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Antifungal activity and biocompatibility of α-AgVO3 microcrystals: A promising material against oral Candida disease

dc.contributor.authorPimentel, Bruna Natália Alves da Silva [UNESP]
dc.contributor.authorde Foggi, Camila Cristina [UNESP]
dc.contributor.authorBarbugli, Paula Aboud [UNESP]
dc.contributor.authorde Oliveira, Regiane Cristina
dc.contributor.authorde Avila, Erica Dorigatti [UNESP]
dc.contributor.authorLongo, Elson
dc.contributor.authorVergani, Carlos Eduardo [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.date.accessioned2020-12-12T02:29:22Z
dc.date.available2020-12-12T02:29:22Z
dc.date.issued2020-03-01
dc.description.abstractThe number of studies on microcrystals containing silver has increased in recent decades. Among the silver-containing microcrystals, α-AgVO3 has gained prominence owing to its polymorphism that allows it to exert interesting antimicrobial activity against pathogenic microorganisms. The aim of this study was to evaluate the antifungal activity and cytotoxicity of three different α-AgVO3 microcrystals when in solution. α-AgVO3 microcrystals were synthesized using the co-precipitation method at three different temperatures (10 °C, 20 °C, and 30 °C), and then characterized by X-ray diffraction and scanning electron microscopy. The antifungal activity of α-AgVO3 microcrystals against Candida albicans was determined by estimating the minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC). Fluorescence images were obtained to confirm antifungal concentrations. To assess the biocompatibility of microcrystals applied at MIC and MFC on keratinocytes cells (NOK-si), an Alamar Blue assay, scanning electron microscopy, and a DNA gel integrity test were carried out. The quantitative and qualitative results showed that, regardless of the co-precipitation method used to synthetize α-AgVO3 microcrystals, C. albicans growth was visibly inhibited at 3.9 μg/mL (MIC) and completely inhibited at 15.62 μg/mL (MFC). The cytotoxic and genotoxic outcomes revealed that the MIC and MFC concentrations did not affect NOK-si cell morphology, proliferation, or DNA integrity. The search for new antimicrobial materials has been the focus of the research community recently because of increases in microbial resistance. The findings reported herein demonstrate a novel antifungal and non-cytotoxic material that could be used in biomedical and dental applications.en
dc.description.affiliationSão Paulo State University (UNESP) School of Dentistry Araraquara, Rua Humaita, 1680
dc.description.affiliationCDMF-UFSCar - Universidade Federal de São Carlos, Washington Luis km 235, P.O. Box 676
dc.description.affiliationUnespSão Paulo State University (UNESP) School of Dentistry Araraquara, Rua Humaita, 1680
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2013/07296-2
dc.description.sponsorshipIdFAPESP: 2015/03567-7
dc.description.sponsorshipIdFAPESP: 2015/03654-7
dc.description.sponsorshipIdFAPESP: 2015/13834-2
dc.description.sponsorshipIdFAPESP: 2015/25124-0
dc.identifierhttp://dx.doi.org/10.1016/j.msec.2019.110405
dc.identifier.citationMaterials Science and Engineering C, v. 108.
dc.identifier.doi10.1016/j.msec.2019.110405
dc.identifier.issn1873-0191
dc.identifier.issn0928-4931
dc.identifier.scopus2-s2.0-85074684916
dc.identifier.urihttp://hdl.handle.net/11449/201310
dc.language.isoeng
dc.relation.ispartofMaterials Science and Engineering C
dc.sourceScopus
dc.subjectAntifungal agents
dc.subjectBiocompatibility
dc.subjectCandida albicans
dc.subjectKeratinocytes
dc.titleAntifungal activity and biocompatibility of α-AgVO3 microcrystals: A promising material against oral Candida diseaseen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublication3936e2e2-946a-42ab-8b9d-9521513200fc
relation.isDepartmentOfPublication.latestForDiscovery3936e2e2-946a-42ab-8b9d-9521513200fc
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.author.lattes3003130522427820[7]
unesp.author.orcid0000-0002-7375-4714[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentMateriais Odontológicos e Prótese - FOARpt

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