An insight of in vitro transport of PEGylated non-ionic surfactant vesicles (NSVs) across the intestinal polarized enterocyte monolayers

Eur J Pharm Biopharm. 2018 Jun:127:432-442. doi: 10.1016/j.ejpb.2018.03.013. Epub 2018 Mar 29.

Abstract

PEGylated non-ionic surfactant-based vesicles (NSVs) are promising drug delivery systems for the local, oral and systemic administrations of therapeutics. The aim of this study was to test the cellular biocompatibility and transport of Nile Red-loaded NSVs (NR-NSVs) across the Caco-2-cell monolayers, which represent an in vitro model of human intestinal epithelium. The NR-NSVs assumed a spherical shape with a mean size of 140 nm, and a narrow size distribution. The NR-NSVs did not modify Caco-2 cell viability, which remained unaltered in vitro up to a concentration of 1 mM. The transport studies demonstrated that the NR-NSVs moved across the Caco-2 monolayers without affecting the transepithelial electrical resistance. These results were supported by flow cytometry analysis, which demonstrated that NR-NSVs were internalized inside the Caco-2 cells. Nanoparticle tracking and Transmission Electron Microscopy (TEM) analysis showed the presence of NR-NSVs in the basolateral side of the Caco-2 monolayers. TEM images also showed that NSVs were transported intact across the Caco-2 monolayers, thus demonstrating a predominant transcytosis mechanism of transport through endocytosis. The NSVs did not affect the integrity of the membrane barrier in vitro, and can potentially be used in clinics to increase the oral bioavailability and delivery of therapeutics.

Keywords: Caco-2-cell monolayers; In vitro biological barrier transport; Nanoparticle tracking analysis; PEGylated non-ionic surfactant vesicles; Transepithelial electrical resistance analysis.

MeSH terms

  • Biological Availability
  • Biological Transport / physiology
  • Caco-2 Cells
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Drug Carriers / metabolism
  • Drug Delivery Systems / methods
  • Endocytosis / physiology
  • Enterocytes / metabolism*
  • Humans
  • Intestinal Absorption / physiology*
  • Intestinal Mucosa / metabolism*
  • Nanoparticles / metabolism
  • Polyethylene Glycols / metabolism*
  • Surface-Active Agents / metabolism*

Substances

  • Drug Carriers
  • Surface-Active Agents
  • Polyethylene Glycols