Peptide-conjugated micelles as a targeting nanocarrier for gene delivery

被引:11
作者
Lin, Wen Jen [1 ,2 ]
Chien, Wei Hsuan [1 ]
机构
[1] Natl Taiwan Univ, Grad Inst Pharmaceut Sci, Sch Pharm, Taipei 10050, Taiwan
[2] Natl Taiwan Univ, Coll Med, Drug Res Ctr, Taipei 10050, Taiwan
关键词
Peptide; Epidermal growth factor receptor; Micelles; DNA; Nanomedicine; BREAST-CANCER CELLS; TUMOR-BEARING MICE; DRUG-DELIVERY; POLYMERIC NANOPARTICLES; PLGA NANOPARTICLES; EGFR; DOXORUBICIN; BIODISTRIBUTION; NANOMEDICINE; RECEPTOR;
D O I
10.1007/s11051-015-3132-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The aim of this study was to develop peptide-conjugated micelles possessing epidermal growth factor receptor (EGFR) targeting ability for gene delivery. A sequence-modified dodecylpeptide, GE11(2R), with enhancing EGF receptor binding affinity, was applied in this study as a targeting ligand. The active targeting micelles were composed of poly(D,L-lactide-co-glycolide)-poly(ethylene glycol) (PLGA-PEG) copolymer conjugated with GE11(2R)-peptide. The particle sizes of peptide-free and peptide-conjugated micelles were 277.0 +/- 5.1 and 308.7 +/- 14.5 nm, respectively. The peptide-conjugated micelles demonstrated the cellular uptake significantly higher than peptide-free micelles in EGFR high-expressed MDA-MB-231 and MDA-MB-468 cells due to GE11(2R)-peptide specificity. Furthermore, the peptide-conjugated micelles were able to encapsulate plasmid DNA and expressed cellular transfection higher than peptide-free micelles in EGFR high-expressed cells. The EGFR-targeting delivery micelles enhanced DNA internalized into cells and achieved higher cellular transfection in EGFR high-expressed cells.
引用
收藏
页数:14
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