Potential Comparison of Anti-inflammatory Activities of Quercetin and Diclofenac Mouthwash Formulations

Introduction: Periodontitis is a pandemic, with about 14% of people worldwide already suffering from severe periodontitis. Early intervention in the disease could probably reduce its progression and eliminate the need for the extraction of affected teeth. Quercetin is a probable candidate as it has exemplary anti-inflammatory properties. The presence of phenolic hydroxyl groups in them greatly contributes to their antioxidant and anti-inflammatory activities. Objectives: The study introduces the formulation of Quercetin mouthwash and assesses its anti-inflammatory properties in comparison to Diclofenac sodium. Methods: Quercetin mouthwash was prepared using a commercially procured bioactive agent. One standard nonsteroidal anti-inflammatory drug, Diclofenac was used as a reference drug. The percentage inhibition of protein denaturation was calculated and its anti-inflammatory properties were evaluated through Bovine Serum Albumin Assay and Egg Albumin Assay. Results: Quercetin mouthwash showed parallel anti-inflammatory properties and showed a proportionate increase in anti-inflammatory properties with the increase in the concentration of the mouthwash. Comparable inhibition of protein denaturation at 10µl and 50µl concentrations with a proportionate variation of 1% (p>0.05) to the control in Egg Albumin Assay and 47% and 83% denaturation at 10µl and 50µl of Bovine Serum Albumin Assay were observed. Conclusion: Quercetin mouthwash has shown significant anti-inflammatory activity and hence is considered a potent anti-inflammatory agent comparable to Diclofenac sodium. It is found to be a suitable agent as an oral formulation for reducing the progression of inflammatory conditions.

Introducción: La periodontitis es una pandemia, ya que alrededor del 14 % de las personas en todo el mundo padecen periodontitis grave. Una intervención precoz en la enfermedad podría, probablemente, reducir su progresión y eliminar la necesidad de extraer los dientes afectados. La quercetina es un candidato probable, ya que tiene propiedades antiinflamatorias ejemplares. Su presencia de grupos hidroxilos fenólicos contribuye en gran medida a sus actividades antioxidantes y antiinflamatorias. Objetivos: El estudio presenta la formulación del colutorio de quercetina y evalúa sus propiedades antiinflamatorias en comparación con el diclofenaco sódico. Métodos: Se preparó un colutorio de quercetina, utilizando un agente bioactivo obtenido comercialmente. Se utilizó como fármaco de referencia un antiinflamatorio no esteroideo estándar, el diclofenaco. Se calculó el porcentaje de inhibición de la desnaturalización de proteínas y se evaluaron sus propiedades antiinflamatorias mediante ensayo con albúmina de suero bovino y con albúmina de huevo. Resultados: El colutorio de quercetina mostró propiedades antiinflamatorias paralelas y mostró un aumento proporcional de las propiedades antiinflamatorias con el aumento de la concentración del colutorio. Se observó una inhibición comparable de la desnaturalización de proteínas a concentraciones de 10µl y 50µl con una variación proporcional del 1 % (p > 0,05), respecto al control en el ensayo de albúmina de huevo y una desnaturalización del 47 % y 83 % a 10µl y 50µl del ensayo de albúmina de suero bovino. Conclusiones: El enjuague bucal de quercetina ha mostrado una actividad antiinflamatoria significativa, por lo que se considera un potente agente antiinflamatorio comparable al diclofenaco sódico. Se considera un agente adecuado como formulación oral para reducir la progresión de las afecciones inflamatorias.

Silver nanoparticles in mouthwashes against infection caused by SARS-CoV-2: a scoping review / Nanopartículas de prata em enxaguatórios bucais para uso em infecções por SARS-CoV-2: uma revisão de escopo

The Silver nanoparticle (AgNPs) have received attention for their antiviral potential against SARS-CoV-2. The objective is to conduct a scope review and map the scientific evidence on the use of AgNPs in mouthwashes as an adjunct in decreasing the viral load in the oral cavity of patients with SARS-CoV-2. A search was performed in the PubMed, Medline, Scielo databases, and a manual search in the reference lists, following the standards of the Joanna Briggs Institute for Scoping Review without restriction of year, language or sample size. Thus, 14 articles were included, where they researched the use of AgNPs with antiviral effect against SARS-CoV-2, mouthwashes for SARS-CoV-2 and AgNPs as mouthwashes. We can suggest that AgNPs are likely antiviral therapies for SARS-CoV-2 and its use in mouthwashes associated with other therapies are promising strands for decreasing viral load and infection by the vírus (AU)

As nanopartículas de prata (AgNPs) têm recebido atenção por seu potencial antiviral no SARS-CoV-2. O objetivo deste trabalho é realizar uma revisão de escopo e mapear as evidências científicas sobre o uso de AgNPs em bochechos como adjuvante na diminuição da carga viral na cavidade oral de pacientes com SARS-CoV-2. Foi realizada busca nas bases de dados PubMed, Medline, Scielo e busca manual nas listas de referências, seguindo os padrões do Joanna Briggs Institute for Scoping Review sem restrição de ano, idioma ou tamanho da amostra. Assim, foram incluídos 14 artigos, onde pesquisaram o uso de AgNPs com efeito antiviral contra SARS-CoV-2, enxaguatórios bucais para SARS-CoV-2 e AgNPs como enxaguatórios bucais, vertentes promissoras para diminuição da carga viral e infecção pelo vírus.(AU)

Efficacy of mouthrinses in reducing oral SARS-COV-2 load: a review

Abstract Accumulated evidence has shown that the oral cavity may be an important reservoir for SARS-CoV-2. Some authors have suggested that the use of mouthrinses could reduce SARS-CoV-2 viral load in the saliva. Thus, the aim of this review was to synthesize evidence about the efficacy of mouthrinses in reducing the salivary viral load of SARS-CoV-2. 2. Nine randomized controlled trials (RCTs) have investigated the efficacy of different mouthrinses in reducing salivary SARS-CoV-2 loads. Various active ingredients have been tested in these trials: 0.5%,1% and 2% povidone-iodine, 0.2% and 0.12% chlorhexidine (CHX), 0.075% cetylpyridinium chloride (CPC), 0.075% CPC with Zinc lactate, 1% and 1.5% hydrogen peroxide (HP), 1.5% HP + 0.12% CHX and ß-cyclodextrin and citrox. The studies reported an intra-group reduction in the salivary levels of the virus, when compared with the baseline. However, the majority of these trials failed to demonstrate a significant inter-group difference between active groups and the control group relative to the decrease in salivary SARS-CoV-2 loads. Although promising, these results should be confirmed by larger trials.

