Mesoporous iron oxide nanoparticles prepared by polyacrylic acid etching and their application in gene delivery to mesenchymal stem cells

被引:23
作者
Cao, Binrui [1 ]
Qiu, Penghe [1 ]
Mao, Chuanbin [1 ]
机构
[1] Univ Oklahoma, Dept Chem & Biochem, Stephenson Life Sci Res Ctr, Norman, OK 73019 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
postsynthesis etching; mesoporous nanostructures; iron oxide nanoparticles; gene delivery; INORGANIC HOLLOW NANOPARTICLES; DRUG-DELIVERY; MAGNETIC NANOPARTICLES; CONTROLLED-RELEASE; SILICA NANOPARTICLES; ETHYLENE-GLYCOL; THERAPY; NANOMEDICINE; POLYESTERIFICATION; FUNCTIONALIZATION;
D O I
10.1002/jemt.22251
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Novel monodisperse mesoporous iron oxide nanoparticles (m-IONPs) were synthesized by a postsynthesis etching approach and characterized by electron microscopy. In this approach, solid iron oxide nanoparticles (s-IONPs) were first prepared following a solvothermal method, and then etched anisotropically by polyacrylic acid to form the mesoporous nanostructures. MTT cytotoxicity assay demonstrated that the m-IONPs have good biocompatibility with mesenchymal stem cells (MSCs). Owing to their mesoporous structure and good biocompatibility, these monodisperse m-IONPs were used as a nonviral vector for the delivery of a gene of vascular endothelial growth factor (VEGF) tagged with a green fluorescence protein (GFP) into the hard-to-transfect stem cells. Successful gene delivery and transfection were verified by detecting the GFP fluorescence from MSCs using fluorescence microscopy. Our results illustrated that the m-IONPs synthesized in this work can serve as a potential nonviral carrier in gene therapy where stem cells should be first transfected and then implanted into disease sites for disease treatment. Microsc. Res. Tech. 76:936-941, 2013. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:936 / 941
页数:6
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