Wang Siya, Zhai Yu, Liu Minghan, Cheng Zhuo, Zhang Jiayi, Zhang Haifeng, Wang Haibing, Hu Yan, Li Changqing, Luo Zhong
College of Bioengineering, Chongqing University, Chongqing 400044, China.
Department of Orthopedic Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Acta Biomater. 2025 Jul 15. doi: 10.1016/j.actbio.2025.07.033.
Intervertebral disc degeneration (IDD) is a major cause of low back pain and spinal diseases, characterized by aberrant oxidative stress and inflammation in the affected disc tissues. Celecoxib is the most commonly used drug to treat IDD with significant anti-oxidation and anti-inflammation capacity. However, the poor blood supply of the intervertebral disc (IVD) restricts the bioavailability of celecoxib following oral administration. To address this issue, a hydrogel-based drug delivery system (HPPC) was developed by modifying hyaluronic acid (HA) with adipic dihydrazide (ADH) and 3-aminobenzeneboronic acid (PBA), aldehyde-functionalized polyethylene glycol (PEG-FBA), and celecoxib-loaded polydopamine (CLX@PDA) nanoparticles via dynamic Schiff base and boronic ester ligation. HPPC readily responds to high levels of reactive oxygen species (ROS) and low pH of the degenerated IVD microenvironment, enabling on-demand and sustainable celecoxib release. HPPC also possesses good mechanical properties, degradability, injectability and biocompatibility. In vivo and in vitro studies show the HPPC effectively reduces inflammation and oxidative stress in nucleus pulposus cells (NPCs) and restores disc function in IDD rats by regulating the COX2-PGE2-NFκB and TNFα-P38-MAPK pathways. This hydrogel drug delivery system offers a strategy for improving IDD treatment. STATEMENT OF SIGNIFICANCE: A dynamic hydrogel based on biopolymeric components (HPPC) is developed for treating intervertebral disc degeneration (IDD), which could respond to biochemical cues in degenerated discs to trigger on-demand celecoxib release. The HPPC treatment enables cooperative regulation of NF-κB and MAPK signaling activities in nucleus pulposus cells, which effectively reduces locogerional inflammation and oxidative stress to restore disc structure and function. This study offers an approach for improving IDD treatment in the clinic.
椎间盘退变(IDD)是腰痛和脊柱疾病的主要原因,其特征是受影响的椎间盘组织中存在异常的氧化应激和炎症。塞来昔布是治疗IDD最常用的药物,具有显著的抗氧化和抗炎能力。然而,椎间盘(IVD)的血液供应不足限制了口服给药后塞来昔布的生物利用度。为了解决这个问题,通过己二酸二酰肼(ADH)、3-氨基苯硼酸(PBA)、醛基功能化聚乙二醇(PEG-FBA)和载有塞来昔布的聚多巴胺(CLX@PDA)纳米颗粒对透明质酸(HA)进行修饰,开发了一种基于水凝胶的药物递送系统(HPPC),通过动态席夫碱和硼酸酯连接。HPPC能够对退变的IVD微环境中的高水平活性氧(ROS)和低pH值做出反应,实现塞来昔布的按需和持续释放。HPPC还具有良好的机械性能、可降解性、可注射性和生物相容性。体内和体外研究表明,HPPC通过调节COX2-PGE2-NFκB和TNFα-P38-MAPK途径,有效减轻髓核细胞(NPCs)中的炎症和氧化应激,并恢复IDD大鼠的椎间盘功能。这种水凝胶药物递送系统为改善IDD治疗提供了一种策略。重要意义声明:开发了一种基于生物聚合物成分的动态水凝胶(HPPC)用于治疗椎间盘退变(IDD),它可以对退变椎间盘中的生化信号做出反应,触发塞来昔布的按需释放。HPPC治疗能够协同调节髓核细胞中NF-κB和MAPK信号活性,有效减轻局部炎症和氧化应激,恢复椎间盘结构和功能。本研究为临床改善IDD治疗提供了一种方法。