Strategies for altering lipid self-assembly to trigger liposome cargo release

Chem Phys Lipids. 2020 Oct:232:104966. doi: 10.1016/j.chemphyslip.2020.104966. Epub 2020 Sep 1.

Abstract

While liposomes have proven to be effective drug delivery nanocarriers, their therapeutic attributes could be improved through the development of clinically viable triggered release strategies in which encapsulated drug contents could be selectively released at the sites of diseased cells. As such, a significant amount of research has been reported involving the development of stimuli-responsive liposomes and a broad range of strategies have been explored for driving content release. These have included the introduction of trigger groups at either the lipid headgroup or within the acyl chains that alter lipid self-assembly properties of known lipids as well as the rational design of lipid analogs programed to undergo conformational changes induced by events such as binding interactions. This review article describes advances in the design of stimuli-responsive liposome strategies with an eye towards emerging trends in the field.

Keywords: Drug delivery; Lipids; Liposomes; Self-assembly; Synthetic lipids; Triggered release.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acylation
  • Drug Design
  • Drug Liberation*
  • Lipids / chemistry*
  • Liposomes
  • Molecular Conformation

Substances

  • Lipids
  • Liposomes