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Objectives: The objective was to evaluate the polymerization efficiency of different bulk-fill resin-based composites cured by monowave and polywave light-curing units, by assessment of the degree of conversion and Vickers microhardness at different depths. Method and materials: Two commercially available bulk-fill resin-based composites were used: Filtek One Bulk Fill Restorative (3M ESPE) and Tetric N-Ceram Bulk Fill (Ivoclar Vivadent). The light-curing units utilized were two LED light-curing units: a monowave LED light-curing unit (BlueLEX LD-105, Monitex) and a polywave LED light-curing unit (Twin Wave GT-2000, Monitex). For each test, 20 cylindrical specimens (4 mm diameter, 4 mm thickness) were prepared from each bulk-fill resin-based composite using a split Teflon mold. Ten specimens were light-cured by the monowave light-curing unit and the other ten were light-cured by the polywave light-curing unit according to the manufacturer's recommendations. Attenuated total reflectance-Fourier transform infrared spectroscopy (ATRFTIR) was used to assess the degree of conversion, and a Vickers microhardness tester was used to assess Vickers microhardness. Statistical analysis was performed using three-way ANOVA and Tukey post-hoc tests (P < .05). Results: The degree of conversion and Vickers microhardness in bulk-fill resin-based composites containing only camphorquinone as photoinitiator were similar when cured with either monowave or polywave light-curing units. However, bulk-fill resin-based composites containing a combination of photoinitiators exhibited significantly higher degree of conversion and Vickers microhardness when cured with a polywave light-curing unit. Although all groups showed statistically significant differences between the top and bottom surfaces regarding degree of conversion and Vickers microhardness, all of them showed bottom/top ratios > 80% regarding degree of conversion and Vickers microhardness. Conclusion: The polywave light-curing unit enhanced the polymerization efficiency of bulk-fill resin-based composites especially when the latter contained a combination of photoinitiators, but does not prevent the use of a monowave light-curing unit. [ABSTRACT FROM AUTHOR]

Matrix metalloproteinase (MMP)-induced collagen degradation at the resin-dentin interface remains a significant challenge for maintaining the longevity of dental restorations. This study investigated the effects of epigallocatechin-3-gallate (EGCG), a potent MMP inhibitor, on dental adhesive curing efficiency when encapsulated in halloysite nanotubes (HNTs). EGCG-loaded HNTs were incorporated into a commercial dental adhesive (Adper Scotchbond Multi-Purpose) at 7.5% and 15% w/v concentrations. To isolate the effects of each component, the study included three control groups: unmodified adhesive (negative control), adhesive containing only HNTs, and adhesive containing only EGCG (0.16% and 0.32%, equivalent to the EGCG content in EGCG–HNT groups). Degree of conversion (DC), polymerization conversion (PC), and Vickers micro-hardness (VHN) were assessed to evaluate curing efficiency. The addition of 7.5% EGCG-encapsulated HNTs maintained curing properties similar to the control, showing no significant differences in DC (80.97% vs. 81.15%), PC (86.59% vs. 85.81%), and VHN (23.55 vs. 24.12) (p > 0.05). In contrast, direct incorporation of EGCG at 0.32% significantly decreased DC (73.59%), PC (80.63%), and VHN (20.56) values compared to both control and EGCG–HNT groups (p < 0.05). Notably, HNT encapsulation mitigated these negative effects on polymerization, even at higher EGCG concentrations. These findings demonstrate that EGCG encapsulation in HNTs can maintain the curing efficiency of dental adhesives while potentially preserving the MMP-inhibitory benefits of EGCG. [ABSTRACT FROM AUTHOR]

This study evaluated the degree of conversion (DC), polymerization kinetics, and temperature of a new self-cure bulk-fill resin-based composite (Stela Automix, SDI). The study was divided into seven groups: (1) Stela Primer, (2) Stela Automix, (3) Stela Automix exposed to light for 20 s after 100 s, (4) Stela Primer with Stela Automix, (5) Stela Primer with Stela Automix and exposed to light for 20 s after 100 s, (6) Scotchbond Universal with Stela Automix, and (7) Scotchbond Universal with Stela Automix and exposed to light for 20 s after 100 s. The real-time reaction rates and DC at the bottom of 2 mm thick specimens at ∼32 °C were measured at 720 s after insertion using a spectrometer with an Attenuated Total Reflectance detector. The temperature of Stela, Stela exposed to light, Stela Primer with Stela, and Stela Primer with Stela exposed to light were measured by an infrared thermal camera in human molar teeth with Class I cavities. The temperature was recorded in real-time every 0.03 s for 720 s. The results were compared with ANOVA and Tukey's multiple comparison test (α = 0.05). The highest degree of conversion (DC) at the 2 mm depth was achieved when Stela Primer was combined with Stela (72.4 ± 3.5 % at 720 s). Stela could self-cure independently, but not as rapidly or effectively as when used with its Primer. The greatest temperature increase was for the light-cured Stela, followed by Stela Primer with Stela RBC exposed to light for 20 s. The Scotchbond Universal bonding system did not significantly increase the DC compared to Stela alone, except when exposed to light for 20 s, which slightly increased the final DC. Exposing Stela to light for 20 s did not improve the final DC of Stela as much as using the Stela Primer, but it did increase the temperature and prolonged the time taken to return to 37 °C. The Stela primer accelerates the degree of conversion of Stela. The reaction occurred rapidly and achieved a higher DC at the bottom of the specimens where the Stela was in contact with the Stela primer. Exposing Stela to light for 20 s is not recommended. Instead, Stela should be used with Stela Primer. [ABSTRACT FROM AUTHOR]

Objective: The aim of this study was to evaluate the cure efficiency and biocompatibility of a novel iron-based coordination complex used as a photoinitiator in comparison to conventional ethyl (2,4,6-trimethylbenzoyl) phenylphosphinate (TPO-L) and camphorquinone (CQ) as photoinitiators in dental 3D-printed resins. Materials and Methods: Experimental dental resin formulations were prepared by blending 1:1 ratio of Bis-GMA and TEGDMA, to which 0.2 wt% of either the iron-based coordination complex or CQ were added, along with 0.2 wt% EDAB and 0.4 wt% IOD, and the TPO-L. The degree of conversion (DC) was measured using Fourier transform infrared spectroscopy (FTIR). Biocompatibility was assessed by evaluating the viability of L929 fibroblast-like cells using the MTT assay 24 h post-exposure. Statistical analyses included a two-way ANOVA followed by Tukey's test for post hoc comparisons, with significance at p < 0.05. Results: The degree of conversion for the iron-based coordination complex (84.54% ± 1.69%) was significantly higher than that for the TPO-L (78.77% ± 1.25%) and CQ-based resins (73.21% ± 0.47%) (p < 0.001). The iron-based coordination complex and TPO-L resins exhibited significantly higher conversion than CQ-based resins (p < 0.001). Regarding biocompatibility, the cell viability test revealed that the iron-based coordination complex demonstrated the highest cell viability at 86.5% ± 10.24%, followed by TPO-L with 80.03% ± 11.07%. CQ showed the lowest cell viability of 51.29% ± 8.44% (p < 0.05). Tukey's test confirmed significant differences between CQ and other photointiators (p < 0.05), while no significant difference was found between TPO-L and the iron-based coordination complex. Conclusions: This study introduces a novel iron-based coordination complex photoinitiator that demonstrates enhanced cure efficiency and comparable biocompatibility to TPO-L, while significantly reducing the cytotoxicity associated with CQ. Its longer absorption wavelength supports deeper layer curing, making it a promising alternative for dental 3D printing, particularly in bioactive scaffold applications requiring minimized cytotoxicity. [ABSTRACT FROM AUTHOR]

