Nanoparticle-modified PMMA to prevent denture stomatitis: a systematic review.

This systematic review aimed to evaluate the antifungal effectiveness of polymethylmetacrylate (PMMA) modified by nanoparticles (NPs) and to compare it with conventional acrylic resins for denture bases. The present study was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). Searches were performed using PubMed, SCOPUS, SciELO, EMBASE, and LILACS. Eligibility criteria were as recommended by PRISMA. The studies presented great variability regarding NP type, synthesis method, antifungal evaluation method, and antifungal effect. The most commonly used NPs were silver (AgNP) and zinc oxide (ZnONP), ranging in size from 10 to 100 nm. The incorporation methods were mechanical or agitated. Despite PMMA modification by ZnONP being shown in vitro to be a combination with the best antifungal effect, future studies are still needed to determine the minimum inhibitory concentration for Candida spp. and assess its biocompatibility before the protocol is clinically tested.

The effectiveness of microwave disinfection in treating Candida-associated denture stomatitis: a systematic review and metaanalysis.

OBJECTIVE: To evaluate the effectiveness of microwave disinfection in treating Candida-associated denture stomatitis (CADS). MATERIALS AND METHODS: The PubMed/MEDLINE, Embase, and Scopus databases were searched for reports on randomized clinical trials (RCTs) published in English until May 2020 (PROSPERO CRD42020192062) that evaluated the treatment of CADS by using microwave disinfection. The main outcomes were the improvement of clinical signs and/or the decrease in the residual yeast present on the dentures and palatal mucosa. The mean differences, standard deviations, risk ratio, and 95% confidence interval were calculated by using the random-effects model. Heterogeneity was assessed by using Cochran's Q test and I2 values. The level of significance was set at α = 0.05. RESULTS: Five RCTs with 245 participants were included. The descriptive investigations demonstrated that microwave disinfection was as effective (p > 0.05) as 0.2% chlorhexidine, 0.02% sodium hypochlorite, and topical nystatin (100.000 IU/mL), and was superior to topical miconazole in treating CADS. The metaanalysis did not show a statistical difference between microwave disinfection and nystatin (100.000 IU/mL) treatment in terms of mycological counts, cure, and recurrence rates (p > 0.05). CONCLUSION: Microwave disinfection showed comparable results with those of conventional therapies for treating CADS. In addition, treatment with 650 W for 3 min once a week for 14 days had better cost-effect results, indicating both the prevention and treatment of CADS. CLINICAL RELEVANCE: Our findings provide evidence regarding the treatment of CADS using microwave disinfection, and also indicating the best cost-effective option for this treatment modality.

Caracterización de la estomatitis subprotésica en portadores de prótesis removible en clínicas de la Universidad San Gregorio de Portoviejo, Ecuador / Characterization of subprosthetic stomatitis in patients with removable prosthesis. San Gregorio de Portoviejo University

RESUMEN Introducción: La estomatitis subprotésica es un proceso inflamatorio de la mucosa bucal que se encuentra cubierta por una prótesis removible, de causa multifactorial y alta prevalencia. Objetivo: Caracterizar la estomatitis subprotésica en pacientes portadores de prótesis removible atendidos en las clínicas odontológicas de la Universidad San Gregorio de Portoviejo en el período marzo-noviembre de 2019. Método: Se realizó un estudio descriptivo transversal, con los criterios de inclusión siguientes: mayores de 18 años, ambos sexos, buen estado de salud general, no practicar hábitos tóxicos, usar prótesis removible, total o parcial, confeccionada de acrílico o metales. Todos los sujetos de la investigación firmaron el consentimiento informado antes de realizarles la historia clínica de odontología del Ministerio de Salud Pública del Ecuador de donde se extrajeron los datos sociodemográficos, signos clínicos y características de la prótesis. Resultados: Fueron evaluados 100 pacientes. El 45 %, presentaba signos clínicos de estomatitis subprotésica; predominó el sexo femenino con el 33 % y el grupo de edad de 40 a 59 años con un 26 %. La mayoría de las prótesis no se ajustan ni adaptan de manera correcta, y tienen un mal estado físico, en el 80, 82,2 y el 91 %, respectivamente. El 84,4 % de los pacientes utilizaba prótesis parcial removible, confeccionadas con acrílico, por un periodo de 1 a 6 años en el 60 % de los casos. Conclusiones: El diagnóstico de estomatitis subprotésica se asocia con el mal estado físico, desajuste e inadecuada adaptación de las prótesis removibles, lo que indica la necesidad de la institución para el establecimiento de estrategias docentes hacia la comunidad para su prevención y diagnóstico temprano.

ABSTRACT Introduction: Subprosthetic stomatitis is an inflammatory process of the mucosa in the oral cavity covered by a removable prosthesis, with a multifactorial cause and high prevalence. Objective: To characterize subprosthetic stomatitis in patients with removable prosthesis treated at the dental clinics of San Gregorio University in Portoviejo in the period March-November 2019. Method: A cross-sectional descriptive study was conducted, with the following inclusion criteria: patients over 18 years old, both sexes, good general health, no toxic habits, use of removable prosthesis, total or partial, made of acrylic or metals. All the patients involved in the research signed their consent, information given to them before taking their dental records taken by the Ministry of Public Health of Ecuador, from which socio-demographic data, clinical signs and characteristics of the prosthesis were extracted. Results: 100 patients were evaluated. Forty-five per cent showed clinical signs of subprosthetic stomatitis; the female sex (33%) predominated and the age group 40-59 years with (26%). Most of the prosthesis did not fit or adapt correctly and were in poor physical condition in 80%, 82.2% and 91% respectively. 84.4% of the patients used removable partial prosthesis, made of acrylic, for a period of 1 to 6 years, (60%) of the cases. Conclusions: The diagnosis of subprosthetic stomatitis is associated with poor physical condition, maladjustment and inadequate adaptation of removable prostheses, which indicates the need for the institution to establish educational strategies towards the community for prevention and early diagnosis.

