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Mesoporous Iron Oxide Nanoparticles Prepared by Polyacrylic Acid Etching and Their Application in Gene Delivery to Mesenchymal Stem Cells

机译:聚丙烯酸蚀刻制备的介孔氧化铁纳米粒子及其在间充质干细胞基因传递中的应用

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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.
机译:通过后合成刻蚀法合成了新型单分散介孔氧化铁纳米粒子(m-IONPs),并通过电子显微镜对其进行了表征。在这种方法中,首先按照溶剂热法制备固体氧化铁纳米粒子(s-IONPs),然后通过聚丙烯酸各向异性蚀刻形成介孔纳米结构。 MTT细胞毒性试验表明,m-IONP与间充质干细胞(MSC)具有良好的生物相容性。由于其介孔结构和良好的生物相容性,这些单分散的m-IONPs被用作非病毒载体,用于将带有绿色荧光蛋白(GFP)的血管内皮生长因子(VEGF)基因递送至难以转染的细胞中干细胞。通过使用荧光显微镜检测来自MSC的GFP荧光来验证成功的基因递送和转染。我们的结果表明,在这项工作中合成的m-IONPs可以作为潜在的非病毒载体,在基因治疗中应先转染干细胞,然后将其植入疾病部位进行疾病治疗。

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