Mouthwash use and oral cancer: a systematic review and meta-analysis

ABSTRACT OBJECTIVE This study aimed to investigate the effect of mouthwash use on the development of oral cancer. METHODS Observational studies with adult/older adult populations that have examined the association between mouthwash use and oral cancer were included. Electronic search was performed in July 2022, with no time or language restrictions. PubMed/Medline, Embase, and Web of Science databases were used, and the search was extended to theses and dissertations libraries, Google Scholar, reference lists, and other sources. Methodological quality was assessed using the Newcastle-Ottawa Scale and quantitative data synthesis was performed by random effects meta-analysis, with different subgroup analyses and meta-regression. This revision was registered in Prospero (CRD42020143307). RESULTS Of the 4,094 studies identified in the search, 15 case-control studies were included in the review, totaling 6,515 cases and 17,037 controls. The meta-analysis included 17 measures of effect from 15 case-control studies. The pooled OR was 1.00 (95%CI: 0.79-1.26, n = 17 studies), but it was 2.58 (95%CI: 1.38-4.82, n = 2 studies) among those who had used mouthwashes three times or more times a day, and 1.30 (95%CI: 1.10-1.54, n = 4 studies) among those who had used mouthwashes for more than 40 years. CONCLUSIONS We found evidence that a high frequency of mouthwash use may be associated with an increased risk of oral cancer. However, despite the biological plausibility for this association, we suggest caution upon interpretation of our findings due to the few number of studies that have investigated the mouthwash use frequency, which should be considered. Therefore, we recommend that future studies assess, in detail, the frequency, duration, and content of mouthwashes to increase the strength of evidence for a possible dose-response effect of mouthwashes on oral cancer risk.

Ação clareadora e microbiológica do enxaguante bucal com peróxido de hidrogênio: ensaio clínico / Whitening and microbiological action of mouthwash with hydrogen peroxide: clinical trial

Introdução: os enxaguantes bucais clareadores tem sido muito utilizados, porém sua eficiência e efeitos colaterais trazem questionamentos. Objetivo: este ensaio clínico teve como objetivo avaliar se o enxaguante bucal clareador, contendo peróxido de hidrogênio a 1,5%, apresenta ação clareadora e se há algum efeito secundário na cavidade bucal. Metodologia: foram selecionados 10 voluntários com idade média de 21,5 anos, submetidos a avaliação da cor dos dentes com auxílio do espectrômetro em 3 momentos: inicial; com 15 e com 30 dias de uso do enxaguante. A avaliação dos efeitos colaterais foi realizada a partir da coleta de saliva estimulada em 4 momentos: antes e depois ao primeiro uso do produto, com 15 e com 30 dias, e realizadas as análises laboratoriais: fluxo salivar; pH; quantidade de Streptococcus mutans e de Lactobacillus. A normalidade dos dados foi verificada pelo teste de Shapiro-Wilk, comparação de cor pelo teste t dependente, comparação dos microrganismos pelos testes ANOVA de medidas repetida e Tukey. Resultados: as análises de cor dos dentes não evidenciaram nenhuma alteração significativa em nenhum dos tempos investigados. No fluxo salivar, pH e Lactobacillus não houveram alterações significativas. Na quantidade de Streptococcus mutans notou-se um aumento significativo quando comparado os valores após o primeiro uso e com 30 dias. Conclusão: a solução de enxague bucal contendo peróxido de hidrogênio a 1,5% não apresentou alteração significativa na coloração dos dentes e nenhum efeito colateral significativo na atividade cariogênica de acordo com os testes e períodos avaliados.

Introduction: whitening mouthwashes have been widely used, but their efficiency and side effects raise questions. Objective: this clinical trial aimed to assess whether the bleaching mouthwash, containing 1.5% hydrogen peroxide, has a bleaching action and whether there are any side effects in the oral cavity. Methods: 10 volunteers were selected, with a mean age of 21.5 years, who underwent tooth color evaluation with the aid of a spectrometer in 3 moments: initial; with 15 and 30 days of using the washes. The evaluation of side effects was performed from the collection of stimulated saliva in 4 moments: before and after the first use of the product, at 15 and 30 days, and laboratory analyzes were carried out: salivary flow; pH; the number of Streptococcus mutans and Lactobacillus. Normal distribution was verified with Shapiro-Wilk test, comparisons of color were performed with t-test, comparisons of the microorganisms were performed with repeated measures ANOVA and Tukey tests. Results: the analysis did not show any significant changes in any of the investigated times. There were no significant changes in the salivary flow, pH and Lactobacillus. The number of Streptococcus mutans, was noted a significant increase when comparing the values after the first use and with 30 days. Conclusion: the mouthwash containing 1.5% hydrogen peroxide was not shown any significant alterations in the color teeth. There were not significant collateral effects on the cariogenic activity according to the tests and periods evaluated.

Antibacterial and antifungal capacity of three commercially available mouthwashes with different concentrations of chlorhexidine / Efecto antibacteriano y antifúngico de tres enjuagues bucales comerciales con diferentes concentraciones de clorhexidina

Abstract Chlorhexidine was introduced almost seven decades ago and has a myriad of applications in dentistry. Few studies have evaluated the antimicrobial and antifungal capacity of different concentrations of chlorhexidine mouthwashes. Therefore, the aim of this study, was to evaluate in vitro, the antibacterial and antifungal capacity of three commercially available mouthwashes in Costa Rica, with different concentrations of chlorhexidine, 0.12%, 0.06%, and 0.03%. The experimental method selected was the Kirby-Bauer method to evaluate the antibacterial and antifungal effect of each compound by measuring the inhibitory effect on Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, and Candida albicans strains, exposed to the antiseptic solutions. All samples showed some degree of antibacterial and antifungal effect. Even though we provide in vitro results, our findings are of relevance since all the species used in our experiment are microorganisms that may be present in dental plaque. Our results further support evidence that oral hygiene regimens may include mouthwashes with low doses of chlorhexidine and maintain reasonable antibacterial and antifungal efficacy.

