透明质酸
骨关节炎
体内
微球
药物输送
双氯芬酸钠
微流控
材料科学
体外
药品
荧光寿命成像显微镜
靶向给药
纳米技术
关节软骨
生物医学工程
荧光
临床前影像学
软骨
控制释放
毒品携带者
化学
生物相容性材料
分子成像
从长凳到床边
脚手架
作者
Jingying Dai,Xiaoxuan Wang,Cong Shao,Jiawei Liu,Chenxi Lian,Honglian Dai
标识
DOI:10.1002/adhm.202503349
摘要
Osteoarthritis (OA) is a common degenerative joint disease, and early diagnosis and effective treatment are essential for managing its progression. This study focuses on the development of a novel drug delivery system using aggregation-induced emission (AIE) probe for enhanced fluorescence imaging and targeted therapy in OA. TPE-S-BTD, an AIE probe, is synthesized and characterized for its photophysical properties, demonstrating significant aggregation-induced fluorescence enhancement. FPTD (FA-PEG-DSPE@TPE-S-BTD@DS) nanomicelles, which encapsulate TPE-S-BTD and diclofenac sodium (DS), are designed to target M1 macrophages via folate (FA) receptor-mediated endocytosis. These nanomicelles are incorporated into methacrylanhydride-modified hyaluronic acid (HAMA) hydrogel microspheres using microfluidic technology, creating a sustained drug release system (HAMA@FPTD). In vitro and in vivo experiments demonstrated the ability of this system to target M1 macrophages, reduce inflammation, and enhance cartilage repair in an OA rat model. This approach shows promise for the treatment and imaging of OA through a minimally invasive strategy, utilizing both FA-mediated targeting and controlled drug release.
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