Release of Plasmid DNA from Intravascular Stents Coated with Ultrathin Multilayered Polyelectrolyte Films
| Autor: | Christopher M. Jewell, Matthew R. Wolff, Jingtao Zhang, David M. Lynn, Nathaniel J. Fredin, Timothy A. Hacker |
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| Rok vydání: | 2006 |
| Předmět: |
Fabrication
Materials science Polymers and Plastics Scanning electron microscope Green Fluorescent Proteins Biocompatible Materials Bioengineering Nanotechnology Article Biomaterials Electrolytes Coated Materials Biocompatible Chlorocebus aethiops Microscopy Polyamines Materials Chemistry Animals Thin film Drug Administration Routes technology industry and agriculture DNA equipment and supplies Controlled release Polyelectrolyte Models Chemical COS Cells Microscopy Electron Scanning Stents Self-assembly Drug carrier Biotechnology Plasmids |
| Zdroj: | Biomacromolecules. 7:2483-2491 |
| ISSN: | 1526-4602 1525-7797 |
| DOI: | 10.1021/bm0604808 |
| Popis: | Materials that permit control over the release of DNA from the surfaces of topologically complex implantable devices, such as intravascular stents, could contribute to the development of new approaches to the localized delivery of DNA. We report the fabrication of ultrathin, multilayered polyelectrolyte films that permit both the immobilization and controlled release of plasmid DNA from the surfaces of stainless steel intravascular stents. Our approach makes use of an aqueous-based, layer-by-layer method for the assembly of nanostructured thin films consisting of alternating layers of plasmid DNA and a hydrolytically degradable polyamine. Characterization of coated stents using scanning electron microscopy (SEM) demonstrated that stents were coated uniformly with an ultrathin film ca. 120 nm thick that adhered conformally to the surfaces of stent struts. These ultrathin films did not crack, peel, or delaminate substantially from the surface after exposure to a range of mechanical challenges representative of those encountered during stent deployment (e.g., balloon expansion). Stents coated with eight bilayers of degradable polyamine and a plasmid encoding enhanced green fluorescent protein (EGFP) sustained the release of DNA into solution for up to four days when incubated in phosphate buffered saline at 37 degrees C, and coated stents were capable of mediating the expression of EGFP in a mammalian cell line without the aid of additional transfection agents. The approach reported here could, with further development, contribute to the development of localized gene-based approaches to the treatment of cardiovascular diseases or related conditions. |
| Databáze: | OpenAIRE |
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