School of Engineering, University of Vermont, Burlington, VT, USA.
Eur Cell Mater. 2011 Apr 18;21:373-83. doi: 10.22203/ecm.v021a28.
Treatment of damaged intervertebral discs is a significant clinical problem and, despite advances in the repair and replacement of the nucleus pulposus, there are few effective strategies to restore defects in the annulus fibrosus. An annular repair material should meet three specifications: have a modulus similar to the native annulus tissue, support the growth of disc cells, and maintain adhesion to tissue under physiological strain levels. We hypothesized that a genipin crosslinked fibrin gel could meet these requirements. Our mechanical results showed that genipin crosslinked fibrin gels could be created with a modulus in the range of native annular tissue. We also demonstrated that this material is compatible with the in vitro growth of human disc cells, when genipin:fibrin ratios were 0.25:1 or less, although cell proliferation was slower and cell morphology more rounded than for fibrin alone. Finally, lap tests were performed to evaluate adhesion between fibrin gels and pieces of annular tissue. Specimens created without genipin had poor handling properties and readily delaminated, while genipin crosslinked fibrin gels remained adhered to the tissue pieces at strains exceeding physiological levels and failed at 15-30%. This study demonstrated that genipin crosslinked fibrin gels show promise as a gap-filling adhesive biomaterial with tunable material properties, yet the slow cell proliferation suggests this biomaterial may be best suited as a sealant for small annulus fibrosus defects or as an adhesive to augment large annulus repairs. Future studies will evaluate degradation rate, fatigue behaviors, and long-term biocompatibility.
治疗受损的椎间盘是一个重大的临床问题,尽管在修复和替换髓核方面取得了进展,但很少有有效的策略来修复纤维环的缺陷。环形修复材料应满足三个规格:具有与天然纤维环组织相似的模量,支持椎间盘细胞的生长,并在生理应变水平下保持与组织的黏附。我们假设,京尼平交联纤维蛋白凝胶可以满足这些要求。我们的力学结果表明,可以用京尼平交联纤维蛋白凝胶来创建具有天然环形组织范围内模量的凝胶。我们还证明,当京尼平:纤维蛋白比为 0.25:1 或更低时,这种材料与体外人类椎间盘细胞的生长是兼容的,尽管细胞增殖较慢,细胞形态更圆,而不是单独的纤维蛋白。最后,进行了搭接试验来评估纤维蛋白凝胶和环形组织片之间的黏附力。没有京尼平的标本处理性能差,容易分层,而京尼平交联纤维蛋白凝胶在超过生理水平的应变下仍黏附在组织片上,在 15-30%时失效。这项研究表明,京尼平交联纤维蛋白凝胶作为一种具有可调材料性能的填补间隙黏附生物材料具有很大的潜力,但是细胞增殖缓慢表明这种生物材料可能最适合作为小的纤维环缺陷的密封剂,或作为增强大的纤维环修复的黏合剂。未来的研究将评估降解率、疲劳行为和长期生物相容性。