A novel acrylic resin palatal device contaminated with Candida albicans biofilm for denture stomatitis induction in Wistar rats

Abstract Denture stomatitis is the most frequent oral lesion in removable prosthesis wearers, with high recurrence rates and a complex treatment. Objective This study describes a protocol to obtain and to contaminate a palatal device with Candida albicans biofilm that could be used for an animal model of denture stomatitis. Methodology Acrylic resin devices (N=41) were obtained from impressions of the palates of Wistar rats with individual trays and polyether. The efficacy of microwave irradiation (MW), ultraviolet light (UV), or ultrasonic bath (US) was assessed by colony viability and spectrophotometric analyses (n=5) in order to select the most appropriate method for sterilizing the devices. Then, different devices (n=5) were contaminated with C. albicans and evaluated by CFU/mL determination, scanning electron microscopy, and laser confocal microscopy. Device stabilization was assessed with either autopolymerizing acrylic resins or a self-adhesive resin cement (n=2). The spectrophotometric data were analyzed by one-way ANOVA followed by the Tukey's HSD post-hoc test (α=0.05). Results MW was the only method capable of sterilizing the devices, and the contamination protocol developed a mature and viable C. albicans biofilm (~1.2 x 106 CFU/mL). The self-adhesive resin cement was the best stabilization material. Conclusions This acrylic resin palatal device was designed to be similar to the clinical situation of contaminated prostheses, with easy manufacturing and handling, effective stabilization, and satisfactory contamination. Thus, the acrylic device can be a valuable tool in the development of denture stomatitis in rats.

Influence of radiant exposure values from two third generation LED curing units on polymerization profile and microhardness of orthodontic composite under ceramic and metallic brackets

ABSTRACT Introduction: Third generation of LED light curing units might be used in short exposure periods for orthodontic brackets bonding. Objective: This study evaluated the effect of the different radiant exposure (RE) values: Manufacturers' instructions (MI), ½ MI, 1/4 MI and Turbo mode. Two third-generation LED curing units were used: VALO® and Bluephase 20i® . The degree of conversion (DC) and Vickers hardness (VHN) of an orthodontic composite (OC) (Transbond XT) under metallic (MB) or ceramic brackets (CB) were measured. Methods: OC was applied to the bracket base, which was then placed over an attenuated total reflectance (ATR) table coupled to an infrared light spectroscope, or to a glass surface for the VHN analysis. The specimens were light-cured and DC values were calculated. The VHN was obtained in a microhardness tester. The data were analyzed with 2-way ANOVA followed by Tukey's post-hoc test (pre-set α=0.05). Linear regression analysis evaluated the relationship between RE values and dependent variables. Results: CB allowed higher DC and VHN values than MB (p< 0.001). No significant difference was noted among groups when CB were used. For MB, MI groups showed the highest DC and VHN values. A significant, but weak relationship was found between delivered RE values and dependent variables. Conclusions: The decrease in RE values from third generation LED CU did not jeopardize the DC values when CB were used, but can compromise DC and VHN values when MB are used.

RESUMO Introdução: A terceira geração de LEDs fotopolimerizadores pode ser utilizada em curtos períodos de exposição para a colagem de braquetes ortodônticos. Objetivo: O presente estudo avaliou o efeito dos diferentes valores de irradiância (IR): instruções do fabricante (IF), ½ IF, » IF e modo Turbo. Dois fotopolimerizadores LED de terceira geração (VALO® e Bluephase20i®) foram utilizados. Foram mensurados o grau de conversão (GC) e a dureza Vickers (VHN) de um compósito ortodôntico (CO) (Transbond XT) sob braquetes metálicos (BM) ou cerâmicos (BC). Métodos: O compósito ortodôntico foi aplicado na base do braquete e foi posicionado sobre uma mesa de refletância total atenuada (ATR) acoplada a um espectroscópio de infravermelho ou a uma superfície de vidro para análise de VHN. As amostras foram fotopolimerizadas e os valores de GC foram calculados. O VHN foi obtido em um microdurômetro. Os dados foram analisados com ANOVA de 2 fatores seguida do teste post-hoc de Tukey (predefinido α = 0,05). A análise de regressão linear avaliou a relação entre os valores de IR e as variáveis dependentes. Resultados: BC permitiu valores maiores de GC e VHN do que BM (p<0,001). Nenhuma diferença significativa foi observada entre os grupos quando BC foi utilizado. Para BM, os grupos de IF mostraram os maiores valores de GC e VHN. Uma relação significativa, mas fraca, entre os valores de IR entregue e as variáveis dependentes foi encontrada. Conclusões: A diminuição dos valores de IR dos fotopolimerizadores LED de terceira geração não prejudicou os valores de GC quando BC foram utilizados, mas pode comprometer os valores de GC e VHN quando BM são utilizados.

