Insights on the role of cytokines in carious lesions / Insights sobre o papel das citocinas em lesões cariosas

Objetivo: A resposta imune da dentina-polpa à patogênese da cárie ainda é pouco compreendida devido à complexa interação dos processos envolvidos. O objetivo desta revisão foi explorar o papel das citocinas e sua relevância na patogênese da cárie dental. Resultados: A cárie dentária pode resultar em uma resposta inflamatória do hospedeiro na polpa dental, caracterizada pelo acúmulo de células inflamatórias levando à liberação de citocinas inflamatórias como, Interleucina-4 (IL-4), Interleucina (IL-6), Interleucina-8 (IL-8) e fator de necrose tumoral­α(TNF-α). IL-4 parece estar correlacionada com a profundidade das lesões cariosas; IL-6 está fortemente correlacionada com a doença cárie e é considerada um potente biomarcador; IL-8 pode ser um potente biomarcador tanto para cárie quanto para outras alterações presentes na polpa e sua liberação está correlacionada com TNF-α e IL-6; TNF-α desempenha um papel importante não apenas na progressão da cárie, mas também em outros processos patológicos. Conclusao: Mediadores específicos têm um grande potencial para servir como biomarcadores quanto à presença e progressão da doença cárie, o que incita a necessidade de mais investigações nesse campo (AU).

Objectives: The dentin-pulp immune response to caries pathogenesis is still poorly understood due to the complex interplay of the involving processes. The aim of this review was to explore the role of cytokines and its relevance in the pathogenesis of dental caries. Results: Dental caries can result in a host inflammatory response in the dental pulp, characterized by the accumulation of inflammatory cells leading to the release of inflammatory cytokines such as Interleukin-4 (IL-4), Interleukin (IL-6), Interleukin-8 (IL-8) and Tumor necrosis factor­ α (TNF- α ). IL-4 seems to be correlated to the depth of carious lesions; IL-6 is strongly correlated to caries disease and is considered a potent biomarker; IL-8 can be a potent biomarker for both caries and other changes present in the pulp and, its release is correlated to TNF- α and IL-6; TNF-α plays an important role not only in caries progression, but also in other pathological processes. Conclusion: Specific mediators have a great potential to serve as biomarkers alluding to the presence and progress of caries disease, urging further investigations in the field (AU)

Clinical performance of 6% hydrogen peroxide containing TiO2N nanoparticles activated by LED in varying wavelengths-a randomized clinical trial.

This randomized, controlled, and double-blinded clinical trial evaluated the clinical performance of dental bleaching performed with 6% hydrogen peroxide containing TiO2-N nanoparticles exposed to blue and violet activation lights. Forty volunteers, selected according to the inclusion and exclusion criteria, were randomly distributed into four experimental groups (n = 10): 35% hydrogen peroxide (PH35)-control; 6% hydrogen peroxide (PH6) containing TiO2-N nanoparticles without light activation; PH6 activated with a blue LED (PH6A); and PH6 activated with a violet LED (PH6V). The three bleaching sessions consisted of 3 consecutive 16-min applications of the bleaching agent described for each group. The groups receiving LED activation were exposed to light intermittently every 1 min, with a total exposure time of 8 min in each application. Efficacy was determined by the color variation in the upper central incisors and canines, using reflectance spectroscopy analysis performed by a calibrated evaluator (ICC = 0.83). Tooth sensitivity was characterized according to the presence and intensity (SI) self-recorded in specific forms. The group treated with PH6V was as effective as the control group (PH35), whereas the groups PH6A and PH6 showed lower efficacy. Regardless of the activation, all groups treated with 6% hydrogen peroxide were less likely to cause sensitivity compared to the control group (PH35). The use pf PH6 activated by LED violet resulted in an effective and safe clinical protocol for in-office dental bleaching.Trial registration number: RBR-8pbydg; registration date: 08/29/2017.

Methacrylation of epigallocatechin-gallate for covalent attachment with a dental polymer.