This research assessed the effects of pre-heating on the physical–mechanical–chemical properties of different resin composites. For this, resin composites were evaluated in 6 levels: Admira/ADM, Vitra/VIT, Filtek Supreme/FS, Filtek Supreme Flowable/FSF, Filtek One/FO, and Filtek Bulk Fill Flowable/FBF; temperature was evaluated in 4 levels using a composite heater: room temperature/22 ºC, 37 ºC, 54 ºC, and 68 ºC. Response variables were: degree of conversion/DC, flexural strength/FS and color stability/ΔE (immediately after light curing/LC, after 7 days of dark-dry-storage, and after 24 h and 3 days of artificial aging in water at 60 ºC). Data were subjected to 2-way ANOVA (DC and FR) and 3-way repeated measurements ANOVA (ΔE), all followed by Tukey's test (α = 5%). DC were similar (FBF, FS, and FSF) or increased (ADM, FO, and VIT) as the temperature increased. Results of FR were unchanged or increased for all composites except VIT and ADM. High-viscosity composites (VIT and FS) showed higher FR values than low-viscosity composite (FSF). For bulk-fill composites, FBF and FO showed similar results, but lower than high-viscosity composites. Results of color stability showed acceptable values up to 3 days aging except for ADM and FSF. ΔE was not influenced by pre-heating and, overall, ΔE: FS < VIT < FO < FSF < ADM < FBF. Only VIT and FS showed ΔE ≤ 3.3 (clinical threshold). Therefore, the effects of pre-heating depend on the material. The tested materials generally showed similar or enhanced properties after pre-heating (except ADM and VIT). [ABSTRACT FROM AUTHOR]

To assess micro‐tensile bond strength (μTBS), degree of conversion (DC), microleakage (ML) antibacterial efficacy, and adhesive remnant index (ARI) of orthodontic brackets to enamel with different concentrations of photoactivated riboflavin‐doped hydroxyapatite (HA) nanospheres (NS) (0%,1%,5% and 10%) and 0.5 wt% RF alone in orthodontic adhesive. Samples were included on the predefined inclusion criteria and positioned up to the cementoenamel junction (CEJ). Hydroxy apatite nanospheres (HANS) commercially bought were doped with RF. Surface characterization of HANS and RF‐doped HANS were assessed along with EDX analysis. Samples were grouped based on experimental orthodontic adhesive modification. Group 1: Transbond XT no modification, Group 2: experimental Transbond XT 0.5 wt% RF, Group 3: experimental Transbond XT 0.5 wt% RF‐doped 1% HANS, Group 4: experimental Transbond XT 0.5 wt % RF‐doped 5% HANS and Group 5: Experimental Transbond XT 0.5 wt% RF‐doped 10% HANS. Brackets were placed based on different adhesive modifications and samples underwent thermocycling. Samples were evaluated for μTBS, DC, and ML. The type of failure was assessed using ARI. Adhesive modified and un‐modified in four different concentrations (0%, 1%, 5%, and 10%) and 0.5 wt% RF only were used to test efficacy against Streptococcus mutans (S.mutans). The survival rate of S.mutans and ML was determined using the Kruskal–Wallis Test. For the analysis of μTBS, ANOVA was employed, followed by a post‐hoc Tukey HSD multiple comparisons test. The highest μTBS and lowest ML were observed in Group 2 experimental Transbond XT 0.5 wt% RF only. The lowest μTBS, highest ML, and lowest DC was seen in Group 5 experimental Transbond XT 0.5 wt% RF‐doped 10% HANS. Samples in Group 1 in which Transbond XT was used as adhesive demonstrated significantly the highest microbial count of S.mutans and DC. Photoactivated RF‐doped HANS in 1% and 0.5 wt% Riboflavin alone in orthodontic adhesive for metallic bracket bonding improved micro tensile bond strength, ML, DC, and antibacterial scores. Research Highlights: The highest μTBS and lowest ML were observed in Group 2 experimental Transbond XT 0.5 wt% RF only.The lowest μTBS, highest ML, and lowest DC was seen in Group 5 experimental Transbond XT 0.5 wt% RF‐doped 10% HA‐NS.Samples in Group 1 in which Transbond XT was used as adhesive demonstrated significantly the highest microbial count of S.mutans and DC [ABSTRACT FROM AUTHOR]

The aim of this study was to evaluate the mechanical properties and degree of conversion of a novel 3D-printing model resin and compare it to eight commercially available model resins. An experimental resin formulated by our proprietary resin technology along with DentaModel, NextDent 2, KeyModel Ultra, Rodin Model, Die and Model 2, DMR III, LCD Grey, and Grey Resin were used in this study. Parallelepiped specimens (2 × 2 × 25 mm, n = 5) were printed and measured for their flexural strength (FS), flexural modulus (FM), and modulus of resilience (MR) in accordance with ISO-4049. Dumbbell-shaped specimens (Type V, n = 5) were printed to test tensile strength (TS) and elongation according to ASTM-D638. Barcol hardness (BH) was measured based on ASTM D2583 using broken tensile strength specimens. Izod-type test specimens (3.2 × 12.7 × 63.5 mm, n = 10) were printed, notched, and determined for impact strength according to ASTM D256-10. The degree of conversion was measured using FTIR (n = 5). Data were analyzed using one-way ANOVA and post hoc Tukey tests (p ≤ 0.05). The experimental resin exhibited a similar or significantly greater flexural strength (88.8 MPa), modulus of resilience (2.13 MPa), tensile strength (54.4 MPa), and hardness (82.9) than most model resins (FS 62.6–90.1 MPa, MR 1.37–2.0 MPa, TS 36.3–54.6 MPa, BH 66.1–83.7). The elongation (6.2%) and impact strength (14.2 J/m) of the experimental resin are statistically the same as those of most resins (3.0–7.5%, 13.8–16.4 J/m). However, the experimental resin has a significantly lower flexural modulus (1.97 GPa) than most resins (2.18–3.03 GPa). The experimental resin exhibited a significantly higher degree of conversion (66.58%) than most resins (1.11–62.34%) for 40 s of light curing; however, a similar or higher value (84.87%) than most resins (72.27–82.51%) was obtained for 3D-printed objects. The newly formulated 3D-printing model resin exhibited adequate mechanical properties and degree of conversion, which is comparable to the commercially available 3D-printing model resin materials. The new 3D-printing model resin can be used for modeling applications in restoration, orthodontics, implants, and other cases. [ABSTRACT FROM AUTHOR]

This study examines the effects of varying ultraviolet (UV) exposure times on the properties of UDMA/TEG-DMA composite resins, focusing on degree of conversion, surface morphology, water absorption, shrinkage, hardness, and flexural strength. Composite resin samples were exposed to UV light for 30, 60, 90, and 120 min. The degree of conversion was assessed using Fourier Transform Infrared Spectroscopy (FTIR). Surface morphology was analyzed via Scanning Electron Microscopy (SEM). Water absorption and shrinkage were measured following standard procedures, while mechanical properties, including hardness and flexural strength, were evaluated using a Vickers hardness tester and a 3-point bending test, respectively. The results indicate that a UV exposure time of 90 min optimizes the composite resin properties, achieving the highest degree of conversion at 77 %, optimal surface morphology, minimal water absorption and shrinkage, and superior mechanical properties, including maximum flexural strength and hardness. In contrast, both shorter and longer UV exposure times detrimentally affected these properties, with prolonged exposure causing thermal degradation and reduced performance. This research underscores the importance of precise UV curing time control to enhance the performance and durability of UDMA/TEG-DMA composite resins, providing valuable insights and practical guidelines for their application in dental and industrial fields. [ABSTRACT FROM AUTHOR]

This study investigated the effects of resin composites (RCs) containing surface pre-reacted glass ionomer (S-PRG) filler on the dentin microtensile bond strength (μTBS) of HEMA-free and HEMA-containing universal adhesives (UAs). Water sorption (WS) and solubility (SL), degree of conversion (DC), and ion release were measured. The UAs BeautiBond Xtreme (BBX; 0% HEMA), Modified Adhesive-1 (E-BBX1; 5% HEMA), Modified Adhesive-2 (E-BBX2; 10% HEMA), and two 2-step self-etch adhesives (2-SEAs): FL-BOND II (FBII; with S-PRG filler) and silica-containing adhesive (E-FBII) were used. Teeth were restored with Beautifil Flow Plus F00 with S-PRG filler (BFP) and flowable resin composite with silica filler (E-BFP). μTBS was evaluated after 24 h and 6 months of water storage. WS and SL measurement followed ISO 4049:2019; spectroscopy measured DC; ICP-MS evaluated ion release. BBX and FBII presented the highest DC. The adhesives did not comply with the WS ISO requirements, but the bonding resin of 2-SEAs complied with the SL threshold. BFP released more ions than E-BFP. BFP positively affected the μTBS of UAs, regardless of HEMA concentration after 24 h, comparable to the 2-SEAs. The 6 months μTBS decrease depended on the adhesive and RC combination. HEMA did not affect the μTBS of UAs, while bioactive resins had a positive impact. [ABSTRACT FROM AUTHOR]

