃中添加骨骼或细胞可将骨化面积分别增加至42.7%和30.2%。由于强烈的细胞介导的生物降解过程,被生物玻璃替代的缺陷表现出不同程度的炎症反应。基于这些发现,不建议使用生物玻璃颗粒修复大的颅面缺陷。

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