Changes of pH produced by immersion of endodontic sealers.

When evaluating the antimicrobial effect of endodontic sealers it is important to study the variation of pH, since this is one of the properties that may inhibit the microbial growth and influence biocompatibility. The aim of this study was to evaluate the capacity of several endodontic sealers without calcium hydroxide to modify the pH of the solution in which they were immersed. The sealers used were: Endomethasone C-Septodont (EC), Bio Seal-Ogna (BS), Diaket-Espe (D), Procosol-StarDental (P), AH26-Dentsply (AH), Ketac Endo-Espe (KE), AHPlus-Dentsply (AHP), Endion-Voco (E), Endomethasone-Septodont (EM), EZ Fill-Essential Dental Systems (EZ). Samples of each material were placed in tubes with phosphate saline solution (PBS). The pH was determined at 2, 5, 12, 20, 30, 60, and 90 days. A tube with solution alone was taken as control. Statistical analysis of the results was performed by ANOVA. Material, sample, time and material-time interaction elicited statistically significant differences (p < 0.05). The variation of pH produced by immersion of endodontic sealers depends on the composition of the material.

Changes of pH produced by immersion of endodontic sealers

When evaluating the antimicrobial effect of endodontic sealers it is important to study the variation of pH, since this is one of the properties that may inhibit the microbial growth and influence biocompatibility. The aim of this study was to evaluate the capacity of several endodontic sealers without calcium hydroxide to modify the pH of the solution in which they were immersed. The sealers used were: Endomethasone C-Septodont (EC), Bio Seal-Ogna (BS), Diaket-Espe (D), Procosol-StarDental (P), AH26-Dentsply (AH), Ketac Endo-Espe (KE), AHPlus-Dentsply (AHP), Endion-Voco (E), Endomethasone-Septodont (EM), EZ Fill-Essential Dental Systems (EZ). Samples of each material were placed in tubes with phosphate saline solution (PBS). The pH was determined at 2, 5, 12, 20, 30, 60, and 90 days. A tube with solution alone was taken as control. Statistical analysis of the results was performed by ANOVA. Material, sample, time and material-time interaction elicited statistically significant differences (p < 0.05). The variation of pH produced by immersion of endodontic sealers depends on the composition of the material.

Changes of pH produced by immersion of endodontic sealers.

When evaluating the antimicrobial effect of endodontic sealers it is important to study the variation of pH, since this is one of the properties that may inhibit the microbial growth and influence biocompatibility. The aim of this study was to evaluate the capacity of several endodontic sealers without calcium hydroxide to modify the pH of the solution in which they were immersed. The sealers used were: Endomethasone C-Septodont (EC), Bio Seal-Ogna (BS), Diaket-Espe (D), Procosol-StarDental (P), AH26-Dentsply (AH), Ketac Endo-Espe (KE), AHPlus-Dentsply (AHP), Endion-Voco (E), Endomethasone-Septodont (EM), EZ Fill-Essential Dental Systems (EZ). Samples of each material were placed in tubes with phosphate saline solution (PBS). The pH was determined at 2, 5, 12, 20, 30, 60, and 90 days. A tube with solution alone was taken as control. Statistical analysis of the results was performed by ANOVA. Material, sample, time and material-time interaction elicited statistically significant differences (p < 0.05). The variation of pH produced by immersion of endodontic sealers depends on the composition of the material.

Antimicrobial effect of six endodontic sealers: an in vitro evaluation.

