Long Rose G, Bürki Alexander, Zysset Philippe, Eglin David, Grijpma Dirk W, Blanquer Sebastien B G, Hecht Andrew C, Iatridis James C
Leni & Peter W. May Department of Orthopaedics, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Collaborative Research Partner Annulus Fibrosus Rupture Program of AO Foundation, Davos, Switzerland.
Institute for Surgical Technology & Biomechanics, University of Bern, Bern, Switzerland.
Acta Biomater. 2016 Jan;30:116-125. doi: 10.1016/j.actbio.2015.11.015. Epub 2015 Nov 11.
Unrepaired defects in the annulus fibrosus of intervertebral disks are associated with degeneration and persistent back pain. A clinical need exists for a disk repair strategy that can seal annular defects, be easily delivered during surgical procedures, and restore biomechanics with low risk of herniation. Multiple annulus repair strategies were developed using poly(trimethylene carbonate) scaffolds optimized for cell delivery, polyurethane membranes designed to prevent herniation, and fibrin-genipin adhesive tuned to annulus fibrosus shear properties. This three-part study evaluated repair strategies for biomechanical restoration, herniation risk and failure mode in torsion, bending and compression at physiological and hyper-physiological loads using a bovine injury model. Fibrin-genipin hydrogel restored some torsional stiffness, bending ROM and disk height loss, with negligible herniation risk and failure was observed histologically at the fibrin-genipin mid-substance following rigorous loading. Scaffold-based repairs partially restored biomechanics, but had high herniation risk even when stabilized with sutured membranes and failure was observed histologically at the interface between scaffold and fibrin-genipin adhesive. Fibrin-genipin was the simplest annulus fibrosus repair solution evaluated that involved an easily deliverable adhesive that filled irregularly-shaped annular defects and partially restored disk biomechanics with low herniation risk, suggesting further evaluation for disk repair may be warranted.
Lower back pain is the leading cause of global disability and commonly caused by defects and failure of intervertebral disk tissues resulting in herniation and compression of adjacent nerves. Annulus fibrosus repair materials and techniques have not been successful due to the challenging mechanical and chemical microenvironment and the needs to restore biomechanical behaviors and promote healing with negligible herniation risk while being delivered during surgical procedures. This work addressed this challenging biomaterial and clinical problem using novel materials including an adhesive hydrogel, a scaffold capable of cell delivery, and a membrane to prevent herniation. Composite repair strategies were evaluated and optimized in quantitative three-part study that rigorously evaluated disk repair and provided a framework for evaluating alternate repair techniques.
椎间盘纤维环未修复的缺陷与退变和持续性背痛相关。临床上需要一种椎间盘修复策略,该策略能够密封纤维环缺陷,在手术过程中易于实施,并能以低疝出风险恢复生物力学性能。利用针对细胞递送进行优化的聚碳酸三亚甲酯支架、设计用于防止疝出的聚氨酯膜以及根据纤维环剪切特性调整的纤维蛋白-京尼平粘合剂,开发了多种纤维环修复策略。这项三部分研究使用牛损伤模型,评估了在生理和超生理负荷下,扭转、弯曲和压缩时生物力学恢复、疝出风险和失效模式的修复策略。纤维蛋白-京尼平水凝胶恢复了一些扭转刚度、弯曲活动度和椎间盘高度损失,疝出风险可忽略不计,并且在严格加载后,在纤维蛋白-京尼平中间物质处组织学观察到失效。基于支架的修复部分恢复了生物力学性能,但即使使用缝合膜稳定后,疝出风险仍很高,并且在支架与纤维蛋白-京尼平粘合剂的界面处组织学观察到失效。纤维蛋白-京尼平是所评估的最简单的纤维环修复解决方案,它涉及一种易于递送的粘合剂,该粘合剂可填充不规则形状的纤维环缺陷,并以低疝出风险部分恢复椎间盘生物力学性能,这表明可能有必要对椎间盘修复进行进一步评估。
下背痛是全球残疾的主要原因,通常由椎间盘组织的缺陷和失效导致相邻神经的疝出和压迫引起。由于具有挑战性的机械和化学微环境,以及在手术过程中实施时需要恢复生物力学行为并促进愈合且疝出风险可忽略不计,纤维环修复材料和技术一直未取得成功。这项工作使用包括粘性水凝胶、能够进行细胞递送的支架和防止疝出的膜在内的新型材料,解决了这一具有挑战性的生物材料和临床问题。在一项三部分定量研究中评估并优化了复合修复策略,该研究严格评估了椎间盘修复,并为评估替代修复技术提供了框架。