Influence of Specimen Dimension, Water Immersion Protocol, and Surface Roughness on Water Sorption and Solubility of Resin-Based Restorative Materials.

The evaluation of water sorption and solubility is pivotal for the development of new resin-based restorative materials with the potential for clinical application. The purpose of the present study was to evaluate the influence of the specimen dimension, water immersion protocol, and surface roughness on the water sorption and solubility of three resin-based restorative materials. Disk-shaped specimens of 15 mm × 1 mm, 10 mm × 1 mm, and 6 mm × 1 mm were produced with a composite resin (Z100), a resin cement (RelyX ARC), and an adhesive system (Single Bond 2-SB2). The specimens were immersed in distilled water according to four protocols: ISO (all the specimens for each group were vertically immersed in 50 mL); IV-10 (the specimens were individually and vertically immersed in 10 mL); IH-10 (the specimens were individually and horizontally immersed in 10 mL); and IH-2 (the specimens were individually and horizontally immersed in 2 mL). The surface roughness (Sa and Sp) was evaluated using an atomic force microscope, and the degree of conversion was determined using FT-IR spectrometry. The specimen dimension and water immersion protocol had no effect on water sorption and solubility. For the three resin-based restorative materials, Sp was higher than Sa. The degree of conversion was not influenced by the specimen dimension. The variations in the specimen dimension and water immersion protocol compared to those determined by ISO 4049 did not prevent the comparison between the values of water sorption and solubility obtained for a given resin-based restorative material.

Characterization and Anti-Caries Effect of an Experimental Adhesive Containing Natural Antimicrobial Agents.

PURPOSE: To characterize experimental adhesives containing natural antimicrobial agents (proanthocyanidins, apigenin, tt-farnesol) in the primer and to evaluate their anti-caries effect. MATERIALS AND METHODS: Natural agents were incorporated in the primer of an experimental adhesive: 4.5% proanthocyanidins (PA), 1 mM apigenin (API), 1 mM apigenin + 5 mM tt-farnesol (API + FAR), and primer without antimicrobial agent (control). Microtensile bond strength (µTBS) to dentin and nanoleakage were measured immediately (n = 7) and after 1 year of storage (n = 7). Water sorption (WS), solubility (SO), and degree of conversion (DC%) of the adhesives were measured. The hardness loss of enamel (n = 6) and dentin (n = 6) at the restorative margin was evaluated after biofilm formation. RESULTS: DC%, nanoleakage, and immediate µTBS were similar for all groups. After 1 year, API + FAR showed higher nanoleakage and lower µTBS than the other groups, which were similar. WS and SO of API + FAR were lower than in the other groups. PA, API, and API + FAR presented less hardness loss than did the control group. At enamel, PA and API presented less hardness loss than the control and API + FAR groups at distances 50 µm and 100 µm; the hardness loss of enamel was similar for all groups 150 µm from the margin. CONCLUSION: The addition of proanthocyanidins and apigenin to the adhesives decreased the hardness loss of dentin and enamel submitted to biofilm formation, without jeopardizing the physical properties of the adhesives. The combination of apigenin + tt-farnesol decreased the hardness loss of dentin but not of enamel, and decreased the µTBS after 1 year of storage.

Characterization and Antibacterial Effect of an Experimental Adhesive Containing Different Concentrations of Proanthocyanidin.