Resumen La clorhexidina se introdujo hace casi siete décadas y tiene una gran variedad de aplicaciones en odontología. Pocos estudios han evaluado la capacidad antimicrobiana y antifúngica de diferentes concentraciones de enjuagues bucales con clorhexidina. Por lo tanto, el objetivo de este estudio fue evaluar in vitro, la capacidad antibacteriana y antifúngica de tres enjuagues bucales disponibles comercialmente en Costa Rica, con diferentes concentraciones de clorhexidina, 0.12%, 0.06% y 0.03%. El método experimental seleccionado fue el método Kirby-Bauer para evaluar el efecto antibacteriano y antifúngico de cada compuesto midiendo el efecto inhibidor sobre Staphylococcus aureus, Enterococcus faecalis, Escherichia coli y Candida albicans, expuestos a la solución antiséptica. Todas las muestras mostraron algún grado de efecto antibacteriano y antifúngico. Aunque proporcionamos resultados in vitro, nuestros hallazgos son de relevancia, ya que todas las especies utilizadas en nuestro experimento son microorganismos que pueden estar presentes en la placa dental. Nuestros resultados respaldan aún más la evidencia de que los regímenes de higiene bucal pueden incluir enjuagues bucales con dosis bajas de clorhexidina y mantener una eficacia antibacteriana y antifúngica razonable.

Efectividad de los enjuagues bucales para reducir la carga viral de SARS-CoV-2. Una revisión sistemática

Introducción: El propósito del presente es sistematizar y analizar artículos científicos, acerca de la efectividad de ciertos enjuagues bucales para reducir la carga viral contra SARS-COV-2. Metodología: Las búsquedas se realizaron en las bases de datos científicas como PubMed y SciELO, entre otros, utilizando algoritmos de búsqueda, términos MeSH y booleanos. También se aplicaron criterios de inclusión/exclusión, seleccionando artículos provenientes de estudios primarios, publicados entre los meses de enero a septiembre de 2020, en idiomas inglés y español. Se utilizó un diseño metodológico mixto mediante el uso de los criterios de calidad PRISMA y de la Teoría Fundamentada (codificación abierta y central). Resultados: Se encontraron 144 artículos que coincidían con los algoritmos de búsqueda y criterios de calidad, de los cuales sólo ocho fueron analizados en la etapa de elegibilidad. Conclusiones: Se pudo determinar que los enjuagues más frecuentemente investigados en el último tiempo, para la desinfección oral inicial preoperatoria y/o de uso rutinario como enjuague oral contra SARS-COV-2 fueron la povidona yodada 0.2%; clorhexidina 0.12% y 0.2%, aceites esenciales con etanol al 21.6% y peróxido de hidrógeno 1.5% y 3.0%. La clorhexidina 0.2% temperada a 47°C demostró mayor efectividad que clorhexidina 0.12% a temperatura normal y que povidona yodada.

Introduction: The purpose of this research was systematize and analyze scientific articles, about the effectiveness of certain mouthwashes to reduce the viral load against SARS-COV-2. Methodology: The searches were performed in the PubMed and SciElo scientific databases, among others, using search algorithms, MeSH and Boolean terms. Certain criteria of inclusion/exclusion were also applied, selecting articles from primary studies, published between the months of January and September of 2020, in both English and Spanish. A mixed methodological design was used through the employment of quality criteria such as PRISMA and the Grounded Theory (open and central coding). Software based on texts and numbers were used for the data analysis plan. Results: 144 articles matching the search algorithms and quality criteria were found, of which only eight were analyzed in the eligibility stage. Conclusions: It was determined that the most frequently investigated mouthwashes in recent times, for preoperative initial oral disinfection and/or for a daily basis use as an oral rinse were the povidone iodine 0.2%; chlorhexidine 0.12% and 0.2%; essential oils with ethanol 21.6% and hydrogen peroxide 1.5% and 3.0%. The chlorhexidine 0.2% tempered at 47°C proved to be more effective than the chlorhexidine 0.12% at normal temperature and the povidone iodine.

Use of dentifrices and mouthwashes during orthodontic treatment in the clinical management of orthodontists / Utilização de dentifrícios e colutórios durante o tratamento ortodôntico na conduta clínica dos ortodontistas

ABSTRACT Objective: To evaluate the knowledge of orthodontic professionals regarding the prescription of dentifrices and antiseptics during orthodontic treatment. Methods: An observational and descriptive exploratory study of national scope was conducted with 440 Brazilian orthodontists, based on previous sample calculations, to evaluate the clinical practice of orthodontists in prescribing dentifrices and antiseptics. Self-managed electronic questionnaires were sent to orthodontic professionals. The data were analyzed by means of absolute and relative frequency distribution tables. Results: It was verified that the most indicated mouthwash (39.8%) was Colgate Periogard® and 421 of the participants (95.7%) know its active ingredient (chlorhexidine digluconate). Besides Colgate Periogard® antiseptic, the participants were also questioned about which active ingredient present on the following antiseptics, whose assertive answers were in the following order of %, Cepacol® (Sanofi-Aventis®) with 60.7%, Colgate Plax® (Colgate®) with 54.5% and Listerine® (Jhonson&Jhonson®) with 51.6%. As for the chlorhexidine therapeutic regime, 63.9% have stated assertively its use, being this one of 2 times a day during 7 to 10 days. The most indicated tooth was Colgate Total 12®, and 60.18% of these individuals correctly indicated its active compound. Conclusion: According to the methodology employed, it could be concluded that orthodontic professionals know and prescribe methods of chemical control to patients during orthodontic treatment and most identify the active chemical compounds present in antiseptic and tooth formulas.

