Release of Plasmid DNA from Intravascular Stents Coated with Ultrathin Multilayered Polyelectrolyte Films

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 polyelectro...

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Veröffentlicht in:Biomacromolecules 2006-09, Vol.7 (9), p.2483-2491
Hauptverfasser: Jewell, Christopher M, Zhang, Jingtao, Fredin, Nathaniel J, Wolff, Matthew R, Hacker, Timothy A, Lynn, David M
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container_issue 9
container_start_page 2483
container_title Biomacromolecules
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creator Jewell, Christopher M
Zhang, Jingtao
Fredin, Nathaniel J
Wolff, Matthew R
Hacker, Timothy A
Lynn, David M
description 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 °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.
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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 °C, and coated stents were capable of mediating the expression of EGFP in a mammalian cell line without the aid of additional transfection agents. 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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 °C, and coated stents were capable of mediating the expression of EGFP in a mammalian cell line without the aid of additional transfection agents. 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source MEDLINE; American Chemical Society Journals
subjects Animals
Application fields
Applied sciences
Biocompatible Materials - chemistry
Biological and medical sciences
Biotechnology - methods
Chlorocebus aethiops
Coated Materials, Biocompatible - chemistry
COS Cells
DNA - chemistry
Drug Administration Routes
Electrolytes - chemistry
Exact sciences and technology
General pharmacology
Green Fluorescent Proteins - chemistry
Medical sciences
Microscopy, Electron, Scanning
Models, Chemical
Pharmaceutical technology. Pharmaceutical industry
Pharmacology. Drug treatments
Plasmids - metabolism
Polyamines - chemistry
Polymer industry, paints, wood
Stents
Technology of polymers
title Release of Plasmid DNA from Intravascular Stents Coated with Ultrathin Multilayered Polyelectrolyte Films
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