Sandwich-Type Au-PEI/DNA/PEI-Dexa Nanocomplex for Nucleus-Targeted Gene Delivery in Vitro and in Vivo

被引:64
作者
Chen, Zhenzhen [1 ]
Zhang, Lifen [1 ]
He, Yuling [1 ]
Li, Yanfeng [1 ]
机构
[1] Lanzhou Univ, State Key Lab Appl Organ Chem, Key Lab Nonferrous Met Chem & Resources Utilizat, Coll Chem & Chem Engn,Inst Biochem Engn & Environ, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
gold nanoparticle; layer-by-layer; nucleus-targeted; polyethylenimine; dexamethasone; MODIFIED GOLD NANOPARTICLES; MEDIATED TRANSFECTION; ANTITUMOR-ACTIVITY; DNA; POLYMERS; THERAPY; CELLS; BARRIERS; VECTORS; RNA;
D O I
10.1021/am503483w
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Many synthetic Au-based cationic nanoparticles (AuNPs) for nonviral gene delivery show high efficiency in vitro, but their excessive charge density, harsh reducing conditions, and nontarget delivery prevent their application in vivo. Herein, we constructed a sandwich-type layered polyethylenimine (PEI)-coated gold nanocomposite outerlaid with a nucleus-targeted Dexamethasone (Dexa), namely, Au-PEI/DNA/PEI-Dexa nanocomplex, for DNA delivery system using a low molecular weight PEI as a mild reducing agent. The nucleus-targeting Au-PEI/DNA/PEI-Dexa nanocomplex with low positive charge and low cytotoxicity condensed DNA and protected from enzymatic degradation. In vitro transfection studies demonstrated that Au-PEI/DNA/PEI-Dexa nanocomplex exhibited much more efficient nucleus transfection than Au-PEI/DNA/PEI without nucleus-targeted residues and commercially available PEI 25 kDa due to the Dexa targeting of the nucleus. Furthermore, the nanocomplex markedly transfected pTRAIL (TRAIL = tumor-necrosis-factor-related apoptosis-inducing ligand) to tumors in vivo and subsequently inhibited the tumor growth with minimal side effects. These findings suggest that nucleus-targeting Au-PEI/DNA/PEI-Dexa ternary complexes have promising potential in gene delivery.
引用
收藏
页码:14196 / 14206
页数:11
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