The degree of conversion (DC) is crucial in determining the mechanical and clinical performance of resin-based composites (RBCs). This in vitro study aimed to evaluate the effect of the resin type and placement technique on the DC of RBCs (micro-hybrid, packable, hybrid, ormocer-based and flowable) polymerized with a second-generation LED light-curing unit (LCU). A total of 75 RBC samples were divided into three groups. Each RBC was placed into 4 mm diameter and 2 and 8 mm heigh Teflon molds with conventional standard, bulk, and incremental techniques (n = 5) and polymerized by LED LCU (229.153 mW/cm2) using the standard mode. After 24 h, DC was determined by FTIR spectrophotometry. The data were analyzed with two-way ANOVA and Tukey's HSD test (p < 0.05). The DC of the RBCs varied between 62.8 and 29.2%. While the same DC was obtained for 2 mm samples at the top and the bottom surfaces, the DC of the 8 mm samples gradually diminished from the top surface to the bottom surface. Significant differences were observed in the DC of the RBCs. An optimal DC was obtained for packable, micro-hybrid and ormocer-based RBCs polymerized by LED LCU with the recommended curing times. Considering that the polymerization process is versatile, further in vitro studies are needed. [ABSTRACT FROM AUTHOR]

Assessment of the antimicrobial, micro tensile bond strength (μTBS), and degree of conversion (DC) of fifth‐generation adhesive modified using photoactivated 0.5% rose bengal (RB) and photoactivated RB‐doped titanium dioxide nanoparticles (TiO2NPs) in different concentrations (2% and 5%) as compared with the unmodified adhesive bonded to the carious affected dentin (CAD). Forty mandibular molars with caries progression up to the middle third of the dentin, as per the International Caries Detection and Assessment System (ICDAS) score of 4 and 5 were included. Specimens were divided into four groups based on etch and rinse adhesive (ERA) modification group 1: unmodified ERA, group 2: photoactivated 0.5% RB photosensitizer (PS) modified ERA, group 3: photoactivated RB‐doped 2 wt% TiO2NPs adhesive, group 4: photoactivated RB‐doped 5 wt% TiO2NPs adhesive. Followed by adhesive and composite restoration on the CAD surface. All the specimens were thermocycled and an assessment of μTBS and failure pattern analysis was performed. The antibacterial potency of RB and RB‐doped TiO2NPs (2% and 5%) followed by their activation using visible light against Streptococcus mutans (S.mutans) were tested. The survival rate of S.mutans was assessed using the Kruskal–Wallis test. The analysis of μTBS involved the use of ANOVA, followed by a post‐hoc Tukey honestly significant difference (HSD) multiple comparisons test. Group 1 (Unmodified ERA) (0.52 ± 0.31 CFU/mL) treated samples unveiled the highest means of bacterial survival and lowest μTBS (11.32 ± 0.63 MPa). Nevertheless, group 4: photoactivated RB‐doped 5 wt% TiO2NPs adhesive displayed the lowest outcomes of S.mutans survival (0.11 ± 0.02 CFU/mL) and highest bond strength (18.76 ± 1.45 MPa). The photoactivated RB‐doped 2 wt% TiO2NPs in adhesive demonstrated promising enhancements in both μTBS and antibacterial efficacy against S.mutans. However, it is noteworthy that this modification led to a decrease in the DC of the adhesive. Research Highlights: Unmodified ERA‐treated samples unveiled the highest bacterial survival and the lowest μTBS.Photoactivated RB‐doped 5 wt% TiO2NPs adhesive displayed the lowest S.mutans survival rate and highest bond strength.DC decreased with an increase in concentration of TiO2. [ABSTRACT FROM AUTHOR]

Objective: To evaluate the effects of preheating procedure and polymerization modes on degree of conversion (DC) of resin composites.Methods: Three different types of composites - a conventional (GrandioSO - [GSO]), a bulkfill (GrandioSO x-tra - [GSX]), and a thermoviscous bulkfill (VisCalor bulk - [VCB]) - were investigated. Three specimens were prepared for each combination of the variables (composite type*preheating procedure*polymerization mode). Photo-polymerization was performed using an LED operated in standard (SM), high power plus (HM), and x-tra power (XM) modes. DC was measured with Fourier Transform Infrared Spectroscopy after 5 min and 24 h post-irradiation. Furthermore, three-way analysis of variance followed by a Tukey test at a significance level of P SM > XM.Conclusion: Preheating generally exhibited favorable effects on the DC of all tested composites, with the most significant impact observed in VCB. Additionally, polymerization with x-tra power mode is not recommended to achieve a sufficient DC required for clinically acceptable restorations.Keywords: bulk fill composite; degree of conversion; FTIR; polymerization mode; preheating; thermoviscousity

Abstract Aim This in-vitro study aimed to evaluate the degree of conversion (DC) of dual-cured luting cement (Bifix QM, VOCO) and flowable composite (Grandio Flow, VOCO) under lithium disilicate glass-ceramic (IPS e.max CAD, Ivoclar Vivadent) and hybrid ceramic (Grandio Blocs, VOCO; Cerasmart, GC) CAD-CAM blocks with different thicknesses. Materials and methods Contrast ratio (CR), translucency (TPab, TP00), and opalescence (OP) parameters of 30 disc-shaped CAD-CAM blocks (n = 5) prepared with two different thicknesses (1.5 and 2 mm) and 8 mm diameters were calculated using a spectrophotometer (VITA Easyshade V, Zahnfabrik). A total of 36 Bifix QM and Grandio Flow samples were prepared at 100 μm thickness using a specific setup by polymerizing from the top of the blocks. Following immersion in distilled water at 37 °C for 24 h, luting materials were examined by Fourier Transform Infrared Spectroscopy for DC calculation. Data were analyzed using One-way ANOVA, Kruskal Wallis, Mann Whitney U, and Independent Samples t-tests (p 0.05). DC of Grandio Flow was significantly higher than Bifix QM under 2 mm-IPS e.max CAD (p = 0.011). Conclusion The translucency of the CAD-CAM blocks varies depending on their thickness. However, there was no significant difference in the DC of the luting materials depending on the block thickness. Further studies are needed on the use of flowable resin composites as luting material.

Abstract Background Using infection control barriers (ICBs) on light curing units (LCUs) became mandatory to achieve proper infection control measures without jeopardizing the integrity of the restorations, especially at deeper layers. This study explored the effect of two ICBs on the irradiance of the LCU, as well as the degree of conversion (DC) and flexural strength (FS) of two types of bulk-fill composites. Water vapor permeability (WVP) of both barriers was also assessed to evaluate the capability of such barriers to prevent transmission of blood and saliva droplets and aerosols. Methods Two bulk-fill composites (X-tra fil and Tetric N- ceram) and two ICBs (Pinnacle Cure sleeve and Sanita wrapping film) were used in this study. Light irradiance was recorded per experimental condition using spectroradiometer. For DC and FS, specimens of 4 mm thickness were prepared. Each specimen was composed of two separable upper and lower layers of thickness 2 mm. DC and FS were measured using Infra-red spectroscopy and three-point loading test respectively. WVP was investigated using the cup method. Means and standard deviations were calculated, and the data were statistically analyzed using factorial analysis of variance test (α = 0.05). Results Light irradiance showed highest values using no ICBs and lowest values using Pinnacle curing sleeve. Both bulk-fill composites showed higher DC mean values without ICBs and when using Sanita wrapping film for both upper and lower layers of the specimens compared to Pinnacle curing sleeve. The upper layers of composite specimens showed higher DC compared to lower layers for all experimental conditions. Both ICBs had no adverse effect on FS of both composites’ upper layers. Pinnacle sleeve significantly reduced FS of both composites’ lower layers. X-tra fil showed higher DC and FS compared to Tetric N-Ceram for all experimental conditions. Regarding WVP; the wrapping film showed higher WVP compared to the curing sleeve. Conclusions Sanita wrapping film can be used as a successful ICB, without jeopardizing the concept of bulk-fill composites. Pinnacle cure sleeve can be considered an effective ICB, however its influence on properties and serviceability of bulk-fill composites remains questionable.

