Gene transfer into the lung by nanoparticle dextran-spermine/plasmid DNA complexes

J Biomed Biotechnol. 2010:2010:284840. doi: 10.1155/2010/284840. Epub 2010 Jun 30.

Abstract

A novel cationic polymer, dextran-spermine (D-SPM), has been found to mediate gene expression in a wide variety of cell lines and in vivo through systemic delivery. Here, we extended the observations by determining the optimal conditions for gene expression of D-SPM/plasmid DNA (D-SPM/pDNA) in cell lines and in the lungs of BALB/c mice via instillation delivery. In vitro studies showed that D-SPM could partially protect pDNA from degradation by nuclease and exhibited optimal gene transfer efficiency at D-SPM to pDNA weight-mixing ratio of 12. In the lungs of mice, the levels of gene expression generated by D-SPM/pDNA are highly dependent on the weight-mixing ratio of D-SPM to pDNA, amount of pDNA in the complex, and the assay time postdelivery. Readministration of the complex at day 1 following the first dosing showed no significant effect on the retention and duration of gene expression. The study also showed that there was a clear trend of increasing size of the complexes as the amount of pDNA was increased, where the sizes of the D-SPM/pDNA complexes were within the nanometer range.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • DNA
  • Deoxyribonuclease I
  • Dextrans / chemistry*
  • Electrophoresis, Agar Gel
  • Flow Cytometry
  • Gene Expression
  • Gene Transfer Techniques*
  • Genes, Reporter
  • Luciferases
  • Lung / metabolism*
  • Macromolecular Substances
  • Mice
  • Mice, Inbred BALB C
  • Microscopy, Fluorescence
  • Nanoparticles*
  • Particle Size
  • Plasmids / genetics*
  • Spermine / chemistry*

Substances

  • Dextrans
  • Macromolecular Substances
  • Spermine
  • DNA
  • Luciferases
  • Deoxyribonuclease I