透明质酸
甲氨蝶呤
类风湿性关节炎
药理学
关节炎
化学
体内
内吞作用
联合疗法
医学
受体
免疫学
生物化学
生物
解剖
生物技术
作者
Shenghui Zhong,Peng Liu,Jinsong Ding,Wenhu Zhou
出处
期刊:Crystals
[Multidisciplinary Digital Publishing Institute]
日期:2021-03-24
卷期号:11 (4): 321-321
被引量:21
标识
DOI:10.3390/cryst11040321
摘要
Methotrexate (MTX) is an anchor drug for the treatment of rheumatoid arthritis (RA); however, long-term and high-dose usage of MTX for patients can cause many side effects and toxic reactions. To address these difficulties, selectively delivering MTX to the inflammatory site of a joint is promising in the treatment of RA. In this study, we prepared MTX-PEI@HA nanoparticles (NPs), composed of hyaluronic acid (HA) as the hydrophilic negative electrical shell, and MTX-linked branched polyethyleneimine (MTX-PEI) NPs as the core. MTX-PEI@HA NPs were prepared in the water phase by a one-pot method. The polymeric NPs were selectively internalized via CD44 receptor-mediated endocytosis in the activated macrophages. In the in vivo mice mode study, treatment with MTX-PEI@HA NPs mitigated inflammatory arthritis with notable safety at a high dose of MTX. We highlight the distinct advantages of aqueous-synthesized NPs coated with HA for arthritis-selective targeted delivery, thus verifying MTX-PEI@HA NPs as a promising MTX-based nanoplatform for treatment of RA.
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