Jiang Yanan, Liao Haixia, Yan Liwei, Jiang Shengxi, Zheng Yujia, Zhang Xin, Wang Kefeng, Wang Qiguang, Han Lu, Lu Xiong
Department of General Surgery, The Third People's Hospital of Chengdu, The Affiliated Hospital of Southwest Jiaotong University, College of Medicine, Southwest Jiaotong University, Chengdu, Sichuan 610031, China.
Institute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu, Sichuan 610031, China.
ACS Appl Mater Interfaces. 2023 Oct 11;15(40):46598-46612. doi: 10.1021/acsami.3c06706. Epub 2023 Sep 28.
The treatment of osteoarthritis (OA)-related cartilage defects is a great clinical challenge due to the complex pathogenesis of OA and poor self-repair ability of cartilage tissue. Combining local and long-term anti-inflammatory therapies to promote cartilage repair is an effective method to treat OA. In this study, a zinc-organic framework-incorporated extracellular matrix (ECM)-mimicking hydrogel platform was constructed for the inflammatory microenvironment-responsive delivery of neobavaisoflavone (NBIF) to promote cartilage regeneration in OA. The NBIF was encapsulated in situ in zeolitic imidazolate frameworks (ZIF-8 MOFs). The NBIF@ZIF-8 MOFs were decorated with polydopamine and incorporated into a methacrylate gelatin/hyaluronic acid hybrid network to form the NBIF@ZIF-8/PHG hydrogel. The hydrogel featured excellent cell/tissue affinity, providing a favorable microenvironment for recruiting cells and cytokines to the defect sites. The hydrogel enabled the on-demand NBIF released in response to a weakly acidic microenvironment at the injured joint site to resolve inflammatory responses during the early stages of OA. Consequently, the cooperativity of the loaded NBIF and hydrogel synergistically modulated the immune response and assisted in cartilage defect repair. In summary, the NBIF@ZIF-8/PHG hydrogel delivery platform represents an effective treatment strategy for OA-related cartilage defects and may attract attentions for applications in other inflammatory diseases.
由于骨关节炎(OA)发病机制复杂且软骨组织自我修复能力差,OA相关软骨缺损的治疗是一项重大的临床挑战。结合局部和长期抗炎疗法以促进软骨修复是治疗OA的有效方法。在本研究中,构建了一种包含锌有机框架的细胞外基质(ECM)模拟水凝胶平台,用于对新补骨脂异黄酮(NBIF)进行炎症微环境响应递送,以促进OA中的软骨再生。NBIF原位包封于沸石咪唑酯骨架(ZIF-8金属有机框架)中。将NBIF@ZIF-8金属有机框架用聚多巴胺修饰,并掺入甲基丙烯酸明胶/透明质酸混合网络中,形成NBIF@ZIF-8/PHG水凝胶。该水凝胶具有优异的细胞/组织亲和力,为将细胞和细胞因子募集到缺损部位提供了有利的微环境。该水凝胶能够响应受损关节部位的弱酸性微环境按需释放NBIF,以解决OA早期阶段的炎症反应。因此,负载的NBIF与水凝胶的协同作用可协同调节免疫反应并协助软骨缺损修复。总之,NBIF@ZIF-8/PHG水凝胶递送平台代表了一种治疗OA相关软骨缺损的有效策略,可能会吸引在其他炎症性疾病中的应用关注。