Evidence map›Paper›PMID 18838346›Full record

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.

Eric M Saurer, Christopher M Jewell, Jon M Kuchenreuther, David M Lynn

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Review
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  11. Degradable polyelectrolyte multilayers that promote the release of siRNA.Langmuir : the ACS journal of surfaces and colloids · 2011
    Article
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Eric M SaurerDepartment of Chemical and Biological Engineering, University of Wisconsin - Madison, 1415 Engineering Drive, Madison, WI 53706, USA.
Christopher M Jewell
Jon M Kuchenreuther
David M Lynn

Funding

Controlled Release of DNA from SurfacesR01EB006820 · NIBIB · UNIVERSITY OF WISCONSIN-MADISON · PI LYNN, DAVID M · 2008 to 2011
$1.3M
Controlled Release of DNA from SurfacesR21EB002746 · NIBIB · UNIVERSITY OF WISCONSIN MADISON · PI LYNN, DAVID M · 2003 to 2004
$465k
NIBIB NIH HHS 1 R01 EB006820NIBIB NIH HHS 1 R21 EB002746NIBIB NIH HHS R01 EB006820NIBIB NIH HHS R21 EB002746
6 · The paper itself

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.

Indexed as

AnimalsAntigen-Presenting CellsBiotechnologyCarbocyaninesCell LineChlorocebus aethiopsCoated Materials, BiocompatibleCOS CellsDNAElectrolytesFluorescent DyesGene Transfer TechniquesGoldGreen Fluorescent ProteinsMacrophagesMiceCarbocyaninesCoated Materials, Biocompatiblecyanine dye 3DNAElectrolytesFluorescent DyesGoldGreen Fluorescent ProteinsPolymersPolystyrenesWater

Identifiers

PMID18838346
PMCPMC2667125

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.