Antimicrobial Efficacy of the Use of Mouthwash with Cetylpiridinium Chloride for Aerosol Producing Procedures. A Systematic Review / Eficacia antimicrobiana del uso del enjuague bucal con cloruro de cetilpiridinio en procedimientos que generan aerosoles. Revisión sistemática

Abstract The present research aims to determine the antimicrobial efficacy of the mouthwashes based on cetylpyridinium chloride (CPC), before aerosol producing dental procedures. A data search was performed during August 2021 in five databases MEDLINE (PubMed), SCOPUS, SCIELO, Cochrane Central Register of Controlled Trials (CENTRAL) and Google Scholar. Randomized clinical trials (RCTs) were included based on the PICO question, comparing the efficacy of the mouthwashes based on cetylpyridinium chloride (CPC), versus other mouthwashes and water, before aerosol producing dental procedures, papers in English, Spanish and Portuguese were included without time limits. The risk of the included studies was evaluated with the tool RoB 2.0. Number of registration PROSPERO N° CRD42021275982. 120 papers were obtained in the preliminary search, discarding those that didn't comply with the selection criteria, leaving only 3 studies. These papers reported the use of cetylpyridinium chloride (CPC) was effective for the reduction of bacteria during the ultrasonic prophylactic procedure. The use of CPC mouthwashes previous to the dental treatment with ultrasonic prophylaxis showed only antibacterial capacity.

Resumen El presente trabajo de investigación tiene como objetivo determinar la eficacia antimicrobiana de los colutorios a base de cloruro de Cetilpiridinio (CPC), previo a tratamientos dentales que generen aerosol. Se realizó una búsqueda bibliográfica hasta agosto del 2021 en cinco bases de datos: MEDLINE (vía PubMed), SCOPUS, SCIELO, Cochrane Central Register of Controlled Trials (CENTRAL) y Google Scholar. Se incluyeron ensayos clínicos aleatorizados (ECAs), basándose en la pregunta PICOS, que compare la eficacia del colutorio a base de cloruro de Cetilpiridinio (CPC) con otro colutorio, placebo o agua, previo a un tratamiento dental que genere aerosol, en los idiomas español, inglés o portugués y sin límite de tiempo. El riesgo de los estudios incluidos se evaluó con la herramienta RoB 2.0. Número de registro PROSPERO N° CRD42021275982. Se obtuvo un total de 120 artículos en la búsqueda preliminar, descartando aquellos que no cumplían con los criterios de selección, quedando sólo 3articulos. Estos artículos informaron que el uso de CPC es efectivo para la reducción de bacterias durante el procedimiento de profilaxis con ultrasonido. El uso de los enjuagues bucales a base de CPC previo al tratamiento dental de profilaxis con ultrasonido sólo tiene eficacia antibacteriana.

Use of Ionized Monocalcium phosphate and enameline derivatives to reduce dentin hypersensitivity after periondontal therapy / Uso de Fostato Monocálcio y derivados en Enamelina para reducir la hipersensibilidad dentaria después de terapia periodontal

Abstract This study aimed to evaluate the effectiveness of using an ionized monocalcium phosphate and enamelin derivatives (IMP+ED) based mouthwash for the treatment of dentin hypersensitivity (DH) after scaling and root planing (SRP). 47 patients who reported DH after SRP treatment were included in this prospective cohort study. The Schiff Cold Air Sensitivity Scale (SCASS) was applied to classify their degree of pain in mild, moderate or intense at two times: after SRP (T0), and after one month of using a IMP+ED-based mouthwash (T1). The McNemar-Bowker test was used to compare the correlated proportions between both times (p<0.05). After the SRP therapy (T0), all the sample members reported pain distributed in the following manner: 12.8% were mild, 27.6% moderate, and 59.6% intense. At one month since treatment and with the use of the IMP+ED-based mouthwash (T1), the distribution of pain levels changed to 83% mild, 12.8% moderate, and 4.3% intense, this change was statistically significant (p<0.001). IMP+ED-based mouthwash produces a positive effect in reducing painful responses caused by exposure of the dentin tubules to the oral environment after SRP therapy.

