pH-responsive polyzwitterion covered nanocarriers for DNA delivery

被引:18
|
作者
Shen, Xin [1 ,2 ]
Dirisala, Anjaneyulu [3 ]
Toyoda, Masahiro [1 ,2 ]
Xiao, Yao [1 ,2 ]
Guo, Haochen [1 ,2 ]
Honda, Yuto [1 ,2 ,3 ]
Nomoto, Takahiro [1 ,4 ]
Takemoto, Hiroyasu [1 ,2 ,5 ]
Miura, Yutaka [1 ,2 ]
Nishiyama, Nobuhiro [1 ,2 ,3 ]
机构
[1] Tokyo Inst Technol, Inst Innovat Res, Lab Chem & Life Sci, 4259 Nagatsutacho,Midori Ku, Yokohama, Kanagawa 2268503, Japan
[2] Tokyo Inst Technol, Sch Life Sci & Technol, Dept Life Sci & Technol, 4259 Nagatsutacho,Midori Ku, Yokohama, Kanagawa, Japan
[3] Kawasaki Inst Ind Promot, Innovat Ctr NanoMed iCONM, 3-25-14 Tonomachi,Kawasaki Ku, Kawasaki, Kanagawa 2100821, Japan
[4] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, 3-8-1 Komaba,Meguro Ku, Tokyo 1538902, Japan
[5] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Med Chem, 1-5 Shimogamohangi Cho,Sakyo Ku, Kyoto 6060823, Japan
基金
日本科学技术振兴机构;
关键词
pH-responsiveness; Polyzwitterion; Plasmid DNA; Polyplex; Charge-switchability; Gene therapy; INTRACELLULAR TRAFFICKING; GENE; VECTORS; THERAPEUTICS; POLYPLEXES; SYSTEMS; DESIGN; TUMORS; PEI;
D O I
10.1016/j.jconrel.2023.07.038
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The success of gene therapy relies on gene nanocarriers to achieve therapeutic effects in vivo. Surface shielding of poly(ethylene glycol) (PEG), known as PEGylation, onto gene delivery carriers is a predominant strategy for extending blood circulation and improving therapeutic outcomes in vivo. Nevertheless, PEGylation frequently compromises the transfection efficiency by decreasing the interactions with the cellular membrane of the targeted cells, thereby preventing the cellular uptake and the subsequent endosomal escape. Herein, we developed a stepwise pH-responsive polyplex micelle for the plasmid DNA delivery with the surface covered by ethylenediamine-based polycarboxybetaines. This polyplex micelle switched its surface charge from neutral at pH 7.4 to positive at tumorous and endo-/lysosomal pH (i.e., pH 6.5 and 5.5, respectively), thus enhancing the cellular uptake and facilitating the endosomal escape toward efficient gene transfection. Additionally, the polyplex micelle demonstrated prolonged blood circulation as well as enhanced tumor accumulation, leading to highly effective tumor growth suppression by delivering an antiangiogenic gene. These results suggest the usefulness of a pH-responsive charge-switchable shell polymer on the surface of the polyplex micelle for the efficient nucleic acid delivery.
引用
收藏
页码:928 / 939
页数:12
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