The aim of this study was to determine the in vitro antimicrobial effect of six endodontic sealers after 2, 20 and 40 days. The sealers studied were Apexit, Endion, AH26, AH-Plus. Procosol and Ketac Endo. The microorganisms used were Candida albicans, Staphylococcus aureus, Streptococcus mutans and Actinomyces israelii. Petri dishes were filled with sterile agar and 0.1-ml wells were prepared and filled with the sealers. The agar plates were stored for 24 h at 37 degrees C. The samples were then removed, immersed in 4.5 ml of culture medium and divided into three groups. The samples in group 1 were stored for 2 days at 37 degrees C whereas the samples of groups 2 and 3 were stored at 4 degrees C for 20 and 40 days respectively. The samples were then removed and discarded, and 0.1 ml of the culture medium was seeded on the agar plates in order to perform colony forming unit counts. Apexit, Endion and AH-Plus produced slight inhibition on Streptococcus mutans at 20 days and on Actinomyces israelii at every time interval. No effect was found on Candida albicans and Staphylococcus aureus. Ketac Endo only produced an antimicrobial effect on Actinomyces israelii at 2 and 40 days. AH26 and Procosol showed antimicrobial effect at 40 days on Candida albicans, at 20 and 40 days on Streptococcus mutans and Staphylococcus aureus, and an effective inhibition on Actinomyces israelii at every time interval. Statistical analysis revealed both sealers and microorganisms to be significant factors affecting results in groups 2 and 3. In conclusion, the sealers evaluated in this study showed different inhibitory effects depending on time span. Overall, sealers containing cugenol and formaldehyde proved to be most effective against the microorganisms at the time intervals studied.

Oral microbiota and implant type membranes.

Candida albicans (Ca), Staphylococcus aureus (Sa), Streptococcus sanguis (Ss), Actinomyces naeslundii (An), Actinomyces odontolyticus (Ao), Porphyromona spp (P spp), Candida glabrata (Cg), Candida krusei (Ck), and Rhodotorula spp (R spp) were tested with equal pieces of biodegradable membranes. Membranes pretreated with saliva or clorhexidine and nontreated control membranes were tested in three different culture media containing 0.1 mL homologous suspension for each strain under study. Incubation was performed at 37 degrees C for 48 hours for aerobiosis and for five days for anaerobiosis. Macroscopy and microscopy were carried out. Membranes were removed, washed, and resuspended. Samples were sonicated, and the supernatant was disseminated on brain heart infusion broth or blood agar. Incubation was repeated, colony-forming unit counts were performed, and statistical analysis was carried out using analysis of variance transforming results to Log10 (x + 1), the highest interaction level was used to calculate standard error. Orthogonal contrast was used to compare the different microorganisms under study. Highest adhesion was found with Ca, Cg, Ck, Sa, and Ss. A sufficient quantity of Actinomyces could not be recovered from the membranes. Results with P spp were poor, confirming lower gram-negative adhesion. Replicate flasks with Ss and Ca were cultivated. Membranes were removed after washing and subjected to scanning electron microscopy, as were untreated control pieces. A cavelike surface was observed. Streptococcus sanguis adhering to the membranes showed extracellular projections. Candida and gram-positive cocci showed great recovery capacity.

Germicide effect of several glass ionomer cements.

One the most significant characteristics of glass ionomer cements is their ability to release fluoride compounds. This study was carried out to try establish relationships between this property and the possible effect on the growth of microorganisms that are found in carious lesions, Agar BHI medium containing Petri dishes were flooded with strains of Actinomyces naeslundii, Actinomyces israelii and Actinomyces odontolyticus. Cavities were then prepared in the agar and filled with mixtures of several glass ionomer cements. Some of them were polymerizable resin containing products. A zinc phosphate and a zinc oxide-eugenol cement were used as controls. After a seven day incubation at 37 degrees C under anaerobic conditions the inhibition halos around the specimens were measured in a way similar to that used for antibiograms. The statistical analysis of the results showed no significant differences among Actinomyces strains but a significant difference one among cements. Even when no definitive conclusions could be drawn it is worth taking into consideration the effect of glass ionomer cements on microorganisms such as the Actinomyces and continuing studies to establish more clearly what is required from the material to produce a clinically significant outcome.

Antimicrobial power of composite resin adhesion systems.