Resumen El objetivo de este estudio fue evaluar la efectividad de un enjuague bucal a base de fosfato monocálcico ionizado y derivados de enamelina (FCI+DE) para el tratamiento de hipersensibilidad dentinaria (HD) posterior al tratamiento de raspado y alisado radicular (RAR). 47 pacientes que reportaron tener HD posterior al tratamiento de RAR fueron incluidos en este estudio prospectivo de cohorte. Con el fin de clasificar la HD de los pacientes en leve, moderada o intensa se utilizó la Escala de Sensiblidad al Aire Frío de Schiff (ESAFS). Los pacientes fueron evaluados después del tratamiento de RAR (T0) y posterior al uso de un enjuague bucal basado en FCI+DE (T1). Para comparar las proporciones correlacionadas se utilizó la prueba de McNemar-Bowker (p<0.05). La distribución del dolor de los pacientes posterior al tratamiento de RAR (T0) fue la siguiente: 12.8% fueron leves, 27.6% moderado, and 59.6% intenso. Un mes después del uso del enjuague buccal basado en FCI+DE (T1) la distribución en los niveles de dolor cambio a 83% leve, 12.8% moderado, and 4.3% intenso, este cambio fue estadísticamente significativo (p<0.001). El uso del enjuague bucal basado en FCI+DE produce una reducción significativa a la respuesta de dolor causada por la exposición de la dentina al ambiente oral como consecuencia del tratamiento de RAR.

Development of novel mucoadhesive gels containing nanoparticle for buccal administration of dexamethasone

Abstract This study aimed to develop promising and innovative mucoadhesive gel systems containing dexamethasone-loaded nanoparticle to increase the effectiveness of treatment for oral precancerous lesions and to reduce side effects. In this respect, a dexamethasone-loaded nanoparticle formulation was prepared by using emulsification/solvent evaporation method. The nanoparticle has high zeta potential (-10.3±0.5 mV), low particle size (218.42±2.1), low polydispersity index (0.070±0.014) and high encapsulation efficiency (95.018±2.982%). To improve the mucosal retention time, the dexamethasone-loaded nanoparticle was dispersed in mucoadhesive gel using gellan gum. The developed gels offered appropriate pH value, high drug content, suitable mechanical and mucoadhesive performance and appropriate viscosity for mucosal administration. All formulations exhibited plastic flow and typical gel-type mechanical spectra after the determined frequency value. The developed formulations exhibited extended drug release as intended for these systems. Cytotoxicity was tested by MTT assay in human epithelioid carcinoma cell (HeLa) in vitro. The MTT assay showed that the blank formulations were non-toxic to cells. It was observed that the bioactivity of the free dexamethasone was potentiated by mucoadhesive gels containing dexamethasone-loaded nanoparticle in HeLa cells. Results from this study indicate that mucoadhesive gels are effective for the local treatment of precancerous lesions. Our findings showed that the developed formulations were worthy of further studies.

The Effects of Mouthwashes on the Color Stability of Resin-Based Restorative Materials / Efecto de los enjuagues orales en la estabilidad del color de materiales restauradores a base de resina

Abstract: Objective: This study investigated the effects of three types of mouthwash on the color stability of three resin-based restorative materials (nanohybrid resin composite, sonic-activated bulk-fill material, and compomer). Materials and Methods: To this end, 120 cylindrical disc specimens were prepared and polished, after which they were incubated in distilled water for 24 hours for post-polymerization. The baseline color values of each specimen were measured with a spectrophotometer, then the specimens were randomly divided into four groups. Following immersion in the mouthwashes for 24 hours, the specimens were rinsed with distilled water and dried before the color measurement was repeated. The values of color change (ΔE₀₀) were subsequently calculated. A two-way analysis of variance and Duncan's post hoc multiple comparison tests were conducted to determine statistically significant differences among the restorative materials. Results: All samples showed discoloration after immersion, albeit some instances of discoloration were imperceptible. In this respect, a statistically significant difference was found among the restorative materials and mouthwashes (p<0.05). Imperceptible ΔE₀₀ values were derived on the nanohybrid resin composite and compomer, but perceptible and acceptable ΔE₀₀ values were detected on the sonic-activated bulk-fill materials (p<0.05). The clinically unacceptable discoloration was observed on the sonic-activated bulk-fill composite immersed in Listerine®. Conclusions: Clinicians should make recommendations based on the potential staining capacity of mouthwashes prescribed for daily use in restorative materials. In this way, the need for renewal of restorations due to discoloration could be avoided.

