纳米笼
体内
炎症
癌症研究
关节炎
类风湿性关节炎
药理学
肿瘤坏死因子α
医学
免疫系统
化学
免疫学
生物
生物化学
生物技术
催化作用
作者
Rajiu Venkatesan,Hao Xiong,Yuejun Yao,Jayachandra Reddy Nakkala,Tong Zhou,Shifen Li,Cunyi Fan,Changyou Gao
标识
DOI:10.1016/j.cej.2022.136868
摘要
The chronic autoimmune of rheumatoid arthritis (RA) usually results in inflammation of synovial joint, leading to pain, and destruction of cartilage and bone. Activated macrophages (M1 macrophages) actively take part in the RA pathogenesis, intensifying the inflammation and destruction of bone and cartilage. In this study, a nanoplatform was developed by grafting PEGylated folate acid (FA) and conjugating IL-4 onto gold nanocages (AuNCs), into the nanopores of which anti-inflammatory drug methylprednisolone (MP) was loaded. The [email protected] conjugates (consisting of PEGylated FA, IL-4 and MP) effectively targeted the folate receptors overexpressed on M1 macrophage surface, down-regulating the expression of M1 marker and up-regulating the M2 markers. The expression of pro-inflammatory cytokines such as IL-6, TNF-α, and IL-1β was significantly suppressed by the MP-AuNCs and [email protected] both in vitro and in vivo. The AuNCs conjugates could act as a contrast agent for photoacoustic (PA) phantom and CT imaging. The therapeutic efficacy of different AuNCs conjugates on RA in a model of rat adjuvant-induced arthritis (AIA) was verified by ELISA, histological, and Western blot analyses, revealing the therapeutic potential through immune-modulatory function on macrophages with [email protected] being the best and followed by MP-AuNCs.
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