Comparison of in vivo and in vitro models to evaluate pulp temperature rise during exposure to a Polywave® LED light curing unit

Abstract Objectives: To measure and compare in vivo and in vitro pulp temperature (PT) increase (ΔTEMP) over baseline, physiologic temperature using the same intact upper premolars exposed to the same Polywave® LED curing light. Methodology: After local Ethics Committee approval (#255,945), local anesthesia, rubber dam isolation, small occlusal preparations/minute pulp exposure (n=15) were performed in teeth requiring extraction for orthodontic reasons. A sterile probe of a temperature measurement system (Temperature Data Acquisition, Physitemp) was placed within the pulp chamber and the buccal surface was sequentially exposed to a LED LCU (Bluephase 20i, Ivoclar Vivadent) using the following exposure modes: 10-s low or high, 5-s Turbo, and 60-s high. Afterwards, the teeth were extracted and K-type thermocouples were placed within the pulp chamber through the original access. The teeth were attached to an assembly simulating the in vivo environment, being similarly exposed while real-time temperature (°C) was recorded. ΔTEMP values and time for temperature to reach maximum (ΔTIME) were subjected to two-way ANOVA and Bonferroni's post-hoc tests (pre-set alpha 0.05). Results: Higher ΔTEMP was observed in vitro than in vivo. No significant difference in ΔTIME was observed between test conditions. A significant, positive relationship was observed between radiant exposure and ΔTEMP for both conditions (in vivo: r2=0.917; p<0.001; in vitro: r2=0.919; p<0.001). Conclusion: Although the in vitro model overestimated in vivo PT increase, in vitro PT rise was close to in vivo values for clinically relevant exposure modes.

Porosity, water sorption and solubility of denture base acrylic resins polymerized conventionally or in microwave

Abstract The proper selection of polymerization cycle is important to prevent overheating of the monomer that could cause degradation, porosity and, consequently, deleterious effects on the denture base properties. Objective This study evaluated the porosity, water sorption and solubility of acrylic resins (Vipi Cril-VC and Vipi Wave-VW) after conventional or microwave polymerization cycles. Material and Methods Specimens (n = 10) were made and cured: 1-WB = 65°C during 90 min + boiling during 90 min (VC cycle - control group); 2-M25 = 10 min at 270 W + 5 min at 0 W + 10 min at 360 W (VW cycle); 3-M3 = 3 min at 550 W; and 4-M5 = 5 min at 650 W. Afterward, they were polished and dried in a dessicator until a constant mass was reached. Specimens were then immersed in distilled water at 37°C and weighed regularly until a constant mass was achieved. For porosity, an additional weight was made with the specimen immediately immersed in distilled water. For water sorption and solubility, the specimens were dried again until equilibrium was reached. Data were submitted to 2 way-ANOVA and Tukey HSD (α=0.05). Results Porosity mean values below 1.52% with no significant difference among groups for both materials were observed. Resins showed water sorption and solubility values without a significant difference. However, there was a significant difference among groups for these both properties (P<0.013). The highest sorption (2.43%) and solubility (0.13%) values were obtained for WB and M3, respectively. Conclusions The conventional acrylic resin could be polymerized in a microwave since both the materials showed similar performance in the evaluated properties. Shorter microwave cycles could be used for both the materials without any detectable increase in volume porosity.

Light curing in dentistry and clinical implications: a literature review

Abstract Contemporary dentistry literally cannot be performed without use of resin-based restorative materials. With the success of bonding resin materials to tooth structures, an even wider scope of clinical applications has arisen for these lines of products. Understanding of the basic events occurring in any dental polymerization mechanism, regardless of the mode of activating the process, will allow clinicians to both better appreciate the tremendous improvements that have been made over the years, and will also provide valuable information on differences among strategies manufacturers use to optimize product performance, as well as factors under the control of the clinician, whereby they can influence the long-term outcome of their restorative procedures.