RESUMO Objetivo: Avaliar o conhecimento dos profissionais da ortodontia quanto à prescrição de dentifrícios e antissépticos durante o tratamento ortodôntico. Métodos: Foi realizado um estudo observacional e descritivo exploratório de abrangência nacional com 440 ortodontistas brasileiros, baseado em cálculo amostral prévio, para avaliação da prática clínica dos ortodontistas na prescrição de dentifrícios e antissépticos. Questionários eletrônicos auto administrados foram enviados aos profissionais da Ortodontia. Os dados foram analisados por meio de tabelas de distribuição de frequência absolutas e relativas. Resultados: Verificou-se que o antisséptico bucal mais indicado (39,8%) foi o Colgate Periogard® (Colgate®) e 421 dos participantes (95,7%) conhecem o seu ingrediente ativo (digluconato de clorexidina). Além do antisséptico Colgate Periogard®, os participantes também foram questionados sobre qual o ingrediente ativo presente nos seguintes antissépticos, cujas respostas assertivas estavam na seguinte ordem %, Cepacol® (Sanofi-Aventis®) com 60,7%, Colgate Plax® (Colgate®) com 54,5% e Listerine® (Jhonson&Jhonson®) com 51,6%. Quanto ao regime terapêutico da clorexidina 63,9% indicaram assertivamente sua utilização sendo a mesma de 2 vezes ao dia durante 7 a 10 dias. O dentifrício mais indicado foi o Colgate Total 12®, sendo que 60,18% desses indivíduos indicaram corretamente seu composto ativo. Conclusão: De acordo com a metodologia empregada, pôde-se concluir que os profissionais da ortodontia conhecem e prescrevem métodos de controle químico aos pacientes durante o tratamento ortodôntico e a maioria identifica os compostos químicos ativos presentes nas fórmulas de antissépticos e dentifrícios.

Povidona Yodada como Antiséptico Oral en la Reducción de la Carga Viral del SARS-CoV-2: Revisión de la Literatura

RESUMEN: Se ha sugerido que el uso de antisépticos orales podría reducir la carga viral del virus SARS-CoV-2 en los pacientes durante la atención dental, pero sin evidencia que avale su efectividad. Dada la vulnerabilidad del virus a la oxidac ión, se ha recomendado el uso de colutorios que contengan agentes oxidantes como la povidona yodada. El objetivo de la presente revisión fue determinar la efectividad del uso de povidona yodada como antiséptico oral en la disminución de la carga viral del virus SARS-CoV-2. Se realizó una búsqueda bibliográfica en PubMed, Biblioteca Virtual en Salud, SciELO, Web of Science y EBSCO host. Se incluyeron estudios clínicos en pacientes con COVID-19 y estudios in vitro con cepas del virus que utilizaran colutorios de povidona yodada como forma de intervención, publicados entre enero del 2019 y enero del 2021. La selección de los artículos se realizó en dos etapas por dos autores de manera independiente. Luego de eliminar los artículos duplicados, se mantuvieron 53 referencias. Finalmente se incluyeron 2 estudios in vivo y 5 estudios in vitro para la revisión cualitativa. En los estudios in vitro, todas las concentraciones de povidona yodada evidenciaron una actividad virucida eficaz en los distintos tiempos de exposición, donde la mínima concentración efectiva correspondió a 0,5 % en 15 segundos. Los estudios in vivo presentaron resultados positivos hacia el uso de povidona yodada, pero con tamaños muestrales pequeños y una gran heterogeneidad en su metodología. En conclusión el uso profiláctico de povidona yodada como colutorio contra el virus SARS-CoV-2 es respaldado por los trabajos in vitro, con tiempos de aplicación fácilmente realizables en la atención dental, pero se requiere de un mayor número de ensayos controlados aleatorizados para comprobar su efectividad en la práctica clínica.

ABSTRACT: It has been suggested that the use of oral antiseptics could reduce the viral load of SARS-CoV-2 virus in patients during dental care, but without evidence to support its effectiveness. The objective of this study was to determine the effectiveness of povidone iodine mouthwash in reducing the viral load of SARS-CoV-2 virus. A literature search was conducted in PubMed, Biblioteca Virtual enSalud, SciELO, Web of Science and EBSCOhost. Clinical studies in patients with COVID-19 or in vitro studies with SARS-CoV-2 strains that used povidone-iodine mouthwash as a form of intervention, published between January 2019 and January 2021, were included. The selection of articles was carried out in two phases by two authors independently. After removing duplicate articles, 53 references were kept. Finally, 2 in vivo studies and 5 in vitro studies were included for the qualitative review. In the in vitro studies, all concentrations of povidone iodine showed effective virucidal activity at the different exposure times, where the minimum effective concentration corresponded to 0.5 % in 15 seconds. In vivo studies showed positive results towards the use of povidone iodine, but with small sample sizes and great heterogeneity in their methodology. The prophylactic use of povidone iodine mouthwash against the SARS-CoV- 2 virus is supported by in vitro studies, with application times easily achievable in dental care, but a large number of randomized controlled trials are required to verify its effectiveness in clinical practice.

Relación del uso de colutorios bucales con la disminución de la carga viral del SARS-CoV-2 en la práctica odontológica: tema de revision / Relationship of the use of mouthwashes with the decrease in the viral load of SARS-CoV-2 in dental practice: review topic

Resumen Actualmente, el odontólogo es uno de los profesionales de la salud con mayor riesgo de contagio de la COVID-19 debido a su contacto directo con la cavidad bucal. La alta exposición a los aerosoles, generados por los instrumentos rotatorios, en pacientes con la COVID-19, eleva el contacto con la carga viral del SARS-CoV-2 en los procedimientos de rutina. Se ha descrito que los colutorios bucales, previos a la atención odontológica, podrían ser soluciones efectivas para la reducción del contagio pese a su poca evidencia clínica. Los colutorios con cloruro de cetilpiridinio (CPC), peróxido de hidrógeno (H2O2), povidona yodada (PVP-I) y gluconato de clorhexidina (CHX) muestran un gran potencial para reducir la carga viral del SARS- CoV-2 en los aerosoles generados a partir de la saliva durante la consulta odontológica. Por lo expuesto, el presente artículo tuvo por objetivo hacer una revisión de la información científica actual sobre la relación del uso de los colutorios bucales con la disminución de la carga viral del SARS-CoV-2.

Abstract It is currently known that the dentist is one of the health professionals with the highest risk of contagion of COVID-19 due to its direct contact with the oral cavity. High exposure to aerosols generated by rotating instruments in COVID-19 patients increases contact with the SARS-CoV-2 viral load in routine procedures. It has been described that mouthwashes prior to dental care could be effective solutions to reduce contagion despite their little clinical evidence. Mouthwashes with cetylpyridinium chloride (CPC), hydrogen peroxide (H2O2), povidone-iodine (PVP-I) and chlorhexidine gluconate (CHX) show great potential to reduce the viralload of SARS-CoV-2 in the aerosols generated from saliva during the dental visit. Therefore, the objective of this article was to review the current scientific information on the relationship of the use of mouthwashes with the decrease in the viral load of SARS-CoV-2.