The adherence of microorganisms to dentin that had been contaminated and then treated with conditioning substances was evaluated. The germicide effect of those products and their possible substantivity was also evaluated. Dentin slices were contaminated with Candida albicans, Streptococcus mutans and Actinomyces naeslundii and then treated with the following substances: 1. Experimental Blue Solution A, 2. Experimental Red Solution B; 3 Tubulicid Blue Label; 4. Tubulicid Red Label; 5 Scotchprep Dentin Primer; 6 ventura Dentin Bond Cleaner; 7 ventura Dentin Bond Primer, 8. Gluma dentin Bond; 9 Tenure Conditioner; 10. All Bond Dentin Conditioner; 11 Syntac Primer; 12. Clearfil New Bond acid + adhesive; 13 Prisma Universal Bond 3 Primer; 14. Denthesive Cleaner; 15. Control (Distilled water). Adherence was evaluated using scanning electron microscopy and viability tests were performed. Substances 1, 2, 3, 4, 5, 7, 8, and 11 impair adherence; the control and substances 6 and 9 produced no afforded intermediate results effect while substances 10, 12, 13 and 14. Viability tests afforded results similar to those obtained for adherence. Several substances that are used for dentin treatment or for dentin priming for adhesion could be useful in preventing microorganism viability and so contribute to the protection of pulp vitality.

Antimicrobial power of composite resin adhesion systems

The adherence of microorganisms to dentin that had been contaminated and then treated with conditioning substances was evaluated. The germicide effect of those products and their possible substantivity was also evaluated. Dentin slices were contaminated with Candida albicans, Streptococcus mutans and Actinomyces naeslundii and then treated with the following substances: 1. Experimental Blue Solution A, 2. Experimental Red Solution B; 3 Tubulicid Blue Label; 4. Tubulicid Red Label; 5 Scotchprep Dentin Primer; 6 ventura Dentin Bond Cleaner; 7 ventura Dentin Bond Primer, 8. Gluma dentin Bond; 9 Tenure Conditioner; 10. All Bond Dentin Conditioner; 11 Syntac Primer; 12. Clearfil New Bond acid + adhesive; 13 Prisma Universal Bond 3 Primer; 14. Denthesive Cleaner; 15. Control (Distilled water). Adherence was evaluated using scanning electron microscopy and viability tests were performed. Substances 1, 2, 3, 4, 5, 7, 8, and 11 impair adherence; the control and substances 6 and 9 produced no afforded intermediate results effect while substances 10, 12, 13 and 14. Viability tests afforded results similar to those obtained for adherence. Several substances that are used for dentin treatment or for dentin priming for adhesion could be useful in preventing microorganism viability and so contribute to the protection of pulp vitality.

Antimicrobial power of composite resin adhesion systems.

The adherence of microorganisms to dentin that had been contaminated and then treated with conditioning substances was evaluated. The germicide effect of those products and their possible substantivity was also evaluated. Dentin slices were contaminated with Candida albicans, Streptococcus mutans and Actinomyces naeslundii and then treated with the following substances: 1. Experimental Blue Solution A, 2. Experimental Red Solution B; 3 Tubulicid Blue Label; 4. Tubulicid Red Label; 5 Scotchprep Dentin Primer; 6 ventura Dentin Bond Cleaner; 7 ventura Dentin Bond Primer, 8. Gluma dentin Bond; 9 Tenure Conditioner; 10. All Bond Dentin Conditioner; 11 Syntac Primer; 12. Clearfil New Bond acid + adhesive; 13 Prisma Universal Bond 3 Primer; 14. Denthesive Cleaner; 15. Control (Distilled water). Adherence was evaluated using scanning electron microscopy and viability tests were performed. Substances 1, 2, 3, 4, 5, 7, 8, and 11 impair adherence; the control and substances 6 and 9 produced no afforded intermediate results effect while substances 10, 12, 13 and 14. Viability tests afforded results similar to those obtained for adherence. Several substances that are used for dentin treatment or for dentin priming for adhesion could be useful in preventing microorganism viability and so contribute to the protection of pulp vitality.

