Characterization, Antifungal Evaluation against Candida spp. Strains and Application of Nystatin: β-cyclodextrin Inclusion Complexes

Author:

Urban Vanessa Migliorini1ORCID,Urban Amanda Migliorini2ORCID,Morikava Francine Sumie1,Schoeffel Amanda Cristina1ORCID,Novatski Andressa3ORCID,Moraes Gustavo Simão1ORCID,Cachoeira Victoria Schlumberger1ORCID,Matioli Graciette4,Sanches Ito Carmen Antonia5ORCID,Ferrari Priscileila Colerato2ORCID,Neppelenbroek Karin Hermana6ORCID,Farago Paulo Vitor7ORCID

Affiliation:

1. Department of Dentistry, State University of Ponta Grossa, Ponta Grossa, PR, Brazil.

2. Department of Pharmaceutical Sciences, State University of Ponta Grossa, Ponta Grossa, PR, Brazil

3. Department of Physics, State University of Ponta Grossa, Ponta Grossa, PR, Brazil

4. Department of Pharmacy, State University of Maringa, Maringa, PR, Brazil

5. Laboratory of Clinical Analyses, State University of Ponta Grossa,, Paraná, Brazil

6. Department of Prosthodontics and Periodontics, Bauru School of Dentistry, University of São Paulo, Bauru, São Paulo, Brazil.

7. Department of Pharmaceutical Sciences, State University of Ponta Grossa, Ponta Grossa, PR, Brazil.

Abstract

Background: Nystatin (Nys) is a fungicidal drug commonly prescribed for candidiasis disease in several administration routes. However, Nys is a class IV drug according to the Biopharmaceutical Classification System, that possesses limited bioavailability, and is used for local activity. Objective: This study developed and characterized nystatin:β-cyclodextrin (Nys:βCD) inclusion complexes and evaluated their activity against Candida spp. Methods: Complexes were characterized by physicochemical techniques and drug dissolution profiles. The susceptibility of C. albicans, C. krusei, C. parapsilosis, C. glabrata, C. guilliermondii, C. tropicalis, and C. auris was assessed using the broth microdilution method. The applicability of Nys:βCD inclusion complex was evaluated by incorporating it into a temporary soft material for denture stomatitis treatment Results: Nys was better complexed in a 1:1 molar ratio by freeze-drying and spray-drying methods. The inclusion complexes show bi-exponential release, an initial burst release followed by a sustained manner, presenting higher dissolution efficiency than raw Nys. The 1:1 freeze-drying Nys:βCD complex presents antifungal activity against all evaluated Candida strains, showing the maintenance of the drug effectiveness. The inclusion complex incorporated into a tissue conditioner material for denture stomatitis treatment effectively inhibited more than 90% of C. albicans biofilm growth during 7 and 14 days, in a half dose compared to raw Nys. Conclusion: This work represents a significant contribution to treating a wide variety of diseases caused by the Candida species, optimizing the drug bioavailability and compliance to the treatment due to improved drug solubility, dissolution, and sustained delivery.

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmaceutical Science

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