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Material properties in unconfined compression of human nucleus pulposus injectable hyaluronic acid-based hydrogels and tissue engineering scaffolds

机译:人体髓核可注射的透明质酸基水凝胶和组织工程支架无限制压缩的材料特性

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摘要

Surgical treatment for lower back pain related to degenerative disc disease commonly includes discectomy and spinal fusion. While surgical intervention may provide short-term pain relief, it results in altered biomechanics of the spine and may lead to further degenerative changes in adjacent segments. One non-fusion technique currently being investigated is nucleus pulposus (NP) support via either an injectable hydrogel or tissue engineered construct. A major challenge for either approach is to mimic the mechanical properties of native NP. Here we adopt an unconfined compression testing configuration to assess toe-region and linear-region modulus and Poisson’s ratio, key functional parameters for NP replacement. Human NP, experimental biocompatible hydrogel formulations composed of hyaluronic acid (HA), PEG-g-chitosan, and gelatin, and conventional alginate and agarose gels were investigated as injectable NP replacements or tissue engineering scaffolds. Testing consisted of a stress-relaxation experiment of 5% strain increments followed by 5-min relaxation periods to a total of 25% strain. Human NP had an average linear-region modulus of 5.39 ± 2.56 kPa and a Poisson’s ratio of 0.62 ± 0.15. The modulus and Poisson’s ratio are important parameters for evaluating the design of implant materials and scaffolds. The synthetic HA-based hydrogels approximated NP well and may serve as suitable NP implant materials.
机译:与变性椎间盘疾病相关的下背部疼痛的外科治疗通常包括椎间盘切除术和脊柱融合术。尽管外科手术可以短期缓解疼痛,但会导致脊柱生物力学改变,并可能导致相邻节段的进一步退行性改变。当前正在研究的一种非融合技术是通过可注射水凝胶或组织工程构建体的髓核(NP)支持。两种方法的主要挑战是模拟天然NP的机械性能。在这里,我们采用无限制的压缩测试配置来评估趾区和线性区的模量以及泊松比,这是NP替代的关键功能参数。研究了人类NP,由透明质酸(HA),PEG-g-壳聚糖和明胶组成的实验性生物相容性水凝胶制剂,以及常规的藻酸盐和琼脂糖凝胶作为可注射的NP替代物或组织工程支架。测试包括以5%的应变增量进行应力松弛实验,然后进行5分钟的松弛时间以达到25%的应变。人类NP的平均线性区域模量为5.39±2.56 kPa,泊松比为0.62±0.15。模量和泊松比是评估植入物材料和支架设计的重要参数。合成的基于HA的水凝胶非常接近NP,可以用作合适的NP植入材料。

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