Curcumin-containing liposomes stabilized by thin layers of chitosan derivatives

Colloids Surf B Biointerfaces. 2013 Sep 1:109:307-16. doi: 10.1016/j.colsurfb.2013.03.059. Epub 2013 Apr 22.

Abstract

Stable vesicles for efficient curcumin encapsulation, delivery and controlled release have been obtained by coating of liposomes with thin layer of newly synthesized chitosan derivatives. Three different derivatives of chitosan were obtained and studied: the cationic (by introduction of the stable, quaternary ammonium groups), the hydrophobic (by attachment of N-dodecyl groups) and cationic-hydrophobic one (containing both quaternary ammonium and N-dodecyl groups). Zeta potential measurements confirmed effective coating of liposomes with all these chitosan derivatives. The liposomes coated with cationic-hydrophobic chitosan derivative are the most promising curcumin carriers; they can easily penetrate cell membrane and release curcumin in a controlled manner. Biological studies indicated that such systems are non-toxic for murine fibroblasts (NIH3T3) while toxic toward murine melanoma (B16F10) cell line.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / toxicity
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Chitosan / analogs & derivatives*
  • Chitosan / chemistry*
  • Curcumin / pharmacology*
  • Curcumin / toxicity
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor
  • Hydrophobic and Hydrophilic Interactions
  • Liposomes / chemistry*
  • Mice
  • NIH 3T3 Cells
  • Particle Size
  • Structure-Activity Relationship
  • Surface Properties

Substances

  • Antineoplastic Agents
  • Liposomes
  • Chitosan
  • Curcumin