Effects of radiant exposure values using second and third generation light curing units on the degree of conversion of a lucirin-based resin composite

Abstract Alternative photoinitiators with different absorption wavelengths have been used in resin composites (RCs), so it is crucial to evaluate the effectiveness of light-curing units (LCUs) on these products. Objective Using Fourier transform infrared analysis (FTIR) in vitro, the effects of varying radiant exposure (RE) values generated by second and third generation LED LCUs on the degree of conversion (DC) and maximum rate of polymerization (Rpmax) of an experimental Lucirin TPO-based RC were evaluated. Material and Methods 1 mm or 2 mm thick silicon molds were positioned on a horizontal attenuated total reflectance (ATR) unit attached to an infrared spectroscope. The RC was inserted into the molds and exposed to varying REs (18, 36 and 56 J/cm2) using second (Radii Plus, SDI) and third generation LED LCUs (Bluephase G2/Ivoclar Vivadent) or a quartz tungsten based LCU (Optilux 501/SDS Kerr). FTIR spectra (n=7) were recorded for 10 min (1 spectrum/s, 16 scans/spectrum, resolution 4 cm-1) immediately after their application to the ATR. The DC was calculated using standard techniques for observing changes in aliphatic to aromatic peak ratios both prior to, and 10 min after curing, as well as during each 1 second interval. DC and Rpmax data were analyzed using 3-way ANOVA and Tukey’s post-hoc test (p=0.05). Results No significant difference in DC or Rpmax was observed between the 1 mm or 2 mm thick specimens when RE values were delivered by Optilux 501 or when the 1 mm thick composites were exposed to light emitted by Bluephase G2, which in turn promoted a lower DC when 18 J/cm2 (13 s) were delivered to the 2 mm thick specimens. Radii Plus promoted DC and Rpmax values close to zero under most conditions, while the delivery of 56 J/cm2 (40 s) resulted in low DC values. Conclusions The third generation LCU provided an optimal polymerization of Lucirin TPO-based RC under most tested conditions, whereas the second generation LED-curing unit was useless regardless of the RE.

Influence of resin cement shade on the color and translucency of ceramic veneers

ABSTRACT Objective This in vitro study evaluated the effect of two different shades of resin cement (RC- A1 and A3) layer on color change, translucency parameter (TP), and chroma of low (LT) and high (HT) translucent reinforced lithium disilicate ceramic laminates. Material and Methods One dual-cured RC (Variolink II, A1- and A3-shade, Ivoclar Vivadent) was applied to 1-mm thick ceramic discs to create thin RC films (100 µm thick) under the ceramics. The RC was exposed to light from a LED curing unit. Color change (ΔE) of ceramic discs was measured according to CIEL*a*b* system with a standard illuminant D65 in reflectance mode in a spectrophotometer, operating in the light range of 360-740 nm, equipped with an integrating sphere. The color difference between black (B) and white (W) background readings was used for TP analysis, while chroma was calculated by the formula C*ab=(a*2+b*2)½. ΔE of 3.3 was set as the threshold of clinically unacceptable. The results were evaluated by two-way ANOVA followed by Tukey's post hoc test. Results HT ceramics showed higher ΔE and higher TP than LT ceramics. A3-shade RC promoted higher ΔE than A1-shade cement, regardless of the ceramic translucency. No significant difference in TP was noted between ceramic discs with A1- and those with A3-shade cement. Ceramic with underlying RC showed lower TP than discs without RC. HT ceramics showed lower chroma than LT ceramics, regardless of the resin cement shade. The presence of A3-shade RC resulted in higher chroma than the presence of A1-shade RC. Conclusions Darker underlying RC layer promoted more pronounced changes in ceramic translucency, chroma, and shade of high translucent ceramic veneers. These differences may not be clinically differentiable.

Influence of photo-activation source on enamel demineralization around restorative materials

This study evaluated the effects of the photoactivation source and restorative material on the development of caries-like lesions on human enamel after an in vitro pH challenge. Enamel cavities were prepared in 36 blocks, which were assigned to two groups according to the restorative material: resin-modified glass ionomer (RMGI) and composite resin (CR). Samples were exposed to quartz-tungsten-halogen lamp, argon-ion laser, or light-emitting diode (n = 6). The Knoop microhardness (KHN) values of the top surface of all materials were evaluated. Restored enamel blocks were thermocycled and subjected to 10 demineralization-remineralization cycles at 37°C. KHN analysis of the superficial enamel was performed by four indentations located 100 mm from the restoration margin. The material KHN was not affected by the photoactivation source. No significant difference in KHN was noted between CR and RMGI. The enamel surface around RMGI exhibited a higher KHN (272.8 KHN) than the enamel around CR (93.3 KHN), regardless of the photoactivation source. Enamel demineralization around the dental restoration was not influenced by the photoactivation source. Less enamel demineralization was observed around the RMGI than around the CR restoration.