The effect of nanodiamonds on candida albicans adhesion and surface characteristics of PMMA denture base material - an in vitro study.

Candida albicans is the main causative pathogen of denture stomatitis, which affects many complete denture patients. OBJECTIVE: To evaluate the effect of different concentrations of nanodiamonds (NDs) added to polymethyl methacrylate (PMMA) denture base material on Candida albicans adhesion as well as on surface roughness and contact angle. METHODOLOGY: Acrylic resin specimens sized 10×10×3 mm3 were prepared and divided into four groups (n=30) according to ND concentration (0%, 0.5%, 1%, 1.5% by wt). Surface roughness was measured with a profilometer, and the contact angle with a goniometer. The effect of NDs on Candida albicans adhesion was evaluated using two methods: 1) slide count and 2) direct culture test. Analysis of variance (ANOVA) and Tukey's post hoc test were used in the statistical analyses. RESULTS: Addition of NDs decreased the Candida albicans count significantly more than in the control group (p<0.05), with a lowest of 1% NDs. Addition of NDs also significantly decreased the surface roughness (p<0.05), but the contact angle remained the same. Incorporation of NDs into the PMMA denture base material effectively reduced Candida albicans adhesion and decreased surface roughness. CONCLUSION: PMMA/NDs composites could be valuable in the prevention of denture stomatitis, which is considered one of the most common clinical problems among removable denture wearers.

The effect of nanodiamonds on candida albicans adhesion and surface characteristics of PMMA denture base material - an in vitro study

Abstract Candida albicans is the main causative pathogen of denture stomatitis, which affects many complete denture patients. Objective: To evaluate the effect of different concentrations of nanodiamonds (NDs) added to polymethyl methacrylate (PMMA) denture base material on Candida albicans adhesion as well as on surface roughness and contact angle. Methodology: Acrylic resin specimens sized 10×10×3 mm3 were prepared and divided into four groups (n=30) according to ND concentration (0%, 0.5%, 1%, 1.5% by wt). Surface roughness was measured with a profilometer, and the contact angle with a goniometer. The effect of NDs on Candida albicans adhesion was evaluated using two methods: 1) slide count and 2) direct culture test. Analysis of variance (ANOVA) and Tukey's post hoc test were used in the statistical analyses. Results: Addition of NDs decreased the Candida albicans count significantly more than in the control group (p<0.05), with a lowest of 1% NDs. Addition of NDs also significantly decreased the surface roughness (p<0.05), but the contact angle remained the same. Incorporation of NDs into the PMMA denture base material effectively reduced Candida albicans adhesion and decreased surface roughness. Conclusion: PMMA/NDs composites could be valuable in the prevention of denture stomatitis, which is considered one of the most common clinical problems among removable denture wearers.

Properties of an acrylic resin after immersion in antiseptic soaps: Low-cost, easy-access procedure for the prevention of denture stomatitis.

Denture stomatitis triggered by Candida species requires better preventive measures. This study evaluated the physical and biological properties of a denture base acrylic resin after immersion in antiseptic soaps. Acrylic resin specimens were prepared and stored in distinct solutions for 0, 7, 14, 21, and 28 days. The solutions were as follows: DW: distilled water at 37°C (control group); DS: cycles of daily immersion in Dettol soap for 8 hours at room temperature, followed by immersion in distilled water for 16 hours at 37°C; PS: cycles of daily immersion in Protex soap, as described for the previous group; LS: cycles of daily immersion in Lifebuoy soap, as described for the DS group. The parameters evaluated at each time point were the following: biofilm formation capacity by Candida albicans and reduction of preformed fungal biofilms, cytotoxicity, surface roughness, hardness, and color change. For the fungal adhesion phase, the type of soap had a statistically significant effect (p = 0.0292), but after 24 hours, no differences were found between solutions or between storage times. Regarding the efficacy of biofilm reduction, there was a significant difference when the groups were compared to each other (p = 0.014). Dettol and Lifebuoy eliminated the preformed biofilm on the specimens. Moreover, all the soaps were classified as non-cytotoxic (on HaCaT cell line) because there was no difference in cell viability between the different groups, except after 21 days, when a decrease in cell viability occurred, regardless of the type of soap. Regarding the roughness, there was no statistically significant difference (p > 0.05) between the groups. Lifebuoy decreased resin hardness regardless of storage time (p = 0.003). After 21 and 28 days of storage, there was an increase in hardness value, regardless of the type of soap. The specimens' color, according to the National Bureau of Standards values, ranged from 0.27 to 0.58 (i.e., imperceptible or mild color changes). In general, the disinfectant soaps were not able to prevent biofilm formation, but all the soaps were effective in reducing the preformed biofilm. In addition, all soaps were non-cytotoxic and did not change surface roughness, hardness (except Lifebuoy), and color (except Lifebuoy). Therefore, immersion in two antiseptic soaps (Protex and Dettol) may be a cheap and easy procedure for preventing denture stomatitis.

