化学
自愈水凝胶
明胶
软骨发生
肿瘤微环境
胶粘剂
生物医学工程
巨噬细胞极化
纳米复合材料
细胞外基质
药物输送
再生(生物学)
生物物理学
极限抗拉强度
纳米技术
间充质干细胞
生物相容性
软骨
控制释放
透明质酸
细胞迁移
细胞生物学
细胞内
巨噬细胞
细胞粘附
细胞
作者
Shaowei Zheng,Jiang Guo,Nianwu Li,Yang-Chi-Dung Lin,Peng Zhang,Wenqiang Li,Xintao Zhang
摘要
Abstract Natural functional regeneration of the tendon–bone interface in rotator cuff repair surgery remains a major challenge and requires the development of innovative therapeutic strategies. Hydrogels with biomechanical adaptability and regenerative microenvironment modulation are promising candidates for treating such injuries. In this study, an ROS-responsive adhesive nanocomposite hydrogel (TPGA@CZB) was developed to enhance tendon-to-bone interface repair by on-demand drug release to modulate the inflammatory microenvironment and promote cell differentiation. The hydrogel consisted of baicalin (Ba)-loaded Cu-Zn bimetallic-organic framework (CZB), N-[tris(hydroxymethyl) methyl] acrylamide (THMA), poly(ethylene glycol) diacrylate (PEGDA) and phenylboronic acid modified methacrylated gelatin (GelMA-CPBA). Owing to its multi-crosslinked structure, TPGA@CZB exhibits excellent adhesive properties (lap shear strength reaching 110.90 ± 15.38 kPa) and mechanical adaptability (compressive strain exceeding 80% and tensile strain of 196.24 ± 3.87%). Additionally, TPGA@CZB demonstrated favorable ROS-responsive release characteristics, with the cumulative release of Ba in H2O2 solution (63.90 ± 4.76% at 96 h) being significantly higher than that in PBS solution (48.39 ± 1.56% at 96 h). Furthermore, cellular experiments revealed that TPGA@CZB effectively scavenged intracellular ROS, inhibits the NF-κB signaling pathway, regulates macrophage polarization and promotes osteogenic differentiation and chondrogenesis. In vivo studies confirmed that TPGA@CZB treatment effectively optimized collagen remodeling, enhanced osteogenesis and cartilage formation, as well as modulated the inflammatory microenvironment at the injury site. In conclusion, this nanocomposite hydrogel integrates “mechanical support—controlled drug release—microenvironment regulation” into a single platform, offering a promising multifunctional therapeutic strategy for enhancing tendon–bone interface regeneration.
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