Effect of Spondias mombin L. extract on the wettability, roughness, color and morphology of bovine enamel

Although Spondias mombin L. extract has an excellent antimicrobial effect against oral microorganisms, it should be clarified how it affects enamel surface properties. Aim: To evaluate the color change, wettability/contact angle, surface roughness and morphology of bovine enamel submitted to the Spondias mombin L. extract. Methods: Thirty bovine teeth were distributed into the following groups: 0.12% chlorhexidine digluconate, 1:32 Spondias mombin L. extract and distilled water. Color change (CC) was evaluated after immerging specimens into the solutions for 14 days. Surface roughness (Ra) was measured using a roughness meter; wettability/contact angles (CA) were determined by the sessile drop method, and scanning electron microscopy images were obtained to characterize the morphology (SMA). The pH of the solutions was evaluated using a pHmeter. The Ra, CA, and CC data were parametric (Kolmogorov-Smirnov; p>0.05). Two-way ANOVA (for Ra and CA) and one-way ANOVA (for CC) with Tukey's posthoc tests at a significance level of 5% were used. SMA was analyzed descriptively. Results: The Spondias mombin L. extract revealed an acidic pH, and when in contact with the bovine teeth, it increased the wettability, but it did not cause statistically significant differences in the Ra. Spondias mombin L. extract caused the highest color change. The SEM images showed differences in the specimens' surface submitted to the extract compared to the other groups. Conclusion: Spondias mombin L. extract provided negative effects on bovine enamel's surface, including a high color change and a more wettable substrate

Effect of whitening mouth rinses on the chemical and physical properties of a nanofilled composite

Aim: This study analyzed the effect of whitening mouth rinses on water sorption (WS), solubility (SL), color change, and surface roughness of a nanofilled composite. Whitening perceptibility and acceptability (WID) were also studied. Methods: Forty specimens of Filtek Z350XT, shade EA2 were produced and randomly distributed (n=8) to AS ­ artificial saliva (control); LWE ­ Listerine Whitening Extreme; CLW ­ Colgate Luminous White; LCM ­ Listerine Cool Mint; and CP ­ Colgate Plax. They were immersed in the mouth rinses 2x/day, for one minute, during 28 days. The color was assessed using an Easyshade spectrophotometer (CIE-L*a*b* system). Surface roughness (Ra-µm) was measured with three parallel measures, using an RP-200 roughness meter. The WS and SL (µg/mm-3) were analyzed based on the ISO 4049 recommendations. The data were analyzed using one- and two-way ANOVA/Tukey tests (α=0.05). Results: Surface roughness significantly increased after immersion in AS and LCM, with no significant differences between the groups either before or after immersion. The ΔE* was not significantly different between the groups. All substances produced a ΔWID higher than the 50%:50% perceptibility and acceptability thresholds. The WS and SL were not significantly affected by the mouth rinses. Conclusion: Whitening mouth rinses did not affect WS, SL, surface roughness, and color stability of a nanofilled composite, regardless of the presence of ethanol in the composition

Antimicrobial potential of essential oils mouthrinses with and without alcohol: a randomized clinical trial

Aim: This study aimed to compare the microbiological potential and gustatory perception of essential oils (EO) mouthrinses containing and not containing alcohol. Methods: Twenty healthy adult volunteers rinsed with 10mL of the following test solutions: EO with alcohol, EO without alcohol, or a control solution (saline solution with mint essence). A washout period of at least seven days was adopted after a single-use protocol of the respective solution. All participants used all three tested substances. Antimicrobial potential was assessed by counting salivary total viable bacteria both before and after each rinse. Gustatory perception was evaluated using the Visual Analogue Scale (VAS). Multiple comparisons were performed with the Wilcoxon test, using Bonferroni correction. Results: Both EO solutions presented a higher antimicrobial potential in comparison to the control solution (p<0.017). However, no significant difference in antimicrobial potential was observed between EO containing or not containing alcohol (p=0.218). VAS of EO with alcohol (median: 2.7) was similar to control solution (median: 1.6) (p=0.287). A better gustatory perception was observed of the EO without alcohol (median 7.6) when compared to the control solution (p<0.0001). When EO groups were compared, EO without alcohol also demonstrated a significantly better gustatory perception (p=0.001). Conclusion: Mouthrinse containing EO without alcohol presented a better taste perception when compared to the EO with alcohol, but no difference was observed in the antimicrobial potential of both EO solutions after a single rinse protocol

Estudio preliminar de un enjuague bucal de solución salina como muestra diagnóstica para SARS-CoV-2 / Preliminary study of a saline mouthwash as a diagnostic sample for SARS-CoV-2

Resumen Objetivo: Evaluar la utilidad de un enjuague bucal con solución salina (EBSS) como muestra diagnóstica para la detección de SARS-CoV-2 en pacientes ambulatorios. Material y métodos: Este fue un estudio prospectivo realizado en el Hospital Regional de Alta Especialidad "Dr. Juan Graham Casasús", se seleccionaron 34 muestras aleatorias pareadas EBSS/MNF (enjuague bucal con solución salina/muestra (clínica) de la nasofaringe) que se recolectaron durante la visita al centro de evaluación ambulatoria de dicho hospital. Las muestras se analizaron mediante la reacción en cadena de la polimerasa con transcripción inversa en tiempo real (RT-PCR) y se calculó la concordancia entre EBSS y MNF, la sensibilidad y especificidad del EBSS. Resultados: De las 34 muestras pareadas EBSS/MNF, 14 fueron positivas para SARS- CoV-2; 4 muestras de EBSS y 10 muestras de MNF. Los resultados concordantemente positivos en las muestras pareadas EBSS/MNF fueron 3 y las medias de CT de cada gen (RdRp, N, E) no mostraron diferencia significativa entre las muestras. Se observaron 8 discordancias entre los dos tipos de muestras (7 individuos dieron positivo por MNF y 1 por EBSS). La concordancia observada entre EBSS y MNF fue aceptable (coeficiente kappa 0.31). La sensibilidad de EBSS fue de 30% con una especificidad del 95.8%. Conclusiones: La sensibilidad de EBSS no es comparable con la sensibilidad de MNF para la detección de SARS-CoV-2, pero nuestros datos sugieren al EBSS como una herramienta no invasiva, permite la autocolección y no requiere personal de salud capacitado para su muestreo: asimismo, esta muestra podría ser alternativa ante la escasez de hisopos y medios de transporte viral. Además, el EBSS puede tener beneficio para poblaciones remotas, vulnerables o facilitar las pruebas a un gran número de individuos.