Abstract Minimally invasive access cavities have been proposed in the last decade to reduce tooth tissue loss during endodontic treatment and mitigate compromised fracture resistance of endodontically treated teeth. Fracture resistance of molars with different types of access cavity design may be affected by restorative materials and aging. Insufficient literature data exist on the effect of cavity design and type of restorative materials on restorative aspects such as material adaptation or photo-polymerization in restricted access cavities. This study analyses quality of polymerization, material adaptation and fracture resistance of molars with different types of access cavities restored with glass-ionomer, high-viscosity fiber-reinforced bulk-fill and nanofilled resin composite. Plastic molar teeth with truss (TREC) and traditional endodontic access cavity (TEC) were restored with nanofilled composite (Filtek Supreme), glass-ionomer Fuji IX and Filtek or fiber-reinforced everX Posterior and Filtek. Porosity was determined using microcomputer tomography and the degree of conversion of resin-based materals using micro-Raman spectroscopy. Human molars prepared and restored in the same way were used for fracture resistance testing at baseline and after thermocycling. The results demonstrate that high-viscosity fiber-reinforced composite was difficult to adapt in TREC cavity leading to greater porosity than Filtek or Fuji. TREC design did not affect composite polymerization and led to higher fracture resistance of restored molars compared to TEC but also more unrestorable fractures.

Aim: This in-vitro study aimed to evaluate the degree of conversion (DC) of dual-cured luting cement (Bifix QM, VOCO) and flowable composite (Grandio Flow, VOCO) under lithium disilicate glass-ceramic (IPS e.max CAD, Ivoclar Vivadent) and hybrid ceramic (Grandio Blocs, VOCO; Cerasmart, GC) CAD-CAM blocks with different thicknesses. Materials and methods: Contrast ratio (CR), translucency (TPab, TP00), and opalescence (OP) parameters of 30 disc-shaped CAD-CAM blocks (n = 5) prepared with two different thicknesses (1.5 and 2 mm) and 8 mm diameters were calculated using a spectrophotometer (VITA Easyshade V, Zahnfabrik). A total of 36 Bifix QM and Grandio Flow samples were prepared at 100 μm thickness using a specific setup by polymerizing from the top of the blocks. Following immersion in distilled water at 37 °C for 24 h, luting materials were examined by Fourier Transform Infrared Spectroscopy for DC calculation. Data were analyzed using One-way ANOVA, Kruskal Wallis, Mann Whitney U, and Independent Samples t-tests (p < 0.05). Results: It was observed that, as the block thickness increased TPab, TP00, and OP decreased, while CR increased. There was no significant difference between the DC of Bifix QM and Grandio Flow when 1.5 mm blocks were used in all groups (p > 0.05). DC of Grandio Flow was significantly higher than Bifix QM under 2 mm-IPS e.max CAD (p = 0.011). Conclusion: The translucency of the CAD-CAM blocks varies depending on their thickness. However, there was no significant difference in the DC of the luting materials depending on the block thickness. Further studies are needed on the use of flowable resin composites as luting material. [ABSTRACT FROM AUTHOR]

Background: Using infection control barriers (ICBs) on light curing units (LCUs) became mandatory to achieve proper infection control measures without jeopardizing the integrity of the restorations, especially at deeper layers. This study explored the effect of two ICBs on the irradiance of the LCU, as well as the degree of conversion (DC) and flexural strength (FS) of two types of bulk-fill composites. Water vapor permeability (WVP) of both barriers was also assessed to evaluate the capability of such barriers to prevent transmission of blood and saliva droplets and aerosols. Methods: Two bulk-fill composites (X-tra fil and Tetric N- ceram) and two ICBs (Pinnacle Cure sleeve and Sanita wrapping film) were used in this study. Light irradiance was recorded per experimental condition using spectroradiometer. For DC and FS, specimens of 4 mm thickness were prepared. Each specimen was composed of two separable upper and lower layers of thickness 2 mm. DC and FS were measured using Infra-red spectroscopy and three-point loading test respectively. WVP was investigated using the cup method. Means and standard deviations were calculated, and the data were statistically analyzed using factorial analysis of variance test (α = 0.05). Results: Light irradiance showed highest values using no ICBs and lowest values using Pinnacle curing sleeve. Both bulk-fill composites showed higher DC mean values without ICBs and when using Sanita wrapping film for both upper and lower layers of the specimens compared to Pinnacle curing sleeve. The upper layers of composite specimens showed higher DC compared to lower layers for all experimental conditions. Both ICBs had no adverse effect on FS of both composites' upper layers. Pinnacle sleeve significantly reduced FS of both composites' lower layers. X-tra fil showed higher DC and FS compared to Tetric N-Ceram for all experimental conditions. Regarding WVP; the wrapping film showed higher WVP compared to the curing sleeve. Conclusions: Sanita wrapping film can be used as a successful ICB, without jeopardizing the concept of bulk-fill composites. Pinnacle cure sleeve can be considered an effective ICB, however its influence on properties and serviceability of bulk-fill composites remains questionable. [ABSTRACT FROM AUTHOR]

The objective of this study was to evaluate the influence of light‐curing time and increment thickness on the microhardness and degree of conversion (DC) of bulk fill composite resins with different application systems. Translucency parameter (TP) was also measured. Specimens of resin composites were prepared in a circular matrix using a single increment with different thicknesses (2, 4, and 6 mm) and light‐cured with distinct times (10, 20, and 40 s). The materials tested (n = 5 pergroup) were Filtek One (FO) bulk fill, Tetric N‐Ceram (TC) bulk fill, SonicFill 3 (SF), VisCalor (VC) bulk. After 24 h, Knoop microhardness (KN) was measured, and the bottom/top ratio (B/Tratio) was calculated. The DC was measured using Fourier transformed infrared (FTIR) spectroscopy. The TP was assessed in additional specimens with 1 mm thick (n = 5). The data were statistically analyzed with analysis of variance (ANOVA) and Tukey's tests (5%). Significant differences were observed for all factors, for both B/Tratio and DC (p < 0.05). The higher increment thickness and the lower curing times resulted in lower B/Tratio and DC means. The VC and TC resins exhibited the overall higher B/Tratio, and the highest TP. SF presented the lowest values of B/Tratio and DC, with compromised polymerization at 6 mm depth. TP (means ± SD) were FO (12.85 ± 1.0)1, SF (15.62 ± 0.73)2, TC (20.32 ± 0.49)3, and VC (20.53 ± 0.73)3. We concluded that the greater the thickness of the increment, the lower the DC. Higher light curing times resulted on increased DC of the tested composites. The higher translucent materials VC and TC showed the greater B/Tratio; and FO resin exhibited the higher DC values. [ABSTRACT FROM AUTHOR]

Aim: To prepare experimental adhesive (EA) with 1% and without chitosan nanoparticles on dentin conditioned with a conventional technique phosphoric acid (PA) compared with two different contemporary techniques: photodynamic therapy (PDT) and femtosecond laser (FSL). Method: The methodology consisted of synthesis of EA and 1% chitosan-modified adhesive (CMA). Scanning electron microscopy, dentin adhesive interface assessment, energy-dispersive spectroscopy, shear bond strength (SBS), degree of conversion (DC), and bond failure were assessed. Teeth were selected, disinfected, and mounted in acrylic up to the cementoenamel junction. Occlusal enamel was removed and teeth were randomly allocated into groups and conditioned. These included Group 1: samples treated with PA; Group 2: specimens conditioned with methylene blue photosensitizer (MBP) activated by PDT; and Group 3: samples conditioned with FSL. Following different conditioning regimes, specimens were bonded using 1% CMA and EA. The composite buildup was followed by SBS testing and a bond failure assessment. DC was assessed for both EA and CMA. Analysis of variance and Tukey's post hoc test were used to compare the mean and standard deviation of SBS and DC in different experimental groups, with a significance level of p < 0.05. d Results: Dentin pretreated with etch and rinse demonstrated the highest bond strength with 1% CMA. Dentin conditioned with MBP activated by PDT and bonded to EA showed the lowest bond scores. Overall SBS values of 1% CMA were better than EA irrespective of the conditioning regime of dentin. The DC was higher in EA adhesive. This was followed by DC in 1% CMA. DC in EA was found to be comparable with 1% CMA. Conclusions: PA remains the gold standard for dentin conditioning. The incorporation of 1% chitosan in adhesive improves SBS and results in no change in DC. The use of FSL in dentin conditioning can be used as an alternative approach as it results in SBS within acceptable limits. The study was approved by the ethical board of King Saud University. [ABSTRACT FROM AUTHOR]