OBJECTIVE: Synthesize novel epigallocatechin-gallate (EGCG) methacrylate monomers with the ability to copolymerize with dental methacrylate resins. METHODS: EGCG was reacted with 1/3 (E33), 2/3 (E67) and 1 (E100) molar equivalents of methacyloyl chloride introducing three degrees of polymerizablility. EGCG-methacrylates were characterized by Fourier Transform Infrared Spectroscopy (FTIR) and Nuclear Magnetic Resonance (NMR). E33, E67, E100 and neat EGCG were incorporated into TEGDMA at 0.5-20% ratios (m/m). Copolymers were tested for degree of conversion (%DC), EGCG release, gel content (%GC), degree of swelling (%DS), flexural properties and bacterial viability (Streptococcus mutans, baseline/30-days). Neat TEGDMA and TEGDMA passively loaded with EGCG (E0) were used as controls. Data were analysed by one-way ANOVA, Tukey, and Dunnett's method (α=5%). Two-way ANOVA and Bonferroni were used to investigate factor interaction. RESULTS: FTIR/NMR confirmed synthesis of desired compounds. All of E100 incorporated ratios had %DC similar to TEGDMA. Remaining groups had reduction in %DC at 2% in E0, 10% in E33 and 20% in E67 ratios. EGCG was stable within ECGC-methacrylate copolymers. Release of EGCG from E0 significantly increased with higher EGCG ratios. Except for E100, higher EGCG or EGCG-methacrylate ratios led to decreased %CG and %DS. At baseline, E0 had the lowest bacterial survival rates (1-10% survival) at all ratios compared to E33, E67, E100, and neat TEGDMA. However, E33, E67 and E100 still had statistically lower survival rates (7-53%) compared with neat TEGDMA. After 30-days, all compounds had similar survival rates for all ratios, which were lower than that of neat TEGDMA. SIGNIFICANCE: Demonstration of methacrylate functionalized EGCG- with inherited antibacterial activity for improved restoration longevity.

Blue Covarine Toothpaste versus Office Whitening: Which is the Most Effective on Stained Teeth? / Creme Dental de Blue Covarine Versus Clareamento de Consultório: Qual é o Mais Efetivo em Dentes Pigmentados?

Alternative whitening strategies to hydrogen peroxide have been proposed, such as the inclusion of abrasive and/or pigmented particles in the toothpaste. This study compared the whitening effectiveness of a toothpaste containing Blue Covarine (BC) vs. an in-office whitening treatment using 35% hydrogen peroxide (HP) in teeth stained. Bovine incisors blocks (6.0x6.0x2.0 mm) were stained with green tea (GT), orange soda (OS), or red wine (RW). The samples were randomly assigned into 8 groups (n=15), according to the type of staining and whitening treatment: G1 ­ no staining, BC (Control); G2 ­ no staining, HP (Control); G3 ­ GT, BC; G4 ­ GT, HP; G5 ­ OS, BC; G6 ­ OS, HP; G7 ­ RW, BC; G8 ­ RW, HP. Color change (ΔE), luminosity (L*), green-red axis (a*), and blue-yellow axis (b*) were recorded with spectroscopy at T0 ­ baseline, T1 ­ immediately after toothbrushing or in office tooth whitening, and T2 ­ after the conclusion of the treatments. The whiteness index for dentistry (WID) was calculated. Data were analyzed by two-way repeated measured mixed ANOVA and Bonferroni test (α=0.05). HP showed a better whitening performance (ΔE) (p ≤ 0.042). Otherwise, no effects of the whitening agent were observed (p = 1.000). Data from ΔL, Δa, and Δb showed statistically significant differences for experimental groups (p < 0.001). In the WID analysis, BC and HP had similar effects within control and RW groups. In conclusion, blue covarine toothpaste may be a viable option for extrinsically stained teeth. However, for severe staining, HP-based whitening agents proved to be the most effective treatment strategy. (AU)

Estratégias de clareamento alternativas ao peróxido de hidrogênio têm sido propostas, como a inclusão de partículas abrasivas e/ou pigmentadas nos cremes dentais. Este estudo comparou a eficácia clareadora de um creme dental contendo Blue Covarine (BC) com um tratamento de clareamento em consultório com peróxido de hidrogênio a 35% (HP) em dentes pigmentados. Blocos de incisivos bovinos (6,0x6,0x2,0 mm) foram pigmentados com chá verde (GT), refrigerante de laranja (OS) ou vinho tinto (RW). As amostras foram distribuídas aleatoriamente em 8 grupos (n = 15), de acordo com o tipo de pigmento e tratamento clareador: G1 - sem coloração, CB (Controle); G2 - sem coloração, HP (Controle); G3 - GT, BC; G4 - GT, HP; G5 - OS, BC; G6 - SO, HP; G7 - RW, BC; G8 - RW, HP. Mudança de cor (ΔE), luminosidade (L *), eixo verde-vermelho (a*) e eixo azul-amarelo (b*) foram registrados com espectroscopia em T0 - baseline, T1 - imediatamente após a escovação ou clareamento dental em consultório, e T2 - após a conclusão dos tratamentos. O índice de brancura para odontologia (WID) foi calculado. Os dados foram analisados por ANOVA mista de duas vidas para medidas repetidas e teste de Bonferroni (α = 0,05). HP apresentou melhor desempenho de clareamento (ΔE) (p ≤ 0,042). Os dados de ΔL, Δa e Δb mostraram diferenças estatisticamente significativas para os grupos experimentais (p <0,001). Na análise WID, BC e HP tiveram efeitos semelhantes nos grupos controle e RW. Em conclusão, o creme dental covarine azul pode ser uma opção viável para dentes com coloração extrínseca. No entanto, para manchas graves, os agentes de clareamento à base de HP provaram ser a estratégia de tratamento mais eficaz. (AU)