Abstract Objective: To assess the usefulness of a saline mouth rinse (SMR) as a diagnostic tool for the detection of SARS-CoV-2 in outpatients. Method: This was a prospective study carried out at the Hospital Regional de Alta Especialidad "Dr. Juan Graham Casasús", 34 SMR/SNP (saline mouth rinse/sample (clinical) of nasopharyngeal) randomized paired samples were selected and collected in the outpatient clinic. The samples were analyzed by real-time reverse transcription polymerase chain reaction (RT-PCR) and the concordance between SMRs and SNP samples and the sensitivity and specificity of SMR were calculated. Results: Out of the 34 SMR/SNP paired samples, 14 samples were positive for SARS- CoV-2; 4 SMR samples and 10 SNP samples. We found 3 positive concordant results in the SMRs/SNP paired samples, the mean CT for each gene (RdRp, N, E) did not show a significant difference between the samples. Eight discrepancies were observed between the two types of samples (7 individuals were positive by SNP and 1 for SMR). The concordance observed between SMR and SNP was acceptable (kappa coefficient 0.31). The sensitivity of EBSS was 30% with a specificity of 95.8%. Conclusions: The SMR sensitivity is not comparable with SNP sensitivity for SARS- CoV-2 detection, but our data suggest SMR as a non-invasive tool that allows self- collection, and it does not require health trained personnel for its collection. Also, this sample could be an alternative to the lack of swabs and/or viral transportation media. Additionally, SMR may be of benefit in remote and vulnerable populations, and/or to facilitate the screening of SARS-CoV-2 in a large number of individuals.

Efficacy of intraoral antiseptics in SARS-CoV-2 infection control in dental clinics / Eficácia de antissépticos intraorais no controle da infecção por SARS-CoV-2 na clínica odontológica / Eficacia de los antisépticos intraorales en el control de la infección por SARS-CoV-2 en la clínica dental

Justificativa e Objetivos: No contexto da pandemia de COVID-19, em que a principal rota de transmissão da doença se dá pelo contato com saliva contaminada, procedimentos odontológicos de rotina representam um risco potencial de contágio para profissionais e pacientes. Para diminuir a ocorrência de infecção cruzada, são necessárias formas de controle da carga microbiana oral, como o uso de enxaguantes bucais pré-operatórios. Dessa forma, o objetivo desta revisão de literatura foi avaliar a potencial eficácia de diferentes antissépticos intraorais no controle de infecção por SARS-CoV-2 na clínica odontológica. Conteúdo: Trata-se de uma revisão da literatura, realizada nas bases de dados LILACS, Biblioteca Cochrane, CAPES e MEDLINE, através dos termos de busca "mouth rinse", "dental care", "COVID-19", "cetylpiridinium cloride", "povidoneiodine", "chlorhexidine" e "hydrogen peroxide". Entre os 46 artigos potencialmente relevantes, foram selecionados 14 artigos, com textos completos publicados, nos últimos 5 anos. Esses foram analisados e categorizados conforme o tipo de estudo (revisão de literatura, estudos in vitro e estudos in vivo). Os antissépticos destacados como mais relevantes em termos de eficácia antiviral foram iodopovidona, cloreto de cetilpiridínio, peróxido de hidrogênio e clorexidina. Conclusão: Poucas evidências foram encontradas em relação à eficácia de antissépticos orais contra o SARS-CoV-2. Vale ressaltar que alguns estudos realizados com iodopovidona e clorexidina demonstram resultados promissores no combate à infecção pelo SARS-CoV-2. Contudo, a realização de estudos clínicos randomizados é de extrema importância para determinar a eficácia desses compostos no controle da COVID-19 na prática odontológica.(AU)

Background and Objectives: In the context of the COVID-19 pandemic, in which the main route of transmission is through contact with contaminated saliva, routine dental procedures represent a potential risk of contagion for professionals and patients. To reduce the occurrence of cross-infection, ways of controlling oral microbial load are necessary, such as the use of preoperative mouthwashes. Thus, the aim of this literature review was to assess the potential efficacy of different intra-oral antiseptics in SARSCoV-2 infection control in dental clinics. Content: This is a literature review, carried out in the LILACS, Cochrane Library, CAPES and MEDLINE databases, using the search terms "mouth rinse", "dental care", "COVID-19", "cetylpiridinium chloride", "povidoneiodine", "chlorhexidine", and "hydrogen peroxide". Among the 46 potentially relevant articles, fourteen articles were selected, with full texts published in the last 5 years. These were analyzed and categorized according to the type of study (literature review, in vitro and in vivo studies). The antiseptics highlighted as most relevant in terms of antiviral efficacy were povidone-iodine, cetylpyridinium chloride, hydrogen peroxide and chlorhexidine. Conclusion: Little evidence has been found regarding the effectiveness of oral antiseptics against SARS-CoV-2. It is worth mentioning that some studies conducted with povidone-iodine and chlorhexidine show promising results in combating SARSCoV-2 infection. However, conducting randomized clinical studies is extremely important to determine the effectiveness of these compounds in controlling COVID-19 in dental practice.(AU)

Justificación y objetivos: En el contexto de la pandemia de COVID-19, en la que la principal vía de transmisión de la enfermedad es a través del contacto con saliva contaminada, los procedimientos dentales representan un riesgo de contagio para profesionales y pacientes. Para reducir la infección cruzada, son necesarias formas de controlar la carga microbiana oral, como el uso de enjuagues bucales preoperatorios. Por lo tanto, el propósito de esta revisión de la literatura fue evaluar la efectividad de diferentes antisépticos intraorales para controlar la infección por SARS-CoV-2 en la clínica dental. Contenido: Esta es una revisión de la literatura, realizada en las bases de datos LILACS, Cochrane Library, CAPES y MEDLINE, utilizando los términos de búsqueda "mouth rinse", "dental care", "COVID-19", "cetylpiridinium cloride", "povidone-iodine", "chlorhexidine" y "hydrogen peroxide". Entre los 46 artículos potencialmente relevantes, se seleccionaron 14 artículos, con textos completos publicados en los últimos 5 años. Estos fueron analizados y categorizados según el tipo de estudio (revisión de la literatura, estudios in vitro y in vivo). Los antisépticos destacados como más relevantes en términos de eficacia antiviral fueron povidona yodada, cetilpiridinio cloruro, peróxido de hidrógeno y clorhexidina. Conclusión: Se encontró poca evidencia con respecto a la efectividad de los antisépticos orales contra el SARS-CoV-2. Vale la pena mencionar que algunos estudios realizados con povidona yodada y clorhexidina muestran resultados prometedores contra el SARS-CoV-2. Sin embargo, realizar estudios clínicos aleatorios es importante para determinar la efectividad de estos compuestos en el control de COVID-19 en la práctica dental.(AU)