Resumen: Objetivo: Este estudio investigó los efectos de tres tipos de enjuague bucal en la estabilidad del color de tres materiales de restauración a base de resina (resina nanohíbrida, resina bulk-fill de activación sónica y compómero). Materiales y Métodos: Para ello se prepararon y pulieron 120 muestras de discos cilíndricos, después de lo cual se incubaron en agua destilada durante 24 horas pospolimerización. Los valores de color de base de cada muestra se midieron con un espectrofotómetro, después las muestras se dividieron aleatoriamente en cuatro grupos. Tras la inmersión en los enjuagues bucales durante 24 horas, los especímenes se enjuagaron con agua destilada y se secaron antes de repetir la medición del color. Posteriormente se calcularon los valores de cambio de color (ΔE₀₀). Se llevó a cabo un análisis bidireccional de la varianza y las pruebas de comparación múltiple post hoc de Duncan para determinar las diferencias estadísticamente significativas entre los materiales de restauración. Resultados: Todas las muestras mostraron decoloración después de la inmersión, aunque algunos casos esta fue imperceptible. Se encontró una diferencia estadísticamente significativa entre los materiales de restauración y los enjuagues bucales (p<0,05). Se obtuvieron valores imperceptibles de ΔE₀₀ en el compuesto de resina nanohíbrida y el compómero, pero se detectaron valores perceptibles y aceptables de ΔE₀₀ en la resina bulk-fill activada sónicamente (p<0,05). Se observó una decoloración clínicamente inaceptable en la resina bulk-fill activada sónicamente inmersa en Listerine®. Conclusiones: Los clínicos deben hacer recomendaciones basadas en la capacidad potencial de coloración de los enjuagues bucales prescritos para uso diario en los materiales de restauración. De esta manera, se podría evitar la necesidad de renovar las restauraciones debido a la decoloración.

Effect of Listerine Mouthwash with Green Tea on the Inhibition of Streptococcus Mutans: A Microbiologic Study

Abstract Objective: To evaluate in vitro the antimicrobial effect of Listerine-green tea mouthwash on Streptococcus mutans (SM) in comparison with 0.12% Chlorhexidine (CHX) and Listerine-Zero. Material and Methods: The sensitivity and growth inhibition of SM bacterial species were evaluated and compared between Listerine-green tea, 0.12% CHX and Listerine-Zero mouthwashes. Sixty plates containing SM colonies were prepared in three groups (n=20), and growth inhibition zones were measured using the disk diffusion agar test in mm. Data were analyzed with SPSS 21. One-way ANOVA was used to compare the efficacy of the three mouthwashes tested. Post hoc Tukey tests were used for two-by-two comparisons. Statistical significance was defined at P<0.05. Results: Analysis of data showed significant differences between the three groups (p<0.001); 0.12% CHX was the most effective mouthwash, and Listerine-Zero exhibited the least effect on the growth inhibition of SM (p<0.004). Conclusion: All three mouthwashes were significantly effective in inhibiting the growth of SM. The effect of Listerine-green tea mouthwash was higher than that of Listerine-Zero and less than that of 0.12% CHX.

Formulation and evaluation of a mucoadhesive buccal tablet of mefenamic acid

Buccal route of administration has many advantages such as improving patient compliance, bypassing the GIT and hepatic first pass effect. The objectives are to formulate mucoadhesive buccal tablet using Mefenamic acid and compatible excipients, and to evaluate the product using quality control tests and in vitro tests. The ingredients were subjected to Differential Scanning Calorimetry and Fourier Transform Infrared Spectroscopy studies for compatibility test and the results showed no interaction. Two batches of mefenamic buccal tablet were prepared. The tablet thickness and diameter are 3.75 mm and 12 mm respectively. All tablets are within the specification of +/- 5%. The in-house tablet hardness is 6.8-15kg and percent friabilation is not more than 0.8%. The disintegration test showed that all tablets disintegrated within 4 hours. The content uniformity showed that tablets are within the range of 85%-115%. The tablet weight is within the 5% range. The percent swelling is 53.83% to 58.86% and moisture absorption is 14.79% to 15.56%. The surface pH of the tablet is close to the salivary pH, which means that it would not irritate the buccal mucosa. The buccal tablet has a mucoadhesiveness of 0.196 to 0.200. There was no change in pH and size after subjecting it to stability studies in human saliva. Drug release studies showed 80.7% to 83.4% after 3 hours. Even after 3 months of subjecting the tablets to 40 ºC and 75% RH, results are within acceptable range. The results show the potential of the formulation as a mucoadhesive buccal tablet.

