Supramolecular core-shell nanosilica@liposome nanocapsules for drug delivery

Langmuir. 2012 Jul 24;28(29):10725-32. doi: 10.1021/la3021645. Epub 2012 Jul 13.

Abstract

The fabrication of core-shell structural nanosilica@liposome nanocapsules as a drug delivery vehicle is reported. SiO(2) nanoparticles are encapsulated within liposomes by a W/O/W emulsion approach to form supramolecular assemblies with a core of colloidal particles enveloped by a lipid bilayer shell. A nanosilica core provides charge compensation and architectural support for the lipid bilayer, which significantly improves their physical stability. A preliminary application of these core-shell nanocapsules for hemoglobin (Hb) delivery is described. Through the H-bonding interaction between the hydroxyl groups on nanosilicas and the amino nitrogens of Hb, Hb-SiO(2) nanocomplexes in which the saturated adsorption amount of Hb on SiO(2) is 0.47 g g(-1) are coated with lipids to generate core-shell Hb-SiO(2)@liposome nanocapsules with mean diameters of 60-500 nm and Hb encapsulation efficiency of 48.4-87.9%. Hb-SiO(2)@liposome supramolecular nanovehicles create a mode of delivery that stabilizes the encapsulated Hb and achieves long-lasting release, thereby improving the efficacy of the drug. Compared with liposome-encapsulated Hb and Hb-loaded SiO(2) particles, such core-shell nanovehicles show substantially enhanced release performance of Hb in vitro. This finding opens up a new window of liposome-based formulations as drug delivery nanovehicles for widespread pharmaceutical applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Drug Delivery Systems*
  • Hemoglobins / chemistry*
  • Liposomes / chemistry*
  • Macromolecular Substances / chemistry
  • Models, Molecular
  • Molecular Conformation
  • Nanostructures / chemistry*
  • Particle Size
  • Silicon Dioxide / chemistry*
  • Surface Properties

Substances

  • Hemoglobins
  • Liposomes
  • Macromolecular Substances
  • Silicon Dioxide