Borem Ryan, Madeline Allison, Walters Joshua, Mayo Henry, Gill Sanjitpal, Mercuri Jeremy
The Laboratory of Orthopaedic Tissue Regeneration & Orthobiologics, Department of Bioengineering, Clemson University, Clemson, SC, USA.
The Laboratory of Orthopaedic Tissue Regeneration & Orthobiologics, Department of Bioengineering, Clemson University, Clemson, SC, USA; Department of Orthopaedic Surgery, Medical Group of the Carolinas-Pelham, Spartanburg Regional Healthcare System, Greer, SC, USA.
Acta Biomater. 2017 Aug;58:254-268. doi: 10.1016/j.actbio.2017.06.006. Epub 2017 Jun 3.
Annulus fibrosus (AF) damage commonly occurs due to intervertebral disc (IVD) degeneration/herniation. The dynamic mechanical role of the AF is essential for proper IVD function and thus it is imperative that biomaterials developed to repair the AF withstand the mechanical rigors of the native tissue. Furthermore, these biomaterials must resist accelerated degradation within the proteolytic environment of degenerate IVDs while supporting integration with host tissue. We have previously reported a novel approach for developing collagen-based, multi-laminate AF repair patches (AFRPs) that mimic the angle-ply architecture and basic tensile properties of the human AF. Herein, we further evaluate AFRPs for their: tensile fatigue and impact burst strength, IVD attachment strength, and contribution to functional spinal unit (FSU) kinematics following IVD repair. Additionally, AFRP resistance to collagenase degradation and cytocompatibility were assessed following chemical crosslinking. In summary, AFRPs demonstrated enhanced durability at high applied stress amplitudes compared to human AF and withstood radially-directed biaxial stresses commonly borne by the native tissue prior to failure/detachment from IVDs. Moreover, FSUs repaired with AFRPs and nucleus pulposus (NP) surrogates had their axial kinematic parameters restored to intact levels. Finally, carbodiimide crosslinked AFRPs resisted accelerated collagenase digestion without detrimentally effecting AFRP tensile properties or cytocompatibility. Taken together, AFRPs demonstrate the mechanical robustness and enzymatic stability required for implantation into the damaged/degenerate IVD while supporting AF cell infiltration and viability.
The quality of life for millions of individuals globally is detrimentally impacted by IVD degeneration and herniation. These pathologies often result in the structural demise of IVD tissue, particularly the annulus fibrosus (AF). Biomaterials developed for AF repair have yet to demonstrate the mechanical strength and durability required for utilization in the spine. Herein, we demonstrate the development of an angle-ply AF repair patch (AFRP) that can resist the application of physiologically relevant stresses without failure and which contributes to the restoration of functional spinal unit axial kinematics following repair. Furthermore, we show that this biomaterial can resist accelerated degradation in a simulated degenerate environment and supports AF cell viability.
纤维环(AF)损伤通常由于椎间盘(IVD)退变/突出而发生。AF的动态力学作用对于IVD的正常功能至关重要,因此开发用于修复AF的生物材料必须能够承受天然组织的机械应力。此外,这些生物材料必须在退变IVD的蛋白水解环境中抵抗加速降解,同时支持与宿主组织的整合。我们之前报道了一种开发基于胶原蛋白的多层AF修复补片(AFRP)的新方法,该补片模仿了人类AF的角向铺层结构和基本拉伸性能。在此,我们进一步评估AFRP的:拉伸疲劳和冲击破裂强度、IVD附着强度以及在IVD修复后对功能脊柱单元(FSU)运动学的贡献。此外,在化学交联后评估AFRP对胶原酶降解的抗性和细胞相容性。总之,与人类AF相比,AFRP在高施加应力幅度下表现出更高的耐久性,并且在从IVD失效/脱离之前能够承受天然组织通常承受的径向双轴应力。此外,用AFRP和髓核(NP)替代物修复的FSU的轴向运动学参数恢复到完整水平。最后,碳二亚胺交联的AFRP抵抗加速的胶原酶消化,而不会对AFRP的拉伸性能或细胞相容性产生不利影响。综上所述,AFRP展示了植入受损/退变IVD所需的机械稳健性和酶稳定性,同时支持AF细胞浸润和活力。
全球数百万人的生活质量受到IVD退变和突出的不利影响。这些病理情况通常导致IVD组织的结构破坏,特别是纤维环(AF)。为AF修复开发的生物材料尚未证明在脊柱中使用所需的机械强度和耐久性。在此,我们展示了一种角向铺层AF修复补片(AFRP)的开发,该补片能够抵抗生理相关应力的施加而不失效,并且有助于修复后功能脊柱单元轴向运动学的恢复。此外,我们表明这种生物材料能够在模拟退变环境中抵抗加速降解并支持AF细胞活力。