Triggering bilayer to inverted-hexagonal nanostructure formation by thiol-ene click chemistry on cationic lipids: consequences on gene transfection

Soft Matter. 2016 May 18;12(20):4516-20. doi: 10.1039/c6sm00609d.

Abstract

The ramification of cationic amphiphiles on their unsaturated lipid chains is readily achieved by using the thiol-ene click reaction triggering the formation of an inverted hexagonal phase (HII). The new ramified cationic lipids exhibit different bio-activities (transfection, toxicity) including higher transfection efficacies on 16HBE 14o-cell lines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Cell Line
  • Click Chemistry
  • Drug Carriers / chemistry*
  • Lipids / chemistry*
  • Nanostructures / chemistry*
  • Sulfhydryl Compounds / chemistry*
  • Transfection*

Substances

  • Alkenes
  • Drug Carriers
  • Lipids
  • Sulfhydryl Compounds