Minimally invasive access cavities have been proposed in the last decade to reduce tooth tissue loss during endodontic treatment and mitigate compromised fracture resistance of endodontically treated teeth. Fracture resistance of molars with different types of access cavity design may be affected by restorative materials and aging. Insufficient literature data exist on the effect of cavity design and type of restorative materials on restorative aspects such as material adaptation or photo-polymerization in restricted access cavities. This study analyses quality of polymerization, material adaptation and fracture resistance of molars with different types of access cavities restored with glass-ionomer, high-viscosity fiber-reinforced bulk-fill and nanofilled resin composite. Plastic molar teeth with truss (TREC) and traditional endodontic access cavity (TEC) were restored with nanofilled composite (Filtek Supreme), glass-ionomer Fuji IX and Filtek or fiber-reinforced everX Posterior and Filtek. Porosity was determined using microcomputer tomography and the degree of conversion of resin-based materals using micro-Raman spectroscopy. Human molars prepared and restored in the same way were used for fracture resistance testing at baseline and after thermocycling. The results demonstrate that high-viscosity fiber-reinforced composite was difficult to adapt in TREC cavity leading to greater porosity than Filtek or Fuji. TREC design did not affect composite polymerization and led to higher fracture resistance of restored molars compared to TEC but also more unrestorable fractures. [ABSTRACT FROM AUTHOR]

Oral bacteria cause tooth caries and periodontal disease. Much research is being conducted to prevent both major oral diseases by rendering dental materials' antimicrobial potential. However, such antimicrobial materials are regarded as 'combination' products and face high hurdles for regulatory approval. We loaded inorganic montmorillonite with the antimicrobial agent cetylpyridinium chloride, referred to below as 'CPC-Mont'. CPC-Mont particles in a 1, 3 and 5 wt% concentration were added to the considered gold-standard self-etch adhesive Clearfil SE Bond 2 ('CSE2'; Kuraray Noritake) to render its antibacterial potential (CSE2 without CPC-Mont served as control). Besides measuring (immediate) bonding effectiveness and (aged) bond durability to dentin, the antibacterial activity against S. mutans and the polymerization-conversion rate was assessed. Immediate and aged bond strength was not affected by 1 and 3 wt% CPC-Mont addition, while 5 wt% CPC-Mont significantly lowered bond strength and bond durability. The higher the concentration of the antimicrobial material added, the stronger the antimicrobial activity. Polymerization conversion was not affected by the CPC-Mont addition in any of the three concentrations. Hence, adding 3 wt% CPC-Mont to the two-step self-etch adhesive rendered additional antimicrobial potential on top of its primary bonding function. [ABSTRACT FROM AUTHOR]

(1) Background: To compare the degree of conversion of resin cores in various types of cavities and determine an effective irradiation method for achieving a higher degree of conversion. (2) Methods: Four different-sized cavities (narrow–shallow, narrow–deep, wide–shallow, and wide–deep) were simulated using a Teflon mold. The light irradiance reaching the bottom of each mold was measured by positioning a radiometer. The degree of conversion of the dual-cure resin core after irradiation (400 mW/cm2 for 20 s, 400 mW/cm2 for 40 s, and 800 mW/cm2 for 20 s) was measured using Fourier-transform near-infrared spectroscopy. (3) Results: The highest light irradiance was found at the bottom of wide–shallow cavities, followed by wide–deep, narrow–shallow, and narrow–deep ones (p < 0.001). In narrow cavities, irradiation at 800 mW/cm2 for 20 s led to a significantly higher degree of conversion (p < 0.001). In wide cavities, irradiation at 400 mW/cm2 for 40 s and 800 mW/cm2 for 20 s both led to a significantly higher degree of conversion (p < 0.001). (4) Conclusions: Less curing light reaches the bottom of cavities with a smaller diameter and greater depth. Providing a higher irradiance of light can induce a higher degree of conversion of resin composites in narrower cavities. [ABSTRACT FROM AUTHOR]

The objectives of this study were to evaluate the bonding durability of four different self-etch adhesives to dentin after 24 h and thermal cycling (TC) and to measure the degree of polymerization conversion (DC) in situ. Two-step self-etch adhesives, Clearfil SE Bond 2 (SE2, Kuraray Noritake Dental) and G2-Bond Universal (G2B, GC), and one-step self-etch adhesives, Scotchbond™ Universal Plus Adhesive (SBU, 3M ESPE) and Clearfil Universal Bond Quick (UBQ, Kuraray Noritake Dental), were used. The labial surfaces of bovine teeth were ground to create flat dentin surfaces. The adhesives were applied according to the manufacturers' instructions. After resin composite buildup and 24 h water storage, the specimens were sectioned into beams and all groups were subjected to thermal stress for 0, 10,000 (10k), or 20,000 (20k) cycles followed by micro-tensile bond strength (µTBS) testing. In situ DC was investigated with a laser Raman microscope. The µTBS data were statistically analyzed and subjected to a Weibull analysis. The different groups were compared at the characteristic strength (63.2% probability of failure) (α = 0.05). Two-Way ANOVA was used to show the effect of different adhesives and thermal cycling on the mean DC% followed by Tukey's multiple comparison post hoc test. G2B/TC10k resulted in a significant increase in the µTBS compared to TC0. SBU/TC20k showed significantly higher µTBS compared to TC0. For comparison between different tested adhesives, SBU showed a significantly lower µTBS compared to G2B after TC10k. G2B and SBU showed a greater number of adhesive failures after TC. Mean DC% was different for each adhesive. The newly developed MDP- and HEMA-free 2-SEA showed similar bonding performance with the gold-standard 2-SEA. However, there is still room for further improvement in terms of SEAs. [ABSTRACT FROM AUTHOR]

This study investigated the influence of photoinitiator types on degree of conversion (DC), rate of polymerization (RP), flexural strength (FS), flexural modulus (FM), and light transmittance (LT) of filled and unfilled light-curable resin cements through different thicknesses and shades of lithium disilicate ceramics. Lithium disilicate ceramic discs (IPS Emax Press, background [0.0], 0.5, 1.0, 2.0, 3.0, and 4.0 mm, shades A1 and BL3) were prepared. Experimental resin-based cements [TEGDMA/BisGMA (50/50 mass%)] were prepared using either camphorquinone (CQ)/amine (0.44/1.85 mol%) or TPO (0.44 mol%)], and a micro and nanofiller loads of nil (unfilled); 40/10 mass%; and 50/10 mass%). Resin cements (0.2 mm thick) were placed on the lower surface of the ceramic specimens and light-activated for 30 s from the upper surface using a Bluephase Style curing light (exitance at tip: 1236 mW/cm2 ± 1.20). LT and distribution of irradiance through the ceramics were measured using a UV–vis spectrometer and a beam profile camera, respectively (n = 3). The DC and RP were measured in real-time using mid infrared spectroscopy in attenuated total reflectance (ATR) mode (n = 3). FS and FM were measured using a universal testing machine (n = 5). Statistical analyses were performed on LT, DC, RP, FS, and FM data using a general linear model, and supplementary ANOVA and post hoc Tukey multiple comparison test were also performed (α =.05). Thicknesses, shades, photoinitiator type, and fillers load significantly influenced the optical and mechanical characteristics of the resin-based materials (p < 0.05). The BL3 shade ceramic provided higher values of DC, RP, FS, FM, and LT compared with the A1 shade (p < 0.05). Increasing ceramic thickness decreased the properties of the resin-based materials (p < 0.05). Generally, TPO improved mechanical properties of the resin cement compared with CQ (p < 0.05). The luting process of indirect restorations may be improved by using high molar absorptivity, more reactive, and more efficient photoinitiators such as TPO, as opposed to conventional CQ. The use of such initiator may allow the placement of thicker and more opaque indirect restorations. • TPO is a satisfactory alternative as photoinitiator (PI) to the conventional combination of camphorquinone/amine system. • Light-curable resin cements (LCRC) could be useful on luting of thicker and more opaque materials. • Physico-mechanical properties of LCRC are affected by shade and thickness of ceramic. • Fillers load have a different performance on LCRC according to the PI type used. [ABSTRACT FROM AUTHOR]

