Plasmid size influences chitosan nanoparticle mediated gene transfer to chondrocytes

J Biomed Mater Res A. 2008 Mar 15;84(4):1038-48. doi: 10.1002/jbm.a.31479.


The objective of the present study was to prepare chitosan nanoparticles incorporating a relatively large plasmid encoding for osteogenic protein (OP)-1 and to determine the ability of these nanoparticles to transfect adult canine articular chondrocytes in vitro. The positive charge of chitosan acted to condense the relatively large negatively-charged OP-1 plasmid such that it could be incorporated into nanoparticles. Incorporation of the plasmid into the chitosan nanoparticles did not affect the structural integrity of the plasmid as demonstrated by gel electrophoresis. The morphology and size of the nanoparticles were found to vary with the chitosan:plasmid weight ratio. Nanoparticles formulated with a chitosan:plasmid ratio of 10:1 were of uniformly small size (less than 250 nm) and spherical shape. These nanoparticles had a positive charge of about 20 mV. FITC-labeled chitosan nanoparticles were found in virtually all of the cells after 24 h of incubation with the nanoparticles, and confocal microscopy revealed FITC-related fluorescence in the nucleus of the chondrocytes. Although transfection of the chondrocytes was demonstrated by the fluorescence of cells treated with chitosan nanoparticles containing the plasmid for the enhanced green fluorescence protein, cells transfected with nanoparticles incorporating the larger OP-1 plasmid did not show OP-1 expression measured by ELISA for up to 2 weeks in culture. These results indicate that although a large plasmid can be successfully incorporated within chitosan nanoparticles, the size of the plasmid incorporated within the nanoparticles may still significantly affect gene transfer to cells.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Biocompatible Materials / chemistry*
  • Bone Morphogenetic Protein 7
  • Bone Morphogenetic Proteins / metabolism*
  • Chitosan / chemistry
  • Chitosan / metabolism*
  • Chondrocytes / metabolism*
  • Fluorescein-5-isothiocyanate / chemistry
  • Fluorescent Dyes / pharmacology
  • Gene Transfer Techniques*
  • Green Fluorescent Proteins / metabolism
  • Humans
  • Light
  • Microscopy, Confocal
  • Microscopy, Electron, Scanning
  • Nanoparticles / chemistry*
  • Plasmids / metabolism
  • Scattering, Radiation
  • Transforming Growth Factor beta / metabolism*


  • BMP7 protein, human
  • Biocompatible Materials
  • Bone Morphogenetic Protein 7
  • Bone Morphogenetic Proteins
  • Fluorescent Dyes
  • Transforming Growth Factor beta
  • Green Fluorescent Proteins
  • Chitosan
  • Fluorescein-5-isothiocyanate