Crosslinked linear polyethylenimine enhances delivery of DNA to the cytoplasm

被引:50
作者
Bonner, Daniel K. [1 ,2 ,3 ]
Zhao, Xiaoyong [1 ,2 ]
Buss, Hilda [1 ,2 ]
Langer, Robert [1 ,2 ,3 ]
Hammond, Paula T. [1 ,2 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Gene delivery; Polyethylenimine; Bioresponsive; Reducible; Endosomal escape; LOW-MOLECULAR-WEIGHT; TRANSFECTION EFFICIENCY; FREE POLYCATIONS; NUCLEIC-ACIDS; GENE; POLYMER; VECTOR; OLIGOETHYLENIMINE; COMPLEXATION; TOXICITY;
D O I
10.1016/j.jconrel.2012.09.004
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Crosslinked polyethylenimines (PEIs) have been frequently examined over the past decade since they can maintain the transfection efficiency of commercially available, 25 k branched PEI, but exhibit less cytotoxicity. The argument is often made that the degradability of such polymers, generally synthesized with either disulfide or hydrolytically degradable crosslinkers, is critical to the high efficiency and low toxicity of the system. In this work, we present a crosslinked linear PEI (xLPEI) system in which either disulfide-responsive or non-degradable linkages are incorporated. As with previous systems, strong transfection efficiency in comparison with commercial standards was achieved with low cytotoxicity. However, these properties were shown to be present when either the degradable or non-degradable crosslinker was used. Uncomplexed polymer was demonstrated to be the critical factor determining transfection efficiency for these polymers, mediating efficient endosomal escape without signs of cell membrane damage. While several crosslinked PEI systems in the literature have demonstrated the effect of the disulfide moiety, this work demonstrates that disulfide-mediated unpackaging may not be as important as conventionally thought for some PEI systems. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:101 / 107
页数:7
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