This in vitro study evaluated the influence of radiant exposure and material shade on the degree of conversion (DC) and microhardness of a resin-based composite (RBC). Sixty-four RBC specimens in shades A1E (enamel) and A4D (dentin) were light cured at a calibrated exitance of 1000 mW/cm² for 5, 10, 15, or 20 seconds, resulting in radiant exposure levels of 5. 10. 15 or 20 J/cm². The DC was determined using Fourier-transform infrared spectroscopy (n = 3 per shade per exposure level). The Knoop hardness number (KHN) was measured on the top and bottom surfaces of each specimen (n = 5 per shade per exposure level). Data were analyzed using 2- and 3-way analyses of variance and post hoc Tukey tests (α = 0.05). The RBC shade did not affect the DC (P = 0.860), and the lowest DC values were achieved with an exposure level of 5 J/cm² (P < 0.001). The shade did not affect the KHN on the top surface, but the radiant exposure level did, with the application of 5 J/cm² resulting in significantly lower values (P< 0.05). For the bottom surface, shade A1E showed significantly higher KHN values than A4D (P < 0.001). An increase in the radiant exposure led to increased DC and KHN for both shades of RBC until reaching a saturation point of 10 J/cm² for A1E and the top surface of A4D. The darker and more opaque shade was not adequately polymerized at a 2-mm depth, even when the highest radiant exposure level was applied. [ABSTRACT FROM AUTHOR]

Enhancing the degree of polymerization can mitigate the cytotoxic effects of resinous materials, as residual monomers have been identified as a significant contributor to cytotoxicity. Hence, the aim of the current research was to evaluate the influence of preheating self-adhesive cements at 39 °C on cell migration, cytotoxicity, and degree of conversion. RelyX U200, Set PP, and MaxCem Elite were subjected to Fourier Transform Infrared Spectroscopy–Attenuated Total Reflection (FTIR–ATR). Self-adhesive resin cements were applied onto an ATR device, with samples subjected to either heated or room temperature conditions, followed by photoactivation. For the cytotoxicity analysis, extracts (24 h and 7 days) were placed in contact with NIH/3T3 cells. For cell migration, images were captured of each sample until the possible closure of the cleft occurred. A two-way analysis of variance (ANOVA) was conducted to assess the effect of preheating on the degree of conversion and cell viability within the self-adhesive cements tested. A significance level of 5% was set for statistical purposes. In the results of the degree of conversion, preheating did not improve the conversion of cements (p > 0.05). For the 3-(4-5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT), preheating did not improve the results within 24 h, however, it generated positive results within 7 days for the Set PP resin cement (p < 0.05). For cell migration, high rates of cell death were found in all groups. It is concluded that preheating at 39 °C causes a positive effect only in increasing the cell viability of the Set PP resin cement and that both materials analyzed are highly cytotoxic. [ABSTRACT FROM AUTHOR]

The aim of the study was to evaluate changes in the degree of C=C conversion (DC%), chemical structure, optical properties and roughness of one-shade composites before/after photoaging. Τhe one-shade materials tested were Charisma Topaz One (CHT), Clearfil Majesty ES-2 Universal (MES), Essentia Universal (ESU) and Omnichroma (OMN), with G-aenial Anterior (CNA) serving as control. Specimens (2 mm thickness) were prepared and tested for DC% and chemical structure (ATR–FTIR spectroscopy), optical properties (L*a*b*–ΔΕ, translucency parameter–TP, opalescence parameter–OP, contrast ratio–CR and total transmittance–TT by UV–Vis spectroscopy) and roughness (Sa, Sz, Sdr, Sds and Sc by optical profilometry) before and after photoaging (Xe-arc weatherometer). Significant differences were found in DC% between top–bottom surfaces (ESU, OMN before; ESU, CNA after). Photoaging improved DC%, reduced ester peaks implying photodegradation, reduced L* (CHT, OMN, CNA), a* (CHT, CNA), b* (OMN, CNA), TP (all, except for MES), OP (only MES), CR (only MES, but an increase in CNA) and TT (CHT, OMN). OMN, CNA and MES demonstrated ΔΕ > 3.3. Photoaging significantly increased all roughness parameters in all materials, except for MES (Sz, Sdr, Sc) and OMN (Sdr). Although listed in the same group, significant differences were found in one-shade composites before and after photoaging. Several products were strongly affected by photoaging, demonstrating evidence of photodegradation, an increased roughness and color changes exceeding the clinically acceptable levels. [ABSTRACT FROM AUTHOR]

Abstract Objectives To investigate the effect of neutral 10-methacryloyloxydecyl dihydrogen phosphate salt (MDP-Na) on the dentin bond strength and remineralization potential of etch-&-rinse adhesive. Methods Two experimental etch-&-rinse adhesives were formulated by incorporating 0 wt% (E0) or 20 wt% (E20) neutral MDP-Na into a basic primer. A commercial adhesive, Adper Single Bond 2 (SB, 3 M ESPE), served as the control. Sixty prepared teeth were randomly allocated into three groups (n = 20) and bonded using either one of the experimental adhesives or SB. Following 24 h of water storage, the bonded specimens were sectioned into resin-dentin sticks, with four resin-dentin sticks obtained from each tooth for microtensile bond strength (MTBS) test. Half of the sticks from each group were immediately subjected to tensile loading using a microtensile tester at a crosshead speed of 1 mm/min, while the other half underwent tensile loading after 6-month incubation in artificial saliva (AS). The degree of conversion (DC) of both the control and experimental adhesives (n = 6 in each group) and the adsorption properties of MDP-Na on the dentin organic matrix (n = 5 in each group) were determined using Fourier-transform infrared spectrometry. Furthermore, the effectiveness of neutral MDP-Na in promoting the mineralization of two-dimensional collagen fibrils and the adhesive-dentin interface was explored using transmission electron microscopy and selected-area electron diffraction. Two- and one-way ANOVA was employed to assess the impact of adhesive type and water storage on dentin bond strength and the DC (α = 0.05). Results The addition of MDP-Na into the primer increased both the short- and long-term MTBS of the experimental adhesives (p = 0.00). No difference was noted in the DC between the control, E0 and E20 groups (p = 0.366). The MDP-Na remained absorbed on the demineralized dentin even after thorough rinsing. The intra- and extra-fibrillar mineralization of the two-dimensional collagen fibril and dentin bond hybrid layer was confirmed by transmission electron microscopy and selected-area electron diffraction when the primer was added with MDP-Na. Conclusions The use of neutral MDP-Na results in high-quality hybrid layer that increase the dentin bond strength of etch-&-rinse adhesive and provides the adhesive with remineralizing capability. This approach may represent a suitable bonding strategy for improving the dentin bond strength and durability of etch-&-rinse adhesive.

Enhancing the degree of polymerization can mitigate the cytotoxic effects of resinous materials, as residual monomers have been identified as a significant contributor to cytotoxicity. Hence, the aim of the current research was to evaluate the influence of preheating self-adhesive cements at 39 °C on cell migration, cytotoxicity, and degree of conversion. RelyX U200, Set PP, and MaxCem Elite were subjected to Fourier Transform Infrared Spectroscopy–Attenuated Total Reflection (FTIR–ATR). Self-adhesive resin cements were applied onto an ATR device, with samples subjected to either heated or room temperature conditions, followed by photoactivation. For the cytotoxicity analysis, extracts (24 h and 7 days) were placed in contact with NIH/3T3 cells. For cell migration, images were captured of each sample until the possible closure of the cleft occurred. A two-way analysis of variance (ANOVA) was conducted to assess the effect of preheating on the degree of conversion and cell viability within the self-adhesive cements tested. A significance level of 5% was set for statistical purposes. In the results of the degree of conversion, preheating did not improve the conversion of cements (p > 0.05). For the 3-(4-5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT), preheating did not improve the results within 24 h, however, it generated positive results within 7 days for the Set PP resin cement (p < 0.05). For cell migration, high rates of cell death were found in all groups. It is concluded that preheating at 39 °C causes a positive effect only in increasing the cell viability of the Set PP resin cement and that both materials analyzed are highly cytotoxic.

