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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.
Abstract:
Amphotericin B possesses high activity against Candida spp. with low risk of resistance. However, Amphotericin B's high molecular weight compared to other antifungal drugs, such as miconazole and clotrimazole, and poor water solubility hampers its efficacy at the physiological conditions of the oropharyngeal cavity (saliva pH, limited volume for dissolution) and thereby limits its clinical use in oropharyngeal candidiasis. We have prepared fast-dissolving orodispersible films with high loading (1% w/w) using solvent casting that enables amphotericin B to remain solubilised in saliva in equilibrium between the monomeric and dimeric states, and able to produce a local antifungal effect. Optimisation of the amphotericin B-loaded orodispersible films was achieved by quality by design studies combining dextran and/or maltodextrin as dextrose-derived-polymer film formers with cellulose-derived film formers (hydroxypropylmethyl/hydroxypropyl cellulose in a 1:4 weight ratio), sorbitol for taste masking, microcrystalline cellulose (Avicel 200) or microcrystalline cellulose-carboxymethylcellulose sodium (Avicel CL-611) for enhancing the mechanical strength of the film, and polyethylene glycol 400 and glycerol (1:1 w/w) as plasticizers. The optimised amphotericin B orodispersible films (containing 1% AmB, 25% dextran, 25% maltodextrin, 5% sorbitol, 10% Avicel 200, 10% polyethylene glycol 400, 10% glycerol, 3% hydroxypropylmethyl cellulose acetate succinate, 12% hydroxypropyl cellulose) possessed a fast disintegration time (60 ± 3 s), quick release in artificial saliva (>80% in 10 min), high burst strength (2190 mN mm) and high efficacy against several Candida spp. (C. albicans, C. parapsilosis and C. krusei) (>15 mm inhibition halo). Amphotericin B orodispersible films are stable for two weeks at room temperature (25 °C) and up to 1 year in the fridge. Although further toxicological and in vivo efficacy studies are required, this novel Amphotericin B orodispersible films is a promising, physicochemically stable formulation with potential wide application in clinical practice, especially for immunocompromised patients suffering from oropharyngeal candidiasis.
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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