Oral Manifestation COVID-19 and the Rapid Resolution of Symptoms Post-Phtalox Treatment: a Case Series

ABSTRACT: The mouth plays a critical role in the transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) owing to the fact that both the tongue and salivary glands are conducive environments for the storage and spread of the virus. This case series aimed to describe the oral manifestations of coronavirus disease (COVID-19) and report the rapid response to Phtalox® treatment in all patients who tested positive for the virus. The patients were grouped based on whether according to convenience as soon as they tested positive for COVID-19. All patients had mouth ulcers and were advised to use 5 mL of Phtalox® mouthwash for 1 min, five times daily, in addition to standard COVID-19 treatment. Complete healing of mouth ulcers occurred in all patients diagnosed with COVID-19, and the mean duration for complete healing was 2.37 days. General improvement of COVID-19 symptoms was also observed. Based on the rapid recovery of mouth ulcers observed, we suggest that Phtalox® is effective as a complementary oral treatment for ulcers associated with COVID-19.

RESUMEN: La cavidad oral juega un papel fundamental en la transmisión del síndrome respiratorio agudo severo coronavirus 2 (SARS-CoV-2) debido al hecho de que tanto la lengua como las glándulas salivales son entornos propicios para el almacenamiento y la propagación del virus. Esta serie de casos tuvo como objetivo describir las manifestaciones orales de la enfermedad por coronavirus (COVID-19) e informar la rápida respuesta al tratamiento con Phtalox® en todos los pacientes que dieron positivo al virus. Los pacientes se agruparon en función de su conveniencia tan pronto como dieron positivo a COVID-19. Todos los pacientes tenían úlceras en la boca y se les recomendó utilizar 5 ml de enjuague oral Phtalox® durante 1 minuto, cinco veces al día, además del tratamiento estándar de COVID-19. La curación completa de las úlceras orales ocurrió en todos los pacientes diagnosticados con COVID-19, y la duración media para la curación completa fue de 2,37 días. También se observó una mejoría general de los síntomas de COVID-19. Con base en la rápida recuperación de las úlceras orales observadas, sugerimos que Phtalox® es eficaz como tratamiento oral complementario para las úlceras asociadas con COVID-19.

Chromatic analysis of orthodontic resin bonding agents exposed to different antiseptic mouthrinses

ABSTRACT Objective: To assess the color of different orthodontic resin bonding agents exposed to three antiseptic mouthrinses for a prolonged time interval (10-year aging simulation). Methods: 160 specimens were distributed into four groups, according to the orthodontic resin bond agent (Concise, Transbond XT, Transbond Plus Color Change, and Natural Ortho). Each group was exposed to different antiseptic mouthrinses: alcohol-based (Listerine®), alcohol-free (Oral-B®), chlorhexidine (Periogard®) and distilled water as the control. Specimens were submitted to two cycles of staining and artificial aging. Color was evaluated by means of a digital spectrophotometer at the beginning of the experiment and after every cycle. The system used to assess color changes was the CIE L*a*b*. Data was analyzed using the ANOVA and Tukey post-hoc test. Results: After simulation of 10 years of aging, Transbond XT and Natural Ortho composites presented no statistically significant differences in ∆E when exposed to different mouthrinses. The Concise composite specimens exposed to alcohol-free mouthrinse presented a significant difference when compared with specimens from the same group exposed to other antiseptic mouthrinses. Transbond Plus Color Change specimens exposed to chlorhexidine mouthrinse and to alcohol-containing mouthrinse presented a significant difference when compared with the specimens from the group exposed to water and alcohol-free antiseptic. Conclusion: All orthodontic resin bonding agents tested presented clinically perceptible color changes when exposed to at least one of the mouthrinses, except for the Natural Ortho composite. The Concise composite exposed to the alcohol-free solution was the resin that presented the highest color change values.

RESUMO Objetivo: Avaliar a cor de diferentes resinas ortodônticas expostas a três enxaguantes bucais, por um intervalo de tempo prolongado (simulação de 10 anos de envelhecimento). Métodos: 160 espécimes foram distribuídos em quatro grupos, de acordo com a resina de colagem ortodôntica (Concise, Transbond XT, Transbond Plus Color Change e Natural Ortho). Cada grupo foi exposto a diferentes tipos de enxaguantes bucais: à base de álcool (Listerine®), isento de álcool (Oral-B®), clorexidina (Periogard®) ou água destilada, como controle. Os espécimes foram submetidos a dois ciclos de manchamento e envelhecimento artificial. A cor foi avaliada por meio de um espectrofotômetro digital no início do experimento e após cada ciclo. O sistema utilizado para avaliar as alterações de cor foi o CIE L*a*b*. Os dados foram analisados utilizando-se o teste ANOVA e o teste post-hoc de Tukey. Resultados: Após a simulação de 10 anos de envelhecimento, as resinas Transbond XT e Natural Ortho não apresentaram diferenças estatisticamente significativas no ∆E, quando expostas a diferentes enxaguantes bucais. Os espécimes do grupo Concise expostos ao enxaguante bucal sem álcool apresentaram diferença significativa quando comparados aos espécimes do mesmo grupo expostos aos outros enxaguantes bucais. Os espécimes do grupo Transbond Plus Color Change expostos à clorexidina e ao enxaguante bucal à base de álcool apresentaram diferença significativa quando comparados aos espécimes dos grupos expostos à água e ao enxaguante bucal sem álcool. Conclusão: Todas as resinas ortodônticas avaliadas apresentaram alterações de cor clinicamente perceptíveis quando expostas a pelo menos um dos enxaguantes bucais, com exceção da resina ortodôntica Natural Ortho. A resina Concise exposta à solução isenta de álcool foi a que apresentou os maiores valores de alteração de cor.