Antimicrobial activity of denture adhesive associated with Equisetum giganteum- and Punica granatum-enriched fractions against Candida albicans biofilms on acrylic resin surfaces.

Candida biofilms adhere to the internal surface of removable dentures, which is an etiological factor in the pathogenesis of denture stomatitis (DS). Adhesive materials are used at the base of maxillary complete dentures to improve their retention and chewing qualities. This article reports the antimicrobial activity of the enriched fractions of Equisetum giganteum and Punica granatum incorporated into a denture adhesive against C. albicans biofilm. The biofilms were induced on the surface of heat-cured acrylic resin specimens that were previously treated with a mixture of adhesive/herb extracts. The antimicrobial activity was evaluated by CFU counts, XTT reduction, and SEM and CLSM analysis. Both herb extracts amplified the anti-biofilm action of the adhesive on the acrylic resin by up to 12 h. Therefore, when these extracts were combined with COREGA®, they played a collaborative and innovative role in biofilm control and can be considered alternatives for temporary use in the treatment and/or prevention of DS.

Effect of sodium hypochlorite and Ricinus communis solutions on control of denture biofilm: A randomized crossover clinical trial.

STATEMENT OF PROBLEM: The prevalence of complete edentulism remains high in the elderly, and previous data have shown that poor denture hygiene is common among patients with edentulism. PURPOSE: The purpose of this randomized crossover trial was to evaluate the efficacy of denture cleansers in terms of biofilm removal, antimicrobial action, and the remission of denture stomatitis. MATERIAL AND METHODS: Fifty denture wearers with denture stomatitis were instructed to brush their dentures (brush and soap) and to soak them (20 minutes/14 days) in 4 solutions, as follows: C (control), 0.85% saline; SH1, 0.1% sodium hypochlorite; SH2, 0.2% sodium hypochlorite; and RC, 8% Ricinus communis. The biofilm in the intaglio surface of maxillary dentures was stained, photographed, and quantified by software (Image Tool). It was then collected (brushed with saline solution), and the obtained suspension was diluted (100 to 10-3) and seeded (50 µL) in CHROMagar for Candida spp. After incubation, colony-forming units per milliliter values were calculated. Denture stomatitis remission was classified according to the Newton classification. Data were analyzed by Friedman (α=.05) and Wilcoxon tests and corrected by the Bonferroni test (α=.005). RESULTS: SH1 (mean rank [MR]=1.98) and SH2 (MR=1.64) showed lower biofilm coverage than C (MR=3.73) that was similar to RC (MR=2.92). SH1 (MR=2.43) and SH2 (MR=2.10) showed antimicrobial action for Candida spp, and RC (MR=3.36) showed similar results to C (MR=3.51) and baseline (MR=3.50). Clinical signs of denture stomatitis were reduced by SH1 (MR=2.44), while SH2 (MR=2.56) and RC (MR=2.74) showed intermediate results. CONCLUSIONS: The two sodium hypochlorite solutions were the most effective means of biofilm control. All tested solutions were effective in reducing the signs of denture stomatitis.

Influence of melaleuca and copaiba oils on Candida albicans adhesion.

OBJECTIVE: To evaluate the efficacy of Melaleuca alternifolia and Copaifera officinalis in inhibiting the adhesion of Candida albicans biofilm. BACKGROUND: Over 65% of denture wearers suffer from denture stomatitis, which is one of the most prevalent forms of oral candidiasis. This disease is characterised by the inflammation of the oral mucosa in contact with the contaminated denture. The contaminated denture contributes to the switch of C. albicans from yeast to its pathogenic hyphal form. Candida albicans adheres and colonises the polymethylmethacrylate resin surfaces and thus contributes to the development of denture stomatitis. MATERIALS AND METHODS: The minimal inhibitory concentration (MIC) of M. alternifolia and Co. officinalis was assessed by the agar dilution method. Sixty-six thermopolymerised acrylic resin squares were used and treated with phosphate-buffered saline, sodium hypochlorite 1%, melaleuca 0.75%, melaleuca 0.375%, melaleuca 0.188% and copaiba 10%. For adherence and biofilm formation, the treated squares were placed in six-well tissue culture plates containing 1 × 10(7)  cells/ml of ATCC1023 or SC5314 in Roswell Park Memorial Institute (RPMI) medium, and after 12 h, the planktonic cells were counted. RESULTS: Copaiba oil did not inhibit C. albicans growth. However, melaleuca oil showed an MIC value of 0.375% (3.4 mg/ml) for ATCC10231 and 0.093% (0.84 mg/ml) for SC5314. CONCLUSIONS: Our results demonstrated that M. alternifolia oil inhibited the growth of C. albicans. Moreover, both oils promoted significant adhesion reduction in the tested strains. These findings suggest the possibility of using these oils in prophylaxes against candidiasis.