Silorane- and high filled-based"low-shrinkage" resin composites: shrinkage, flexural strength and modulus

This study compared the volumetric shrinkage (VS), flexural strength (FS) and flexural modulus (FM) properties of the low-shrinkage resin composite Aelite LS (Bisco) to those of Filtek LS (3M ESPE) and two regular dimethacrylate-based resin composites, the microfilled Heliomolar (Ivoclar Vivadent) and the microhybrid Aelite Universal (Bisco). The composites (n = 5) were placed on the Teflon pedestal of a video-imaging device, and VS was recorded every minute for 5 min after 40 s of light exposure. For the FS and FM tests, resin discs (0.6 mm in thickness and 6.0 mm in diameter) were obtained (n = 12) and submitted to a piston-ring biaxial test in a universal testing machine. VS, FS, and FM data were submitted to two-way repeated measures and one-way ANOVA, respectively, followed by Tukey's post-hoc test (a = 5%). Filtek LS showed lower VS than did Aelite LS, which in turn showed lower shrinkage than did the other composites. Aelite Universal and Filtek LS exhibited higher FS than did Heliomolar and Aelite LS, both of which exhibited the highest FM. No significant difference in FM was noted between Filtek LS and Aelite Universal, while Heliomolar exhibited the lowest values. Aelite LS was not as effective as Filtek LS regarding shrinkage, although both low-shrinkage composites showed lower VS than did the other composites. Only Filtek LS exhibited FS and FM comparable to those of the regular microhybrid dimethacrylate-based resin composite.

Surface roughness evaluation of in vitro refinished dental ceramics followed by bleaching treatment / Avaliação in vitro da rugosidade superficial de ceramicas após repolimento e tratamento clareador

Objetivo: O objetivo deste estudo foi avaliar o efeito do processo de repolimento na rugosidade de cerâmicas dentais e o efeito do tratamento clareador com peróxido de carbamida 16%. Material e métodos: espécimes de 5 x 3 x 1 mm foram produzidos em dois grupos (n = 14 por grupo) de cerâmicas odontológicas seguindo as instruções dos fabricantes: IPS D.Sign (Ivoclar-Vivadent) e VMK-95 (Vita). Um rugosímetro foi usado para avaliar a rugosidade superficial (Ra) de todas as cerâmicas adquirindo 3 perfis com cinco cortes de 0,25 mm (λc) a 0,1 mm/s, em 4 tempos. O primeiro tempo foi o valor inicial (controle negativo), seguido pelo segundo tempo no qual foi realizada a asperização por broca (granulação 91-126 μm) para simular um ajuste oclusal no segundo tempo (controlo positivo). Depois disso, as amostras foram submetidas a tratamentos sequenciais de repolimento com pontas diamantadas finas (2135F - granulação 37-44 μm) e extra finas (2135FF - granulação 20-40 μm), terceiro tempo; e polimento com taças abrasivas e pasta (quarto tempo). Após o repolimento, as cerâmicas foram divididas em 2 subgrupos: clareadas (BL) e não clareadas (NB), totalizando 4 sub-grupos (n = 7 por grupo). O clareamento foi realizado diariamente por 6 h, com peróxido de carbamida 16%, durante 21 dias, enquanto os grupos NB foram armazenados em saliva artificial. O efeito dos procedimentos de repolimento foram avaliados por 2-way ANOVA e teste de Tukey; o efeito do clareamento nas cerâmicas repolidas foi avaliado pelo teste T. Resultados: Não houve diferenças estatisticamente significativas na rugosidade superficial entre as cerâmicas entre os tempos em que foi avaliado o repolimento. O ajuste de cerâmicas odontológicas com pontas diamantadas aumenta drasticamente a rugosidade superficial. O tratamento apenas com a ponta diamantada fina e extra fina reduziu, mas não reverteu a rugosidade superficial das cerâmicas...

