RGD4C modified ferritin nanocages for rat hepatic stellate cells-targeted drug delivery
10.3969/j.issn.1006-5725.2015.18.004
- VernacularTitle:RGD4C修饰的铁蛋白纳米笼用于大鼠肝星状细胞的靶向药物输送
- Author:
Li HE
;
Jun ZHANG
;
Chun WU
;
Xuhui XIA
;
Gang LIU
;
Dan LI
;
Hong SHAN
- Publication Type:Journal Article
- Keywords:
Liver fibrosis;
Hepatic stellate cells;
Ferritin nanocages;
Integrin αvβ3;
Targeted drug delivery
- From:
The Journal of Practical Medicine
2015;(18):2950-2953
- CountryChina
- Language:Chinese
-
Abstract:
Objective The purpose of this study was to prepare RGD4C modified ferritin nanocages (RGD4C-FRT) for targeted drug delivery to rat hepatic stellate cells (HSC-T6). Methods RGD4C modified human H-chain ferritin was expressed and purified. Doxorubicin (Dox) was encapsulated into the cavity of RGD4C-FRT through ion channels, which resulted in RGD4C-FRT-Dox. The target of RGD4C-FRT-Dox to HSC-T6 was detected using fluorescence microscopy. Results Transmission electron microscopy showed that RGD4C-FRT was hollow spherical-structured with uniform size and good dispersion. The average particle diameters of RGD4C-FRT and RGD4C-FRT-Dox were 12.57 nm and 20.13 nm , respectively. The drug encapsulation efficiency and loading percentage of RGD4C-FRT-Dox were 77.32% and 15.88% respectively. RGD4C-FRT-Dox was significantly uptaken by HSC-T6, and the uptake could be blocked by the empty carrier RGD4C-FRT. Conclusion RGD4C-FRT-Dox can specifically target HSC-T6. Further animal experiments are needed to inspect its therapeutic effect on liver fibrosis.