Polymer-Functionalized Nanodiamond Platforms as Vehicles for Gene Delivery

被引:314
作者
Zhang, Xue-Qing [1 ]
Chen, Mark [2 ,3 ]
Lam, Robert [4 ]
Xu, Xiaoyang [3 ]
Osawa, Eiji [5 ]
Ho, Dean [1 ,4 ,6 ]
机构
[1] Northwestern Univ, Dept Biomed Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Biol Sci, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Mech Engn, Evanston, IL 60208 USA
[5] Shinshu Univ, NanoCarbon Res Inst, Nagano 3868567, Japan
[6] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
nanodiamonds; gene delivery; nanocarrier; transfection; low molecular weight polyethyleneimine (LMW PEI); LOW-MOLECULAR-WEIGHT; PHOTOTHERMAL CANCER-THERAPY; DIAMOND THIN-FILMS; IN-VIVO; FLUORESCENT NANODIAMONDS; BIOLOGICAL APPLICATIONS; CARBON NANOTUBES; DNA; POLYETHYLENIMINE; NANOCRYSTALS;
D O I
10.1021/nn900865g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gene therapy holds great promise for treating diseases ranging from inherited disorders to acquired conditions and cancers. Nonetheless, because a method of gene delivery that is both effective and safe has remained elusive, these successes were limited. Functional nanodiamonds (NDs) are rapidly emerging as promising carriers for next-generation therapeutics with demonstrated potential. Here we introduce NDs as vectors for in vitro gene delivery via surface-immobilization with 800 Da polyethyleneimine (PEI800) and covalent conjugation with amine groups. We designed PEI800-modified NDs exhibiting the high transfection efficiency of high molecular weight PEI (PEI25K), but without the high cytotoxicity inherent to PEI25K. Additionally, we demonstrated that the enhanced delivery properties were exclusively mediated by the hybrid ND-PEI800 material and not exhibited by any of the materials alone. This platform approach represents an efficient avenue toward gene delivery via DNA-functionalized NDs, and serves as a rapid, scalable, and broadly applicable gene therapy strategy.
引用
收藏
页码:2609 / 2616
页数:8
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