Objective: The objective of this study was to evaluate the effect of refinishing process on dental ceramics roughness and the effect of bleaching treatment with 16% carbamide peroxide. Material and methods: Specimens of 5 x 3 x 1 mm were produced in two groups (n = 14 per group) of dental ceramics following manufacturers’ instructions: IPS d.Sign (Ivoclar- Vivadent); and VMK-95 (Vita). A profilometer was used to evaluate the surface roughness (Ra values) of all ceramics acquiring 3 profiles with five 0.25 mm cut-off (λc) at 0.1 mm/s, in four times. The first time was baseline as a negative control, followed by bur roughening (91-126 μm-grit) to simulate an oclusal adjustment in the second time (positive control). After that, the specimens were submitted to refinishing treatments with diamond burs with fine (2135F – 37-44 μm-grit) and extra fine (2135FF – 20-40 μm-grit) diamond burs (third time); and polishing with abrasive cups and paste (fourth time). After refinishing, the two ceramics were divided into a bleached (BL) and non-bleached (NB), with 4 subgroups (n = 7 per group). Bleaching was performed daily for 6-h with 16% carbamide peroxide for 21 days, while NB groups were stored in artificial saliva. The effect of refinishing treatment on ceramics were evaluated by to 2 way ANOVA and Tukey’s test; bleaching effect on refinished ceramics were evaluated by T test. Results: There were no statistical significant differences on surface roughness between ceramics on each refinishing treatments times. The adjustment of dental ceramics with diamond burs drastically increases the surface roughness. The solely treatment with fine and extra fine diamond bur reduced but did not reverse the ceramic surface roughness...

Effect of pre-heated dual-cured resin cements on the bond strength of indirect restorations to dentin

This study evaluated the effects of resin luting agents (LA) polymerized using increased temperature on the in vitro microtensile bond strength (mTBS) of indirect restorations to dentin. The occlusal dentin surfaces of 40 human third molars were exposed and flattened. The teeth were assigned to 8 groups (n = 5) according to the LA temperature (25°C o r 50°C), curing mode (dual- or self-curing mode), and product (Excite DSC/Variolink II [VII] and XP Bond/Calibra [Cal]). The bonding agents were applied to the dentin surfaces according to manufacturers' instructions. For preheated groups, the LAs were heated to 50°C, subsequently mixed on a heated stirrer surface, and applied to the previously heated pre-polymerized resin discs (2 mm thickness, TPH-Spectrum). The discs were bonded to the dentin surfaces, and the LAs were either exposed to a curing light according to manufacturers' instructions or allowed to self-cure. Specimens were stored in relative humidity at 37°C for 7 days. Specimens were mesio-distally and bucco-lingually sectioned to obtain multiple bonded beams with a 1-mm² cross-sectional area for mTBS testing. Data (MPa) were analyzed by 2-way ANOVA and Tukey's post hoc test (a = 5%) for each product. Specimen failure patterns were analyzed using a scanning electron microscope. VII groups showed higher mTBS at 50°C than at 25°C regardless of curing mode (p = 0.05). Cal groups showed similar mTBS at 25°C and 50°C in all activation modes. The use of some dual-polymerizing LAs at 50°C may improve the mTBS of indirect restorations to dentin.

The effect of viscosity and activation mode on biaxial flexure strength and modulus of dual resin cements / Efeito da viscosidade e modo de ativação na resistência flexural biaxial e módulo em cimentos resinosos duais

PURPOSE: The aim of this study was to evaluate the effects of curing mode and viscosity on the biaxial flexural strength (FS) and modulus (FM) of dual resin cements. METHODS: Eight experimental groups were created (n=12) according to the dual-cured resin cements (Nexus 2/Kerr Corp. and Variolink II/IvoclarVivadent), curing modes (dual or self-cure), and viscosities (low and high). Forty-eight cement discs of each product (0.5 mm thick by 6.0 mm diameter) were fabricated. Half specimens were light - activated for 40 seconds and half were allowed to self-cure. After 10 days, the biaxial flexure test was performed using a universal testing machine (1.27 mm/min, Instron 5844). Data were statistically analyzed by three-way ANOVA and Tukey's test (5%). RESULTS: Light-activation increased FS and FM of resin cements at both viscosities in comparison with self-curing mode. The high viscosity version of light-activated resin cements exhibited higher FS than low viscosity versions. The viscosity of resin and the type of cement did not influence the FM. Light-activation of dual-polymerizing resin cements provided higher FS and FM for both resin cements and viscosities. CONCLUSION: The use of different resin cements with different viscosities may change the biomechanical behavior of these luting materials.

OBJETIVO: O objetivo do estudo é avaliar o efeito do modo de ativação na resistência flexual biaxial (RF) e módulo (MF) em cimentos resinosos duais. METODOLOGIA: Foram formados oito grupos experientais (n=12) de acordo com cimento resinos (Nexus 2/Kerr Corp. and Variolink II/IvoclarVivadent), modo de ativação (dual ou auto-polimerizado) e viscosidade (baixa e alta). Quarenta e oito discos de cada cimento foram fabridados (0,5 mm espessura por 6,0 mm diametro). Metade dos espécimes foram foto-ativados e a outra metade foi deixado para auto-polimerização. Após dez dias, o teste biaxial foi realizado em máquina de ensaio universal (1,27 mm/min, Instron 5844). Os dados foram analisados estatisticamente por ANOVA e teste Tukey (5%). RESULTADOS: A foto-ativação aumentou a RF e RM para os cimentos em ambas as viscosidades em comparação com os grupos auto-polimerizados. A versão alta viscosidade dos cimentos foto-ativados apresentou maior RF que os cimentos em baixa viscosidade. A viscosidade e o tipo de cimento não influenciam o MF. A foto-ativação aumenta os valores de RF e MF para ambos os cimentos e viscosidades. CONCLUSÃO: O uso de diferentes cimentos com diferentes viscosidades pode influenciar o comportamento biomecânico de cimentos resinoso.

