Singh Juhi, Kadir Jacob C, Orlando Jason D, Sydlik Stefanie A
Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, PA, 15213, USA.
Biomater Sci. 2025 Jul 22;13(15):4211-4231. doi: 10.1039/d5bm00296f.
Articular cartilage defects are common, and the progressive deterioration of cartilage frequently results in the onset of osteoarthritis. However, the intrinsic regenerative capacity of articular cartilage is minimal. Synthetic therapeutic solutions for treating cartilage damage are being developed. However, current scaffolds and hydrogels employed in cartilage tissue engineering face limitations in promoting cellular activity and providing sufficient load-bearing strength. This is primarily due to suboptimal crosslinking methods for the synthetic scaffolds composed of natural proteins and glycosaminoglycans (GAGs). Synthetic polypeptides, owing to their customizable reactive functional groups, present an exciting opportunity to enhance crosslinking through both physical and chemical approaches. This study introduces a strategy for the development of injectable, shape-adaptive double network hydrogels that closely replicate the structural integrity and mechanical properties of native cartilage. These hydrogels are composed of photocrosslinkable GAGs, specifically methacrylated chondroitin sulfate A (CSMA), combined with a synthetic polypeptide, poly(L-lysine) (PLL). By varying the degree of polymerization (DP) of PLL and weight percentage of PLL in the composition, the hydrogels can be optimized for desired material properties. Varying DP of PLLs varies the molecular weight between crosslinks, thus leading to tunable rigidity (yield strength, ultimate compression strength, storage modulus) and toughness. We further this tunability through the integration of photoresponsive components, enabling controlled, non-invasive post-injection modifications. Initial testing indicates that these double network hydrogels exhibit significantly improved mechanical strength compared to hydrogels formed solely from CSMA, positioning them as strong candidates for minimally invasive cartilage defect repair. This innovative method offers the potential to accelerate recovery, restore joint function, and improve patients' overall quality of life.
关节软骨缺损很常见,软骨的渐进性退化常常导致骨关节炎的发作。然而,关节软骨的内在再生能力极小。目前正在开发用于治疗软骨损伤的合成治疗方案。然而,当前软骨组织工程中使用的支架和水凝胶在促进细胞活性和提供足够的承重强度方面面临局限性。这主要是由于由天然蛋白质和糖胺聚糖(GAGs)组成的合成支架的交联方法欠佳。合成多肽由于其可定制的反应性功能基团,为通过物理和化学方法增强交联提供了一个令人兴奋的机会。本研究介绍了一种开发可注射、形状适应性双网络水凝胶的策略,该水凝胶能紧密复制天然软骨的结构完整性和力学性能。这些水凝胶由可光交联的GAGs(特别是甲基丙烯酸化硫酸软骨素A,CSMA)与合成多肽聚(L - 赖氨酸)(PLL)组合而成。通过改变PLL的聚合度(DP)和组合物中PLL的重量百分比,可以针对所需的材料性能优化水凝胶。改变PLL的DP会改变交联之间的分子量,从而导致可调节的刚性(屈服强度、极限压缩强度、储能模量)和韧性。我们通过整合光响应成分进一步实现这种可调性,实现可控的、非侵入性的注射后修饰。初步测试表明,与仅由CSMA形成的水凝胶相比,这些双网络水凝胶的机械强度有显著提高,使其成为微创软骨缺损修复的有力候选材料。这种创新方法有可能加速恢复、恢复关节功能并改善患者的整体生活质量。