Abstract Enzymatic degradation of the hybrid layer can be accelerated by the activation of dentin metalloproteinases (MMP) during the bonding procedure. MMP inhibitors may be used to contain this process. Objective To evaluate the degree of conversion (DC%), dentin bond strength (µTBS) (immediate and after 1 year of storage in water), and nanoleakage of an experimental (EXP) and a commercial (SB) adhesive system, containing different concentrations of the MMP inhibitor GM1489: 0, 1 µM, 5 µM and 10 µM. Methodology DC% was evaluated by FT-IR spectroscopy. Dentin bond strength was evaluated by µTBS test. Half of beams were submitted to the µTBS test after 24 h and the other half, after storage for 1 year. From each tooth and storage time, 2 beams were reserved for nanoleakage testing. Data were analyzed using ANOVA and Tukey’s test to compare means (α=0.05). Results All adhesive systems maintained the µTBS after 1 year of storage. Groups with higher concentrations of inhibitor (5 µM and 10 µM) showed higher µTBS values than groups without inhibitor or with 1 µM. The nanoleakage values of all groups showed no increase after 1 year of storage and values were similar for SB and EXP groups, in both storage periods. The inhibitor did not affect the DC% of the EXP groups, but the SB5 and SB10 groups showed higher DC% values than those of SB0 and SB1. Conclusions The incorporation of GM1489 in the adhesive systems had no detrimental effect on DC%. The concentrations of 5 µM GM1489 for SB and 5 µM or 10 µM for EXP provided higher μTBS than groups without GM1489, in the evaluation after 1 year of storage; whereas the concentration of inhibitor did not affect adhesive systems nanoleakage.

Resumo: O objetivo deste trabalho foi avaliar a resistência de união de sistemas adesivos autocondicionantes após estocagem em ácidos presentes no biofilme oral. Foram utilizados três sistemas adesivos: um autocondicionante de dois frascos indicado para uso com a resina composta à base de silorano (P90 System Adhesive- P90), um autocondicionante de dois frascos (Clearfil SE Bond - CSE) e um autocondicionante de frasco único (AdperEasyOne - AEO). Para avaliação da resistência de união à dentina, 90 fragmentos de dentes bovinos foram restaurados de acordo com as recomendações dos fabricantes. Após a confecção de blocos de resina composta (Filtek Z350 para os sistemas adesivos AEO e CSE; Filtek P90 para o sistema adesivo P90) e estocagem em água destilada por 24 h a 37 °C, os fragmentos foram seccionados para a obtenção de palitos (1 mm2) que foram divididos e estocados nos três diferentes meios de imersão (água destilada, ácido lático e ácido propiônico) por períodos de 7 dias e 30 dias (n=5). Em seguida, foi realizado o ensaio de resistência à microtração. Os dados foram submetidos à Análise de Variância (3 fatores) e ao Teste de Tukey (α=0,05). O sistema adesivo CSE apresentou maior resistência de união após imersão em água por 7 ou 30 dias. A resistência de união de todos os sistemas adesivos foi menor após imersão em ácido lático e propiônico do que após imersão em água. Não foi observada diferença significativa entre os tempos de imersão.

Abstract: The aim of this study was to evaluate the microtensile bond strength of self-etch adhesive systems to dentin after storage in acids from oral biofilm. Three adhesive systems were used in the study: a two-step self-etch adhesive for use with a silorane-based resin composite (Filtek P90 adhesive system - P90), a two-step self-etch adhesive (Clearfil SE Bond - CSE) and a one-step self-etch adhesive (Adper Easy One - AEO). The bond strength of these products was evaluated by bonding resin composite (Filtek Z350 for CSE and AEO; and Filtek P90 for P90) to 90 bovine dentin tooth fragments, according to the manufacturer's instructions. After 24 h of water storage at 37 °C, the specimens were sectioned into beams (1 mm2) divided and stored in distilled water, lactic acid and propionic acid, for 7 and 30 days. After storage, the specimens were tested for microtensile bond strength. Data were analyzed by three-way ANOVA and Tukey´s test (α=0.05). CSE presented the highest microtensile bond strength after storage in distilled water for 7 and 30 days. The microtensile bond strength of all adhesive systems was lower after storage in lactic acid and propionic acid than after water storage. Significant difference was not found between storage times.