Equisetum giganteum e Punica granatum Linné associados a adesivo protético: atividade antimicrobiana contra biofilmes de Candida albicans / Equisetum giganteum and Punica granatum Linn associated with denture adhesive: antimicrobial activity against Candida albicans biofilms

Adesivos protéticos inibem a inflamação da mucosa subjacente e podem receber, em sua composição, componentes antimicrobianos, reduzindo o risco do desenvolvimento da estomatite protética (EP), doença relacionada principalmente à colonização das próteses pelo fungo Candida albicans. Tem sido relatada a atividade antifúngica de fitoterápicos, podendo auxiliar no tratamento da EP. Objetivo: Realizar o estudo fitoquímico de substâncias potencialmente ativas de Equisetum giganteum (Eg) (Cavalinha) e de Punica granatum (Pg) (Romã) e avaliar in vitro se a incorporação de extratos hidroalcóolicos de Eg e de Pg a um adesivo protético (COREGA®) influencia no desenvolvimento do biofilme de C. albicans (SC5314) sobre a superfície de resina acrílica termopolimerizável (Lucitone 550). Material e Métodos: Após identificação dos compostos dos fitoterápicos por HPLC-PAD, foi selecionada a fração e a concentração de interesse por meio da concentração inibitória mínima (CIM). Os biofilmes foram induzidos durante 3, 6 ou 12 horas sobre a superfície de corpos de prova de resina acrílica, previamente submetidos ao tratamento com o adesivo associado aos fitoterápicos (AD/Eg ou AD/Pg). Como controles, corpos de prova foram tratados apenas com adesivo (AD), com a associação adesivo/nistatina (AD/Nt) ou não recebam tratamento (PBS). A atividade antimicrobiana foi avaliada por meio da quantificação do biofilme pela contagem de unidades formadoras de colônias por mililitro (UFC/mL) e pelo percentual de redução da atividade metabólica das células fúngicas pelo ensaio colorimétrico de redução de sais de tetrazólio XTT (2,3 Bis (2-Methoxy-4-Nitro-5-Sulfophenil) 5 - [(Phenyl-Amino) Carbonyl] 2H - Tetrazolium Hidroxide). Os resultados foram expressos como média ± desvio padrão, e submetidos ao teste de Kruskal-Wallis para UFC/mL e Mann-Whitney ou análise de variância ANOVA-2 fatores seguido do teste post-hoc de Tukey HSD e teste de Dunnett para XTT. As médias dos valores obtidos pelas duas metodologias (UFC/mL e XTT) foram submetidas ao teste de correlação de Spearman (α= 0,05). Resultados: Foi possível identificar, pela análise em HPLCPAD, compostos derivados de kaempferol e quercetina em Eg e derivados de elagitaninos, como punicalina, em Pg. A associação de ambos os fitoterápicos ao adesivo (AD/Eg ou AD/Pg) reduziram significativamente o biofilme sobre a superfície da resina, em comparação ao grupo AD. Considerando os corpos de prova tratados, o período inicial (3 horas) apresentou os melhores resultados em relação à inibição do crescimento fúngico, comparando-se com os outros períodos. Conclusão: Possivelmente, o potencial antimicrobiano de Eg e de Pg está associado a compostos como flavonoides e taninos, respectivamente. Por fim, é possível que a associação destes fitoterápicos ao adesivo protético COREGA® poderá constituir uma alternativa temporária, viável e inovadora para auxiliar no tratamento e/ou prevenção da EP, desde que a manutenção das propriedades inerentes deste adesivo seja comprovada após estudos posteriores.(AU)

Denture adhesives inhibit inflammation of the underlying mucosal tissue and can receive, in their composition, antimicrobial components, reducing the risk of development of denture stomatitis (DS), a disease related mainly to the colonization of the prosthesis by the fungus Candida albicans. It has been reported the antifungal activity of herbal medicines, which may help in the treatment of DS. Objective: To realize the phytochemical study of potentially active substances of Equisetum giganteum (Eg) (Cola de caballo) and Punica granatum Linne (Pg) (Pomegranate) and evaluate in vitro the incorporation of hydroalcoholic extracts of Eg and Pg to a denture adhesive (COREGA®) influences the development C. albicans biofilm (SC5314) on the surface a polymerized acrylic resin (Lucitone 550). Material and Methods: After identification of compounds of the herbal by HPLC-PAD, the fraction and the concentration were selected by minimum inhibitory concentration (MIC). Biofilms were induced for 3, 6 or 12 hours on the surface of acrylic resin specimens, previously subjected to treatment with the adhesive associated with herbal (AD/Eg or AD/Pg). As controls, samples were treated with adhesive (AD), adhesive/nystatin association (AD/Nt) or not received treatment (PBS). The antimicrobial activity was evaluated by quantifying the biofilm using counting colony forming units per milliliter (CFU/mL) and by reduction percentage of fungal metabolic activity using colorimetric assay XTT (2,3 Bis (2-Methoxy-4-Nitro-5-Sulfophenil) 5 - [(Phenyl-Amino) Carbonyl] 2H - Tetrazolium Hidroxide). The results were expressed as mean ± standard deviation, and subjected to Kruscal-Wallis test for CFU/mL and Mann-Whitney or 2-way analysis of variance (ANOVA) followed by Tukey's HSD post-hoc test and Dunnett test for XTT. The mean values obtained by the two methods (CFU/mL and XTT) were submitted to Spearman correlation test (α=0,05). Results: It was possible to identify, by the analysis on HPLC-PAD, compounds derived from kaempferol and quercetin in Eg and ellagitannins derivatives, as punicalin in Pg. The combination of both herbal medicines to the adhesive (AD/Eg or AD/Pg) significantly reduced the biofilm on the surface of the resin, compared to the AD group. Accordingly, there was an increase in the percentage of reduction of the metabolic activity of biofilm at all periods in the presence of herbal medicines. Considering the treated specimens, the initial period (3 hours) showed the best results in relation to inhibition of fungal growth compared with other periods. Conclusion: Possibly, the antimicrobial potential of E. giganteum and P. granatum is associated with compounds such as flavonoids and tannins, respectively. Finally, we suggest that the combination of these herbal medicines to COREGA® prosthetic adhesive may be a temporary, viable and innovative alternative to assist in the treatment and/or prevention of DS, since the maintenance of the inherent properties of this adhesive is proven after further studies.(AU)

