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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/22677
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dc.contributor.authorSilva, Michelle Peneluppi-
dc.contributor.authorChibebe Junior, Jose-
dc.contributor.authorJorjao, Adeline Lacerda-
dc.contributor.authorda Silva Machado, Ana Karina-
dc.contributor.authorde Oliveira, Luciane Dias-
dc.contributor.authorJunqueira, Juliana Campos-
dc.contributor.authorCardoso Jorge, Antonio Olavo-
dc.date.accessioned2014-05-20T14:04:38Z-
dc.date.available2014-05-20T14:04:38Z-
dc.date.issued2012-01-01-
dc.identifierhttp://dx.doi.org/10.1590/S1806-83242012000100005-
dc.identifier.citationBrazilian Oral Research. São Paulo: Sociedade Brasileira de Pesquisa Odontologica, v. 26, n. 1, p. 24-28, 2012.-
dc.identifier.issn1806-8324-
dc.identifier.urihttp://hdl.handle.net/11449/22677-
dc.description.abstractDue to the increase in life expectancy, new treatments have emerged which, although palliative, provide individuals with a better quality of life. Artificial saliva is a solution that contains substances that moisten a dry mouth, thus mimicking the role of saliva in lubricating the oral cavity and controlling the existing normal oral microbiota. This study aimed to assess the influence of commercially available artificial saliva on biofilm formation by Candida albicans. Artificial saliva I consists of carboxymethylcellulose, while artificial saliva II is composed of glucose oxidase, lactoferrin, lysozyme and lactoperoxidase. A control group used sterile distilled water. Microorganisms from the oral cavity were transferred to Sabouraud Dextrose Agar and incubated at 37 degrees C for 24 hours. Colonies of Candida albicans were suspended in a sterile solution of NaCl 0.9%, and standardisation of the suspension to 10(6) cells/mL was achieved. The acrylic discs, immersed in artificial saliva and sterile distilled water, were placed in a 24-well plate containing 2 mL of Sabouraud Dextrose Broth plus 5% sucrose and 0.1 mL aliquot of the Candida albicans suspension. The plates were incubated at 37 degrees C for 5 days, the discs were washed in 2 mL of 0.9% NaCl and placed into a tube containing 10 mL of 0.9% NaCl. After decimal dilutions, aliquots of 0.1 mL were seeded on Sabouraud Dextrose Agar and incubated at 37 degrees C for 48 hours. Counts were reported as CFU/mL (Log10). A statistically significant reduction of 29.89% (1.45 CFU/mL) of Candida albicans was observed in saliva I when compared to saliva II (p = 0.002, considering p <= 0.05).en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent24-28-
dc.language.isoeng-
dc.publisherSociedade Brasileira de Pesquisa Odontológica (SBPqO)-
dc.sourceWeb of Science-
dc.subjectSaliva, Artificialen
dc.subjectCandida albicansen
dc.subjectBiofilmen
dc.titleInfluence of artificial saliva in biofilm formation of Candida albicans in vitroen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNESP Univ Estadual Paulista, Sch Dent Sao Jose dos Campos, Dept Biosci & Oral Diag, Sao Jose Dos Campos, SP, Brazil-
dc.description.affiliationUnespUNESP Univ Estadual Paulista, Sch Dent Sao Jose dos Campos, Dept Biosci & Oral Diag, Sao Jose Dos Campos, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 10/14434-4-
dc.identifier.doi10.1590/S1806-83242012000100005-
dc.identifier.scieloS1806-83242012000100005-
dc.identifier.wosWOS:000311862300005-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileS1806-83242012000100005.pdf-
dc.relation.ispartofBrazilian Oral Research-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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