PURPOSE: To evaluate the degree of conversion (DC%), water sorption (Sp), solubility (Sl), dentin bond strength (µTBS) (immediate and after 12 months of storage), and the antibacterial effect of an experimental adhesive containing different concentrations (%) of proanthocyanidin (PA): 0, 1%, 2%, 4.5%, and 6% (PA0, PA1%, PA2%, PA4.5% and PA6%, respectively). MATERIALS AND METHODS: DC% was measured by FT-IR and the Sp and Sl were determined based on the ISO 4049 specification. For µTBS, resin composite buildups were constructed incrementally and specimens (n = 8) were sectioned to obtain sticks (1 mm2). The µTBS was evaluated after 24 h and 12 months of water storage at 37°C. The failure mode was analyzed. The antibacterial effects were evaluated by analyzing the bacterial growth (S. mutans) (n = 5) and antibiofilm activity (n = 5) of the adhesives by spectrophotometry. RESULTS: The incorporation of PA did not affect the Sp, Sl, or DC%. Immediate µTBS was similar for all groups. After 12 months, PA4.5% presented significantly higher µTBS than PA0, while the other groups did not differ from PA0 and PA4.5%. Groups PA0 and PA1% underwent significant reduction in µTBS. In the experimental groups PA2%, PA4.5% and PA6%, µTBS was maintained after storage. All groups showed antibacterial activity. CONCLUSION: Incorporation of 2%, 4.5%, and 6% PA maintained the dentin µTBS after 12-month storage, without affecting the Sp, Sl, or DC% of experimental adhesives. PA4.5% presented higher µTBS values than PA0 after 12 months. The adhesive presented antibacterial effect irrespective of PA concentration.

Resin-dentin bond stability of etch-and-rinse adhesive systems with different concentrations of MMP inhibitor GM1489.

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.

Resin-dentin bond stability of etch-and-rinse adhesive systems with different concentrations of MMP inhibitor GM1489

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.

Bond stability of conventional adhesive system with MMP inhibitors to superficial and deep dentin.

PURPOSE: To evaluate the microshear bond strength (µSBS) to deep (DD) or superficial (SD) dentin (µSBS) overtime, nanoleakage (AG%), degree of conversion (DC%), water sorption (WSp), and solubility (WSl) of an adhesive system [Adper Single Bond 2(ASB)] containing matrix metalloproteinases (MMP) inhibitors [GM1489 (ASB-GM), Batimastat (ASB-BAT), or Chlorhexidine diacetate (ASB-CHX)]. ASB without inhibitor was used as control (CONTROL). MATERIALS AND METHODS: WSp and WSL were calculated based on ISO4049. DC% was analyzed using FT-IR spectroscopy. Dentin discs were used for µSBS evaluation. For AG%, resin-dentin beams were analyzed under scanning electronic microscopy. Data were analyzed using three-way ANOVA (AG% and µSBS) or ANOVA (DC%, WSp, WSl) and Tukey's HSD test. RESULTS: ASB-CHX presented the lowest DC%, lowest WSp, and highest WSl. ASB-GM reached the highest immediate µSBS in SD, only different from ASB-CHX. In DD, ASB-BAT and ASB-GM had the highest µSBS, statistically different from ASB-CHX. After twelve months, ASB-GM and ASB-BAT presented higher µSBS in SD when compared to CONTROL and ASB-CHX. In DD, ASB-GM reached the highest value, which was statistically different from CONTROL and ASB-CHX. CONTROL at both dentin depths and ASB-CHX at DD did not maintain bond stability. In SD after 12 months, ASB-BAT and ASB-GM decreased AG%. In DD, only ASB-GM reduced AG%. CONCLUSION: The ASB containing Batimastat and GM1489 maintained resin-dentin bond stability after 12 months for both dentin depths, without jeopardizing WSp, WSl, or DC% of the adhesive system. The ASB-GM presented greater µSBS after 12 months when compared with ASB. CLINICAL SIGNIFICANCE: Batimastat and GM1489 could be suitable for inclusion as an MMP-inhibitor into Single Bond to improve the bond stability to superficial and deep dentin, without jeopardize the physic-mechanical proprieties.

Effect of Calcium Hydroxide on Bonding Performance of an Experimental Self-etch Adhesive.

