Department of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, University of Oklahoma, Norman, Oklahoma, 73019.
Microsc Res Tech. 2013 Sep;76(9):936-41. doi: 10.1002/jemt.22251. Epub 2013 Jul 30.
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.
新型单分散介孔氧化铁纳米粒子(m-IONPs)通过后合成刻蚀法合成,并通过电子显微镜进行了表征。在该方法中,首先通过溶剂热法制备了固体氧化铁纳米粒子(s-IONPs),然后用聚丙烯酸进行各向异性刻蚀,形成介孔纳米结构。MTT 细胞毒性试验表明,m-IONPs 与间充质干细胞(MSCs)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 m-IONPs 被用作携带绿色荧光蛋白(GFP)标记的血管内皮生长因子(VEGF)基因的非病毒载体,转染到难以转染的干细胞中。通过荧光显微镜检测 MSCs 中的 GFP 荧光,验证了成功的基因传递和转染。我们的结果表明,本文合成的 m-IONPs 可用作基因治疗中的潜在非病毒载体,其中应先转染干细胞,然后将其植入疾病部位以治疗疾病。