Objectives: To investigate the effect of neutral 10-methacryloyloxydecyl dihydrogen phosphate salt (MDP-Na) on the dentin bond strength and remineralization potential of etch-&-rinse adhesive. Methods: Two experimental etch-&-rinse adhesives were formulated by incorporating 0 wt% (E0) or 20 wt% (E20) neutral MDP-Na into a basic primer. A commercial adhesive, Adper Single Bond 2 (SB, 3 M ESPE), served as the control. Sixty prepared teeth were randomly allocated into three groups (n = 20) and bonded using either one of the experimental adhesives or SB. Following 24 h of water storage, the bonded specimens were sectioned into resin-dentin sticks, with four resin-dentin sticks obtained from each tooth for microtensile bond strength (MTBS) test. Half of the sticks from each group were immediately subjected to tensile loading using a microtensile tester at a crosshead speed of 1 mm/min, while the other half underwent tensile loading after 6-month incubation in artificial saliva (AS). The degree of conversion (DC) of both the control and experimental adhesives (n = 6 in each group) and the adsorption properties of MDP-Na on the dentin organic matrix (n = 5 in each group) were determined using Fourier-transform infrared spectrometry. Furthermore, the effectiveness of neutral MDP-Na in promoting the mineralization of two-dimensional collagen fibrils and the adhesive-dentin interface was explored using transmission electron microscopy and selected-area electron diffraction. Two- and one-way ANOVA was employed to assess the impact of adhesive type and water storage on dentin bond strength and the DC (α = 0.05). Results: The addition of MDP-Na into the primer increased both the short- and long-term MTBS of the experimental adhesives (p = 0.00). No difference was noted in the DC between the control, E0 and E20 groups (p = 0.366). The MDP-Na remained absorbed on the demineralized dentin even after thorough rinsing. The intra- and extra-fibrillar mineralization of the two-dimensional collagen fibril and dentin bond hybrid layer was confirmed by transmission electron microscopy and selected-area electron diffraction when the primer was added with MDP-Na. Conclusions: The use of neutral MDP-Na results in high-quality hybrid layer that increase the dentin bond strength of etch-&-rinse adhesive and provides the adhesive with remineralizing capability. This approach may represent a suitable bonding strategy for improving the dentin bond strength and durability of etch-&-rinse adhesive. [ABSTRACT FROM AUTHOR]

Objectives: The first aim of this study was to determine whether there is a difference in degree of conversion (DC) of touch-cure cements polymerized by self-curing with adhesive or dual-curing under reduced light. The second aim was to compare interfacial adaptation of zirconia restoration cemented using touch-cure cements self-cured or dual-cured by reduced light. Methods: The DC of touch-cure resin cements with adhesive was measured continuously using Fourier transform infrared spectrometry. Experimental groups differed depending on touch-cure cement. Each group had three subgroups of polymerization method. For subgroup 1, the DC was measured by self-curing. For subgroups 2 and 3, the DCs were measured by dual-curing with reduced light penetrating 3 mm and 1 mm zirconia blocks, respectively. For interfacial adaptation evaluation, Class I cavity was prepared on an extracted third molar, and zirconia restoration was fabricated. The restoration was cemented using the same cement. Groups and subgroups for interfacial adaptation were the same as those of the DC measurement. After thermo-cycling, interfacial adaptation at the tooth-restoration interface was evaluated using swept-source optical coherence tomography imaging. Results: The DC of touch-cure cement differed depending on the measurement time, resin cement, and polymerization method (p < 0.05). Interfacial adaptation was different depending on the resin cement and polymerization method (p < 0.05). Conclusion: For touch-cure cement, light-curing with higher irradiance presented a higher DC and superior interfacial adaptation than light-curing with lower irradiance or self-curing. Clinical relevance: Although some adhesives accelerate the self-curing of touch-cure cement, light-curing for touch-cure cement is necessary for zirconia cementation. [ABSTRACT FROM AUTHOR]

Purpose: The main aim of the present study was to carry out a scoping review on the differences in degree of conversion of monomers regarding several types resin cements, indirect restorative materials, and light-curing procedures used in dentistry. Method: A bibliographic review was performed on PubMed using the following search items: “degree of conversion” OR “filler” AND “resin cement” OR “inorganic cement” AND “organic” OR “radiopacity” OR “refractive” OR “transmittance” OR “type” AND “resin composite.” The search involved articles published in English language within the last thirteen years. A research question has been formulated following the PICO approach as follow: “How different is the degree of conversion of monomers comparing several types of resin-matrix cements?”. Results: Within the 15 selected studies, 8 studies reported a high degree of conversion (DC) of the organic matrix ranging from 70 up to 90% while 7 studies showed lower DC values. Dual-cured resin-matrix cements revealed the highest mean values of DC, flexural strength, and hardness when compared with light- and self-polymerized ones. DC mean values of resin-matrix cements light-cured through a ceramic veneer with 0.4 mm thickness were higher (~ 83%) than those recorded for resin-matrix cements light-cured through a thicker ceramic layer of 1.5 mm (~ 77%). Conclusions: The highest percentage of degree of conversion of monomers was reported for dual-cured resin-matrix cements and therefore both chemical and light-induced pathways promoted an enhanced polymerization of the material. Similar degree of conversion of the same resin-matrix cement were recorded when the prosthetic structure showed a low thickness. On thick prosthetic structures, translucent materials are required to allow the light transmission achieving the resin-matrix cement. Clinical relevance: The chemical composition of resin-matrix cements and the light-curing mode can affect the polymerization of the organic matrix. Thus, physical properties of the materials can vary leading to early clinical failures at restorative interfaces. Thus, the analysis of the polymerization pathways of resin-matrix cements is significantly beneficial for the clinical performance of the restorative interfaces. [ABSTRACT FROM AUTHOR]

Aims: To evaluate hydroxyapatite-silver (HA-Ag) hybrid nanoparticles (NPs), as an antibacterial agent when integrated in self-etch (SE) adhesive. Blue light activated HA-Ag hybrid NP incorporation on mechanical properties, degree of conversion (DC), and microtensile bond strength (lTBS). Method: Eighty primary molar teeth have carious lesions reaching the dentin but not involving the pulp. The infected dentin was removed and carious-affected dentin (CAD) was preserved. Forty samples were inoculated with Streptococcus mutans. All primary teeth (n = 80) were allocated into four groups based on the incorporation of HAAg hybrid NPs in different concentrations (0%, 1%, 5%, and 10%). Group 1: 0% HA-Ag hybrid NPs + Clearfil SE bond primer, group 2: 1% HA-Ag hybrid NPs + Clearfil SE bond primer, group 3: 5 wt% HA-Ag NPs + Clearfil SE bond primer, and group 4: 10 wt% HA-Ag NPs + Clearfil SE bond primer. The survival rate assessment of S. mutans was conducted on 40 inoculated samples. On the remaining primary teeth (n = 40), Clearfil SE bonding agent was applied uniformly via a blue light source. The composite buildup was performed on the samples and lTBS and failure analysis assessed. Fourier transform infrared spectroscopy was performed to assess DC. Survival rates of S. mutans and lTBS among the tested groups were compared using ANOVA and Tukey post hoc analysis. Results: 10 wt % HA-Ag NPs + Clearfil SE bond primer exhibited the highest level of antibacterial efficacy (0.14 -- 0.02 CFU/mL) against S. mutans. The highest lTBS (18.38 - 0.78MPa) at the composite/CAD interface was in group 2 (1 wt % HA-Ag NPs + Clearfil SE bond primer + Clearfil SE bonding agent + activation with a blue light source). The highest DC was observed in the control group with Clearfil SE bond primer + Clearfil SE bonding agent + activationwith a blue light source. Conclusion: 1 wt% HA-Ag hybrid NPs showed enhanced antibacterial effectiveness, DC, and bond strength of the SE adhesive to the primary CAD. [ABSTRACT FROM AUTHOR]