Adherencia de candida modificada por la acción de antisépticos / Adherence of candida albicans modifiqued for the action the antisepsic

La capacidad de los microorganismos para adherirse tiene importancia en el mecanismo de la formación de placa "in vitro". El objetivo de este trabajo fue investigar la posible acción antiadherente de antisépticos, de uso oral; la influencia ejercida por la presencia de sacarosa y las modificaciones que se producirían si se asociara un microorganismo de la flora indígena bucal dominante con otro de la flora accesoria. Se prepararon suspensiones homologadas con el n§3 de la escala de Mac Farland de 10 cepas de Candida albicans y una suspensión de Streptococcus sanguis. Cada suspensión de Candida albicans fue distribuida en 12 tubos a razón de 0,5 ml en 10 de ellos y 0,25 en los tubos restantes; a estos se le completó el volumen con 0,25 ml de la suspensión de Streptococcus sanguis. En cada tubo agregamos 0,5 ml de los distintos antisépticos en estudio (Fluoruro de sodio (NaF) en distintas concentraciones, clorhexidina al 0,2 % floruro estañoso, povidona y agua destilada estéril (testigo)). El conjunto fue incubado 2 hs. en agitación constante a 37§C. Se lavaron las células una vez y se restituyó el volumen. 0,5 ml de cada uno se sembró en tubos que contenían 5 ml de medio base para la formación de placa "in vitro" con y sin el agregado de sacarosa. De los tapones pendían trocitos de diente estéril. Se incubó 5 días a 37§C. Transcurrido este tiempo procedimos a interpretar los resultados por el aspecto macroscópico de los cultivos y se procedió a la fijación de los dientes para su posterior observación por Microscopía electrónica de barrido (M.E.B.). Algunos de los antisépticos ensayados, ejercen una débil acción candicida, no se demostró influencia en la adherencia. La presencia de sacarosa en el medio es un factor importante para la formación de placa "in vitro"; la asociación de Candida albicans y Esteptococcus sanguis no influye en la misma

Adherencia de candida modificada por la acción de antisépticos / Adherence of candida albicans modifiqued for the action the antisepsic

La capacidad de los microorganismos para adherirse tiene importancia en el mecanismo de la formación de placa "in vitro". El objetivo de este trabajo fue investigar la posible acción antiadherente de antisépticos, de uso oral; la influencia ejercida por la presencia de sacarosa y las modificaciones que se producirían si se asociara un microorganismo de la flora indígena bucal dominante con otro de la flora accesoria. Se prepararon suspensiones homologadas con el nº3 de la escala de Mac Farland de 10 cepas de Candida albicans y una suspensión de Streptococcus sanguis. Cada suspensión de Candida albicans fue distribuida en 12 tubos a razón de 0,5 ml en 10 de ellos y 0,25 en los tubos restantes; a estos se le completó el volumen con 0,25 ml de la suspensión de Streptococcus sanguis. En cada tubo agregamos 0,5 ml de los distintos antisépticos en estudio (Fluoruro de sodio (NaF) en distintas concentraciones, clorhexidina al 0,2 % floruro estañoso, povidona y agua destilada estéril (testigo)). El conjunto fue incubado 2 hs. en agitación constante a 37ºC. Se lavaron las células una vez y se restituyó el volumen. 0,5 ml de cada uno se sembró en tubos que contenían 5 ml de medio base para la formación de placa "in vitro" con y sin el agregado de sacarosa. De los tapones pendían trocitos de diente estéril. Se incubó 5 días a 37ºC. Transcurrido este tiempo procedimos a interpretar los resultados por el aspecto macroscópico de los cultivos y se procedió a la fijación de los dientes para su posterior observación por Microscopía electrónica de barrido (M.E.B.). Algunos de los antisépticos ensayados, ejercen una débil acción candicida, no se demostró influencia en la adherencia. La presencia de sacarosa en el medio es un factor importante para la formación de placa "in vitro"; la asociación de Candida albicans y Esteptococcus sanguis no influye en la misma