类风湿性关节炎
药物输送
医学
药品
关节内
药理学
化学
内科学
病理
骨关节炎
替代医学
有机化学
作者
Mong-Hsiu Song,Yunxiang Yan,Bohan Chen,Liming Gong,Liqing Chen,Jing Feng,Mingfeng Han,Chenfei Liu,Congcong Xiao,Mingji Jin,Zhonggao Gao,Wei Huang
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2025-08-27
卷期号:17 (9): 1118-1118
被引量:6
标识
DOI:10.3390/pharmaceutics17091118
摘要
Rheumatoid arthritis (RA) is a systemic autoimmune disorder characterized by chronic inflammation of the synovial membrane, leading to synovial hyperplasia, infiltration of immune cells, and subsequent cartilage and bone erosion. This progressive joint pathology results in persistent pain and functional impairment. Currently, convenient oral traditional disease-modifying anti-rheumatic drugs (DMARDs) are available, and increasingly precise biologic agents and targeted synthetic DMARDs (tsDMARDs) have been developed, offering promising therapeutic options. However, systemic administration generally fails to achieve therapeutic drug concentrations in the joints owing to poor biodistribution and dose-limiting systemic toxicity. Intra-articular (IA) administration has demonstrated promising potential in addressing these challenges. Among the various strategies employed for IA administration, hydrogels have gained significant attention due to their tunable mechanical properties, biocompatibility, and controlled release capabilities. These unique properties enable hydrogel-based IA delivery systems to simultaneously modulate the inflammatory microenvironment and protect cartilage tissue. This review comprehensively summarizes the histopathological changes and associated cellular and molecular events in RA, while also highlighting the design principles of hydrogels and advanced strategies for hydrogel-based IA administration. By addressing the limitations of conventional treatments, hydrogel-based IA injection holds significant promise for improving RA treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI