Effect of cell membrane thiols and reduction-triggered disassembly on transfection activity of bioreducible polyplexes

Jing Li, Devika S. Manickam, Jun Chen, David Oupicky

Research output: Contribution to journalArticle

15 Scopus citations

Abstract

Bioreducible polyplexes are promising vectors for delivery of nucleic acids due to low toxicity and favorable transfection activity. The often improved transfection is usually explained by enhanced intracellular reductive disassembly of the polyplexes. This study evaluated the effect of enhanced reductive disassembly on transfection activity of plasmid DNA and antisense oligonucleotide (AON) polyplexes based on a series of bioreducible poly(amido amine)s (PAA). We found that the presence of disulfide bonds in PAA had no effect on nucleic acid binding, hydrodynamic size and zeta potential of polyplexes. Increasing the disulfide content in PAA increased susceptibility to reduction-triggered DNA and AON release from the polyplexes. Increasing the disulfide content in PAA increased DNA transfection but had no effect on AON transfection. Plasma membrane protein thiols played a key role in the observed enhancement of DNA transfection. The presence of disulfide bonds in PAA had no significant effect on the rate of intracellular DNA clearance, suggesting that enhanced intracellular disassembly of the bioreducible polyplexes is not a major contributing factor to the improved transfection activity.

Original languageEnglish (US)
Pages (from-to)173-180
Number of pages8
JournalEuropean Journal of Pharmaceutical Sciences
Volume46
Issue number3
DOIs
StatePublished - Jun 14 2012

    Fingerprint

Keywords

  • Gene delivery
  • Polyplexes
  • Reducible polycations
  • Transfection

ASJC Scopus subject areas

  • Pharmaceutical Science

Cite this