ArticleActa biomaterialia2009
Assembly of erodible, DNA-containing thin films on the surfaces of polymer microparticles: toward a layer-by-layer approach to the delivery of DNA to antigen-presenting cells.
Article in Acta biomaterialia, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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Who cites it
15 citing papers in PubMed.
- Recent advances in layer-by-layer assembly scaffolds for co-delivery of bioactive molecules for bone regeneration: an updated review.Journal of translational medicine · 2024Review
- Electrical characterization of DNA supported on nitrocellulose membranes.Scientific reports · 2016Article
- Replenishable dendrimer-nanoparticle hybrid membranes for sustained release of therapeutics.Nanoscale · 2013Article
- Polyelectrolyte multilayers promote stent-mediated delivery of DNA to vascular tissue.Biomacromolecules · 2013Article
- Reduction of intimal hyperplasia in injured rat arteries promoted by catheter balloons coated with polyelectrolyte multilayers that contain plasmid DNA encoding PKCδ.Biomaterials · 2013Article
- An influenza virus-inspired polymer system for the timed release of siRNA.Nature communications · 2013Article
- Rapid release of plasmid DNA from surfaces coated with polyelectrolyte multilayers promoted by the application of electrochemical potentials.ACS applied materials & interfaces · 2012Article
- Article
- A pH-sensitive multifunctional gene carrier assembled via layer-by-layer technique for efficient gene delivery.International journal of nanomedicine · 2012Article
- Layer-by-layer nanoparticles with a pH-sheddable layer for in vivo targeting of tumor hypoxia.ACS nano · 2011Article
- Degradable polyelectrolyte multilayers that promote the release of siRNA.Langmuir : the ACS journal of surfaces and colloids · 2011Article
- Design and Synthesis of a Fluorescently End-Labeled Poly(β-amino ester): Application to the Characterization of Degradable Polyelectrolyte Multilayers.Journal of polymer science. Part A, Polymer chemistry · 2011Article
- Delivery of plasmid DNA to vascular tissue in vivo using catheter balloons coated with polyelectrolyte multilayers.Biomaterials · 2011Article
- Layer-by-layer assembly of DNA- and protein-containing films on microneedles for drug delivery to the skin.Biomacromolecules · 2010Article
- Characterization of nanoscale transformations in polyelectrolyte multilayers fabricated from plasmid DNA using laser scanning confocal microscopy in combination with atomic force microscopy.Microscopy research and technique · 2010Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
We report a layer-by-layer approach to the assembly of ultrathin and erodible DNA-containing films on the surfaces of polymer microparticles. DNA-containing multilayered films were fabricated layer-by-layer on the surfaces of polystyrene microspheres (approximately 6 microm) by iterative and alternating cycles of particle suspension, centrifugation and resuspension in solutions of plasmid DNA and a hydrolytically degradable polyamine. Film growth occurred in a stepwise manner, as demonstrated by characterization of the zeta potentials and fluorescence intensities of film-coated particles during film assembly. Characterization of film-coated particles by confocal fluorescence microscopy and scanning electron microscopy revealed the multilayered particle coatings to be smooth, uniform and free of large-scale physical defects. Film-coated microparticles sustained the release of transcriptionally active DNA into solution for approximately three days when incubated in physiologically relevant media. Previous studies have demonstrated that the adsorption of DNA onto the surfaces of cationic microparticles can be used to target the delivery of DNA to antigen-presenting cells. As a first step toward the application of this layer-by-layer approach to the development of methods for the delivery of DNA to antigen-presenting cells, we demonstrated that film-coated microparticles could be used to transport DNA into macrophage cells in vitro using a model mouse macrophage cell line. Our results suggest the basis of a general approach that could, with further development, prove useful for the delivery of DNA-encoded antigens to macrophages, or other antigen-presenting cells, and provide new materials-based methods for the formulation and delivery of DNA vaccines.
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