Biocompatibilidade in vivo de material resiliente temporário para base de prótese modificado por antimicrobianos para tratamento da estomatite protética / Biocompatibility in vivo of temporary soft denture liner for denture base modified by antimicrobials agents for denture stomatitis treatment

Reembasadores resilientes temporários contendo fármacos antifúngicos foram sugeridos como um tratamento adjunto para estomatite protética. No entanto, antes de utilizar clinicamente estes reembasadores modificados em humanos, é importante avaliar a sua biocompatibilidade em modelos animais. Este estudo avaliou a biocompatibilidade in vivo de um reembasador resiliente temporário para base de prótese (Trusoft) modificado por agentes antimicrobianos em suas mínimas concentrações inibitórias (MCIs) para biofilme de Candida albicans. Dispositivos acrílicos intra-orais (DIOs) foram confeccionados individualmente para 60 ratos Wistar. Os ratos foram divididos em 6 grupos (n=5): 3 grupos controle (Negativo: sem DIO; Geral: DIO sem reembasamento; Positivo: DIO reembasado com Trusoft sem fármacos) e 3 grupos experimentais (DIOs reembasados com Trusoft modificados por fármacos em suas respectivas MCIs: 0,032 g de nistatina, 0,064 g de diacetato de clorexidina e 0,128 g de cetoconazol). Os ratos com ou sem os DIOs foram eutanasiados após 7 e 14 dias de avaliação. A análise histopatológica qualitativa foi realizada comparando-se fotomicrografias de secções histológicas, que foram obtidas utilizando um microscópio óptico que abrangeu transversalmente a região intermolares. As alterações morfológicas no epitélio e queratina foram analisadas quantitativamente através da realização de planimetria computadorizada. Os dados quantitativos foram analisados utilizando ANOVA 2-fatores e teste de Tukey (=0,05). A análise quantitativa mostrou que apenas o grupo com DIO contendo cetoconazol diminuiu significativamente a espessura e a área do estrato córneo em comparação com os outros grupos (p<0,05), que não apresentaram diferenças significativas entre si (p>0,05). Estes resultados estiveram de acordo com os obtidos para análise qualitativa. A incorporação de MCIs de nistatina e diacetato de clorexidina no Trusoft não induziram alterações histopatológicas na mucosa palatina de ratos, sugerindo a biocompatibilidade in vivo deste protocolo para o tratamento de estomatite protética.(AU)

Temporary resilient denture liners containing antifungal drugs have been suggested as an adjunct treatment for denture stomatitis. However, before clinically using these modified liners in humans, it is important to assess their biocompatibility in animal models. This study evaluated the in vivo biocompatibility of a temporary soft denture liner (Trusoft) modified by antimicrobial agents at their minimum inhibitory concentrations (MICs) for biofilm formation by Candida albicans. Methods: Acrylic intraoral devices (IODs) were individually made for 60 Wistar rats. The rats were divided into the following 6 groups (n=5): 3 control groups (Negative: without IOD; General: IOD without relining; Positive: IOD relined with Trusoft without drugs) and 3 experimental groups (IOD relined with Trusoft modified by drugs at MICs: 0.032 g for nystatin, 0.064 g for chlorhexidine diacetate, and 0.128 g for ketoconazole). The rats with or without the IODs were sacrificed after 7 or 14 days of evaluation. Histopathological qualitative analysis was performed by comparing photomicrographs of histological sections, which were obtained using an optical microscope that transversely covered the inter-molar region. Morphological changes in the epithelium and keratin were quantitatively analyzed by performing computerized planimetry. Quantitative data were analyzed using 2-way ANOVA and Tukey's test (=0.05). Quantitative analysis showed that only the group with IOD containing ketoconazole significantly decreased the thickness and area of the stratum corneum compared with the other groups (p<0.05), which showed no significant differences between each other (p>0.05). These results were in accordance with those obtained for qualitative analysis. Incorporation of MICs of nystatin and chlorhexidine diacetate in Trusoft did not induce histopathological changes in the palatal mucosa of rats, suggesting the in vivo biocompatibility of this protocol for treating denture stomatitis.(AU)

Susceptibilidad in vitro de Candida albicans y no albicans Aisladas de Prótesis Dentales de Pacientes con Estomatitis Protésica a Tres Sustancias de Desinfección / In vitro Susceptibility of Candida albicans and Non-albicans Isolated fro Dental Prothesis in Patients with Denture Stomatitis to Three Disinfectants

A pesar del gran número de productos disponibles para la limpieza de prótesis dentales, el 60% de los portadores hace uso de ellos, posiblemente por la situación económica. El objetivo fue determinar la susceptibilidad antifúngica in vitro que presenta Candida y sus especies a tres sustancias utilizadas para la desinfección de prótesis (hipoclorito de sodio, ácido acético y solución de superoxidación). Se obtuvieron aislados clínicos de Candida de pacientes portadores de prótesis diagnosticados con estomatitis protésica, para su posterior estudio de susceptibilidad in vitro a las diferentes sustancias. El hipoclorito de sodio al 0,5% mostró in vitro una mayor inhibición para las cepas de Candida albicans y Candida no albicans. El ácido acético y la solución de superoxidación no mostraron inhibición in vitro frente a ambas cepas. El hipoclorito de sodio al 0,5% tiene un efecto inhibitorio in vitro sobre las cepas de C. albicans y Candida no albicans.

