Folate-PEG coated cationic modified chitosan--cholesterol liposomes for tumor-targeted drug delivery

Biomaterials. 2010 May;31(14):4129-38. doi: 10.1016/j.biomaterials.2010.01.089. Epub 2010 Feb 16.

Abstract

In this paper, a folate-PEG coated polymeric liposome (FPL) formed from octadecyl-quaternized lysine modified chitosan (OQLCS) and cholesterol has been prepared successfully. The OQLCS and its derivatives were characterized using (1)H NMR and infrared spectrum analysis. The FPLs properties were extensively studied by dynamic light scattering (DLS), fluorescence spectroscopy, and transmission electron microscopy (TEM). Due to the amphiphilic property and positive zeta potential of OQLCS, the OQLCS and cholesterol can form stable core-shell FPLs with small size (effective diameter: 163.5 nm) and narrow distribution (polydispersity: 0.108) in aqueous solutions. The PLs could form multi-lamellar structure similar to that of traditional liposomes prepared from phosphatidylcholine/cholesterol (PC/Chol). Compared with traditional liposome, calcein-loaded Polymeric Liposome exhibited high encapsulation efficiency in aqueous solution and slow, controlled release under different pH conditions. Most important, in cellular uptake experiment, folate coated FPLs showed significant higher uptake by MCF-7 cells as compared to FPLs without folate and traditional liposomes, because of the folate-receptor mediated endocytosis. The data suggest that the folate-PEG coated polymeric liposomes (FPLs) may be a useful drug delivery system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cations / pharmacology
  • Cell Line, Tumor
  • Chitosan / chemistry
  • Chitosan / pharmacology*
  • Cholesterol / chemistry
  • Cholesterol / pharmacology*
  • Drug Delivery Systems / methods*
  • Flow Cytometry
  • Fluoresceins / metabolism
  • Folic Acid / chemistry
  • Folic Acid / pharmacology*
  • Humans
  • Hydrogen-Ion Concentration / drug effects
  • Kinetics
  • Liposomes / chemistry
  • Magnetic Resonance Spectroscopy
  • Micelles
  • Microscopy, Fluorescence
  • Neoplasms / drug therapy*
  • Neoplasms / pathology
  • Particle Size
  • Permeability / drug effects
  • Polyethylene Glycols / chemistry
  • Polyethylene Glycols / pharmacology*
  • Spectrometry, Fluorescence
  • Spectroscopy, Fourier Transform Infrared
  • Time Factors

Substances

  • Cations
  • Fluoresceins
  • Liposomes
  • Micelles
  • Polyethylene Glycols
  • Chitosan
  • Folic Acid
  • Cholesterol
  • fluorexon