Overcoming intestinal barriers by heparanase-responsive charge-converting nanocarriers

Int J Pharm. 2024 Feb 15:651:123817. doi: 10.1016/j.ijpharm.2024.123817. Epub 2024 Jan 17.

Abstract

In this study, we present a novel approach for overcoming intestinal barriers by utilizing heparanase-responsive charge-converting nanocarriers (NCs). These NCs are designed to undergo charge conversion in response to the activity of heparanase (HPSE), an enzyme commonly overexpressed in cancer cells. Nanostructured lipid carriers (NLCs) and solid lipid nanocarriers (SLNs) with a positively charged core were coated with heparin (Hep), resulting in a negative surface charge and a size between 195 and 220 nm. However, upon encountering heparanase, heparin undergoes enzymatic cleavage, resulting in zeta potential shift from -22.1 to +8.3 mV for NLC-Hep and from -19.8 to +5.1 mV for SLN-Hep. Heparin-coated NCs showed more than 6-fold higher mucus permeating properties compared to the uncoated NCs. In vitro experiments using the heparanase-expressing cancer cell line HT29 demonstrated an up to 4-fold improved cellular uptake of the heparin coated NCs compared to co-incubation with the HPSE inhibitor suramin. Furthermore, cellular uptake was investigated on Caco-2 cells and on a Caco-2/HT29-MTX co-culture. Overall, this study highlights the potential of heparanase-responsive charge-converting NCs as a promising strategy for overcoming intestinal barriers and enhancing cellular uptake.

Keywords: Charge conversion; Heparanase; Heparin; Nanostructured lipid carrier; Solid lipid nanocarrier.

MeSH terms

  • Caco-2 Cells
  • Drug Carriers*
  • Glucuronidase*
  • Heparin
  • Humans
  • Lipids
  • Nanoparticles*
  • Particle Size

Substances

  • Drug Carriers
  • heparanase
  • Lipids
  • Heparin
  • Glucuronidase