血尿素氮
化学
硫酸软骨素
药物输送
肾
药理学
CD44细胞
靶向给药
癌症研究
纤维化
细胞外基质
肾脏疾病
肌酐
药品
活性氧
急性肾损伤
受体
肌成纤维细胞
医学
联合疗法
毒品携带者
肾毒性
肾功能
软骨素
去唾液酸糖蛋白受体
终末期肾病
作者
Wei Zhao,Jie Zhou,Yan Xia,Jingwei Li,Jiahao Chen,Xinghe Ji,Lingling Wang,Jinhang Zhang,Shuting Qiu,Yimin Xiong,Lunzhi Liu,Jinhan He,Yanping Li
标识
DOI:10.1021/acs.molpharmaceut.5c01524
摘要
studies demonstrated that CEL@CB nanoparticles facilitate targeted CEL delivery to activated myofibroblasts, achieving a drug accumulation in fibrotic kidneys more than 2-fold higher than in healthy controls. Treatment with CEL@CB reduced the expression of key fibrotic markers (α-SMA and Col1a1) by approximately 30-70% at both mRNA and protein levels and decreased serum creatinine and blood urea nitrogen (BUN) levels by about 50%, thereby significantly attenuating folic acid-induced renal fibrosis, restoring renal function, and mitigating histological damage. Importantly, this targeted strategy markedly minimized the toxicity to the heart, testis, and hematological systems associated with free CEL. This dual-functional nanoparticle combines CD44-mediated renal targeted delivery with ROS-responsive drug release, offering a novel approach for antifibrotic therapy.
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