Whitening toothpaste containing activated charcoal, blue covarine, hydrogen peroxide or microbeads: which one is the most effective?

The efficacy of whitening toothpastes is questionable and controversial. Clinicians, patients and researchers have expressed concern with whitening toothpastes due to the risk of wearing the dental structure and the potential for disappointment if the advertised cosmetic results are not achieved. OBJECTIVE: This study compared the whitening performance of toothpastes with different whitening technologies after initial and continued use. MATERIAL AND METHODS: Ninety bovine incisors were stained using a concentrated solution of black tea. They were randomly distributed into 6 groups, according to the toothpaste whitening technology: activated charcoal (B&W), blue covarine (WAD), hydrogen peroxide (LWA), microbeads (Oral B 3D White Perfection - 3DW) and optimized abrasives (XW4D). They were compared to a traditional toothpaste without a whitening agent (TA - control). Specimens underwent a brushing machine with controlled pressure, time and temperature. A calibrated examiner measured the color using a VITA-Classical scale before the first brushing cycle (T0), after the first brushing cycle (TI), and after a brushing cycle that simulates continuous use (TCU). Whitening performance was evaluated by the difference of shades (ΔSGU) between T0-TI and T0-TCU timepoints, using the Kruskal-Wallis and Dunn's non-parametric test. The Wilcoxon test was used to evaluate the cumulative effect (α=0.05). RESULTS: Statistically significant differences were observed between toothpastes in both TI and TCU (p<0.05). The time of use also had a significant effect (p<0.05). CONCLUSION: Only WAD and 3DW showed whitening performance after the first use (TI). The greatest whitening performance after continuous use was obtained by WAD, followed by LWA and 3DW. The use of conventional toothpaste (TA) promotes no tooth whitening. CLINICAL RELEVANCE: Microbead abrasives (3DW) and blue covarine (WAD) were the active technology tested that presented the best global tooth whitening performance.

Whitening toothpaste containing activated charcoal, blue covarine, hydrogen peroxide or microbeads: which one is the most effective?

Abstract The efficacy of whitening toothpastes is questionable and controversial. Clinicians, patients and researchers have expressed concern with whitening toothpastes due to the risk of wearing the dental structure and the potential for disappointment if the advertised cosmetic results are not achieved. Objective: This study compared the whitening performance of toothpastes with different whitening technologies after initial and continued use. Material and Methods: Ninety bovine incisors were stained using a concentrated solution of black tea. They were randomly distributed into 6 groups, according to the toothpaste whitening technology: activated charcoal (B&W), blue covarine (WAD), hydrogen peroxide (LWA), microbeads (Oral B 3D White Perfection - 3DW) and optimized abrasives (XW4D). They were compared to a traditional toothpaste without a whitening agent (TA - control). Specimens underwent a brushing machine with controlled pressure, time and temperature. A calibrated examiner measured the color using a VITA-Classical scale before the first brushing cycle (T0), after the first brushing cycle (TI), and after a brushing cycle that simulates continuous use (TCU). Whitening performance was evaluated by the difference of shades (ΔSGU) between T0-TI and T0-TCU timepoints, using the Kruskal-Wallis and Dunn's non-parametric test. The Wilcoxon test was used to evaluate the cumulative effect (α=0.05). Results: Statistically significant differences were observed between toothpastes in both TI and TCU (p<0.05). The time of use also had a significant effect (p<0.05). Conclusion: Only WAD and 3DW showed whitening performance after the first use (TI). The greatest whitening performance after continuous use was obtained by WAD, followed by LWA and 3DW. The use of conventional toothpaste (TA) promotes no tooth whitening. Clinical relevance: Microbead abrasives (3DW) and blue covarine (WAD) were the active technology tested that presented the best global tooth whitening performance.