PURPOSE: To investigate the effect of Ca(OH)2 concentration on pH neutralization, degree of conversion (DC%), and bonding performance of experimental self-etch adhesives (SEAs). MATERIALS AND METHODS: Four different concentrations of Ca(OH)2 (0 wt%, 1 wt%, 2 wt%, and 4 wt%) were added to the bond of an experimental two-step SEA consisting of primer (10-MDP [30 wt%], TEG-DMA [30 wt%], ethanol [35 wt%], water [5 wt%], camphorquinone [0.5 wt%], and tertiary amine [0.5 wt%]) and bond (bis-GMA [50 wt%], TEG-DMA [30 wt%], HEMA [20 wt%], camphorquinone [0.5 wt%], and tertiary amine [0.5 wt%]) to form four groups: E0, E1, E2 and E4. pH neutralization was evaluated until it reached equilibrium, and DC% within the hybrid layer was analyzed by micro-Raman spectroscopy. Human molars were wet ground until the occlusal dentin was exposed, SEAs were applied, and composite buildups were constructed. After storage in distilled water at 37°C for 24 h, the teeth were cut into composite-dentin beams. Microtensile bond strength (µTBS) was evaluated after 24 h of water storage at 37°C. Nanoleakage was evaluated by SEM. Data were analyzed using ANOVA and Tukey's HSD test (a = 0.05). RESULTS: All the SEAs reached pH equilibrium after thirteen days, with E1 and E4 presenting the highest pH (p < 0.05). E0 and E1 presented lower DC% than did E2 and E4 (p < 0.05). All the SEAs showed statistically similar mTBS and nanoleakage (p > 0.05). CONCLUSION: The incorporation of Ca(OH)2 endowed the SEAs with pH-neutralization ability and improved their DC%, without interfering with the bond strength to dentin or nanoleakage extent.

Resin-dentin Bond Stability of Experimental 4-META-based Etch-and-rinse Adhesives Solvated by Ethanol or Acetone.

PURPOSE: To investigate the influence of 4-META concentration and type of solvent on the degree of conversion (DC%) and resin-dentin bond stability of experimental etch-and-rinse adhesives. MATERIALS AND METHODS: Four different concentrations of 4-META (12 wt%, 20 wt%, 30 wt%, 40 wt%) were added to a model adhesive system consisting of TEG-DMA (25 wt%), UDMA (20 wt%), HEMA (30 wt%), water (4 wt%), camphorquinone (0.5 wt%), and tertiary amine (0.5 wt%) dissolved in 20% acetone (A12, A20, A30 and A40) or 20% ethanol (E12, E20, E30 and E40). DC% was evaluated by FT-IR spectroscopy. Human molars were wet ground until the occlusal dentin was exposed, the adhesive systems were applied after 37% phosphoric acid etching, and resin composite buildups were incrementally constructed. After storage in distilled water at 37°C for 24 h, the teeth were cut into resin-dentin beams (cross-sectional area 1 mm2). Microtensile bond strength (µTBS) was evaluated after 24 h, 6 months, and 1 year of water storage at 37°C. The failure mode was categorized as adhesive, mixed, or cohesive. Data were analyzed using ANOVA and Tukey's HSD test (α = 0.05). RESULTS: A12 presented the lowest DC% (p < 0.05). All the other adhesive systems showed statistically similar DC% (p > 0.05). All adhesive systems maintained resin-dentin bond stability after 6 months of water storage, while only A40 and E40 maintained it after 1 year. CONCLUSION: Irrespective of the type of organic solvent, the incorporation of high concentrations of 4-META (40 wt%) improved the resin-dentin bond stability of the experimental etch-and-rinse adhesive systems over a period of 1 year.

Characterization of an experimental resin composite organic matrix based on a tri-functional methacrylate monomer.

This study evaluated the potential of a tri-functional monomer (trimethylolpropane trimethacrylate -TMPTMA) for inclusion in a dental composite organic matrix. Initially, four ternary matrixes with different concentrations (wt%) of bi-functional monomers [BisGMA (G), Bis-EMA (E) and TEGDMA (T)] were analyzed: GET523, GET532, EGT523 and EGT532 (the numbers (n) represent n×10 wt% of each monomer). The following properties were evaluated: degree of conversion, flexural strength, elastic modulus, hardness, absorption, solubility, diffusion coefficient of water and crosslink density. Based on the best overall results obtained for EGT532, all properties were re-evaluated in a matrix where TEGDMA (T) was replaced by a tri-functional monomer, TMPTMA (A)-EGA532. EGA532 presented the best results for flexural strength, hardness, absorption and crosslink density. EGT523, EGT532 and EGA532 presented the lowest diffusion coefficients of water. The overall results indicated that TMPTMA could be useful in formulating organic matrixes suitable for dental restorative composites.

