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Gellan-Based Hydrogel as a Drug Delivery System for Caffeic Acid Phenethyl Ester in the Treatment of Oral Candida albicans Infections

dc.contributor.authorGarcia, Maíra Terra [UNESP]
dc.contributor.authorCarmo, Paulo Henrique Fonseca do [UNESP]
dc.contributor.authorFigueiredo-Godoi, Lívia Mara Alves [UNESP]
dc.contributor.authorGonçalves, Natália Inês [UNESP]
dc.contributor.authorLima, Patrícia Michelle Nagai de [UNESP]
dc.contributor.authorRamos, Lucas de Paula [UNESP]
dc.contributor.authorOliveira, Luciane Dias de [UNESP]
dc.contributor.authorBorges, Alexandre Luiz Souto [UNESP]
dc.contributor.authorShukla, Anita
dc.contributor.authorJunqueira, Juliana Campos [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionBrown University
dc.date.accessioned2025-04-29T20:03:22Z
dc.date.issued2024-03-01
dc.description.abstractCandida albicans can cause various types of oral infections, mainly associated with denture stomatitis. Conventional therapy has been linked to high recurrence, toxicity, and fungal resistance, necessitating the search for new drugs and delivery systems. In this study, caffeic acid phenethyl ester (CAPE) and gellan gum (GG) were studied as an antifungal agent and carrier system, respectively. First, we observed that different GG formulations (0.6 to 1.0% wt/vol) were able to incorporate and release CAPE, reaching a controlled and prolonged release over 180 min at 1.0% of GG. CAPE-GG formulations exhibited antifungal activity at CAPE concentrations ranging from 128 to >512 µg/mL. Furthermore, CAPE-GG formulations significantly decreased the fungal viability of C. albicans biofilms at short times (12 h), mainly at 1.0% of GG (p < 0.001). C. albicans protease activity was also reduced after 12 h of treatment with CAPE-GG formulations (p < 0.001). Importantly, CAPE was not cytotoxic to human keratinocytes, and CAPE-GG formulations at 1.0% decreased the fungal burden (p = 0.0087) and suppressed inflammation in a rat model of denture stomatitis. Altogether, these results indicate that GG is a promising delivery system for CAPE, showing effective activity against C. albicans and potential to be used in the treatment of denture stomatitis.en
dc.description.affiliationDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology São Paulo State University (UNESP), SP
dc.description.affiliationDepartment of Dental Materials and Prosthodontics Institute of Science and Technology São Paulo State University (UNESP), SP
dc.description.affiliationCenter for Biomedical Engineering School of Engineering Brown University
dc.description.affiliationUnespDepartment of Biosciences and Oral Diagnosis Institute of Science and Technology São Paulo State University (UNESP), SP
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics Institute of Science and Technology São Paulo State University (UNESP), SP
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipOffice of Naval Research Global
dc.description.sponsorshipIdCNPq: CNPq 310265/2022-3
dc.description.sponsorshipIdOffice of Naval Research Global: N62909-20-1-2034
dc.identifierhttp://dx.doi.org/10.3390/pharmaceutics16030298
dc.identifier.citationPharmaceutics, v. 16, n. 3, 2024.
dc.identifier.doi10.3390/pharmaceutics16030298
dc.identifier.issn1999-4923
dc.identifier.scopus2-s2.0-85188750635
dc.identifier.urihttps://hdl.handle.net/11449/305540
dc.language.isoeng
dc.relation.ispartofPharmaceutics
dc.sourceScopus
dc.subjectantifungal
dc.subjectcaffeic acid phenethyl ester
dc.subjectCandida albicans
dc.subjectdenture stomatitis
dc.subjectgellan gum
dc.subjectoral candidiasis
dc.titleGellan-Based Hydrogel as a Drug Delivery System for Caffeic Acid Phenethyl Ester in the Treatment of Oral Candida albicans Infectionsen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0003-3186-885X[2]
unesp.author.orcid0000-0002-6690-9650[3]
unesp.author.orcid0000-0001-7870-0005[5]
unesp.author.orcid0000-0001-9956-7768[7]
unesp.author.orcid0000-0002-5707-7565[8]
unesp.author.orcid0000-0001-6646-6856[10]

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