An in Vitro Effectiveness Evaluation of Chemical Agents for Toothbrushes Disinfection

Objective: To evaluate in the vitro effectiveness of three chemical agents for toothbrush disinfection. Material and Methods: Sixteen new toothbrushes were evaluated, previously sterilized and classified in five experimental groups (n=3) and one item as control. Three chemical agents were assessed: 0.12% Chlorhexidine gluconate (CHX), essential oil mouth rinse (Listerine) and 3.5% Sodium hypochlorite (NaOCl). The five selected strains were inoculated on toothbrushes and incubated for a 24 hours period and 37°C temperature in aerobic conditions. The incubated toothbrushes were immersed for a 15 min period into selected chemical agents and after drying in a controlled air stream, again re-cultured into enriched broth. A comparison was made between the initial and final microorganisms density recovered after chemical disinfection based on Mc Farland scale. The data obtained was compared by descriptive analysis and ANOVA methodology. Results: 3.5% NaOCl was the most effective chemical agent for toothbrush disinfection followed by CHX; Listerine was not effective to eliminate the inoculated bacteria in toothbrushes. Conclusion: 3.5% NaOCl and 0.12% CHX are the most effective chemical agents for toothbrush disinfection and Listerine was only effective against C. albicans.

Efficacy of Mouthwash from Aloe vera Juice after Scaling Treatment on Patient with Gingivitis: A Clinical Study

Objective: To determine the effectiveness effectivity of mouthwash from Aloe vera juice after scaling treatment on patient with gingivitis. Material and Methods: This was an experimental research using pretest and posttest design with control group. The number of samples of 30 people selected using sampling method quota sampling. Samples were divided into two groups: test (n = 15 skeletons with Aloe vera juice) and control (n = 15 just scaling). Gingival inflammation is measured using a gingival index according to Loe and Sillness on the first day before scaling treatment and 7th day after scaling. Data analysis was conducted using SPSS version 20. Independent-samples t-test and paired-samples t-test were used for data analysis. The statistical test performed has a significance level of 0.05 (p = 0.05) and confidence level of 95% (α = 0,05). Results: There was a significant decrease in the mean score of the gingival index in the control group (1.1 to 0.5) and the test group (1.2 to 0.4) significantly (p<0.05). Conclusion: The use of mouthwash from Aloe vera juice can decrease gingival inflammation, which can be seen from the gingival index score on all test subjects. The decrease in gingival index in the test group using the Aloe vera juice was greater than that of the control group, which was not given the mouthwash.

Short-term evaluation of a green tea extract-based mouthrinse / Avaliação de curto prazo de um enxaguatório bucal à base de extrato de chá verde

Introduction: mechanical hygiene is still the best method forthe maintenance of oral health and prevention of biofilm formation. However, mouthrinses have been increasingly used as an adjunct support especially for post-operatory conditions or when periodontal conditions require. In this way, a number of mouthrinses are available, presenting different active ingredients with predominant antimicrobial action. Objectives: the aim of the present study was to evaluate the topical action of a green-tea extract-based mouthwash on gingival tissue. Materials and Methods: a longitudinal double-blind comparison was performed with two groups of patients clinically evaluated and diagnosed as suffering from gingivitis (n= 40). The patients were divided into two groups, according to the mouthrinse used: GT - green tea (concentration of 20mg/ml), and P - placebo, 0.9% saline solution. Clinical examination of the mucosa, tooth staining, plaque and gingival indices were peformed before and 15 days after the continuous use of the products twice a day. Results: no mucosal or tasting alterations were found, neither tooth staining regardless the mouthrinse used. Statistical assessment did not detect differences on gingival indexes between the groups before and after mouthrinses use; however, plaque indexes were significant lower in patients of GT group, compared to the P group. Conclusions: the use of phytotherapic products with active ingredients should be investigated for biofilm control, responsible for the onset and progression of periodontal disease, as well as other various oral pathologies. Considering the period of evaluation pro-posed in this study, relevant decrease in initial phase of plaque for-mation could be observed with the green tea mouthrinse. Further long-term evaluation studies should be carried-out in order to eluci-date its continuous effects on oral structures.