Despite the large number of products available for denture cleaning, less than 60% of denture wearers use them, possibly due to the economic situation. The aims were to determine the in vitro anti-fungal susceptibility of Candida species to three denture disinfectants (Sodium hypochlorite, acetic acid and super oxidized solution). Clinical isolates were obtained from denture wearers diagnosed with denture stomatitis for its posterior in vitro susceptibility study to the different substances. 0.5% Sodium hypochlorite showed the higher in vitro inhibitory effect on Candida albicans and non-albicans. Acetic acid and super oxidized solution showed no inhibition in both species. 0.5% Sodium hypochlorite has an in vitro inhibitory effect on Candida species.

Evaluación de conocimientos sobre estomatitis subprotésica en pacientes y profesionales de la Clínica Docente de Especialidades / Evaluation of knowledge about subprosthesis stomatitis in patients and professionals of the Specialty Teaching Clinic

Se muestra un estudio observacional descriptivo de corte transversal realizado en la Clínica Docente de Especialidades Victoria de Santa Clara, entre septiembre de 2013 y febrero de 2014, en una muestra conformada por 53 pacientes y 23 estomatólogos que respondieron a una serie de encuestas sobre la estomatitis subprotésica, con el objetivo de identificar el nivel de conocimiento de los pacientes y profesionales sobre esta enfermedad. El nivel de conocimiento de los pacientes se clasificó como malo, y las mayores dificultades se presentaron en la categoría de la autorresponsabilidad; los especialistas mostraron un nivel bueno, y solo se manifestaron ligeras deficiencias en cuanto a la clasificación de la afección. Se diseñó un plan de acción a partir de las principales deficiencias encontradas dirigido a los pacientes, con un enfoque educativo, para mejorar la promoción y prevención de la enfermedad(AU)

Intervención educativa sobre estomatitis subprótesis en el adulto mayor / Educational Intervention on Denture Stomatitis in the Elderly

Introducción: el bienestar físico-psíquico y social del adulto mayor requiere intervenciones educativas adecuadas.Objetivo: evaluar la efectividad de una intervención educativa sobre de la estomatitis subprótesis.Método: se realizó una intervención educativa en 98 adultos mayores de ambos sexos, con prótesis estomatológicas, que residen en la casa de abuelos del municipio Mayarí, Holguín, entre 2012 y 2013. Se aplicó un cuestionario diagnóstico para medir el nivel de conocimientos antes y después de la intervención.Resultados: antes de la intervención, el nivel de conocimiento predominante fue regular (61,2 %). Después de la intervención, los valores mayores se desplazaron hacia la categoría bueno (95,9 %). La higiene bucal de la prótesis antes de la intervención fue regular en el 67 % y después de la intervención fue buena en el 92 % de los pacientes.Conclusiones: los resultados favorables, obtenidos en la intervención a partir del uso de diferentes técnicas y medios educativos, demostraron la efectividad de la estrategia utilizada y los métodos empleados para su ejecución.(AU)

Introduction: the physical-mental and social well-being of elderly people need adequate educational interventions.Objective: to evaluate educative intervention effectiveness on dental prosthesis stomatitis.Methods: an educational intervention was carried out in 98 elderly patients with dental prosthesis at a Nursing home from Mayarí, Holguín Province, between 2012-2013. A questionnaire was applied to know the level of knowledge before and after the intervention.Results: the prevailing level of knowledge before intervention was of moderate category (61.2 %). After that the highest values enriched to good category (95.9 %). Prosthesis oral hygiene was of moderate category (67 %) before the intervention and improved to good category (92 %) after intervention.Conclusion: favorable results achieved after the intervention from the application of different techniques and educational means showed the effectiveness of the strategy and methods applied.(AU)

Caracterización de pacientes adultos mayores con estomatitis subprótesis / Characterization of elderly patients with stomatitis denture

Se realizó un estudio descriptivo con el propósito de caracterizar los pacientes adultos mayores que asistieron a consulta con estomatitis subprótesis en Hospital General Docente Dr Agostinho Neto de Guantánamo en el período enero de 2013 a enero de 2014. Se aplicó un cuestionario, se emplearon técnicas cualitativas de investigación, se revisaron documentos impresos y digitales donde se analizaron variables, tales como: edad, sexo, nivel de escolaridad, relación con hábito de fumar, frecuencia de cepillado de prótesis y frecuencia de visita al estomatólogo. Los datos cuantitativos obtenidos fueron procesados por medios computarizados, se utilizó el porcentaje (por ciento) como medida de resumen y se presentaron los resultados en tablas. Fueron frecuentemente afectados por esta lesión los pacientes portadores de prótesis total que los portadores de prótesis parcial removible. Candida albicans fue la especie más identificada en los evaluados en este estudio. Se arribó a recomendaciones y conclusiones(AU)

