Red blood cell membrane-camouflaged prednisolone acetate-loaded PLGA nanoparticles for kidney-targeted drug delivery

被引:4
|
作者
Yang, Jing [1 ,2 ]
Zhang, Rongtao [3 ]
Wang, Fangliang [1 ,2 ]
Shang, Jinlu [1 ,2 ]
Wu, Siqiong [1 ,2 ]
Ding, Qian [1 ,2 ]
Yang, Liuxuan [1 ,2 ]
Fan, Qingze [1 ]
Ye, Yun [1 ,4 ]
Zhou, Meiling [1 ,4 ]
机构
[1] Southwest Med Univ, Affiliated Hosp, Dept Pharm, Luzhou, Peoples R China
[2] Southwest Med Univ, Sch Pharm, Dept Clin Pharm, Luzhou, Peoples R China
[3] Xingwen Hosp Tradit Chinese Med, Dept Pharm, Yibin, Peoples R China
[4] Southwest Med Univ, Affiliated Hosp, Dept Pharm, 25 Taiping St, Luzhou 646000, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Red blood cell membrane; PLGA; Biomimetic nanoparticles; Prednisolone acetate; Kidney-targeted;
D O I
10.1016/j.jddst.2023.104693
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The lack of renal targeting and adverse drug reactions are key issues in the treatment of glomerulonephritis. Here, we present the development of red blood cell membrane-camouflaged nanoparticles (RBC-PA-NPs) as a targeted drug delivery system for delivering prednisolone acetate (PA) to the glomerular mesangium. We successfully coated erythrocyte membranes onto PA-loaded PLGA nanoparticles (PA-NPs), and the resultant RBCPA-NPs exhibited a well-defined core-shell structure with a favourable particle size of 104.20 & PLUSMN; 0.35 nm and a surface charge of -15.07 & PLUSMN; 2.13 mV. Toxicity was evaluated by cell viability assays using rat glomerular mesangial cells, and the RBC-PA-NPs showed good biocompatibility. RBC-PA-NPs exhibited reduced uptake by RAW 264.7 cells and greater uptake by rat glomerular mesangial cell lines than PA and PA-NPs. Biodistribution studies revealed that RBC-Cy5-NPs displayed the highest fluorescence intensity in renal tissue and effectively accumulated in the kidney, indicating their targeting effect. In summary, RBC-PA-NPs are a potential system for the kidney-targeted delivery of traditional drugs to improve their efficacy.
引用
收藏
页数:7
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