Color stability of conventional and bulk fill composite resins / Estabilidade cromática de resinas convencionais e resinas bulk fill

ABSTRACT Objective: This study compared the color stability of different dental composite resins after prolonged exposure to a coffee solution. Methods: Sixty-four cylindrical discs (10 mm diameter x 2 mm thickness) were prepared using 8 different dental composite resins (n=8, per group). The specimens were first immersed in artificial saliva for 24 h followed by immersion in a coffee solution for 14 days. The assessment of chromatic variation (ΔE) was performed with the aid of a Vita Easyshade Advanced spectrophotometer (VITA Zahnfabrik, Bad Sackingen, Germany). The color of each specimen was calculated based on the L*, a* and b* coordinates of the CIELab system. Results: Grandio SO had the lowest average chromatic variation (ΔE=7.77) after immersion in coffee solution. Durafill VS, Grandio and Z350 XT (ΔE=8.58; ΔE=9.52; ΔE=10.39, respectively) showed similar chromatic variation, with no statistical difference in relation to Grandio SO. However, the other dental composite resins evaluated showed statistically higher values of ΔE compared to Grandio SO, and Enamel HRi (ΔE=20.56) demonstrated the highest chromatic variation. Conclusion: The Bulk Fill and hybrid composite resins from the same manufacturer (Micerium, Avegno, Italy) showed greater chromatic variation than the other composite resins tested. Grandio SO (Voco, Cuxaven, Germany) had the lowest ΔE variation.

RESUMO Objetivo: Comparar diferentes resinas compostas em relação á estabilidade de cor após exposição prolongada em solução de café. Métodos: Sessenta e quatro discos cilíndricos (10mm x 2mm) foram confeccionados a partir de 8 diferentes marcas comerciais de compósitos (n= 8 por grupo); os espécimes foram imersos em saliva artificial, e posteriormente em café, sendo por conseguinte feita a avaliação da variação cromática (ΔE), utilizando espectrofotômetro Vita Easyshade Advanced (VITA Zahnfabrik, Bad Sackingen, Germany). O padrão de cada espécime foi medido examinando as coordenadas L*, a* e b* do sistema CIELab. Resultados: A resina composta Grandio SO apresentou a menor média de variação cromática (ΔE= 7,77) após a imersão em solução de café. Semelhantemente, a variação cromática das resinas compostas Durafill VS, Grandio e Z350 XT (ΔE=8,58; ΔE=9,52; ΔE=10.39) que não apresentaram diferença estatística. Todavia, as demais resinas compostas avaliadas apresentaram valores estatisticamente maiores de ΔE em relação a resina Grandio SO, sendo que a resina Enamel HRi (ΔE= 20,56) apresentou a maior variação cromática registrada. Conclusão: As resinas da categoria bulk fill e as resinas híbridas produzidas pelo mesmo fabricante (Micerium, Avegno, Itália) tiveram alterações cromáticas superiores às demais resinas testadas sendo que a resina GrandioSO (Voco, Cuxaven, Alemanha) foi a que apresentou menor alteração de ∆E.

New Parameter for In-Office Dental Bleaching.

Dental bleaching is considered a conservative and biologically safe treatment for discolored teeth. Despite this, one of the major undesirable effects of bleaching is dentin sensitivity which may occur during and after treatment. To address these sensitivity issues, new dental bleaching preparations with lower concentrations of hydrogen peroxide (H2O2) have recently been introduced to the market. This paper presents a clinical case report of a 20-year-old female patient admitted to the Araraquara Dental School, UNESP, Brazil. The patient underwent dental bleaching using one of the new products with reduced hydrogen peroxide concentration, Lase Peroxide Lite 6%, a 6% H2O2 gel containing titanium oxide nanoparticles doped with nitrogen (6% H2O2/N-doped TiO2).

Does a toothpaste containing blue covarine have any effect on bleached teeth? An in vitro, randomized and blinded study.

The objective of this study was to analyze the effect of bleaching toothpastes, both conventional and those containing the new whitening agent Blue Covarine, on teeth previously bleached by conventional techniques (in-office and at-home). Squared bovine enamel/dentin blocks (6.0 x 6.0 x 2.0 mm) were randomly distributed in 6 groups (n = 15), according to the technique used to bleach them (in-office: HP35%; at-home: PC10%) and the type of bleaching toothpaste (none: control; Blue Covarine containing: BC; and without Blue Covarine: NBC). Experimental groups denominated HP35%, HP35%BC and HP35%NBC received in-office tooth bleaching before toothbrushing, and groups PC10%, PC10%BC and PC10%NBC were subjected to at-home tooth bleaching prior to toothbrushing. After bleaching treatment, groups HP35%BC, PC10%BC, HP35%NBC and PC10%NBC underwent daily tooth brushing in a brushing machine for 3 minutes (150 strokes/min, with a load of 375 g). Tooth color alteration was measured by reflectance spectroscopy (Vita EasyShade, Vident, Brea, CA, USA) at: T0 (baseline) - after in-office or at-home bleaching treatment; T1 - immediately after tooth brushing; T2 - 7 days and T3 - 14 days after tooth brushing. Data was analyzed by repeated measures mixed ANOVA and the Bonferroni post hoc test, with a significance level of 5%. Statistically significant differences were found between different experimental groups, evaluation times and for the interaction between them (p < 0.001). Tooth brushing using either bleaching toothpaste (conventional or with Blue Covarine) showed no color alteration on teeth previously bleached by in-office and at-home tooth bleaching. The use of bleaching toothpastes on previously bleached teeth did not produce a color alteration.

