A polyethylenimine-mimetic biodegradable polycation gene vector and the effect of amine composition in transfection efficiency

被引:37
作者
Shen, J. [1 ]
Zhao, D. J. [1 ]
Li, W. [1 ]
Hu, Q. L. [1 ]
Wang, Q. W. [1 ]
Xu, F. J. [2 ]
Tang, G. P. [1 ]
机构
[1] Hangzhou Univ, Inst Chem Biol & Pharmaceut Chem, Hangzhou 310028, Peoples R China
[2] Beijing Univ Chem Technol, Coll Mat Sci & Engn, Minist Educ, Key Lab Carbon Fiber & Funct Polymers, Beijing 100029, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Gene delivery; Vector; Polyethylenimine; Biodegradable; Mimic; MOLECULAR-WEIGHT; IN-VITRO; DNA DELIVERY; THERAPY; DRUG; VIVO; CYTOTOXICITY; MICELLES; POLYMERS; CARRIER;
D O I
10.1016/j.biomaterials.2013.02.068
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The low toxicity and efficient gene delivery of polymeric vectors remain the major barrier to the clinical application of non-viral gene therapy. Here, we present a poly-D, c-succinimide (PSI)-based biodegradable cationic polymer which mimicked the golden standard, branched polyethylenimine (PEI, similar to 25 kDa). To investigate the influence of 1 degrees, 2 degrees, 3 degrees amine group ratio in the polymer, a series of PSI-based vectors (PSI-NNx'-NNy) grafted with different amine side chains of N,N-dimethyldipropylenetriamine (NN') and bis(3-aminopropyl)amine (NN) were first characterized and contrasted by biophysical measurements. The in vitro and in vivo biological assay demonstrated that PSI-NN0.85'-NN1 exhibited better transfection ability and biocompatibility than PEI. The present results suggest that such PEI-mimic biodegradable PSI-NN0.85'-NN1 possesses a good potential application for clinical gene delivery. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4520 / 4531
页数:12
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