ABSTRACT
ABSTRACT Objective The antimicrobial effect of ultrasonic agitation of calcium hydroxide (CH) pastes in infected bovine dentin and their penetrability were evaluated using confocal laser scanning microscopy (CLSM) and microbiological culture. Material and Methods Fifty-two bovine teeth were infected with Enterococcus faecalis using a new contamination protocol; then they received CH paste and were divided into groups with or without ultrasound. Ultrasonic agitation was conducted for 1 min with a plain point insert. After 15 d, the CLSM analyzed the viable and dead bacteria with Live and Dead assay. The dentinal wall debris was collected by burs, and the colony forming units (CFU/mL) were counted. The penetrability of the paste inside dentinal tubules was tested using the B-rodamine dye. Results The calcium hydroxide paste showed better results with the use of ultrasonic agitation (p<0.05). Conclusion The ultrasonic agitation of CH paste increased its antimicrobial action and was responsible for intradentinal penetration with the fulfilment of the tubules.
Subject(s)
Animals , Cattle , Root Canal Therapy/methods , Ultrasonic Therapy/methods , Calcium Hydroxide/pharmacology , Enterococcus faecalis/drug effects , Dental Pulp Cavity/microbiology , Dentin/microbiology , Anti-Infective Agents, Local/pharmacology , Root Canal Irrigants/pharmacology , Time Factors , Colony Count, Microbial , Reproducibility of Results , Microscopy, Confocal , Dental Pulp Cavity/drug effects , Dentin/drug effects , Microbial Viability/drug effectsABSTRACT
OBJECTIVE: The antimicrobial effect of ultrasonic agitation of calcium hydroxide (CH) pastes in infected bovine dentin and their penetrability were evaluated using confocal laser scanning microscopy (CLSM) and microbiological culture. MATERIAL AND METHODS: Fifty-two bovine teeth were infected with Enterococcus faecalis using a new contamination protocol; then they received CH paste and were divided into groups with or without ultrasound. Ultrasonic agitation was conducted for 1 min with a plain point insert. After 15 d, the CLSM analyzed the viable and dead bacteria with Live and Dead assay. The dentinal wall debris was collected by burs, and the colony forming units (CFU/mL) were counted. The penetrability of the paste inside dentinal tubules was tested using the B-rodamine dye. RESULTS: The calcium hydroxide paste showed better results with the use of ultrasonic agitation (p<0.05). CONCLUSION: The ultrasonic agitation of CH paste increased its antimicrobial action and was responsible for intradentinal penetration with the fulfilment of the tubules.
Subject(s)
Anti-Infective Agents, Local/pharmacology , Calcium Hydroxide/pharmacology , Dental Pulp Cavity/microbiology , Dentin/microbiology , Enterococcus faecalis/drug effects , Root Canal Therapy/methods , Ultrasonic Therapy/methods , Animals , Cattle , Colony Count, Microbial , Dental Pulp Cavity/drug effects , Dentin/drug effects , Microbial Viability/drug effects , Microscopy, Confocal , Reproducibility of Results , Root Canal Irrigants/pharmacology , Time FactorsABSTRACT
Objectives To compare three methods of intratubular contamination that simulate endodontic infections using confocal laser scanning microscopy (CLSM). Material and Methods Two pre-existing models of dentinal contamination were used to induce intratubular infection (groups A and B). These methods were modified in an attempt to improve the model (group C). Among the modifications it may be included: specimen contamination for five days, ultrasonic bath with BHI broth after specimen sterilization, use of E. faecalisduring the exponential growth phase, greater concentration of inoculum, and two cycles of centrifugation on alternate days with changes of culture media. All specimens were longitudinally sectioned and stained with of LIVE/DEAD® for 20 min. Specimens were assessed using CLSM, which provided images of the depth of viable bacterial proliferation inside the dentinal tubules. Additionally, three examiners used scores to classify the CLSM images according to the following parameters: homogeneity, density, and depth of the bacterial contamination inside the dentinal tubules. Kruskal-Wallis and Dunn’s tests were used to evaluate the live and dead cells rates, and the scores obtained. Results The contamination scores revealed higher contamination levels in group C when compared with groups A and B (p<0.05). No differences were observed between group A and B (p>0.05). The volume of live cells in group C was higher than in groups A and B (p<0.05). Conclusion The new protocol for intratubular infection resulted in high and uniform patterns of bacterial contamination and higher cell viability in all specimens when compared with the current methods.