Fluoride concentration in mouth rinses marketed in Chile and Brazil, and a discussion regarding their legislations

Abstract For fluoride to be effective in controlling caries, it should be bioavailable in commercial products, so that it can be released into the mouth in the products it contains. We chemically determined the available fluoride and pH in nine mouth rinses marketed in Chile, and eleven, in Brazil, and then discussed the legislation in force in both countries, regarding the anticaries potential of these oral hygiene products. The fluoride was analyzed with an ion-selective electrode (F-ISE), using the direct technique. The determinations were made in duplicate, and the results were expressed in ppm F (μg F/mL). The total fluoride concentration found in all the mouth rinses evaluated ranged from 94.7 to 233.5 ppm F, and closely matched what was declared by the manufacturers (100.0 to 226.2 ppm F). However, some mouth rinses showed lower fluoride concentrations (90 and 180 ppm F) in both countries. A Na2FPO3-formulated mouth rinse was found only in Chile, with 216.8 ppm F as the FPO32- ion, and 4.9 ppm F as the F-. The findings show that fluoride was potentially bioavailable in all the mouth rinses evaluated. Regarding the national legislations, although the mouthwashes sold in Brazil comply with the Brazilian legislation, discrepancies were found for Chile. However, neither country had a legislation matching the best available evidence on fluoride mouthwash efficacy for caries control. Thus, some products with low fluoride concentrations (below 226 ppm F), or manufactured with a fluoride salt other than NaF (Na2FPO3) are being sold in the Brazilian and Chilean markets.

Mouthwashes and Nasal Sprays as a Way to Prevent the Spread of SARS-CoV-2 / Enjuagues Bucales y Aerosoles Nasales como un Método de Prevenir la Propagación de SARS-CoV-2

ABSTRACT: COVID-19 pandemic has infected millions of people around the world. Due to its large accumulation in the nasopharyngeal region and transmission through respiratory fluids, its spread among people is extremely high. Considering the needed time for treatments and vaccine development, the research of preventive methods, such as the use of mouthwash and nasal spray, that could decrease the viral load in the nasopharyngeal region, and thus the spread of SARS-CoV-2, becomes fundamental. The evidence has shown that there are compounds with antiviral capacity that could be used for this purpose, among which are povidone-iodine, hydrogen peroxide, cyclodextrins, and the synthetic drug PUL-042. Currently, there is no clinical evidence that proves the effectiveness of these substances against SARS-CoV-2. Nevertheless, there are ongoing clinical trials to prove it and generate methods that could help to prevent or, at least, decrease its spread among the population and stop this pandemic.

RESUMEN: La pandemia de COVID-19 ha infectado a millones de personas en el mundo. Su extremadamente alta capacidad de propagación se debe a la gran acumulación en la región nasofaríngea y su transmisión vía fluidos respiratorios.Considerando el tiempo necesario para desarrollar vacunas y tratamientos, se vuelve fundamental la investigación de métodos preventivos como el uso de enjuague bucal y spray nasal, que puedan disminuir la carga viral en la zona nasofaríngea y así también la capacidad de propagación de SARS-CoV-2La evidencia presenta compuestos con capacidad antiviral como la povidona iodada, peróxido de hidrógeno, ciclodextrinas y la droga sintética PUL-042, que podrían ser usados para dicho propósito. Actualmente no existe evidencia clínica que demuestre la efectividad de estas sustancias contra SARS-Cov-2, sin embargo, se están desarrollando estudios clínicos para probarlos y generar métodos que ayuden a disminuir o prevenir su transmisión en la población, y así detener esta pandemia.

Enjuagues bucales con carbohidratos y su efecto en el rendimiento de carreras contrarreloj: Revisión sistemática / Carbohydrate mouthwashes and their effect on running time trial performance: Systematic review

Resumen Introducción: Actualmente, los efectos del enjuague bucal con carbohidratos sobre el rendimiento son controvertidos, algunos estudios plantean efectos ergogénicos, mientras que otros no han reportado efecto luego de suministrar enjuague bucal con carbohidratos. Objetivo: Determinar si existe evidencia científica que avale los distintos protocolos de enjuagues bucales con carbohidratos y su efecto sobre el rendimiento deportivo en carreras de ciclismo contrarreloj. Materiales y métodos: se realizó una búsqueda bibliográfica entre el 2015 y 2019 en las bases de datos Medline, Biblioteca Cochrane y Scopus utilizando los términos Carbohydrates, Mouth rinse y Athletic performance. Resultados: Se revisaron 96 estudios y se seleccionaron 7 en diversos grupos poblacionales, con diferentes métodos de evaluación y diversas dosis de enjuague con carbohidratos. Los resultados obtenidos fueron controversiales, en algunos casos se demostró efecto ergogénico y en otros no. Conclusiones: Los efectos de los enjuagues bucales con carbohidratos son controvertidos, por lo que no se puede asegurar que provoquen mejoras de rendimiento en carreras de ciclismo contrarreloj. Se requiere de más estudios aleatorizados controlados que logren homogeneizar e identificar los mecanismos de acción específicos mediante el cual los enjuagues bucales con carbohidratos actúan sobre distintas poblaciones de estudio.

Abstract Introduction: Currently, the effects of carbohydrate mouthwash use on sports performance are controversial. While some studies have shown ergogenic effects, others have not demonstrated any advantage. Objective: To determine whether there is scientific evidence to support the different protocols for carbohydrate mouthwashes use and their effect on sports performance in cycling races time trial. Materials and methods: A search of literature published between 2015 and 2019 was conducted in the Medline, Cochrane Library, and Scopus databases using the terms Carbohydrates, Mouth rinses and Athletic performance. Results: 7 out of 96 reviewed studies were selected, which included different population groups, evaluation methods, and doses of rinsing carbohydrates. The results obtained on the impact of carbohydrate mouthwashes on sport performance were controversial as only some studies demonstrated an ergogenic effect. Conclusions: As the effects of carbohydrate mouthwashes are debatable, it cannot be assured that they improve performance in different cycling races time-trial. More randomized controlled studies are required to homogenize and identify the specific action mechanisms through which carbohydrate mouthwashes act on different study populations.