(PhSe)2 and (pCl-PhSe)2 organochalcogen compounds inhibit Candida albicans adhesion to human endocervical (HeLa) cells and show anti- biofilm activities
dc.contributor.author | Silva, Bruna Marques da | |
dc.contributor.author | Braga, Marília Toledo | |
dc.contributor.author | Passos, Juliene Cristina da Silva | |
dc.contributor.author | Carvalho, Moisés Lopes | |
dc.contributor.author | Rosseti, Isabela Bueno | |
dc.contributor.author | Amorim, Laís Mayara Machado de | |
dc.contributor.author | Rocha, João Batista Teixeira da | |
dc.contributor.author | Silva, Carlos Alberto | |
dc.contributor.author | Costa, Maricilia Silva | |
dc.date.accessioned | 2025-06-13T16:32:52Z | |
dc.date.available | 2025-06-13T16:32:52Z | |
dc.date.issued2 | 2021 | |
dc.description.abstract | Adhesion capacity on biological surfaces and biofilm formation is considered an important step in the infection process by Candida albicans. The ability of (PhSe)2 and (pCl-PhSe)2, two synthetic organic selenium (organochalcogen) compounds, to act on C. albicans virulence factors related to adhesion to human endocervical (HeLa) cell surfaces and their anti-biofilm activities was ana- lyzed. Both organochalcogen compounds inhibited C. albicans adhesion to HeLa cells, depend- ent on compound concentrations. (PhSe)2 (at 20 mM; p 1⁄4 0.0012) was significantly more effective than (pCl-PhSe)2 (at 20 mM; p 1⁄4 0.0183) compared with the control. (PhSe)2 inhibited biofilm for- mation and decreased biofilm viability in both early and mature biofilms more efficiently than (pCl-PhSe)2. Overall, the organochalcogen compounds, especially (PhSe)2, were demonstrated to be effective antifungal drugs against C. albicans virulence factors related to epithelial cell surface adhesion and the formation and viability of biofilms. | |
dc.description.physical | 12 p. | |
dc.description.sponsorship | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description.uri | CAPES – Finance Code 001 | |
dc.format.mimetype | ||
dc.identifier.affiliation | Universidade do Vale do Paraíba | |
dc.identifier.affiliation | Universidade Federal de Santa Maria | |
dc.identifier.affiliation | Universidade Federal do ABC | |
dc.identifier.bibliographicCitation | SILVA, B. M. et al. (PhSe)2 and (pCl-PhSe)2 organochalcogen compounds inhibit Candida albicans adhesion to human endocervical (HeLa) cells and show anti-biofilm activities. Biofouling, v. 37, n. 2, p. 235-245, 2021. Disponível em: https://www.tandfonline.com/doi/full/10.1080/08927014.2021.1897110. | |
dc.identifier.doi | 10.1080/08927014.2021.1897110 | |
dc.identifier.uri | https://repositorio.univap.br/handle/123456789/1006 | |
dc.language.iso | en_US | |
dc.publisher | Taylor & Francis | |
dc.rights.holder | Biofouling | |
dc.subject.keyword | Candida albicans | |
dc.subject.keyword | Organochalcogen | |
dc.subject.keyword | Compounds | |
dc.subject.keyword | Biofilm | |
dc.subject.keyword | Antifungal therapy | |
dc.subject.keyword | Cell adhesion | |
dc.subject.keyword | HeLa cells | |
dc.title | (PhSe)2 and (pCl-PhSe)2 organochalcogen compounds inhibit Candida albicans adhesion to human endocervical (HeLa) cells and show anti- biofilm activities | |
dc.type | Artigos de Periódicos |
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