Introdução: higiene mecânica ainda é o melhor método para a manutenção da saúde bucal e prevenção da formação de biofilmes. No entanto, enxagues têm sido cada vez mais usado como um suporte auxiliar especialmente para as condições pós-operatórias ou quando as condições periodontais exigem. Desta forma, um número de bochechos estão disponíveis, apresentando diferentes ingredientes ativos com predominante ação antimicrobiana. Objetivos: o objetivo do presente estudo foi avaliar a ação tópica de um bochecho à base de extrato de chá verde no tecido gengival. Materiais e Métodos: a comparação longitudinal, duplo-cego, foi realizada com dois grupos de pacientes clinicamente avaliados e diagnosticados como portadores de gengivite (n = 40). Os pacientes foram divididos em dois grupos, de acordo com o enxaguatório oral usado: CV - chá verde (concentração de 20 mg / ml), e P - placebo, solução salina a 0,9%. O exame clínico da mucosa, coloração dos dentes, índice de placa e índice gengival foram realizados antes e 15 dias após o uso contínuo dos produtos duas vezes por dia. Resultados: nenhuma alteração na mucosa ou de degustação foi encontrada, assim como não foi identificado modificação na coloração do dente. A Avaliação estatística não detectou diferenças no índice gengival entre os grupos antes e depois de usar enxaguatórios. No entanto, índice de placa inferior foi menor de forma significativa nos pacientes do grupo CV, em comparação com o grupo P. Conclusões: o uso de produtos fitoterápicos com ingredientes ativos deve ser investigado para o controle de biofilme, responsável pelo aparecimento e progressão da doença periodontal. Considerando o período de avaliação proposto, a redução correspondente na fase inicial da formação de placa pôde ser observada com o enxaguatório à base de chá verde. Além disso, estudos de avaliação de longo prazo devem ser realizados, a fim de elucidar seu efeito contínuo em longo prazo sobre as estruturas orais.

Can mouth washes containing chlorhexidine 0.12% be used as synonym of a water solution of chlorhexidine 0.12%? / Pode lavagens da boca contendo 0.12 % de clorexidina ser utilizado como sinónimo de uma solução aquosa de cloro-hexidina 0.12 % ?

Chlorhexidine digluconate (CHX) is a gold standard drug in dentistry and is widely used as a reference in both in vitro and in vivoexperiments. Due to ease of access, mouth washes containing CHX 0.12% are used as a substitute for aqueous CHX 0.12% solution in laboratory experiments. Additionally, it is well known that for product flavor purposes, volatile compounds are added to mouth washes formulations. Volatiles added to CHX 0.12% may improve wash's antibacterial ability. Volatiles add potency to the mouth wash formulation. Compared with an aqueous CHX 0.12% solution, it is proposed that CHX solutions and Periogard^® would have antimicrobial activity. Antimicrobial activity was assessed in the present study via disk diffusion assays against Streptococcus mutans, Streptococcus sanguinisand Escherichia coli. Periogard^® showed a significantly higher antibacterial activity in relation to CHX 0.12% (p<0.05) and a similar activity in relation to CHX 1% (p>0.05). Periogard^(r) volatiles were analyzed by gas-chromatography/mass spectrometry (GCMS) and the presence of antibacterial menthol, menthone, isomenthol, menthyl acetate, trans-anethol and eugenol was verified. Finally, the use of Periogard^® as a synonym of CHX 0.12% must be avoided, because its antibacterial activity is closely related to CHX 1%...