Effects of different concentrations of carbamide peroxide and bleaching periods on the roughness of dental ceramics

The wide use of dental bleaching treatment has brought concern about the possible effects of hydrogen peroxide on dental tissue and restorative materials. The objective of this study was to evaluate in vitro the effect of nightguard bleaching on the surface roughness of dental ceramics after different periods of bleaching treatment. Fifteen specimens of 5 × 3 × 1 mm were created with three dental ceramics following the manufacturers' instructions: IPS Classic (Ivoclar-Vivadent); IPS d.Sign (Ivoclar-Vivadent); and VMK-95 (Vita). A profilometer was used to evaluate baseline surface roughness (Ra values) of all ceramics by five parallel measurements with five 0.25 mm cut off (Λc) at 0.1 mm/s. Afterwards, all specimens were submitted to 6-h daily bleaching treatments with 10 percent or 16 percent carbamide peroxide (Whiteness- FGM) for 21 days, while control groups from each ceramic system were stored in artificial saliva. The surface roughness of all groups was evaluated after 18 h, 42 h, 84 h, and 126 h of bleaching treatment. The surface roughness of each specimen (n = 5) was based on the mean value of five parallel measurements in each time and all data were submitted to two-way repeated measures ANOVA and Tukey's post-hoc test (α = 0.05). No significant differences in ceramic surface roughness were observed between untreated and bleached ceramic surfaces, regardless of bleaching intervals or bleaching treatments. This study provided evidence that at-home bleaching systems do not cause detrimental effects on surface roughness of dental ceramics.

Pre-heated dual-cured resin cements: analysis of the degree of conversion and ultimate tensile strength

This study evaluated the degree of conversion (DC) and ultimate tensile strength (UTS) of dual-cured resin cements heated to 50º C prior to and during polymerization. Disc- and hourglass-shaped specimens of Rely X ARC (RX) and Variolink II (VII) were obtained using addition silicon molds. The products were manipulated at 25º C or 50º C and were subjected to 3 curing conditions: light-activation through a glass slide or through a pre-cured 2-mm thick resin composite disc, or they were allowed to self-cure (SC). All specimens were dark-stored dry for 15 days. For DC analysis, the resin cements were placed into the mold located on the center of a horizontal diamond on the attenuated total reflectance element in the optical bench of a Fourier Transformed Infrared spectrometer. Infrared spectra (n = 6) were collected between 1680 and 1500 cm-1, and DC was calculated by standard methods using changes in ratios of aliphatic-to-aromatic C=C absorption peaks from uncured and cured states. For UTS test, specimens (n = 10) were tested in tension in a universal testing machine (crosshead speed of 1 mm/min) until failure. DC and UTS data were submitted to 2-way ANOVA, followed by Tukey's test (α= 5 percent). Both products showed higher DC at 50º C than at 25º C in all curing conditions. No significant difference in UTS was noted between most light-activated groups at 25º C and those at 50º C. VII SC groups showed higher UTS at 50º C than at 25º C (p < 0.05). Increased temperature led to higher DC, but its effects on resin cement UTS depended on the curing condition.

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 percent). 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.

Effect of curing mode on the hardness of dual-cured composite resin core build-up materials

This study evaluated the Knoop Hardness (KHN) values of two dual-cured composite resin core build-up materials and one resin cement exposed to different curing conditions. Two dual-cured core build-up composite resins (LuxaCore®-Dual, DMG; and FluoroCore®2, Dentsply Caulk), and one dual-cured resin cement (Rely X ARC, 3M ESPE) were used in the present study. The composite materials were placed into a cylindrical matrix (2 mm in height and 3 mm in diameter), and the specimens thus produced were either light-activated for 40 s (Optilux 501, Demetron Kerr) or were allowed to self-cure for 10 min in the dark (n = 5). All specimens were then stored in humidity at 37°C for 24 h in the dark and were subjected to KHN analysis. The results were submitted to 2-way ANOVA and Tukey's post-hoc test at a pre-set alpha of 5 percent. All the light-activated groups exhibited higher KHN values than the self-cured ones (p = 0.00001), regardless of product. Among the self-cured groups, both composite resin core build-up materials showed higher KHN values than the dual-cured resin cement (p = 0.00001). LuxaCore®-Dual exhibited higher KHN values than FluoroCore®2 (p = 0.00001) when they were allowed to self-cure, while no significant differences in KHN values were observed among the light-activated products. The results suggest that dual-cured composite resin core build-up materials may be more reliable than dual-cured resin cements when curing light is not available.