O objetivo deste estudo foi analisar a absorção e a solubilidade de uma resina composta nanopartículada (Filtek Z350) e de uma híbrida (Filtek P60) em substâncias simuladoras do ambiente oral em um modelo de cavidade profunda. Uma cavidade cilíndrica, construída em uma raiz de um incisivo bovino, foi preenchida incrementalmente com as resinas compostas. Os cilindros obtidos foram seccionados perpendicularmente ao eixo para obtenção de discos com 1 mm de espessura, que foram divididos em 15 grupos (n=5) de acordo com a profundidade (1, 2, 3, 4 e 5 mm) e o meio de imersão (água destilada - AD, saliva artificial - SA e ácido lático - AL). A absorção e a solubilidade foram calculadas com base na norma ISO 4049:2000(E). Adicionalmente, o grau de conversão (GC%) foi calculado através de espectroscopia FT-IR. Os dados obtidos foram analisados usando análise de variância multifatorial, teste de Tukey HSD e análise de regressão linear (a=0,05). A resina composta híbrida apresentou o maior grau de conversão, sendo este influenciado pela profundidade da cavidade (p<0,05). A resina composta nanopartículada apresentou maiores valores de absorção e solubilidade (p<0,05). O meio de imersão influenciou a absorção e a solubilidade: AL>SA>AD (p<0,05). Ambos os fenômenos foram influenciados pela profundidade da cavidade, com os valores aumentando de 1 para 5 mm (p<0,05). A degradação de restaurações de resinas compostas pode ser maior em regiões profundas de restaurações classe II e quando o material é exposto à ácidos orgânicos produzidos pelo biofilme oral (ácido lático).

The aim of this study was to analyze the sorption and solubility of a nanofilled (Filtek Z350) and a midifilled (Filtek P60) resin composite in oral environment-like substances, in a simulated deep cavity. A cylindrical cavity prepared in a bovine incisor root was incrementally filled with resin composites. The obtained resin composite cylinders were cut perpendicularly to the axis to obtain 1-mm-thick discs that were divided into fifteen groups (n=5) according to depth (1, 2, 3, 4 and 5 mm) and immersion media (distilled water - DW, artificial saliva - AS and lactic acid - LA). The sorption and solubility were calculated based on ISO 4049:2000. Additionally, the degree of conversion (DC%) was calculated by FT-IR spectroscopy. Data were analyzed using multifactor analysis of variance (MANOVA) followed by Tukey's HSD post-hoc test and linear regression analysis (a=0.05). The DC% was higher for the midifilled resin composite and was negatively influenced by cavity depth (p<0.05). The nanofilled resin composite presented higher sorption and solubility than did the midifilled (p<0.05). The immersion media influenced the sorption and the solubility as follows: LA>AS>DW, (p<0.05). Both phenomena were influenced by cavity depth, with the sorption and solubility increasing from 1 to 5 mm (p<0.05). The degradation of resin composite restorations may be greater in the deepest regions of class II restorations when the composite is exposed to organic acids present in the oral biofilm (lactic acid).