Gluconato de clorexidina (CHX) é um fármaco considerado padrão ouro, em Odontologia, amplamente usado como referência em estudos in vitro e in vivo. Em razão da facilidade de acesso, enxaguatórios bucais que contêm CHX 0,12% são usados em substituição à solução aquosa de clorexidina (CHX 0,12%), em experimentos laboratoriais. É sabido que devido à palatabilidade do produto, os mesmos enxaguatórios bucais contêm compostos voláteis em sua formulação, além da CHX 0.12%. Visto que voláteis adicionados podem acrescentar poder antibacteriano à formulação, a comparação da resposta antibacteriana da solução aquosa de CHX em diferentes concentrações e de Periogard^® é proposta no presente artigo. Para tanto, utilizou-se o ensaio do disco de difusão em ágar com inóculos de Streptococcus mutans, Streptococcus sanguinis e Escherichia coli. Periogard^® mostrou atividade antibacteriana significativa contra as três cepas analisadas, quando comparada à atividade de CHX 0.12% (p<0,05) e atividade similar à CHX diluída a 1% (p>0,05). A presença de compostos voláteis no Periogard^® foi analisada por GC-MS e observou-se que mentol, mentona, isomentol, acetato de mentila, trans-anetol e eugenol estão presentes na formulação. Deste modo, o uso de Periogard^(r) como sinônimo de CHX 0,12% deve ser evitado, uma vez que sua atividade se assemelha àquela da CHX diluída a 1%...

Clinical applicability of natural product(s)-containing mouthwashes as adjunctive treatment of biofilm-induced gingivitis: a systematic review / Aplicabilidade clínica de colutórios à base de produtos naturais como tratamento adjuvante da gengivite induzida por biofilme: uma revisão sistemática

Natural products have emerged as an effective and low-cost alternative for treating various diseases of the oral cavity. This study aimed to evaluate, through a systematic literature review, if there is scientific evidence ensuring the safe and effective use of natural product(s)-containing mouthwashes as adjunctive treatment of biofilm-induced gingivitis. Searches were conducted in the databases Medline, SciELO, LILACS and Cochrane Library, by using combinations of the key words gingivitis/natural products/phytotherapy/mouthwash, in English, Portuguese and Spanish. Studies published until September 2010 were considered. Four examiners analyzed independently: study design and phase, methodological quality (Jadad scale - JE), experimental product and its concentration, dosing interval and time of usage, as well as employed statistical analysis and clinical outcome of interest. From the 503 articles found, 08 were included in the final review as phase II, controlled, randomized and blind clinical trials, scoring 4 (25%) and 5 (75%) in JE. The main natural products assessed were: Azadirachta indica, Garcinia mangostana, Lippia sidoides, Salvadora persica and Sesamum indicum whose concentration, dosing interval, time of usage and adverse effects varied according to each study. The Plaque and Gingival Index were most employed, as well as α = 5% and paired t, Student's t, Wilcoxon and Mann-Whitney tests. A total of 62.5% and 50% of the products significantly reduced supragingival biofilm and gingivitis, respectively. Mouthwashes containing the essential oil from the leaves of L. sidoides (1%) and the extract from the leaves of A. indica (25%) can be indicated as adjunctive treatment of biofilm-induced gingivitis.

Os produtos naturais têm surgido como alternativa eficaz e de baixo custo para o tratamento de várias doenças da cavidade oral. Objetivou-se avaliar, a partir de revisão sistemática da literatura, se há evidências científicas garantindo a utilização segura e eficaz de antissépticos bucais contendo produto(s) natural(is) como tratamento adjuvante da gengivite induzida por biofilme. Foram realizadas buscas nas bases de dados Medline, SciELO, LILACS e Cochrane Library, através de combinações usando as palavras-chave gengivite/produtos naturais/ fitoterápicos/bochechos, em Inglês, Português e Espanhol. Consideraram-se os estudos publicados até setembro de 2010. Quatro examinadores analisaram separadamente: desenho e fase do estudo, qualidade metodológica (escala de Jadad - EJ), produto experimental e a concentração, intervalo de administração e tempo de uso, bem como a análise estatística empregada e os resultados clínicos de interesse. Foram encontrados 503 artigos dos quais 08 foram incluídos na revisão final como sendo ensaios clínicos fase II, controlados, randomizados e cegos, marcando 4 (25%) e 5 (75%) na EJ. Os principais produtos naturais avaliados foram Azadirachta indica, Garcinia mangostana, Lippia sidoides, Salvadora persica e Sesamum indicum, cuja concentração, intervalo de administração, tempo de uso, e efeitos adversos, variaram de acordo com cada estudo. Índice de placa e Índice Gengival foram os mais utilizados, bem como α=5% e testes t-pareado, t-Student, Wilcoxon e Mann-Whitney. 62,5% e 50% dos produtos reduziram significativamente a presença de bioflme supragengival e gengivite, respectivamente. Os colutórios contendo o óleo essencial das folhas de L. sidoides (1%) e o extrato das folhas de A. indica (25%) podem ser indicados como tratamento adjuvante da gengivite induzida por biofilme.

