类风湿性关节炎
关节炎
神经科学
染色质结构重塑复合物
医学
化学
生物
免疫学
基因
组蛋白
生物化学
核小体
作者
Chuan Hu,Jiaqi Ma,Xi Chen,Yaxin Chen,Yujun Song,Qingsong Tang,Xiaoqi He,Yitao Wang,Huile Gao,Jinming Zhang
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-09-03
卷期号:11 (36): eadu5245-eadu5245
被引量:3
标识
DOI:10.1126/sciadv.adu5245
摘要
The aberrant vasculature within the inflamed joint cavity of rheumatoid arthritis (RA) not only exacerbates joint pathology but also restricts the effective delivery of therapeutic drugs. Herein, we propose a strategy that involves the rapid and sustained vasculature repair alongside microenvironment-driven drug delivery to achieve multifaceted RA management. The transformable, self-assembling nanoplatform specifically accumulates in the inflamed joint cavity guided by a vascular targeting peptide (STP). Subsequently, STP detaches and undergoes shape transformation, forming nanofibers on the vascular endothelium, which serve as a rapid-acting physical barrier in the short term and facilitate sustained vascular normalization in the long term. Concurrently, the remaining nanoparticles undergo charge reversal and RGD exposure, enabling precise delivery of anti-RA agent triptolide and the immunomodulatory agent metformin. Collectively, this study provides a potent strategy for rapid, sustained, and precise spatiotemporal remodeling of RA using a simple yet intelligent self-assembling nanoplatform.
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