Indirect restorations in contact with free gingival margins or principally within the gingival sulcus, where the presence of organic acids produced by oral biofilm is higher, may present faster degradation of the resin-based cement pellicle. Objectives To investigate the degradation of four resin-based cements: Rely X ARC (R), Variolink II (V), Enforce (E) and All Cem (A), after immersion in distilled water (DW), lactic acid (LA) and artificial saliva (AS) and to analyze the influence of the activation mode on this response. Material and Methods Two activation modes were evaluated: chemical (Ch) and dual (D). In the dual activation, a two-millimeter thick ceramic disk (IPS Empress System) was interposed between the specimen and light-curing unit tip. Specimens were desiccated, immersed in distilled water, artificial saliva and lactic acid 0.1 M at 37°C for 180 days, weighed daily for the first 7 days, and after 14, 21, 28, 90 and 180 days and were desiccated again. Sorption and solubility (µg/mm 3 ) were calculated based on ISO 4049. The data were submitted to multifactor analysis of variance (MANOVA) and Tukey's HSD test for media comparisons (α=0.05). Results Sorption was higher after immersion in LA (p<0.05) and increased significantly with time (p<0.05). Sorption was influenced by the activation mode: Ch>D (p<0.05). The lowest solubility was presented by R (p<0.05). Conclusions Lactic acid increased the degradation of resin-based cements. Moreover, the physical component of activation, i.e., light-activation, contributed to a low degradation of resin-based cements.

OBJECTIVES: This study evaluated the effects of light exposure through simulated indirect ceramic restorations (SICR) on hardness (KHN) of dual-cured resin cements (RCs), immediately after light-activation and 24 h later. MATERIAL AND METHODS: Three dual-cured RCs were evaluated: Eco-Link (Ivoclar Vivadent), Rely X ARC (3M ESPE), and Panavia F (Kuraray Medical Inc.). The RCs were manipulated in accordance to the manufacturers' instructions and were placed into cylindrical acrylic matrixes (1-mm-thick and 4-mm diameter). The RC light-activation (Optilux 501; Demetron Kerr) was performed through a glass slide for 120 s (control group), or through 2-mm or 4-mm thick SICRs (IPS Empress II; Ivoclar Vivadent). The specimens were submitted to KHN analysis immediately and 24 h after light-activation. The data obtained at the 2 evaluation intervals were submitted to 2-way ANOVA repeated measures and post-hoc Tukey's test (pre-set alpha of 5%). RESULTS: Lower KHN was observed when light-activation was performed through SICRs for Eco-Link at all evaluation intervals and for Rely X ARC 24 h later. For Panavia F, no significant difference in KHN was observed between control and experimental groups, regardless of evaluation interval. Most groups exhibited higher KHN after 24 h than immediately after light-activation, with the exception of Rely X ARC light-activated through SICR, as no significant difference in KHN was found between evaluation intervals. CONCLUSIONS: Light overexposure did not compensate for light intensity attenuation due to the presence of SICR when Rely X and Eco-Link were used. Although hardness of such RCs increased over a 24-h interval, the RCs subjected to light overexposure did not reach the hardness values exhibited after direct light exposure.

O clareamento dental ocorre devido a uma reação de oxidação entre o agente clareador e as macromoléculas de pigmentos presentes nos dentes. Esta reação é inespecífica e o peróxido pode agir na matriz dental causando perdas de mineral. Por outro lado, estudos recentes sugerem que o agente espessante carbopol também pode causar perda mineral. Assim, o objetivo deste trabalho foi avaliar in vitro o efeito do clareamento caseiro sobre a microdureza do esmalte após o uso de agentes clareadores com e sem carbopol como espessante. Fragmentos de esmalte bovino de 3 x 3 x 3 mm foram obtidos, polidos seqüencialmente e aleatoriamente divididos em 4 grupos de acordo com o tratamento experimental: G1: carbopol a 2%; G2: peróxido de carbamida a 10% com carbopol; G3: carbowax; G4: peróxido de carbamida a 10% com poloxamer. O clareamento foi realizado diariamente por 4 semanas em saliva artificial. A microdureza do esmalte foi avaliada antes (T0) e após 7 (T1), 14 (T2), 21 (T3), 28 (T4), e 42 (T5) dias do início do tratamento. A ANOVA e o teste de Tukey revelaram diferenças estatísticas significantes somente para o fator Tempo (F = 5,48; p < 0,01). Os agentes clareadores e espessantes não causaram alterações na microdureza do esmalte.