A novel approach for in-office tooth bleaching with 6% H2O2/TiO_N and LED/laser system-a controlled, triple-blinded, randomized clinical trial.

UNLABELLED: The purpose of this randomized, parallel, triple-blinded clinical trial was to compare efficacy and tooth sensitivity (TS) after use of an in-office bleaching agent of 6% hydrogen peroxide containing nanoparticles of nitrogen-doped titanium oxide (HP6) vs. 35% hydrogen peroxide (HP35). Forty-eight volunteers were randomly divided either a HP6 or HP35. Two clinical sessions were performed with an interval of 7 days between them for each group. In each session, two consecutive applications of each bleaching agent were performed and activated by a hybrid LED/laser light. Efficacy was determined by color alteration (ΔE), recorded with reflectance spectroscopy. It was assessed at baseline and after the first and second bleaching session. TS was characterized according to occurrence, intensity, duration, and type. Efficacy was analyzed by repeated measures analysis of variance (ANOVA) and post hoc Bonferroni test, and TS was analyzed by means of chi(2) test (α = 0.05). For HP35, highest and significant values of ΔE were found after bleaching when compared to HP6 (p = 0.002). However, HP35 showed a significantly higher occurrence of TS than HP6 (p = 0.008). Also, intensity and duration were higher in HP35. The majority of volunteers classified the type experienced in their sensitivity in the form of a "shock." The use of HP6 despite reducing efficacy when compared to an in-office bleaching in higher concentration (35%) produced less tooth sensitivity. CLINICAL RELEVANCE: In terms of tooth sensitivity, the use of lower concentrations of in-office bleaching should be the first choice, suggesting greater biocompatibility and safety compared to a conventional HP35.

Does a toothpaste containing blue covarine have any effect on bleached teeth? An in vitro, randomized and blinded study

Abstract The objective of this study was to analyze the effect of bleaching toothpastes, both conventional and those containing the new whitening agent Blue Covarine, on teeth previously bleached by conventional techniques (in-office and at-home). Squared bovine enamel/dentin blocks (6.0 x 6.0 x 2.0 mm) were randomly distributed in 6 groups (n = 15), according to the technique used to bleach them (in-office: HP35%; at-home: PC10%) and the type of bleaching toothpaste (none: control; Blue Covarine containing: BC; and without Blue Covarine: NBC). Experimental groups denominated HP35%, HP35%BC and HP35%NBC received in-office tooth bleaching before toothbrushing, and groups PC10%, PC10%BC and PC10%NBC were subjected to at-home tooth bleaching prior to toothbrushing. After bleaching treatment, groups HP35%BC, PC10%BC, HP35%NBC and PC10%NBC underwent daily tooth brushing in a brushing machine for 3 minutes (150 strokes/min, with a load of 375 g). Tooth color alteration was measured by reflectance spectroscopy (Vita EasyShade, Vident, Brea, CA, USA) at: T0 (baseline) - after in-office or at-home bleaching treatment; T1 - immediately after tooth brushing; T2 - 7 days and T3 - 14 days after tooth brushing. Data was analyzed by repeated measures mixed ANOVA and the Bonferroni post hoc test, with a significance level of 5%. Statistically significant differences were found between different experimental groups, evaluation times and for the interaction between them (p < 0.001). Tooth brushing using either bleaching toothpaste (conventional or with Blue Covarine) showed no color alteration on teeth previously bleached by in-office and at-home tooth bleaching. The use of bleaching toothpastes on previously bleached teeth did not produce a color alteration.