Evaluation of biaxial flexural strength and modulus of filled and unfilled adhesive systems / Avaliação da resistência flexural biaxial e módulo de flexão de sistemas adesivos

Purpose: The purpose of this study was to evaluate the flexural strength and modulus of two adhesive systems using biaxial flexural strength test. Methods: The bonding agents (Pentron Clinical Technologies) tested were: Bond 1 (B1) and NanoBond (NB). Thirteen disks (6.1 mm diameter and 0.6 mm thick) were prepared with adhesive solutions of each bonding agents using Teflon molds. The adhesive solutions within the molds were light-activated with XL 3000 curing unit (3M ESPE) for 10 s on both sides. The disks were stored for 10 days and were tested in a universal testing machine (1.27 mm/min - Instron 5844). Data were statistically analyzed by one-way ANOVA (á=0.05). Results: The mean values of fracture strength (±SD) for adhesive systems were (in MPa):B1- 89.7±7.6 e NB- 131.1±9.5. Modulus means (±SD) were (in MPa): B1- 1999.9±258.4 e NB- 2314.5±271.0. Conclusion: The filled adhesive system (NB) exhibited higher strength and flexural modulus means than the unfilled adhesive B1.

Objetivo: O objetivo deste estudo foi avaliar a resistência flexural e o módulo de flexão de dois sistemas adesivos, através de ensaio de resistência flexural biaxial. Metodologia: Os adesivos (Pentron Clinical Technologies) estudados foram: Bond 1 (B1) e NanoBond (NB). Treze discos de cada adesivo foram preparados com dimensões aproximadas de 6,1 mm de diâmetro e 0,6 mm de espessura. Os discos de adesivos foram confeccionados utilizando-se moldes de teflon e fotopolimerizados com aparelho XL 3000 (3M ESPE). Após armazenamento por 10 dias, os discos foram testados em máquina universal de ensaio (Instron 5844), com velocidade de 1,27 mm/min. Os dados foram submetidos à análise de variância (1 fator) ao nível de significância de 0,05. Resultados: Os valores médios (±DP) de resistência flexural para os adesivos foram (em MPa): B1- 89,7±7,6 e NB- 131,1±9,5. Os valores médios de módulo flexural (±DP) foram (em MPa): B1- 1999,9±258,4 e NB- 2314,5±271,0.Conclusão: O adesivo contendo partículas de carga (NB) mostrou maiores valores de resistência flexural e módulo de flexão que o adesivo B1.

Degree of conversion of adhesive systems light-cured by LED and halogen light

This study evaluated the effect of blue light emitting diode (LED) and quartz tungsten halogen (QTH) on the degree of conversion (DC) of an etch-and-rinse Single Bond adhesive system (SB) and a mixture composed of primer solution and resin bond from Clearfil SE Bond self-etching adhesive system (CB) using Fourier transform infrared analysis (FTIR). Adhesives were applied to potassium bromide pellet surfaces and FTIR analyses were performed before and after photo-activation for 10 s with either LED (Freelight 1 - 400 mw/cm²) or QTH (XL 3000 - 630 mw/cm²) light-curing units (n=8). Additional FTIR spectra were obtained from photo-activated samples stored in distilled water for 1 week. The DC was calculated by comparing the spectra obtained from adhesive resins before and after photo-activation. The results were analyzed by two-way split-plot ANOVA and Tukey's test (p<0.05). Both adhesive systems exhibited low DC ( percent) immediately after photo-activation (SB/QTH: 18.7 ± 3.9; SB/LED: 13.5 ± 3.3; CF/QTH: 13.6 ± 1.9; CF/LED: 6.1 ± 1.0). The DC of samples light-cured with LED was lower than DC of those light-cured with QTH, immediately after light curing and after 1 week (SB/QTH: 51.3 ± 6.6; SB/LED: 50.3 ± 4.8; CF/QTH: 56.5 ± 2.9; CF/LED: 49.2 ± 4.9). The LED curing unit used to photo-activate the adhesive resins promoted lower DC than the QTH curing unit both immediately after light curing and 1 week after storage in water.

