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• The amine-free dual-activated resin cement demonstrated improved color stability over the traditional one. • The amine-free and the pre-heated composite presented the highest color stability when considering the CIEDE2000 parameter. • The pre-heated composite presented the highest color stability when considering the CIELAB parameter. To determine the curing potential and color stability of resin-based luting materials for aesthetic restorations. Four resin-based luting agents were tested: traditional dual-activated resin cement (RelyX ARC, ARC), amine-free dual-activated resin cement (RelyX Ultimate, ULT), light-activated resin cement (RelyX Veneer, VEN), and pre-heated restorative resin composite (Filtek Supreme, PHC). Degree of C = C conversion was determined by infrared spectroscopy (n = 3) with direct light exposure or with interposition of 1.5-mm-thick ceramic (e.max Press HT) between the luting material and light. The curing potential considered the ratio between these two scenarios. Color difference (n = 6) was determined by CIELAB (Δ E ab) and CIEDE2000 (Δ E 00) methods, by spectrophotometer measurements made 24 h after photoactivation and 90 days after storage in water. Data was submitted to ANOVA and Tukey's test (α = 0.05). The luting agents affected both conversion and color stability. With ceramic, ARC produced the highest conversion among the tested groups (75 ± 1%) and the pre-heated composite (PHC) the lowest one (51 ± 3%), but the curing potential was similar for all materials. ULT produced lower Δ E ab than ARC. PHC presented the lowest color difference when considered both CIELAB and CIE2000 methods (Δ E ab 2.1 ± 0.4; Δ E 00 1.6 ± 0.2). All luting strategies presented high curing potential. Amine-free dual-activated material was able to reduce color difference than that formulated with the amine component. Pre-heated composite produced the least color variation after storage. [ABSTRACT FROM AUTHOR]

Patients with challenging prosthodontic conditions require rehabilitation with a biological, functional, and esthetic approach. When one or more teeth are badly discolored, their restoration is problematic because poor appearance affects not only the crown but also the periodontal tissues. This clinical report describes a complex esthetic rehabilitation with conservative tissue management and ceramic restorations. Subepithelial connective tissue graft surgery and the replacement of a cast metal post with a glass fiber post addressed the problem of a discolored maxillary central incisor. The discolored right maxillary incisor was restored with a combination of a medium-opaque, lithium-disilicate ceramic coping to mask the dark root and to approximate the color of the other incisors. Subsequently, 6 ceramic veneers were placed. A knowledge of the materials' optical properties and adhesion possibilities helped solve this complex problem. [ABSTRACT FROM AUTHOR]

Abstract: Objectives: The purpose of this study was to evaluate the reactivity and polymerization kinetics behavior of a model dental adhesive resin with water-soluble initiator systems. Methods: A monomer blend based on Bis-GMA, TEGDMA and HEMA was used as a model dental adhesive resin, which was polymerized using a thioxanthone type (QTX) as a photoinitiator. Binary and ternary photoinitiator systems were formulated using 1mol% of each initiator. The co-initiators used in this study were ethyl 4-dimethylaminobenzoate (EDAB), diphenyliodonium hexafluorophosphate (DPIHFP), 1,3-diethyl-2-thiobarbituric acid (BARB), p-toluenesulfinic acid and sodium salt hydrate (SULF). Absorption spectra of the initiators were measured using a UV–Vis spectrophotometer, and the photon absorption energy (PAE) was calculated. The binary system camphorquinone (CQ)/amine was used as a reference group (control). Twelve groups were tested in triplicate. Fourier-transform infrared spectroscopy (FTIR) was used to investigate the polymerization reaction during the photoactivation period to obtain the degree of conversion (DC) and maximum polymerization rate (R p max) profile of the model resin. Results: In the analyzed absorption profiles, the absorption spectrum of QTX is almost entirely localized in the UV region, whereas that of CQ is in the visible range. With respect to binary systems, CQ+EDAB exhibited higher DC and values. In formulations that contained ternary initiator systems, the group CQ+QTX+EDAB was the only one of the investigated experimental groups that exhibited an value greater than that of CQ+EDAB. The groups QTX+EDAB+DPIHFP and QTX+DPIHFP+SULF exhibited values similar to those of CQ+EDAB with respect to the final DC; however, they also exhibited lower reactivity. Significance: Water-soluble initiator systems should be considered as alternatives to the widely used CQ/amine system in dentin adhesive formulations. [Copyright &y& Elsevier]

