On the uptake of cationic liposomes by cells: From changes in elasticity to internalization

Colloids Surf B Biointerfaces. 2023 Jan:221:112968. doi: 10.1016/j.colsurfb.2022.112968. Epub 2022 Oct 26.

Abstract

In this study, we assessed the capacity of a previously reported engineered liposomal formulation, which had been tested against model membranes mimicking the lipid composition of the HeLa plasma membrane, to fuse and function as a nanocarrier in cells. We used atomic force microscopy to observe physicochemical changes on the cell surface and confocal microscopy to determine how the liposomes interact with cell membranes and released their load. In addition, we performed viability assays using methotrexate as an active drug to obtain proof of concept of the formulation´s capacity to function as a drug delivery-system. The interaction of engineered liposomes with living cells corroborates the information obtained using model membranes and supports the capacity of the engineered liposomal formulation to serve as a potential nanocarrier.

Keywords: Atomic force microscopy; Confocal microscopy; Drug delivery system; Engineered liposomes; Filopodia; Young´s modulus.

MeSH terms

  • Biological Transport
  • Cations / analysis
  • Cell Membrane / metabolism
  • Drug Delivery Systems*
  • Elasticity
  • Humans
  • Liposomes* / chemistry

Substances

  • Liposomes
  • Cations