Amphotericin B Ocular Films for Fungal Keratitis and a Novel 3D-Printed Microfluidic Ocular Lens Infection Model

Chrysi Rapti1, Francis C Luciano1, Brayan J Anaya1

  • 1Pharmaceutics and Food Technology Department, Faculty of Pharmacy, Universidad Complutense de Madrid, Plaza Ramón y Cajal s/n, 28040 Madrid, Spain.

PubMed

Insights

This study developed a sustained-release amphotericin B ocular film for fungal keratitis treatment. A novel 3D-printed microfluidic model demonstrated the film

Area of Science:

  • Ophthalmology
  • Mycology
  • Materials Science

Background:

  • Fungal keratitis (FK) is a severe eye infection causing vision loss, particularly in contact lens users.
  • Candida albicans is the most common fungal pathogen, with amphotericin B (AmB) as the gold-standard treatment.
  • Current AmB eye drops have limited stability and corneal retention.

Purpose of the Study:

  • To develop a sustained-release AmB ocular film for enhanced FK treatment.
  • To create and utilize a 3D-printed microfluidic device for in vitro ocular drug testing.
  • To evaluate the efficacy of the AmB film against Candida albicans under physiological flow conditions.

Main Methods:

  • A 3D-printed, four-chamber microfluidic device was designed to simulate ocular conditions.
  • Contact lenses inoculated with Candida albicans were exposed to AmB-loaded films under fluid flow for 24 hours.
  • Drug release kinetics and antifungal activity (CFU/mL reduction) were quantified.

Main Results:

  • AmB films formulated with sodium alginate and hyaluronic acid demonstrated sustained release over 24 hours.
  • The AmB films achieved a 1.23-fold and 5.7-fold reduction in Candida albicans CFU/mL, depending on film concentration.
  • The microfluidic model effectively evaluated ocular drug release and antifungal efficacy.

Conclusions:

  • Sustained delivery of dimeric AmB via ocular films offers a promising approach for fungal keratitis treatment.
  • The developed 3D-printed microfluidic system provides a valuable tool for testing ophthalmic antimicrobial therapies.
  • This research paves the way for improved ocular drug delivery systems for infectious eye diseases.