Intra-articular targeted delivery of nanomaterials for the treatment of osteoarthritis: focusing on cell signaling pathway mechanisms

药物输送 靶向给药 再生医学 纳米技术 化学 细胞 药品 纳米毒理学 信号转导 纳米材料 医学 输送系统 毒性 癌症研究 药理学 纳米医学 骨关节炎 毒品携带者 靶向治疗 细胞生物学 药物毒性 药物发现
作者
Bo Gu,Jingjing Qi,Xin Li,Shuya Wang,Yuanqiang Ma,Jiantao Zhang,Tianwen Ma
出处
期刊:Expert Opinion on Drug Delivery [Taylor & Francis]
卷期号:23 (4): 643-659 被引量:1
标识
DOI:10.1080/17425247.2025.2600610
摘要

INTRODUCTION: This review summarizes the application of nanomaterial-mediated intra-articular targeted drug delivery systems in the treatment of osteoarthritis (OA) and their regulatory mechanisms on key cellular signaling pathways. Studies have shown that novel nanocarriers can effectively load, deliver, and controllably release therapeutic agents, significantly enhancing drug bioavailability and reducing systemic toxicity. By precisely modulating signaling pathways, nanomaterials (NM) can effectively suppress inflammatory responses, alleviate oxidative stress, promote chondrocyte anabolism, delay extracellular matrix degradation, and regulate programmed cell death. This study highlights the potential of NM as a multi-target, synergistic therapeutic strategy for OA intervention, providing a theoretical and experimental basis for the development of next-generation precision therapies for OA. AREAS COVERED: This paper reviews the research progress of nano-drug delivery technology in the treatment of joint diseases, focusing on the potential mechanisms of targeted drug delivery and retention, promoting regeneration and repair, and realizing anti-inflammatory and antioxidant effects. We identified relevant literature through PubMed and Web of Science, focusing on studies published over the past five years. EXPERT OPINION: Nanomaterials for osteoarthritis treatment are evolving from passive drug carriers to intelligently responsive, targeted multifunctional systems capable of personalized, proactive, and regenerative therapy, overcoming current limitations in toxicity and delivery precision.
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