Subject(s)
Animals , Cattle , Dental Pulp Cavity/microbiology , Dentin/microbiology , Disease Models, Animal , Enterococcus faecalis , Centrifugation , Culture Media , Dentin/ultrastructure , Gram-Positive Bacterial Infections/microbiology , Microbial Viability , Microscopy, Confocal , Reproducibility of Results , Time FactorsABSTRACT
OBJECTIVES: To compare three methods of intratubular contamination that simulate endodontic infections using confocal laser scanning microscopy (CLSM). MATERIAL AND METHODS: Two pre-existing models of dentinal contamination were used to induce intratubular infection (groups A and B). These methods were modified in an attempt to improve the model (group C). Among the modifications it may be included: specimen contamination for five days, ultrasonic bath with BHI broth after specimen sterilization, use of E. faecalisduring the exponential growth phase, greater concentration of inoculum, and two cycles of centrifugation on alternate days with changes of culture media. All specimens were longitudinally sectioned and stained with of LIVE/DEAD for 20 min. Specimens were assessed using CLSM, which provided images of the depth of viable bacterial proliferation inside the dentinal tubules. Additionally, three examiners used scores to classify the CLSM images according to the following parameters: homogeneity, density, and depth of the bacterial contamination inside the dentinal tubules. Kruskal-Wallis and Dunn's tests were used to evaluate the live and dead cells rates, and the scores obtained. RESULTS: The contamination scores revealed higher contamination levels in group C when compared with groups A and B (p<0.05). No differences were observed between group A and B (p>0.05). The volume of live cells in group C was higher than in groups A and B (p<0.05). CONCLUSION: The new protocol for intratubular infection resulted in high and uniform patterns of bacterial contamination and higher cell viability in all specimens when compared with the current methods.
Subject(s)
Dental Pulp Cavity/microbiology , Dentin/microbiology , Disease Models, Animal , Enterococcus faecalis , Animals , Cattle , Centrifugation , Culture Media , Dentin/ultrastructure , Gram-Positive Bacterial Infections/microbiology , Microbial Viability , Microscopy, Confocal , Reproducibility of Results , Time FactorsABSTRACT
Objetivo: verificar a ação antimicrobiana, solubilidade, tempo de presa, escoamento, pH, liberação de cálcio e característica da superfície do MTA associado as substancias hipoclorito de sodio gel a 1%, clorexidina gel a 2%, água destilada associada a 10% de propilenoglicol (CCPG), K-Y gel, solução salina e, por fim, água destilada. Métodos: para o teste antimicrobiano, utilizou-se o Streptococcus mutans, Lactobacillus casei, Enterococcus faecalis e Candida albicans, por meio do método de contato direto. Para avaliação do tempo de presa e escoamento, foram utilizadas as especificações ASTM 266/08 e ADA 57/2007. Para o pH e liberação de cálcio, os materiais foram inseridos em cavidades retrogradas de dentes de resina acrílica e imersos em água ultrapura, para avaliação em diferentes períodos, utilizando um pHmetro e um espectrofotômetro de absorção atômica. Para a analise das características de superfície, os dentes de acrílico foram analisados com microscopia eletrônica de varredura (MEV). Resultados: os resultados dos testes antimicrobianos mostraram que os diferentes aditivos associados ao MTA apresentaram maior propriedade inibitória do que bactericida, sendo que a clorexidina apresentou os melhores resultados. As amostras que utilizaram o K-Y gel como veiculo apresentaram maiores índices de solubilidade. Houve diferença estatística entre os grupos (p > 0,05) quanto ao escoamento. O grupo que utilizou o CCPG apresentou o menor tempo de presa. O grupo K-Y apresentou os menores pH e liberação de cálcio no período de três horas. Nos outros períodos, houve maior uniformidade entre os grupos. Com relação as características da superfície, o grupo CCPG apresentou a maior porosidade (p < 0,05). Conclusão: o único veiculo avaliado que proporcionou alguma melhora no efeito antimicrobiano foi a clorexidina gel a 2%. Ja o K-Y gel interferiu nas propriedades físico-químicas do MTA, e a adição de CCPG proporcionou a maior porosidade.
