类风湿性关节炎
纳米医学
右旋糖酐
材料科学
甲氨蝶呤
两亲性
内吞作用
纳米颗粒
清道夫受体
结合
药理学
生物物理学
纳米技术
医学
化学
受体
生物化学
免疫学
胆固醇
共聚物
复合材料
数学分析
数学
生物
聚合物
脂蛋白
作者
Roun Heo,Dong Gil You,Wooram Um,Ki Young Choi,Sang‐Min Jeon,Jong Sung Park,Yuri Choi,Seunglee Kwon,Kwangmeyung Kim,Ick Chan Kwon,Dong‐Gyu Jo,Young Mo Kang,Jae Hyung Park
出处
期刊:Biomaterials
[Elsevier BV]
日期:2017-03-26
卷期号:131: 15-26
被引量:148
标识
DOI:10.1016/j.biomaterials.2017.03.044
摘要
With the aim of developing nanoparticles for targeted delivery of methotrexate (MTX) to inflamed joints in rheumatoid arthritis (RA), an amphiphilic polysaccharide was synthesized by conjugating 5β-cholanic acid to a dextran sulfate (DS) backbone. Due to its amphiphilic nature, the DS derivative self-assembled into spherical nanoparticles (220 nm in diameter) in aqueous conditions. The MTX was effectively loaded into the DS nanoparticles (loading efficiency: 73.0%) by a simple dialysis method. Interestingly, the DS nanoparticles were selectively taken up by activated macrophages, which are responsible for inflammation and joint destruction, via scavenger receptor class A-mediated endocytosis. When systemically administrated into mice with experimental collagen-induced arthritis (CIA), the DS nanoparticles effectively accumulated in inflamed joints (12-fold more than wild type mice (WT)), implying their high targetability to RA tissues. Moreover, the MTX-loaded DS nanoparticles exhibited significantly improved therapeutic efficacy against CIA in mice compared to free MTX alone. Overall, the data presented here indicate that DS nanoparticles are potentially useful nanomedicines for RA imaging and therapy.
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