A novel type of self-assembled nanoparticles as targeted gene carriers: an application for plasmid DNA and antimicroRNA oligonucleotide delivery
Yanliang Zhu,1 Gaofeng Liang,2 Bo Sun,1 Tian Tian,3 Feihu Hu,1 Zhongdang Xiao11State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing, 2School of Medical Technology and Engineering, Henan University of Science and Technology, Luoya...
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| Autores principales: | , , , , , |
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| Formato: | article |
| Lenguaje: | EN |
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Dove Medical Press
2016
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| Materias: | |
| Acceso en línea: | https://doaj.org/article/d64106c9bcf24ac0bf48154dd492e7a0 |
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| Sumario: | Yanliang Zhu,1 Gaofeng Liang,2 Bo Sun,1 Tian Tian,3 Feihu Hu,1 Zhongdang Xiao11State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing, 2School of Medical Technology and Engineering, Henan University of Science and Technology, Luoyang, 3Department of Neurobiology, Nanjing Medical University, Nanjing, People’s Republic of ChinaAbstract: In this study, a new type of amphiphilic cetylated polyethyleneimine (PEI) was synthesized, and then polylactic-co-glycolic acid (PLGA)/cetylated PEI/hyaluronic acid nanoparticles (PCPH NPs) were developed by self-assembly as a novel type of gene-delivering vehicle. The PCPH NPs showed good DNA-condensation ability by forming polyplexes with small particle size and positive zeta potential. The transfection efficiency and cytotoxicity of PCPH NPs were evaluated as plasmid DNA vectors to transfect HepG2 in vitro. PCPH NPs exhibited much lower cytotoxicity and higher gene-transfection efficiency than PEI (25,000) and commercial transfection reagents. Furthermore, PCPH NPs were used as an anti-miR-221 vector for transfecting HepG2 cells, and anti-miR-221 was effectively transfected into cells and produced a greater inhibitory effect on cancer-cell growth by PCPH NPs. These results demonstrate that PCPH NPs can be a promising nonviral vector for gene-delivery systems.Keywords: gene delivery, hyaluronic acid, polyethyleneimine, anti-miR-221, PLGA |
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