Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies

Evelyn Osehontue Uroro1, Richard Bright2, Andrew Hayles2

  • 1UniSA STEM, University of South Australia, Mawson Lakes, SA 5095, Australia.

Insights

This study developed novel lipase-sensitive polycaprolactone nanocomposites for amphotericin B delivery. These nanocomposites enable on-demand drug release at infection sites, enhancing antifungal activity and reducing toxicity.

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Pharmacology

Background:

  • Amphotericin B is a critical antifungal agent but suffers from dose-limiting toxicities and poor solubility.
  • Current limitations necessitate innovative drug delivery systems for improved therapeutic outcomes.

Purpose of the Study:

  • To develop a novel nanocomposite system for lipase-triggered, on-demand delivery of amphotericin B.
  • To evaluate the antifungal efficacy and cytotoxicity of the developed nanocomposites.

Main Methods:

  • Amphotericin B was encapsulated into lipase-sensitive polycaprolactone via an oil-in-water emulsion method.
  • Nanocomposite physicochemical properties, in vitro drug release (with/without lipase), antifungal activity against Candida albicans, and cytotoxicity against human dermal fibroblasts were assessed.

Main Results:

  • Nanocomposites demonstrated minimal amphotericin B release in the absence of lipase.
  • Lipase triggered significant drug release, achieving fungicidal concentrations.
  • Enhanced antifungal activity against Candida albicans and reduced cytotoxicity were observed compared to free amphotericin B.

Conclusions:

  • Lipase-sensitive polycaprolactone nanocomposites offer a promising strategy for responsive amphotericin B delivery.
  • This approach can improve antifungal treatment by targeting drug release and minimizing side effects.