Detalhes bibliográficos
Ano de defesa: |
2013 |
Autor(a) principal: |
Nascimento, Camila Almeida [UNESP] |
Orientador(a): |
Não Informado pela instituição |
Banca de defesa: |
Não Informado pela instituição |
Tipo de documento: |
Dissertação
|
Tipo de acesso: |
Acesso aberto |
Idioma: |
por |
Instituição de defesa: |
Universidade Estadual Paulista (Unesp)
|
Programa de Pós-Graduação: |
Não Informado pela instituição
|
Departamento: |
Não Informado pela instituição
|
País: |
Não Informado pela instituição
|
Palavras-chave em Português: |
|
Link de acesso: |
http://hdl.handle.net/11449/108397
|
Resumo: |
The aim of this study was to evaluate the action of conventional endodontic solutions such as sodium hypochlorite and chlorhexidine associated with cetrimide and QMiX, a commercial product composed by chlorhexidine, EDTA and cetrimide, on biofilm and planktonic phase of Enterococcus faecalis (ATCC 29212). The evaluated solutions were: G1: 2.5% Sodium Hypochlorite (NaOCl); G2: 2.5% NaOCl + 0.2% cetrimide (CTR); G3: 2% Chlorhexidine (CLX) 2%; G4: 2% CLX + 0.2% CTR; G5: 0.2% CTR; G6: QMiX. Saline solution was used as negative control. The study was divided into two chapters. In Chapter 1, the antibacterial activity of the solutions on microorganisms in planktonic phase and biofilm was evaluated. For direct contact with E. faecalis in planktonic phase, 50 μL of bacterial suspension were placed in tubes containing 1.45 mL of each irrigation solution or associations and after 1 and 3 minutes, neutralizing solutions were used to stop of the antimicrobial action of endodontic solutions. Decimal serial dilutions were performed and the suspensions were plated in Tryptic Soy agar medium (TSa). Dentin bovine blocks were used as substrate for induction of biofilms for 14 days. The biofilms were placed in contact with the solutions evaluated and transferred to test tubes containing neutralizing solution. After agitation for 60 seconds to suspend the remaining cells, decimal serial dilutions were performed and the suspensions were cultivated in triplicate on TSA plates. The incubation was held in microaerophilic at 37 ° C for 24 hours and the analysis was performed by counting CFU mL-1. The results were submitted to ANOVA and Tukey test, with significance level of 5%. All irrigating solutions and associations evaluated completely eradicated the microorganisms in planktonic phase. On biofilm, only NaOCl and NaOCl+CTR showed 100%- of bacterial elimination. CLX showed similar activity to CLX+CTR, CTR and QMiX after... |