Este estudo avaliou a influência de sistemas de fotoativação no grau de conversão (GC) de sistemas adesivos por meio da análise infravermelha transformada de Fourier (FTIR). Os sistemas adesivos Single Bond (SB) e Clearfil SE Bond (CF) foram aplicados em pastilhas de brometo de potássio e fotoativados com luz halógena (XL 3000 - 630 mw/cm²) (QTH) e LED (Elipar Freelight 1 - 400 mw/cm²) por 10 s (n=8). Foram obtidos espectros de FTIR antes e imediatamente após a fotoativação, e tambem após 1 semana de armazenamento em água destilada. Calculou-se o GC comparando-se a razão entre os picos das bandas dos espectros, antes e após a fotoativação. Os resultados de GC foram submetidos à ANOVA e ao teste de Tukey (p<0,05). Para ambos os sistemas adesivos, o GC ( por cento) obtido imediatamente após a fotoativação com LED foi inferior ao obtido utilizando-se QTH (SB/QTH: 18,7 ± 3,9; SB/LED: 13,5 ± 3,3; CF/QTH: 13,6 ± 1,9; CF/LED: 6,1 ± 1,0). Após uma semana foi observado um aumento significativo no GC de todos os grupos, porém os valores dos grupos fotoativados com LED mantiveram-se inferiores aos obtidos com QTH (SB/QTH: 51,3 ± 6,6; SB/LED: 50,3 ± 4,8; CF/QTH: 56,5 ± 2,9; CF/LED: 49,2 ± 4,9). O GC dos adesivos fotoativados com LED foi inferior ao observado após fotoativação com QTH, imediatamente após fotoativação como após 1 semana de armazenamento em água.

Effect of dentinal surface preparation on bond strength of self-etching adhesive systems

O objetivo deste estudo foi avaliar os efeitos de tratamentos superficiais da dentina na resistência de união (RU) de dois sistemas adesivos autocondicionantes, Clearfil SE Bond (CSE) e One-Up Bond F (OUB). Superfícies dentinárias planificadas de vinte e quatro terceiros molares foram preparadas com pontas diamantadas em alta rotação, brocas "carbide" em baixa rotação ou abrasionadas com lixas de SiC (#600). Os adesivos foram aplicados e fotoativados de acordo com as instruções dos fabricantes. Um bloco de compósito foi construído nas superfícies tratadas e cada incremento de resina foi fotoativado por 40 segundos. Após armazenamento em água (37°C/24 h), os dentes restaurados foram serialmente seccionados paralelamente ao seu longo eixo para obtenção de espécimes com área de secção transversal de aproximadamente 0,8 mm2 (n = 20). Os espécimes foram testados em máquina universal de ensaios (0,5 mm/min). A área de união foi mensurada e os resultados (MPa) foram analisados pela ANOVA (2 fatores) e pelo teste de Tukey (p < 0,05). Os grupos restaurados com o adesivo CSE mostraram os maiores valores de RU para todos os tratamentos. A superfície da dentina preparada com brocas carbide em baixa rotação reduziu a RU para o adesivo CSE; entretanto, a RU do adesivo OUB não foi afetada pelos tratamentos. O efeito da preparação da dentina na RU foi material-dependente.

Influence of curing accelerator for cyanoacrylate glues on physical properties of adhesive resins

The objectives of this study were to evaluate the effect of a curing accelerator (CA) on the ultimate tensile strength (UTS) and degree of conversion (DC) of two adhesive systems, Single Bond and Clearfil SE Bond, as well as to identify the composition of the CA hour-glass adhesive resin samples with a cross sectional area of 0,8 mm² at the "neck" were tested in tension using a Universal Testing Machine. Fourier transform infrared spectroscopy (FTIR) was used to analyse thin films of each adhesive resin. All samples were stored in the dark for 24 hours before they were tested. During the UTS and FTIR analyses, the contact of the CA with samples was either avoided or not. The gas chromatography mass spectrocopy (GC-MS) and the nuclear magnetic resonance (NMR) analyses determined the molecular weight and structure of the CA. UTS and DC were analyzed by ANOVA and Tukey's test at 95% of confidence. The use of the CA did not affect the UST (p=0.5996) but increased the DC of the samples (p<0.0001). The compound identified by GC-MS and NMR was N-dimethyl p-toluidine. The application of CA in microtensile bond strength methodology raises concern regarding its effects on poorly polymerized adhesive systems.