Effective Retinal Penetration of Lipophilic and Lipid-Conjugated Hydrophilic Agents Delivered by Engineered Liposomes

Mol Pharm. 2017 Feb 6;14(2):423-430. doi: 10.1021/acs.molpharmaceut.6b00864. Epub 2016 Dec 27.

Abstract

Efficient delivery of drugs to the retina is critical but difficult to achieve with current methods. There have been a number of attempts to use intravitreal injection of liposomes, artificial vesicles composed of a phospholipid bilayer, to overcome the limitations of conventional intravitreal injection (short retention time, toxicity, poor penetration, etc.). Here, we report an optimal liposomal formulation that can diffuse through the vitreous humor, deliver the incorporated agents to all retinal layers effectively, and maintain them for a relatively long time. We first delivered lipophilic compounds and phospholipid-conjugated hydrophilic agents to the inner limiting membrane using engineered liposomes. Subsequently, the agents penetrated the retina deeply, presumably via extracellular vesicles, nanoscale vesicles secreted from retinal-associated cells. These results suggest that this engineered liposomal formulation can leverage the biological transport system for effective retinal penetration of lipophilic and lipid-conjugated agents.

Keywords: drug delivery; extracellular vesicle; liposome; phospholipid; retina.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chemistry, Pharmaceutical / methods
  • Drug Carriers / administration & dosage
  • Drug Carriers / chemistry
  • Female
  • Hydrophobic and Hydrophilic Interactions
  • Lipid Bilayers / metabolism*
  • Lipids / chemistry*
  • Liposomes / administration & dosage*
  • Liposomes / chemistry*
  • Mice
  • Mice, Inbred C57BL
  • Phospholipids / administration & dosage
  • Phospholipids / chemistry
  • Retina / drug effects*
  • Retina / metabolism*
  • Vitreous Body / drug effects
  • Vitreous Body / metabolism

Substances

  • Drug Carriers
  • Lipid Bilayers
  • Lipids
  • Liposomes
  • Phospholipids