Aerosol delivery of spermine-based poly(amino ester)/Akt1 shRNA complexes for lung cancer gene therapy

被引:46
作者
Jiang, Hu-Lin [3 ]
Hong, Seong-Ho [3 ]
Kim, You-Kyoung [1 ,2 ]
Islam, Mohammad Ariful [1 ,2 ]
Kim, Hye-Joon [3 ]
Choi, Yun-Jaie [1 ,2 ]
Nah, Jae-Woon [4 ]
Lee, Kee-Ho [5 ]
Han, Ki-Won [6 ]
Chae, Chanhee [6 ]
Cho, Chong-Su [1 ,2 ]
Cho, Myung-Haing [3 ,7 ,8 ,9 ]
机构
[1] Seoul Natl Univ, Dept Agr Biotechnol, Seoul 151921, South Korea
[2] Seoul Natl Univ, Res Inst Agr & Life Sci, Seoul 151921, South Korea
[3] Seoul Natl Univ, Toxicol Lab, Coll Vet Med, Seoul 151742, South Korea
[4] Sunchon Natl Univ, Dept Polymer Sci & Engn, Sunchon 540742, South Korea
[5] Korea Inst Radiol & Med Sci, Div Radiat Canc Res, Mol Oncol Lab, Seoul 139240, South Korea
[6] Seoul Natl Univ, Pathol Lab, Coll Vet Med, Seoul 151742, South Korea
[7] Seoul Natl Univ, Grad Sch Convergence Sci & Technol, Dept Nanofus Technol, Suwon 443270, South Korea
[8] Seoul Natl Univ, Adv Inst Convergence Technol, Suwon 443270, South Korea
[9] Seoul Natl Univ, Grad Grp Tumor Biol, Seoul 151742, South Korea
基金
新加坡国家研究基金会;
关键词
Lung cancer; Gene therapy; Poly(amino ester); Spermine; Aerosol delivery; LOW-MOLECULAR-WEIGHT; CHITOSAN-GRAFT-POLYETHYLENIMINE; IN-VIVO; TRANSFECTION EFFICIENCY; POLY(BETA-AMINO ESTERS); CATIONIC POLYMERS; NONVIRAL VECTOR; DNA DELIVERY; CARRIER; CELLS;
D O I
10.1016/j.ijpharm.2011.08.045
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polyethylenimine (PEI) has been commonly used as a cationic polymeric gene carrier due to high transfection efficiency, however, its cytotoxicity has hindered the practical application. In this study, we report the development of poly(amino ester) (PAE) based on glycerol propoxylate triacrylate (GPT) and spermine (SPE) as an alternative gene carrier for lung cancer therapy. GPT-SPE copolymer was prepared by Michael addition reaction between GPT and SPE, and the efficacy was evaluated using shAkt1 as a model therapeutic gene. The molecular weight and composition were characterized using gel permeability chromatography (GPC) and H-1-nuclear magnetic resonance (H-1-NMR), respectively. The GPT-SPE could effectively condense DNA with about 163 nm size and protect the DNA from nucleases. GPT-SPE/DNA complexes showed excellent transfection with low toxicity both in vitro and in vivo. Furthermore, aerosol delivery of GPT-SPE/Akt1 shRNA complexes significantly suppressed lung tumorigenesis in K-ras(LA1) lung cancer model mice. These results suggest that GPT-SPE can be used in shRNA-based lung cancer gene therapy. (c) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:256 / 265
页数:10
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