Influence of Organic Acids from the Oral Biofilm on the Bond Strength of Self-Etch Adhesives to Dentin.

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.

Experimental etch-and-rinse adhesive systems containing MMP-inhibitors: Physicochemical characterization and resin-dentin bonding stability.

OBJECTIVES: To evaluate the degree of conversion (DC%), water sorption (WS), solubility (SO) and the resin-dentin bonding stability (µTBS) of experimental (EXP) etch-and-rinse adhesive systems containing MMP-inhibitors: Galardin-GAL, Batimastat-BAT, GM1489-GM1 and chlorhexidine diacetate-CHX. METHODS: DC% was measured using FT-IR spectroscopy, while WS and SO were calculated based on ISO4049. Thirty-six human molars were wet ground until the occlusal dentin was exposed. The adhesive systems were applied and resin composite buildups were incrementally constructed. After 24 h immersion in distilled water at 37 °C, the specimens were cut into resin-dentin beams with a cross-sectional area of 1 mm(2). The µTBS was evaluated after 24 h, 6 months and 12 months of water storage at 37 °C. Adper Single Bond 2 (SB2) was used as a commercial control. The data were analyzed using ANOVA and Tukey's HSD test. RESULTS: SB2 presented the highest DC% (p<0.05). CHX presented the lowest WS (p<0.05). GM1, GAL and BAT presented similar WS when compared with SB2 (p>0.05). SO was found to be not significant (p>0.05). All adhesive systems maintained µTBS stability after 6 months of water storage. Only BAT, GM1 and CHX maintained µTBs stability after 12 months of water storage. CONCLUSIONS: The experimental adhesive systems with GM1489 and chlorhexidine diacetate presented the best physicochemical properties and preserved resin-dentin bonding stability after 12 months of water storage. CLINICAL SIGNIFICANCE: GM1489 could be suitable for inclusion as an MMP-inhibitor in etch-and-rinse adhesive systems to maintain resin-dentin bonding stability over time.

Influence of Organic Acids from the Oral Biofilm on the Bond Strength of Self-Etch Adhesives to Dentin

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.

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.

Influence of organic acids present in oral biofilm on the durability of the repair bond strength, sorption and solubility of resin composites.

PURPOSE: To evaluate the repair bond strength after storage in water, lactic and propionic acid after 7 days and 6 months and the sorption and solubility of resin composites used. METHODS: Five cylinders of each resin composite (microhybrid, nanofilled and silorane-based composite) were prepared. Specimens were aged with thermocycling (5 and 55°C) 5,000 times. A repair procedure was performed using intraoral sandblasting with 50-µm aluminum oxide, application of an adhesive system and cylinder of composite was fabricated. Specimens were sectioned into beams and stored in three immersion media: water, propionic acid and lactic acid. The microtensile bond strength was measured after periods of 7 days and 6 months. Sorption and solubility were evaluated using 15 specimens (0 = 6 mm; h = 1 mm) of each resin composite, which were prepared and assigned into three groups (n = 5) according to the immersion media (water, propionic acid and lactic acid). Data were analyzed using one-way/two-way/three-way ANOVA and Tukey's test (α = 0.05). RESULTS: The resin composites, immersion media and time of immersion did not affect the repair bond strength (microhybrid 38.3 to 40.9 MPa; nanofilled 38.7 to 42.2 MPa; silorane 41.2 to 51.1 MPa). Additionally, the immersion media did not affect the sorption and solubility. The silorane-based composite presented the lowest sorption (10.5 to 12.1 µg/mm3) and solubility (-2.4 to -2.7 µg/mm3), while the nanofilled methacrylate-based composite showed the highest sorption (32.1 to 33.6 µg/mm3). Regarding solubility, the nanofilled and microhybrid methacrylate-based composites did not present statistically significant differences.

