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A self-organising biomimetic collagen/nano-hydroxyapatite-glycosaminoglycan scaffold for spinal fusion

机译:一种自组织仿生胶原蛋白/纳米羟基磷灰石-糖胺聚糖支架,用于脊柱融合

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摘要

The use of spinal fusion surgery as a treatment for degenerative spinal conditions and chronic back pain is increasing. However, this technique requires use of a bone grafting material to fuse the vertebrae, traditionally autologous bone, which consists of an optimal combination of osteogenic cell precursors, extracellular matrix proteins and mineral components. To date, this remains the ‘gold standard’ material but its supply is limited and is associated with a number of clinical and ethical difficulties; consequently, various combinations of cells with biological scaffold materials have been tested but have failed to achieve fusion rates even comparable to autologous bone. We successfully fabricated a novel collagen-based scaffold using self-organising atelocollagen combined with nano-hydroxyapatite and chondroitin sulphate, cross-linked by microbial transglutaminase. The scaffold was characterised using a range of imaging, chemical composition and thermal analysis techniques. It was found to exhibit appropriate stiffness and suitable pore size for the adhesion, growth and differentiation of MSCs. The low toxicity makes it suitable for clinical application, and its slow degradation profile would enable the scaffold to promote bone growth over an extended period. This material therefore shows promise for clinical use in spinal fusion and other procedures requiring the use of bone grafts.
机译:脊柱融合手术作为退行性脊柱疾病和慢性背痛的治疗方法的使用正在增加。但是,该技术需要使用骨移植材料来融合传统上自体的椎骨,该骨由成骨细胞前体,细胞外基质蛋白和矿物质成分的最佳组合组成。迄今为止,这仍然是“黄金标准”材料,但其供应有限,并伴有许多临床和道德困难;因此,已经测试了细胞与生物支架材料的各种组合,但是未能达到甚至与自体骨相当的融合率。我们成功地使用自组织的端粒胶原蛋白与纳米羟基磷灰石和硫酸软骨素相结合,通过微生物转谷氨酰胺酶交联成功地制备了一种新型的基于胶原蛋白的支架。使用一系列成像,化学成分和热分析技术对支架进行表征。已经发现其对于MSC的粘附,生长和分化表现出合适的刚度和合适的孔径。低毒性使其适合临床应用,并且其缓慢的降解过程将使支架能够在延长的时间内促进骨骼生长。因此,这种材料显示出可用于脊柱融合术和需要使用骨移植物的其他程序的临床应用前景。

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