A descriptive study was conducted in order to characterize elderly patients who attended consultation with stomatitis denture at the General Teaching Hospital Dr Agostinho Neto, Guantanamo, in the period January 2013 to January 2014. A questionnaire was applied, qualitative research techniques, print and digital documents were used variables were reviewed such as : age, sex, and education level, relationship with smoking, frequency of brushing dentures and frequency of visits to the dentist. Quantitative data were obtained and processed by computerized means the percentage (percent) used as a summary measure and the results are presented in tables. They were frequently affected by these injury patients carrying total denture that carriers of removable partial denture. Candida albicans was more identified in species evaluated in this study. Recommendations and conclusions are given(AU)

Prevention and treatment of Candida colonization on denture liners: a systematic review.

STATEMENT OF PROBLEM: Denture liners are well known for their poor physical properties that favor the accumulation of plaque and colonization by Candida species, which can irritate the oral tissues and lead to denture stomatitis. PURPOSE: A systematic review was conducted to determine the feasibility of a prevention protocol for Candida colonization in denture liners and an effective treatment after the fungi has colonized the material. MATERIAL AND METHODS: Clinical and in vitro investigations that assessed the treatment and/or prevention of Candida colonization and biofilm formation in denture liners were selected according to the PRISMA statement. Seven electronic databases were searched from 1950 to April 2012 with the keywords "denture liner" OR "reline*" OR "tissue conditioner" AND "Candida" OR "denture stomatitis" OR "oral candidiasis" OR "antifungal agents" OR "denture clean*". RESULTS: The incorporation of nystatin (in general, 500 000 units) into tissue conditioners to prevent the onset of the disease and immersion in sodium hypochlorite for disinfection were the methods most often described in this systematic review, and both methods were able to prevent or inhibit Candida colonization, depending on their concentrations. The 0.5% sodium hypochlorite concentration can disinfect tissue conditioners and denture liners. Microwave irradiation has also been described an alternative method of disinfection. Because of a lack of standardized results (especially with regard to the method used to perform microbial counts), a meta-analysis could not be performed. CONCLUSIONS: The literature suggests that the use of 0.5% sodium hypochlorite can help disinfect denture liners and tissue conditioners. The incorporation of nystatin in those materials is also able to treat or prevent oral candidiasis. However, as most of the studies were in vitro, there is insufficient reliable evidence to truly provide recommendations regarding the ideal cleaning method or whether the addition of antifungal agents is worthwhile. Well-designed randomized controlled trials are needed to provide answers to these questions.

In vitro adhesion of Candida glabrata to denture base acrylic resin modified by glow-discharge plasma treatment.

This study evaluated the potential of plasma treatments to modify the surface chemistry and hydrophobicity of a denture base acrylic resin to reduce the Candida glabrata adhesion. Specimens (n = 54) with smooth surfaces were made and divided into three groups (n = 18): control - non-treated; experimental groups - submitted to plasma treatment (Ar/50 W; AAt/130 W). The effects of these treatments on chemical composition and surface topography of the acrylic resin were evaluated. Surface free energy measurements (SFE) were performed after the treatments and after 48 h of immersion in water. For each group, half (n = 9) of the specimens were preconditionated with saliva before the adhesion assay. The number of adhered C. glabrata was evaluated by cell counting after crystal violet staining. The Ar/50 W and AAt/130 W treatments altered the chemistry composition, hydrophobicity and topography of acrylic surface. The Ar/50 W group showed significantly lower C. glabrata adherence than the control group, in the absence of saliva. After preconditioning with saliva, C. glabrata adherence in experimental and control groups did not differ significantly. There were significant changes in the SFE after immersion in water. The results demonstrated that Ar/50 W treated surfaces have potential for reducing C. glabrata adhesion to denture base resins and deserve further investigation, especially to tailor the parameters to prolong the increased wettability.

Efeito da incorporação de agentes antimicrobianos sobre propriedades físicas de materiais resilientes temporários para base de prótese / Effect of the incorporation of antimicrobial agents on the physical properties of temporary resilient materials for denture base relining