Can a bleaching toothpaste containing Blue Covarine demonstrate the same bleaching as conventional techniques? An in vitro, randomized and blinded study

ABSTRACT Objective The purpose of this in vitro study was to compare the efficacy of a bleaching toothpaste containing Blue Covarine vs. conventional tooth bleaching techniques using peroxides (both in-office and at-home). Material and Methods Samples were randomly distributed into five experimental groups (n=15): C - Control; BC – Bleaching toothpaste containing Blue Covarine; WBC – Bleaching toothpaste without Blue Covarine; HP35 - In-office bleaching using 35% hydrogen peroxide; and CP10 – At-home bleaching with 10% carbamide peroxide. The dental bleaching efficacy was determined by the color difference (ΔE), luminosity (ΔL), green-red axis (Δa), and blue-yellow axis (Δb). The CIELab coordinates were recorded with reflectance spectroscopy at different times: T0 - baseline, T1 – immediately after bleaching, T2 - 7 days, T3 - 14 days, and T4 - 21 days after the end of treatments. Data were analyzed by a repeated measures mixed ANOVA and post hoc Bonferroni test, with a significance level of 5%. Results No significant differences were found between the treatment groups C, BC, and WBC. The groups HP35 and CP10 showed significantly higher whitening efficacy than groups C, BC, and WBC. Conclusions There were no significant differences in the whitening efficacy between a Blue Covarine containing toothpaste, a standard whitening toothpaste, and a control. Neither of the whitening toothpastes tested were as effective as in-office or at-home bleaching treatments.

Can a bleaching toothpaste containing Blue Covarine demonstrate the same bleaching as conventional techniques? An in vitro, randomized and blinded study.

OBJECTIVE: The purpose of this in vitro study was to compare the efficacy of a bleaching toothpaste containing Blue Covarine vs. conventional tooth bleaching techniques using peroxides (both in-office and at-home). MATERIAL AND METHODS: Samples were randomly distributed into five experimental groups (n=15): C - Control; BC - Bleaching toothpaste containing Blue Covarine; WBC - Bleaching toothpaste without Blue Covarine; HP35 - In-office bleaching using 35% hydrogen peroxide; and CP10 - At-home bleaching with 10% carbamide peroxide. The dental bleaching efficacy was determined by the color difference (ΔE), luminosity (ΔL), green-red axis (Δa), and blue-yellow axis (Δb). The CIELab coordinates were recorded with reflectance spectroscopy at different times: T0 - baseline, T1 - immediately after bleaching, T2 - 7 days, T3 - 14 days, and T4 - 21 days after the end of treatments. Data were analyzed by a repeated measures mixed ANOVA and post hoc Bonferroni test, with a significance level of 5%. RESULTS: No significant differences were found between the treatment groups C, BC, and WBC. The groups HP35 and CP10 showed significantly higher whitening efficacy than groups C, BC, and WBC. CONCLUSIONS: There were no significant differences in the whitening efficacy between a Blue Covarine containing toothpaste, a standard whitening toothpaste, and a control. Neither of the whitening toothpastes tested were as effective as in-office or at-home bleaching treatments.

Eficácia e sensibilidade dental resultante do clareamento dental de consultório com 6% H2O2/TiO_N. Estudo clínico randomizado controlado / Efficacy and tooth sensitivity resulting of 6% H2O2/TiO_N in office dental bleaching. A randomized controlled clinical trial

Este trabalho comparou a eficácia e a sensibilidade dental resultante do uso de um agente clareador composto por 6% peróxido de hidrogênio contendo nanopartículas de dióxido de titânio dopado por nitrogênio (PH6) com um clareador tradicional composto por 35% peróxido de hidrogênio (PH35); ambos fotocatalisados por luz híbrida composta de LED/Laser. Participaram deste estudo clínico controlado, randomizado, com triplo cegamento e amostras pareadas, 48 voluntários, maiores de 18 e menores de 28 anos, distribuídos aleatoriamente em 2 grupos experimentais: PH6 (teste) e PH35 (controle). Foram realizadas 2 sessões clínicas de clareamento com intervalo de 7 dias entre elas. Em cada sessão foram realizadas 2 aplicações consecutivas do clareador. Em cada uma delas, o gel clareador foi aplicado por 12 minutos, sendo fotocatalisado de forma intermitente por metade deste tempo. A eficácia (E) foi determinada pela variação de cor (ΔE), registrada por espectroscopia de refletância avaliada nos tempos T0 (baseline), após a 1ª. sessão de clareamento (T1) e após a 2ª. sessão (T2). A sensibilidade dental (S) foi caracterizada segundo Ocorrência (OS), Intensidade (IS), Tipo (TS) e Duração (DS). A eficácia foi analisada por ANOVA de medidas repetidas e teste post hoc de Bonferroni e a sensibilidade dental foi analisada de forma descritiva e 20 inferencial por meio do teste de Qui-Quadrado (α=0,05). Os testes apontaram valores de ΔE significativamente maiores para PH35 no T2. Para PH6, o clareamento foi o mesmo nos dois momentos. PH35 apresentou maior ocorrência de sensibilidade que PH6. Intensidade e duração da sensibilidade foram maiores para o grupo PH35. O tipo de sensibilidade mais citado pelos voluntários foi em choque. Em pacientes com idade entre 18 e 28 anos de idade, PH35 promoveu maior clareamento e maior sensibilidade dental que PH6. PH6 deve ser a opção de escolha para clareamento dental de consultório.

