4.5 Article

Characterization of Nanoscale Transformations in Polyelectrolyte Multilayers Fabricated From Plasmid DNA Using Laser Scanning Confocal Microscopy in Combination With Atomic Force Microscopy

Journal

MICROSCOPY RESEARCH AND TECHNIQUE
Volume 73, Issue 9, Pages 834-844

Publisher

WILEY
DOI: 10.1002/jemt.20830

Keywords

thin films; nanostructure; polymers; layer-by-layer; DNA delivery

Funding

  1. National Institutes of Health [R21 EB002746, 01 EB006820]
  2. NIH [NIGMS T32 GM008505]
  3. The Arnold and Mabel Beckman Foundation
  4. The National Science Foundation (through the UW Materials Research Science and Engineering Center)
  5. The University of Wisconsin

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Laser scanning confocal microscopy (LSCM) and atomic force microscopy (AFM) were used to characterize changes in nanoscale structure that occur when ultrathin polyelectrolyte multilayers (PEMs) are incubated in aqueous media. The PEMs investigated here were fabricated by the deposition of alternating layers of plasmid DNA and a hydrolytically degradable polyamine onto a precursor film composed of alternating layers of linear poly(ethylene imine) (LPEI) and sodium poly(styrene sulfonate) (SPS). Past studies of these materials in the context of gene delivery revealed transformations from a morphology that is smooth and uniform to one characterized by the formation of nanometer-scale particulate structures. We demonstrate that in-plane registration of LSCM and AFM images acquired from the same locations of films fabricated using fluorescently labeled polyelectrolytes allows the spatial distribution of individual polyelectrolyte species to be determined relative to the locations of topographic features that form during this transformation. Our results suggest that this physical transformation leads to a morphology consisting of a relatively less disturbed portion of film composed of polyamine and DNA juxtaposed over an array of particulate structures composed predominantly of LPEI and SPS. Characterization by scanning electron microscopy and energy-dispersive X-ray microanalysis provides additional support for this interpretation. The combination of these different microscopy techniques provides insight into the structures and dynamics of these multicomponent thin films that cannot be achieved using any one method alone, and could prove useful for the further development of these assemblies as platforms for the surface-mediated delivery of DNA. Microsc. Res. Tech. 73:834-844, 2010. (C) 2010 Wiley-Liss, Inc.

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