O objetivo do presente estudo foi avaliar o efeito da adição de mínimas concentrações inibitórias (MCIs) de agentes antimicrobianos para biofilme de Candida albicans na sorção de água e solubilidade de materiais resilientes temporários (Softone e Trusoft) para reembasamento de próteses removíveis. Os grupos de estudo (n=10) foram formados por corpos de prova circulares (50 mm x 0,5 mm) dos materiais sem (controle) ou com a incorporação das MCIs de três fármacos utilizados para tratamento de estomatite protética: nistatina (Ni)-0,032g/mL; diacetato de clorexidina (Cl)- 0,064g/mL; cetoconazol (Ce)- 0,128g/mL. Para determinar a sorção de água e solubilidade, as amostras foram dessecadas, imersas em água por 24 h, 7 ou 14 dias, pesadas, dessecadas e pesadas novamente. Os dados obtidos (μg/mm3) foram analisados por ANOVA 3 fatores e teste de Tukey (α=0,05). Comparado aos respectivos controles, a sorção de água dos dois materiais avaliados aumentou com a adição de nistatina e clorexidina após 24 h e 7 dias de imersão em água (P<0,0001). Após 14 dias de avaliação, exceto pela clorexidina (P<0,0001) no Softone (483,00 ± 61,00 μg/mm3), a sorção dos materiais não foi afetada (P>0,05) pela adição dos fármacos (Softone: Ni- 310,72 ± 55,00 μg/mm3; Ce- 202,13 ± 52,28 μg/mm3/ Trusoft: Ni- 320,26 ± 22,89 μg/mm3; Ce: 300,45 ± 69,49 μg/mm3; Cl: 331,01 ± 48,18 μg/mm3) em comparação aos respectivos controles (Softone: 244,00 ± 42,00 μg/mm3; Trusoft: 274,85 ± 83,12 μg/mm3). Para todos os grupos, o tempo de imersão aumentou (P<0,0001) a solubilidade do Softone (24h: 18,82 ± 9,80 μg/mm3; 7d: 32,16 ± 4,48 μg/mm3; 14d: 58,81 ± 8,79 μg/mm3), mas não do Trusoft (24h: 12,46 ± 4,51 μg/mm3; 7d: 14,34 ± 5,20 μg/mm3; 14d: 15,48 ± 5,68 μg/mm3) (P>0,05). Em relação aos controles e para todos os períodos, a solubilidade dos dois materiais foi alterada com clorexidina e cetoconazol (P<0,0001), mas não sofreu influência da nistatina (P>0,05). Foi possível concluir após 14 dias de imersão em...

The objective of the present study was to evaluate the addition of minimum inhibitory concentrations (MICs) of antimicrobial agents for C. albicans biofilm on the water sorption and solubility of temporary resilient materials (Softone e Trusoft) for denture base relining. Test groups (n=10) were formed by disc specimens (50 mm x 0.5 mm) of the materials without (control) or with incorporation of the MICs of three drugs for denture stomatitis' treatment: nystatin (Nt)- 0.032g/mL; chlorhexidine diacetate (Cl)- 0.064g/mL; ketoconazole (Kt)- 0.128g/mL. To determine the water sorption and solubility, samples were dried, immersed in water for 24 h, 7 or 14 days, weighed, dried and weighed again. Data (μg/mm3) were analyzed by 3-way ANOVA and Tukeys test (α=.05). Compared to the respective controls, the water sorption of the two materials evaluated increased with the addition of nystatin and ketoconazole after 24 h and 7 days of water immersion (P<.0001). After 14 days of evaluation, except by chlorhexidine (P<.0001) in Softone (483.00 ± 61.00 μg/mm3), the sorption of the materials was not affected (P>.05) by the addition of the drugs (Softone: Nt- 310.72 ± 55.00 μg/mm3; Kt- 202.13 ± 52.28 μg/mm3 / Trusoft: Nt- 320.26 ± 22.89 μg/mm3; Kt: 300.45 ± 69.49 μg/mm3; Cl: 300.45 ± 69.49 μg/mm3) compared to the respective controls (Softone: 244.00 ± 42.00 μg/mm3; Trusoft: 274.85 ± 83.12 μg/mm3). For all groups, the immersion time increased (P<.0001) the solubility of Softone (24h: 18.82 ± 9.80 μg/mm3; 7d: 32.16 ± 4.48 μg/mm3; 14d: 58.81 ± 8.79 μg/mm3), but not of Trusoft (24h: 12.46 ± 4.51 μg/mm3; 7d: 14.34 ± 5.20 μg/mm3; 14d: 15.48 ± 5.68 μg/mm3) (P>.05). In comparison to the controls, and for all periods the solubility of the both materials was affected with chlorhexidine and ketoconazole (P<.0001), but not was influenced by nystatin (P>.05). It can be concluded that after 14 days of water immersion the addition of MICs of nystatin and ketoconazole in the...

Clinical and antimicrobial efficacy of NitrAdineTM-based disinfecting cleaning tablets in complete denture wearers

OBJECTIVE: This study evaluated the efficacy of NitrAdineTM-based disinfecting cleaning tablets for complete denture, in terms of denture biofilm removal and antimicrobial action. MATERIAL AND METHODS: Forty complete denture wearers (14 men and 26 women) with a mean age of 62.3±9.0 years were randomly assigned to two groups and were instructed to clean their dentures according to two methods: brushing (control) - 3 times a day with denture brush and tap water following meals; brushing and immersion (Experimental) - brushing the denture 3 times a day with denture brush and tap water following meals and immersion of the denture in NitrAdineTM-based denture tablets (Medical InterporousTM). Each method was used for 21 days. Denture biofilm was disclosed by a 1 percent neutral red solution and quantified by means of digital photos taken from the internal surface before and after the use of the product. Microbiological assessment was conducted to quantify Candida sp. RESULTS: An independent t-test revealed a significant lower biofilm percentage for the experimental group (4.7, 95 percent CI 2.4 to 7.9) in comparison with the control group (mean 37.5, 95 percent CI 28.2 to 48.1) (t38=7.996, p<0.001). A significant reduction of yeast colony forming units could be found after treatment with Medical InterporousTM denture tablets as compared to the control group (Mann-Whitney test, Z=1.90; p<0.05). CONCLUSION: The present findings suggest that NitrAdineTM-based disinfecting cleaning tablets are efficient in removal of denture biofilm. In addition, a clear antimicrobial action was demonstrated. Therefore, they should be recommended as a routine denture maintenance method for the prevention of the development of microbial biofilm induced denture stomatitis.