Dental bleaching occurs due to an oxidation reaction between the bleaching agents and the macromolecules of pigments in the teeth. This reaction is unspecific and the peroxides can also affect the dental matrix causing mineral loss. On the other hand, recent studies have suggested that the thickener agent carbopol can also cause mineral loss. Thus, the objective of this study was to evaluate in vitro the effect of at-home dental bleaching on dental enamel microhardness after the use of bleaching agents with and without carbopol as a thickener agent. Bovine dental slabs with 3 x 3 x 3 mm were obtained, sequentially polished, and randomly divided into 4 groups according to the experimental treatment: G1: 2% carbopol; G2: 10% carbamide peroxide with carbopol; G3: carbowax; G4: 10% carbamide peroxide with poloxamer. Bleaching was performed daily for 4 weeks, immersed in artificial saliva. Enamel microhardness values were obtained before the treatment (T0) and 7 (T1), 14 (T2), 21 (T3), 28 (T4), and 42 (T5) days after the beginning of the treatment. ANOVA and Tukey's test revealed statistically significant differences only for the factor Time (F = 5.48; p < 0.01). All bleaching and thickener agents caused no alterations on the enamel microhardness.

O objetivo deste trabalho foi avaliar a influência da técnica de ativação e de inserção da resina composta sobre a microinfiltração marginal e microdureza em restaurações classe II. Foram preparadas 180 cavidades que foram divididas em 6 grupos: G1 - incremento único + ativação convencional; G2 - incrementos vestíbulo-linguais + ativação convencional; G3 - incremento único + ativação "soft-start"; G4 - incrementos vestíbulo-linguais + ativação "soft-start"; G5 - incremento único + ativação progressiva; G6 - incrementos vestíbulo-linguais + ativação progressiva. Todas as cavidades foram restauradas com o sistema Z100/Single Bond (3M). Após 1.000 ciclos térmicos (5 e 55ºC), os espécimes foram imersos em solução aquosa de azul de metileno a 2%, por 4 horas e a microinfiltração foi avaliada. Metade dos espécimes foram incluídos em resina de poliestireno e a microdureza Knoop foi avaliada. Após o teste Kruskal-Wallis, não foi observada diferença significativa (p > 0,05) entre todas as técnicas de ativação e de inserção quanto à microinfiltração. Quanto à microdureza, após os testes análise de variância (2 fatores) e Tukey, não houve diferença significativa entre as técnicas restauradoras empregadas (p > 0,05), porém a ativação progressiva (G5 e G6) apresentou menor dureza Knoop (p < 0,05): G1 = 144,11; G2 = 143,89; G3 = 141,14; G4 = 142,79; G5 = 132,15; G6 = 131,67. Concluiu-se que as técnicas de ativação e de inserção da resina composta não afetaram a microinfiltração, mas ocorreu uma diminuição na microdureza do material quando a ativação progressiva foi utilizada.

The aim of this study was to evaluate the influence of techniques of composite resin polymerization and insertion on microleakage and microhardness. One hundred and eighty class II cavities were prepared in bovine teeth and assigned to six groups: G1 - bulk filling + conventional polymerization; G2 - bucco-lingual increments + conventional polymerization; G3 - bulk filling + soft-start polymerization; G4 - bucco-lingual increments + soft-start polymerization; G5 - bulk filling + progressive polymerization; G6 - bucco-lingual increments + progressive polymerization. All cavities were restored with the Z100/Single Bond system (3M). After thermocycling, the samples were immersed in 2% methylene blue dye solution for 4 hours. Half of the samples were embedded in polystyrene resin, and Knoop microhardness was measured. The Kruskal-Wallis test did not reveal statistical differences (p > 0.05) between the polymerization and insertion techniques as to microleakage. Regarding microhardness, the two-way ANOVA and the Tukey test did not reveal statistical differences between the restorative techniques (p > 0.05), but progressive polymerization (G5 and G6) was associated with smaller Knoop microhardness values (p < 0.05): G = 144.11; G2 = 143.89; G3 = 141.14; G4 = 142.79; G5 = 132.15; G6 = 131.67. It was concluded that the evaluated polymerization and insertion techniques did not affect marginal microleakage, but a decrease in microhardness occurred when progressive polymerization was carried out.