4.5 Article

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

Journal

MICROSCOPY RESEARCH AND TECHNIQUE
Volume 76, Issue 9, Pages 936-941

Publisher

WILEY-BLACKWELL
DOI: 10.1002/jemt.22251

Keywords

postsynthesis etching; mesoporous nanostructures; iron oxide nanoparticles; gene delivery

Funding

  1. National Science Foundation [CBET-0854465, CBET-0854414, DMR-0847758]
  2. National Institutes of Health [5R01HL092526-02, 1R21EB015190-01A1, 4R03AR056848-03]
  3. Department of Defense Peer Reviewed Medical Research Program [W81XWH-12-1-0384]
  4. Oklahoma Center for the Advancement of Science and Technology [HR11-006]
  5. Oklahoma Center for Adult Stem Cell Research [434003]
  6. Direct For Mathematical & Physical Scien
  7. Division Of Materials Research [847758] Funding Source: National Science Foundation
  8. Div Of Chem, Bioeng, Env, & Transp Sys
  9. Directorate For Engineering [0854465] Funding Source: National Science Foundation
  10. Div Of Chem, Bioeng, Env, & Transp Sys
  11. Directorate For Engineering [0854414] Funding Source: National Science Foundation

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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.

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