Designing Fast-Dissolving Orodispersible Films of Amphotericin B for Oropharyngeal Candidiasis

Dolores R Serrano1,2, Raquel Fernandez-Garcia1, Marta Mele3

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

Pharmaceutics
|August 4, 2019
PubMed

Insights

New fast-dissolving orodispersible films enhance Amphotericin B

Area of Science:

  • Pharmaceutical Sciences
  • Drug Delivery Systems
  • Mycology

Background:

  • Amphotericin B exhibits potent antifungal activity against Candida species with low resistance risk.
  • Poor water solubility and high molecular weight of Amphotericin B limit its efficacy for oropharyngeal candidiasis.
  • Current formulations face challenges due to physiological conditions in the oropharyngeal cavity.

Purpose of the Study:

  • To develop fast-dissolving orodispersible films for improved Amphotericin B delivery.
  • To enhance the solubilization and local antifungal effect of Amphotericin B in saliva.
  • To optimize film formulation using quality by design principles.

Main Methods:

  • Solvent casting technique used for preparing Amphotericin B-loaded orodispersible films.
  • Quality by Design (QbD) studies employed for formulation optimization.
  • Combination of dextrose-derived and cellulose-derived polymers, plasticizers, and taste-masking agents.

Main Results:

  • Optimized films demonstrated fast disintegration (60 ± 3 s) and rapid drug release (>80% in 10 min).
  • Films exhibited high mechanical strength (2190 mN mm) and potent efficacy against Candida species (>15 mm inhibition halo).
  • Formulation showed stability for two weeks at room temperature and up to one year under refrigeration.

Conclusions:

  • Fast-dissolving orodispersible films offer a promising approach for Amphotericin B delivery in oropharyngeal candidiasis.
  • The developed formulation enhances drug solubility and local antifungal activity.
  • Further in vivo and toxicological studies are warranted to validate clinical potential, especially for immunocompromised patients.

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