Degradation of Resin Composites in a Simulated Deep Cavity

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).

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).

Sodium fluoride and casein phosphopeptide-amorphous calcium phosphate cream plus sodium fluoride efficacy in preventing enamel erosion in a simulated oral environment study model.

AIM: The aim of this study was to evaluate the effectiveness of dentifrices containing high concentrations of sodium fluoride (NaF) and casein phosphopeptide-amorphous calcium phosphate cream plus fluoride (CPP-ACPF) in prevention of the erosion in a simulated oral environment study model. SUBJECTS AND METHODS: Fifteen flat human enamel specimens were polished and half of the surfaces were protected with adhesive tape. Initial Knoop microhardness (KHN) and surface roughness (SR) were measured, and specimens were assigned to four groups: Control (placebo toothpaste - G1); CPP-ACPF (G2), NaF 1450 ppm (G3), and NaF 5000 ppm (G4). Enamel surfaces were brushed 3 times daily in association with demineralization-remineralization cycles (5s in cola drink + 5s in artificial saliva/10 cycles/twice daily) and the specimens were maintained in a salivary flow simulator apparatus. After 14 days, KHN and SR were measured again, and the enamel surfaces were analyzed by scanning electronic microscopy (SEM). STATISTICAL ANALYSIS USED: Data were analyzed using the two-way ANOVA and Student-Newman-Keuls multiple range test (α =0.05). RESULTS: All the tested groups presented a decrease in KHN after 14 days (P < 0.05). There was no statistical significance among materials tested. Significant increase in SR was observed for all groups. SEM analysis showed morphological alterations with honeycomb structures in enamel surfaces in the four experimental groups. CONCLUSIONS: It was concluded that tooth brushing with dentifrices with high concentration of NaF and CPP-ACPF cream was not able to prevent enamel erosion in simulated oral environment.

Sorption and solubility of self-etching adhesives immersed in organic acids present in oral biofilm.

PURPOSE: This study evaluated the sorption and solubility of self-etching adhesive systems after immersion in distilled water, lactic acid, and propionic acid. MATERIALS AND METHODS: Specimens of 2 two-step (P90 System Adhesive [P90], Clearfil SE Bond [CSE]) and 1 single-step (Adper Easy One [AEO]) adhesive systems were prepared and divided into 4 groups: P90 primer ( P90-P), P90 bond (P90-B), AEO, and CSE bond (CSE-B). Specimens were placed in a desiccator and weighed daily until achieving a constant mass (m1). The specimens (n = 5) were then immersed in the respective media and weighed until a achieving a constant mass (m2). The specimens were again desiccated (m3). Sorption and solubility data were analyzed with two-way ANOVA and Turkey's test. Specimens were also observed using SEM without immersion, after 24 h, and at the end of the respective total time of immersion. RESULTS: For all immersion media, the highest sorption values were obtained for AEO and P90-P, followed by CSE-B and P90-B, which presented the lowest sorption. The time required for adhesives to absorb the solutions was: 11 to 19 days for P90-P, 12 to 13 days for P90-B, 15 to 19 days for AEO, and 14 to 18 days for CSE-B. The highest values of solubility were shown for AEO and P90-P in all immersion media. In water and propionic acid, the adhesives with the lowest solubility values were CSE-B and P90-B. CSE-B had the lowest solubility in lactic acid. CONCLUSION: The greatest surface degradation was observed after each respective total time of immersion. AEO specimens presented more evident surface degradation and the highest sorption and solubility.

Degradation of resin composites in a simulated deep cavity.

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).

Long-term degradation of resin-based cements in substances present in the oral environment: influence of activation mode.

UNLABELLED: 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.

Long-term degradation of resin-based cements in substances present in the oral environment: influence of activation mode

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. .

Light-activation through indirect ceramic restorations: does the overexposure compensate for the attenuation in light intensity during resin cement polymerization?

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.