炎症性肠病
甲氨蝶呤
药物输送
结肠炎
靶向给药
医学
炎症
巨噬细胞
免疫系统
细胞毒性
药品
免疫学
药理学
疾病
化学
内科学
体外
生物化学
有机化学
作者
Ying Sun,Bingchao Duan,Huanhuan Chen,Xiaojuan Xu
标识
DOI:10.1002/adhm.201901805
摘要
Abstract Therapy of inflammatory bowel disease (IBD) has been a difficult task in the medical field. There is a great clinical need for more effective treatments for IBD. Herein, a targeted oral delivery system of yeast glucan particles (YGPs) carrying a clinically used anti‐inflammatory drug methotrexate (MTX) to the inflamed sites in IBD mice for therapy is reported. In the findings, MTX is effectively loaded into YGPs through re‐precipitation followed by gelation reaction of alginate to obtain the composite YGPs/MTX, which are internalized into RAW264.7 macrophage cells through dectin‐1 and CR3 receptors. Furthermore, YGPs/MTX can suppress the proliferation of macrophage cells efficiently, leading to down‐regulation of pro‐inflammatory cytokines induced by lipopolysaccharides. Additionally, YGPs accumulate in the inflammation site of colitis mice, enabling YGPs/MTX to target the inflammatory site, significantly improve the efficacy of MTX, and reduce the cytotoxicity of MTX. Therefore, the YGPs‐based drug delivery system provides a new strategy for MTX application in the clinical treatment of IBD.
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