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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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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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.</description><identifier>ISSN: 1525-7797</identifier><identifier>EISSN: 1526-4602</identifier><identifier>DOI: 10.1021/bm0604808</identifier><identifier>PMID: 16961308</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>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. 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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.</description><subject>Animals</subject><subject>Application fields</subject><subject>Applied sciences</subject><subject>Biocompatible Materials - chemistry</subject><subject>Biological and medical sciences</subject><subject>Biotechnology - methods</subject><subject>Chlorocebus aethiops</subject><subject>Coated Materials, Biocompatible - chemistry</subject><subject>COS Cells</subject><subject>DNA - chemistry</subject><subject>Drug Administration Routes</subject><subject>Electrolytes - chemistry</subject><subject>Exact sciences and technology</subject><subject>General pharmacology</subject><subject>Green Fluorescent Proteins - chemistry</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Scanning</subject><subject>Models, Chemical</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Plasmids - metabolism</subject><subject>Polyamines - chemistry</subject><subject>Polymer industry, paints, wood</subject><subject>Stents</subject><subject>Technology of polymers</subject><issn>1525-7797</issn><issn>1526-4602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkU9v1DAQxS1ERUvhwBdAvoDEIWX8L3YuSNVCS6UWKqBny-s4rCsnbm2naL99vXTVLRKnGWl-ejPzHkJvCBwRoOTjcoQWuAL1DB0QQduGt0Cf_-1FI2Un99HLnK8BoGNcvED7pO1awkAdIP_DBWeyw3HAl8Hk0ff487djPKQ44rOpJHNnsp2DSfhncVPJeBFNcT3-48sKX4UKlJWf8MUcig9m7VKdXcawrrK2pNoUh098GPMrtDeYkN3rbT1EVydffi2-NuffT88Wx-eN4YyVpu1Iz4Bz1dneWm4JF7TvhYVu4BIkEMLIErhslVxa1Qni-oEPoAR3Fph07BB9etC9mZej663bPBH0TfKjSWsdjdf_Tia_0r_jnaaCUkZ5FXi_FUjxdna56NFn60Iwk4tz1q1SXFKxAT88gDbFnJMbHpcQ0Jtg9GMwlX379KoduU2iAu-2QPXbhCGZyfq84xShhHCy44zN-jrOaapm_mfhPf24on8</recordid><startdate>200609</startdate><enddate>200609</enddate><creator>Jewell, Christopher M</creator><creator>Zhang, Jingtao</creator><creator>Fredin, Nathaniel J</creator><creator>Wolff, Matthew R</creator><creator>Hacker, Timothy A</creator><creator>Lynn, David M</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200609</creationdate><title>Release of Plasmid DNA from Intravascular Stents Coated with Ultrathin Multilayered Polyelectrolyte Films</title><author>Jewell, Christopher M ; Zhang, Jingtao ; Fredin, Nathaniel J ; Wolff, Matthew R ; Hacker, Timothy A ; Lynn, David M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a433t-691d304489cdcc4c1452dd5c09f470701131b047687bc8951edf4f0854ec037e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Application fields</topic><topic>Applied sciences</topic><topic>Biocompatible Materials - chemistry</topic><topic>Biological and medical sciences</topic><topic>Biotechnology - methods</topic><topic>Chlorocebus aethiops</topic><topic>Coated Materials, Biocompatible - chemistry</topic><topic>COS Cells</topic><topic>DNA - chemistry</topic><topic>Drug Administration Routes</topic><topic>Electrolytes - chemistry</topic><topic>Exact sciences and technology</topic><topic>General pharmacology</topic><topic>Green Fluorescent Proteins - chemistry</topic><topic>Medical sciences</topic><topic>Microscopy, Electron, Scanning</topic><topic>Models, Chemical</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Plasmids - metabolism</topic><topic>Polyamines - chemistry</topic><topic>Polymer industry, paints, wood</topic><topic>Stents</topic><topic>Technology of polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jewell, Christopher M</creatorcontrib><creatorcontrib>Zhang, Jingtao</creatorcontrib><creatorcontrib>Fredin, Nathaniel J</creatorcontrib><creatorcontrib>Wolff, Matthew R</creatorcontrib><creatorcontrib>Hacker, Timothy A</creatorcontrib><creatorcontrib>Lynn, David M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biomacromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jewell, Christopher M</au><au>Zhang, Jingtao</au><au>Fredin, Nathaniel J</au><au>Wolff, Matthew R</au><au>Hacker, Timothy A</au><au>Lynn, David M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Release of Plasmid DNA from Intravascular Stents Coated with Ultrathin Multilayered Polyelectrolyte Films</atitle><jtitle>Biomacromolecules</jtitle><addtitle>Biomacromolecules</addtitle><date>2006-09</date><risdate>2006</risdate><volume>7</volume><issue>9</issue><spage>2483</spage><epage>2491</epage><pages>2483-2491</pages><issn>1525-7797</issn><eissn>1526-4602</eissn><abstract>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.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>16961308</pmid><doi>10.1021/bm0604808</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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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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