Subject(s)
Calcium , Dental Cements , Disk Diffusion Antimicrobial Tests , Chemical Phenomena , SolubilityABSTRACT
O objetivo foi avaliar a influência da agitação ultrassônica (U) na atividade antimicrobiana e penetrabilidade de pastas de hidróxido de cálcio (HC) em propilenoglicol, com ou sem extrato etanólico de própolis (EEP) em propilenoglicol a 10%, através da Microscopia Confocal de Varredura a Laser (MCVL) e cultura microbiológica (CM). Para isso setenta e dois tubos de dentina bovina padronizados foram infectados com Enterococcus faecalis em caldo BHI (Brain Heart Infusion) utilizando um novo protocolo de contaminação com dois ciclos de centrifugação por 5 dias. Durante o período experimental os espécimes foram divididos em 4 grupos e preenchidos com as medicações a seguir: Grupo1- HC, Grupo 2 HC + EEP, Grupo 3 HC + U e Grupo 4 HC + EEP + U. A agitação ultrassônica foi realizada durante 1 minuto nas direções vestíbulo-lingual e mésio-distal, com o auxílio de um inserto liso. As medicações permaneceram no interior dos espécimes por 15 dias. A MCVL analisou as bactérias viáveis (verde) e mortas (vermelho), com o auxílio do corante Live and Dead® nos tubos de dentina após o período de medicação. A contagem de Unidades Formadoras de Colônia (UFCs) foi realizada a partir da cultura microbiológica (CM). As raspas de dentina foram coletadas e diluídas para semeadura em placas de Petri com ágar BHI. Para a penetração foi utilizado o corante Rodamina B durante a manipulação das pastas de HC e as análises feitas por MCVL. O grupo 1 (HC) mostrou a maior viabilidade bacteriana nos tubos de dentina contaminados e o grupo 4 (HC + EEP +U) a menor. A agitação ultrassônica (U) reduziu significativamente a viabilidade bacteriana para todos os grupos. A pasta de HC + EEP mostrou-se mais eficaz que aquela somente com HC (p<0,05%). Concluiu-se que a agitação ultrassônica das pastas de HC aumentou sua atividade antimicrobiana e possibilitou maior penetração intratubular, com preenchimento de túbulos dentinários.
The purpose was to evaluate the influence of ultrasonic agitation (U) on the antimicrobial potential and penetrability of calcium hydroxide (CH) pastes with or without the ethanolic extract of propolis (EEP) in propylene glycol (10%) using Confocal Laser Scanning Microscopy (CLSM) and microbiological cultures (MC) of infected dentin. Seventy two cylindrical dentin specimens were infected with Enterococcus faecalis in BHI broth using a new contamination protocol for 5 days with centrifugations. During the experimental period, the specimens were divided into 4 groups and dressed with the following: Group1- CH paste, Group 2 - CH + EEP, Group 3 CH + U and Group 4 CH + EEP + U. The ultrasonic activation was made during 1 minute in both directions (buccal-lingual / mesio-distal), with the aid of plain point insertion. The medications remained in the root canals for 15 days. The CLSM analyzed the viable (green) and dead (red) bacteria in the infected dentinal tubules, with Live and Dead dye. The colony forming units (CFUs) count was made possible with the MC method. The dentinal wall debris were collected and diluted to be seeded on Petri BHI-agar plates. For the penetration test, the dye Rodamine B was added to CH pastes during the manipulation and analysed by CLSM. Group 1 (CH) showed the greatest bacteria viability in the infected dentinal tubes and Group 4 (CH + EEP+ U) the lowest. Ultrasonic activation created a significant reduction of bacteria viability for all groups. The CH + EEP paste was more bactericidal than the CH (p< 0.05%). It was possible to conclude that ultrasonic activation of CH pastes increased the antimicrobial action and was responsible for better intradentinal penetration with fulfilling of the dentinal tubules.