This study compared the efficacy and tooth sensitivity resulting from use of a bleaching agent composed of 6% hydrogen peroxide containing nanoparticles of nitrogen-doped titanium dioxide (PH6) with a traditional bleaching agent containing 35% hydrogen peroxide (PH35); both agents were activated by a hybrid LED/Laser light. 48 volunteers between 18 and 28 years of age participated in this randomized, controlled, triple-blinded clinical study with paired samples. They were randomly divided in 2 groups: PH6 (test) and PH35 (control). Two clinical sessions were performed with an interval of 7 days between them. In each session, two consecutive applications of the bleaching agent were performed. In each of them, the bleaching agent was applied for 12 minutes, activated intermittently for half of the duration. Efficacy (E) was determined by color alteration (ΔE), recorded with reflectance spectroscopy. It was assessed at T0 (baseline), after the 1st. bleaching session (T1) and after the 2nd. session (T2). Tooth sensitivity (S) was characterized according to Occurrence (OS), Intensity (IS), Type (TS) and Duration (DS). Efficacy was analyzed by repeated measures ANOVA and post hoc Bonferroni test and tooth sensitivity was analyzed descriptively and inferentially by means of chi-squared test (α=0.05). The tests showed significantly higher values of ΔE for PH35 in T2. For PH6, bleaching was the same in both sessions. PH35 showed a higher occurrence of sensitivity than PH6. Intensity and duration of sensitivity were greater for the PH35 group. The majority of volunteers classified the type of pain experienced in their sensitivity in the form of a "shock". For patients aged between 18 and 28 years old, PH35 promoted higher tooth bleaching and greater sensitivity than PH6. PH6 should be the option of choice for dental office bleaching

Efeitos da aplicação de resina hidrofóbica sobre a resistência deunião de adesivos autocondicionantes de frasco único / Effect of additional hydrofobic layer on the microtensile bond strenght of all-in-one adhesive systems

Introdução: Sabe-se que sistemas adesivos autocondicionantes podem atuar como membranas semipermeáveis, o que pode comprometer a adesão. Objetivo: Buscou-se avaliar os efeitos da aplicação adicional de resina hidrofóbica sobre a resistência de união à microtração de sistemas adesivos autocondicionantes de frasco único sobre dentinabovina. Material e método: Sessenta incisivos bovinos tiveram a face vestibular desgastada até se obter superfície dentinária plana. Foram utilizados os seguintes sistemas adesivos: Clearfil Tri S Bond (CTSB), AdheSE One (ADO) e One Coat 7.0 (OC). Os sistemas adesivos foram testados com (G4, G5, G6) e sem (G1, G2, G3) a aplicação de camada adicional de material hidrofóbico do mesmo fabricante (Clearfil SE Bond, AdheSE e One Coat SE, respectivamente), resultando em seis grupos experimentais (n = 10). Após o procedimento adesivo, resinacomposta Z-350 foi inserida em três incrementos de 1 mm. Todo o procedimento adesivo restaurador foi executado sob pressão pulpar simulada e o teste de microtração foi executado imediatamente após a polimerização da resina composta. Os dados obtidos foram submetidos à ANOVA e ao teste de Tukey (p < 0,05). Resultado: Para todos os adesivos testados, os piores resultados foram observados nos grupos em que a camada adicional de resina hidrofóbica não foi aplicada. Conclusão: A aplicação de camada adicional de material hidrofóbico pode melhorar a resistência de união de sistemas adesivos autocondicionantes de passo único.

Introduction: It is known that self-etching adhesive systems can act as semi-permeable membranes. Objective: Evaluate the effects of additional layer of hydrophobic resin on the microtensile bond strength of self-etching one-bottle adhesives. Material and method: Sixty bovine incisors were used in this study. The facial enamel surfaces of the crowns were abraded with silicon carbide paper to expose flat, mid-coronal dentin surfaces. The following adhesives were used: Clearfil Tri S Bond (CTSB), AdheSE One (ADH) and One Coat 7.0 (OC). Each material was tested with and without applying an additional layer of hydrophobic material from the same manufacturer. Z-350 composite resin was inserted in three 1 mm increments. All adhesive restorative procedure was performed under simulated pulpal pressure and the microtensile test was performed immediately after curing the compositeresin. Data were submitted to ANOVA and Tukey test (p < 0.05). Result: For all adhesives tested, the worst results were observed in groups which the additional layer of hydrophobic resin was not applied. Conclusion: The application of additional layer of hydrophobic material can improve the adhesion of self-etching all-in-one adhesive systems.