To investigate the flexural strength (FS), elastic modulus (E), Martens hardness (HM), water sorption (w sp), water solubility (w sl) and degree of conversion (DC) of 3D-printed, milled and injection molded splint materials. Specimens (N = 1140) were fabricated from five 3D-printed (GR-22 flex, GR-10 guide, ProArt Print Splint clear, V-Print Splint, V-Print Splint comfort), five milled (BioniCut, EldyPlus, ProArt CAD Splint clear, Temp Premium Flexible, Thermeo) and two injection molded (PalaXPress clear, Pro Base Cold) materials. FS, E, HM, w sp , w sl and DC were tested initially (24 h, 37 °C, H 2 O), after water storage (90 d, 37 °C, H 2 O) as well as after thermal cycling (5000 thermal cycles, 5/55 °C). Data were analyzed with Kolmogorov-Smirnov, Kruskal- Wallis, Mann-Whitney U test and Spearman's correlation (p < 0.05). Initially, the mean flexural strength values ranged from 1.9 to 90.7 MPa for printed, 3.8 to 107 MPa for milled and 99.7 to 102 MPa for injection molded materials. The initial mean elastic modulus values were 0.0 to 2.4 GPa for printed, 0.1 to 2.7 GPa for milled and 2.8 GPa for injection molded materials. The initial mean Martens hardness values were 14.5 to 126 N/mm2 for printed, 50.2 to 171 N/mm2 for milled and 143 to 151 N/mm2 for injection molded materials. Initially, the mean water sorption values ranged from 23.1 to 41.2 μg/mm3 for printed, 4.5 to 23.5 μg/mm3 for milled and from 22.5 to 23.3 μg/ mm3 for injection molded materials. The initial mean water solubility values ranged from 2.2 to 7.1 μg/mm3 for printed, 0.0 to 0.5 μg/mm3 for milled and 0.1 to 0.3 μg/mm3 for injection molded materials. After water storage and thermal cycling most of the values decreased and some increased. The mean DC values ranged initially from 72.3 to 94.5 %, after water storage from 74.2 to 96.8 % and after thermal cycling from 75.6 to 95.4 % for the printed materials. The mechanical and physical properties of printed, milled and injection molded materials for occlusal devices vary and are influenced by aging processes. For clinical applications, materials need to be chosen according to the specific indications. [ABSTRACT FROM AUTHOR]

This study aimed to assess the key physico-mechanical properties and bonding performance of orthodontic adhesives with graphene addition for bonding a fixed retainer. Transbond LR (3M) and Transbond LV (3M) with no graphene were set as the control groups. Graphene was added into LR and LV at concentrations of 0.01 wt%, 0.05 wt% and 0.1 wt%. The stickiness of the uncured samples (n = 5) and real-time degree of conversion (DC) of the samples (n = 3) were measured over a 24-h period using Fourier-transform infrared spectroscopy. The hardness and other mechanical parameters, including the Martens hardness (HM), indentation modulus (EIT), elastic index (ηIT) and creep (CIT), were measured (n = 5). To measure the shear bond strength (SBS), adhesive composites were applied using a mold to bond the retainer wire to the lingual surfaces of bovine incisors (n = 10). Fracture modes subsequent to the SBS test were examined under light microscopy. Statistical analysis was conducted using ANOVA and Tukey tests (α = 0.05). In the LR groups, the LR + 0.01 showed the highest SBS (12.6 ± 2.0 MPa) and HM (539.4 ± 17.9 N/mm2), while the LV + 0.05 (7.7 ± 1.1 MPa) had the highest SBS and the LV + 0.1 had the highest HM (312.4 ± 17.8 N/mm2) among the LV groups. The most frequent failure mode observed was adhesive fracture followed by mixed fracture. No statistical difference was found between the graphene-added groups and the control groups in terms of the EIT, ηIT and CIT, except that the CIT was significantly lower in the LR + 0.01 than in the control group. Graphene addition had no significant adverse effect on the stickiness and DC of both LR and LV. [ABSTRACT FROM AUTHOR]

To incorporate different concentrations of Al2O9Zr3 (1%, 5%, and 10%) nanoparticles (NP) into the ER adhesive and subsequently assess the impact of this addition on the degree of conversion, μTBS, and antimicrobial efficacy. The current research involved a wide‐ranging examination that merged various investigative techniques, including the application of scanning electron microscopy (SEM) for surface characterization of NP coupled with energy‐dispersive x‐ray spectroscopy (EDX), Fourier‐transform infrared (FTIR) spectroscopy, μTBS testing, and microbial analysis. Teeth were divided into four groups based on the application of modified and unmodified three‐step ER adhesive primer. Group 1 (0% Al2O9Zr3 NPs) Control, Group 2 (1% Al2O9Zr3 NPs), Group 3 (5% Al2O9Zr3 NPs), and Group 4 (10% Al2O9Zr3 NPs). EDX analysis of Al2O9Zr3 NPs was performed showing elemental distribution in synthesized NPs. Zirconium (Zr), Aluminum (Al), and Oxides (O2). After primer application, an assessment of the survival rate of Streptococcus mutans was completed. The FTIR spectra were analyzed to observe the characteristic peaks indicating the conversion of double bonds, both before and after the curing process, for the adhesive Etch and rinse containing 1,5,10 wt% Al2O9Zr3 NPs. μTBS and failure mode assessment were performed using a Universal Testing Machine (UTM) and stereomicroscope respectively. The μTBS and S.mutans survival rates comparison among different groups was performed using one‐way ANOVA and Tukey post hoc (p =.05). Group 4 (10 wt% Al2O9Zr3 NPs + ER adhesive) specimens exhibited the minimum survival of S.mutans (0.11 ± 0.02 CFU/mL). Nonetheless, Group 1 (0 wt% Al2O9Zr3 NPs + ER adhesive) displayed the maximum surviving S.mutans (0.52 ± 0.08 CFU/mL). Moreover, Group 2 (1 wt% Al2O9Zr3 NPs + ER adhesive) (21.22 ± 0.73 MPa) samples displayed highest μTBS. However, the bond strength was weakest in Group 1 (0 wt% Al2O9Zr3 NPs + ER adhesive) (14.13 ± 0.32 MPa) study samples. The etch‐and‐rinse adhesive exhibited enhanced antibacterial activity and micro‐tensile bond strength (μTBS) when 1% Al2O9Zr3 NPs was incorporated, as opposed to the control group. Nevertheless, the incorporation of Al2O9Zr3 NPs led to a decrease in DC. Research Highlights: 10 wt% Al2O9Zr3 NPs + ER adhesive specimens exhibited the minimum survival of S.mutans.1 wt% Al2O9Zr3 NPs + ER adhesive samples displayed the most strong composite/CAD bond.The highest DC was observed in Group 1: 0 wt% Al2O9Zr3 NPs + ER adhesive. [ABSTRACT FROM AUTHOR]

Although self-adhesive resin cements are convenient and less technique-sensitive materials for dental clinicians, they exhibit a lower degree of conversion due to acidic components in their composition. Supplementation of the initiator, accelerator, and activator in self-adhesive resin cements has been suggested to compensate for the lower degree of conversion. This study aimed to evaluate the effects of different combinations of self-curing initiators, self-curing activators, and accelerators on the degree of conversion (DC) of self-adhesive resin cements. A dual-cured self-adhesive resin was prepared using six combinations of initiators, activators, and accelerators. The change in the DC over time was evaluated with and without light curing. The film thickness, flow properties, and cytotoxicity of each formulation were assessed. The results showed that all supplemental components had an effect on increasing the DC, but a greater increase in the DC was observed in the following order: activator, accelerator, and initiator. The cytotoxicity of the resin cements was related to the DC values, as resin cements with lower DC values exhibited higher cytotoxicity. The film thickness met the ISO standards for all groups. The results suggest that utilizing an activator is the most effective approach to enhance the DC in self-adhesive resin cement and that cytotoxicity tended to increase with lower DC values, whereas film thickness and flow properties demonstrated no correlation with DC values. [ABSTRACT FROM AUTHOR]