Eficacia del gluconato de clorhexidina al 0.12 % ante la flora microbiana prevalente en nuestro medio / Efficacy of chlorhexidine gluconate 0.12 % to the microbial flora prevalent in our environment

En la lucha contra la placa bacteriana responsable de las dos enfermedades prevalentes de la cavidad bucal (caries y enfermedad periodontal) se han utilizado numerosas sustancias, entre ellas el gluconato de clorhexidina, a diferentes concentraciones, que hoy en día se supone es el agente más eficaz utilizable. En nuestro mercado se emplea la concentración del 0,12% que según numerosos estudios presenta menos efectos colaterales con la misma eficacia de las concentraciones mayores. Para comprobar dicha eficacia ante las bacterias presentes en la cavidad bucal de individuos residentes en nuestro medio hemos realizado estudios de la sensibilidad, difusibilidad y actividad de la sustancia mencionada, los cuales fueron realizados en placas y en medio líquido en condiciones normales y en anaerobiosis. El trabajo realizado demuestra que el producto es recomendable dado el gran número de bacterias de la flora microbiana normal de la boca que son sensibles a moderadamente sensibles, especialmente en lo que guarda relación a las dos más citadas en la bibliografía como causantes de caries, Streptococcus mutans y Lactobacillus.

Análise do pH e da viscosidade de enxaguatórios bucais fluoretados disponíveis comercialmente na cidade de João Pessoa - PB / Analysis of pH and viscosity of commercially available fluoride mouthrinses in the city of João Pessoa - PB

Objetivo: Avaliar os valores de pH e viscosidade apresentadospor soluções fluoretadas para bochechos disponíveiscomercialmente na cidade de João Pessoa-PB. Método:Constituíram a amostra os produtos Cepacol«, CepacolJúnior«, Fluomint«, Johnson & Johnson«, Malvatricin«, Oral-B«, Plax«, Sanifill« e Sorriso Fresh«. Utilizando-se osaparelhos pHmêtro digital e viscosímetro, com spidle L1 erotação de 220 rpm, puderam ser realizadas as medições dosvalores de pH e de viscosidade de cada produto. Resultados:Analisando-se os dados descritivamente, verificou-se que osvalores de pH variaram entre 5,36 a 7,44. A viscosidadeapresentou uma variação compreendida no intervalo de 4,00 a11,3 mPa.s. Dos 66,7 porcento produtos ácidos que compuseram aamostra apenas o Oral-B« apresentou pH abaixo de 5,5, valorconsiderado crítico para dissolução do esmalte. Além do menorvalor para o pH, o produto Oral-B« apresentou também omenor valor para a viscosidade (4 mPa.s). Conclusão: Dianteda metodologia utilizada e dos resultados obtidos, conclui-seque há uma expressiva variação do pH e da viscosidade dosenxaguatórios bucais analisados

Concentración de fluoruro y pH en colutorios bucales fluorados disponibles en Lima / Concentration and pH of fluorides in fluoridated oral mouthwashes available in Lima

El propósito del presente estudio fue evaluar la concentración de fluoruro y el pH de cuatro marcas comerciales de enjuagues bucales fluorados disponibles en Lima. Los resultados mostraron que las concentraciones de fluoruro de sodio hallados en los diferentes enjuagues bucales fluorados no coincidieron con las indicadas por el fabricante, siendo estas diferencias altamente significativas en dos marcas comerciales y estadísticamente significativas en el caso de una marca comercial. Se halló además un pH ácido en 3 enjuagues bucales, correspondiendo el valor de 6.19 al pH más ácido. Un único enjuague presentó un pH ligeramente alcalino (7.14)

