| Literature DB >> 28371624 |
Roun Heo1, Dong Gil You2, Wooram Um3, Ki Young Choi4, Sangmin Jeon4, Jong-Sung Park5, Yuri Choi6, Seunglee Kwon4, Kwangmeyung Kim7, Ick Chan Kwon7, Dong-Gyu Jo6, Young Mo Kang8, Jae Hyung Park9.
Abstract
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.Entities:
Keywords: Dextran sulfate; Drug delivery; Macrophage; Nanoparticles; Rheumatoid arthritis
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Year: 2017 PMID: 28371624 DOI: 10.1016/j.biomaterials.2017.03.044
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479