Sensibilidade dolorosa e efetividade do clareamento dental de consultório / Painful sensitivity and effectiveness determined by dental bleaching in- office

Vários aspectos da técnica de clareamento dental de consultório permanecem controversos. Neste trabalho foram estudadas a sensibilidade dolorosa e a efetividade determinadas por diferentes tratamentos clareadores. Participaram deste estudo 60 voluntários de ambos os gêneros, com idades variando de 18 a 25 anos que foram aleatoriamente distribuídos em 3 grupos. GI: peróxido de hidrogênio a 35% sem ativação por luz, GII: o mesmo peróxido ativado por dispositivo de luz conjugada LED/LASER e GIII: gel clareador a 15% contendo nanopartículas de óxido de titânio nitrogenado ativado por luz conjugada LED/LASER. A sensibilidade dos pacientes durante as sessões de clareamento foi avaliada utilizando uma escala VAS modificada. A alteração de cor determinada pelos protocolos de clareamento foi mensurada por espectroscopia de reflectância (Vita Easy Shade®,Vident, Brea, CA, USA). Os valores de ∆L (luminosidade), ∆E (variação de cor) e sensibilidade provocada pelos tratamentos (S) foram analisados por meio do método de equações de estimação generalizadas (GEE), comparações múltiplas ad Hoc de Bonferroni com significância de 5%. No estudo 1, realizado para avaliar a eficiência da utilização da luz conjugada LED/Laser, os voluntários de GI relataram maior freqüência e intensidade de sensibilidade provocada pelo tratamento clareador (37,6 ± 5,9% para GI contra 11,1 ± 3,3% de GII). O clareamento em GII foi mais eficiente que em GI (p>0,05). No estudo 2, a utilização do gel clareador H2O2 a 15% contendo TiO_N resultou em menor freqüência e intensidade de sensibilidade provocada que em GI (37,6 ± 6,1% para GI contra 11,9 ± 5,0% de GII) e maior eficiência de clareamento (p>0,05). Concluiu-se que o método de fototermo catalisação com luz conjugada LED/Laser utilizada em conjunto com agente clareadores do tipo processo oxidativo avançado homogêneo (POAHo), permite tanto a redução da sensibilidade provocada como do tempo de tratamento e que o agente de menor concentração reduz a sensibilidade provocada, aumentando a segurança do clareamento dental, com a mesma eficiência do agente tradicional

Several aspects of in-office dental bleaching remain controversial. In this study, we studied the painful sensitivity and effectiveness determined using different bleaching techniques. The study included 60 volunteers of both genres, with ages ranging from 18 to 25 years who were randomly divided into 3 groups. GI: hydrogen peroxide 35% without activation by light, GII: the same peroxide-activated device LED / Laser and GIII: 15% whitening gel containing nanoparticles of titanium oxide nitrogen activated by coupled light LED / Laser. The sensitivity of the patients during the bleaching treatments was evaluated using a modified VAS scale. The color change determined by the protocols of bleaching was measured by reflectance spectroscopy (Vita Easy Shade ®, Seer, Brea, CA, USA). The values of ΔL (brightness), ΔE (color variation) and sensitivity caused by the treatments (S) were analyzed by the method of generalized estimating equations (GEE), multiple comparisons with Bonferroni ad hoc 5% significance. In study 1, conducted to evaluate the efficacy of use of coupled light LED/Laser, GI volunteers reported a higher frequency and intensity of sensitivity caused by bleaching treatment (37.6 ± 5.9% for GI against 11.1 ± 3.3% of GII). The Bleaching was more efficient in GII than GI (p> 0.05). In study 2, the use of gel co 15% H2O2 containing TiO_N resulted in a lower frequency and intensity of sensitivity caused in GI (37.6 ± 6.1% for GI vs. 11.9 ± 5.0% of GII) and greater efficiency of bleaching (p> 0.05). It was concluded that the method of catalyzing photothermo reaction with coupled light LED/Laser used in conjunction with bleaching agent type homogenous advanced oxidation process (POAHo) allows both the reduction of sensitivity caused as time of treatment and the agent of lower concentration reduces sensitivity, increasing safety of tooth whitening, with the same efficiency as the traditional agent