Avaliação clínica da eficácia do listerine na inibição da placa e da gengivite / Clinical evaluation of Listerine efficacy in inhibition of plaque and of gingivitis

Utilizaram-se nove alunos voluntários do 4º ano de odontologia da Universidade Paulista (UNIP) para avaliar a eficácia do Listerine antiséptico na inibição de formação de placa e da gengivite. Foi zerada a presença de placa através da raspagem e polimento. Oito alunos receberam Listerine anti-séptico e um aluno recebeu Listerine placebo, os quais utilizaram como único meio de higiene bucal durante duas semanas, quando foram reavaliados. Os resultados evidenciados mostraram que o Listerine anti-séptico não inibiu a formação de placa bacteriana e da gengivite

Avaliaçäo in vitro de anti-sépticos bucais sobre a microbiota da saliva / In vitro evaluation of the effects of antiseptic mouthrinses on the microflora from saliva

O objetivo do presente estudo foi avaliar a eficácia de diversos anti-sépticos bucais na reduçäo da microbiota da saliva visualizando-se in vitro a sua atividade antimicrobiana. os anti-sépticos avaliados foram: Kolynos, da Kolynos do Brasil; Oral-B, da Gillette do Brasil; Cepacol, da Hoechst Marion Roussel; Periogard, da Colgate-Palmolive; Flogoral, da Asta Médica; Malvatricin, do Laboratório Daudt Oliveira Ltda.; Fluordent, da Johnson e Johnson; Wash, da Abbott Laboratórios do Brasil Ltda.; Plax, da Pfizer do Brasil (atualmente da Colgate-Palmolive) e Listerine, da Warner Lambert. Foram selecionadas 50 amostras de saliva de indivíduos com idade variando de 19 a 54 anos. Após o cultivo dos microrganismos das amostras, procedeu-se à inoculaçäo dos dez diferentes anti-sépticos, em três dosagens (10 µl, 20 µl, 25 µl). Os resultados revelaram que o Periogard se apresentou mais eficaz na reduçäo da microbiota da saliva e que os anti-sépticos Listerine e Flogoral mostram ser ineficazes com relaçäo à atividade antimicrobiana das amostras estudadas

O uso do dentifrício na remoçäo mecânica da placa bacteriana / The use dentifrice in the mechanical removal of bacterial plaque

Este estudo foi realizado com 100 escolares de ambos os sexos com idade de 10-11 anos, objetivando avaliar (a) a influência do uso do dentifrício na remoçäo mecânica da placa bacteriana pela técnica de Fones e (b) o número de movimentos necessários para a remoçäo da placa bacteriana nas diferentes regiöes da cavidade bucal. Os resultados mostraram que a açäo do dentifrício näo influenciou no número de movimentos necessários para a remoçäo da placa bacteriana. Para cada uma das regiöes estudadas, foram necessários 12 movimentos em média com o uso do dentifrício, enquanto que sem o uso do dentifrício foi necessária uma média de 12 movimentos para os dentes da regiäo posterior direita; 11 movimentos para a regiäo anterior e 13 movimentos para a regiäo posterior esquerda

Análisis de triclosán y zinc en productos dentales / Triclosan and zinc analysis in dental products

Se presentan técnicas y metodologías para determinar zinc y triclosán en pastas dentales y enjuagatorios se comparan sus concentraciones en las distintas formulaciones. La determinación de triclosán se realiza espectrofotométricamente a 281 nm (UV) previa extracción con solventes orgánicos, la concentración de triclosán se mide utilizando una curva de calibración. El zinc se tituló espectrofotométricamente con EDTA en presencia de negro de eriocromo T (neT) a 560 nm, La concentración de zinc en las muestras se determina a través de una resolución gráfica de la titulación espectrofotometrica. Los valores de triclosán en el enjuagatorio están en el rango de 0,03 porciento y 0,23 porciento y 0,24 porciento para los dentífricos analizados. El porcentaje promedio de zinc (sulfato) en los enjuagatorios analizados es de 0,23 porciento y de 0,47 porciento para el dentífrico (citrato). El zinc y triclosán presentan concentraciones más bajas en los enjuagatorios al compararlas con dentífricos que los contienen