Abstract: Objectives: Since photoinitiator systems for dental resins based on camphorquinone (CQ) present color disadvantages, trimethylbenzoyl-diphenyl-phosphine oxide (TPO) has been proposed as an alternative. However, there are remaining considerations about its curing efficiency. The aims of the present investigation were: to characterize the relationship between the photoinitiator absorption spectra and the light spectrum emitted from a QTH light (absorbed power density, PDabs); to evaluate the kinetics of polymerization, and the depth of cure for filled dimethacrylate resins formulated with different photoinitiator systems. Methods: CQ+EDMAB (control); TPO and TPO+EDMAB were used in 50:50 Bis-GMA/TEGDMA resins. Photoinitiator absorption and QTH-light emission were evaluated using a spectrophotometer and kinetics of polymerization with differential scanning calorimetry (DSC) (n =3). Depth of cure was analyzed by the scraping method (n =5), as recommended by ISO4049. One-way ANOVA/Tukey''s (p <0.05) was used to analyze the results. Results: CQ presented higher PDabs than TPO (364 and 223mW/cm3, respectively). The DSC revealed that TPO and TPO+EDMAB produced a faster reaction than CQ+EDMAB. Composite formulated with CQ+EDMAB produced higher depth of cure (6.3±0.4mm) than those with TPO (4.3±0.1) or TPO+EDMAB (4.2±0.3). Significance: Although CQ presented higher PDabs than TPO, formulations containing TPO exhibited higher reactivity than that with CQ. On the other hand, materials formulated with TPO demonstrated lower depth of cure than that with CQ. Therefore, its use as an alternative photoinitiator requires further investigation, with higher concentrations. [Copyright &y& Elsevier]

Abstract: Objective: To investigate the surface integrity of solvent-challenged ormocer-matrix composites, photoactivated by different light exposure modes, through surface-hardness measurements at different periods of time; and to compare such behavior with dimethacrylate-based materials. Methods: One hundred percent ormocer-based matrix (experimental ormocer (ORM)), a commercial mixed dimethacrylate-ormocer-based matrix (Admira (ADR)) and two commercial dimethacrylate-based matrix composites (experimental controls, (Grandio (GRD) and Premise (PRE)) were evaluated. Disk specimens (4mm×2mm) were prepared from each material and light-activated using either a standard (S) or soft-start (SS) light exposure protocol with an LED-curing unit. Top, irradiated surface Knoop hardness (KHN) was measured within the following experimental groups (n =5): Group 1: immediately after exposure; Group 2: after dry and dark storage, Group 3: after storage in distilled water, and Group 4: immersion in absolute ethanol. Hardness of Groups 2–4 were measured after 7 days storage. Immediate hardness values were submitted to Student''s t-tests separately for each material. Hardness values after treatments were submitted to two-way ANOVA and Tukey''s post hoc test to compare values among different storage media and light exposure mode protocols. Comparisons among materials were described using percentage of hardness change. Statistical testing was performed at a pre-set alpha of 0.05. Results: Immediate hardness values were not affected by the light exposure mode, regardless of the material. In general, exposure mode did not significantly affect hardness after 7 days storage, regardless of storage media or material. After 7 days dry storage, hardness values increased for all materials relative to immediate testing, and decreased after water and ethanol storage, with ethanol showing the greatest effect. The experimental ormocer-based material had the lowest percentage hardness change and thus proved more resistant to solvent degradation than the other materials, regardless of the light exposure method. Significance: Irradiated surface hardness values and surface integrity were unaffected by light exposure mode, regardless of the material tested. The experimental ormocer-based material presented the least change in hardness as a result of solvent challenge than any of the commercial products: ormocer or conventional resin-based, and thus showed better surface integrity. [Copyright &y& Elsevier]

Abstract: Objectives: Stress development during the polymerization process continues to be a major factor that limits predictability and longevity of resin composite restorations. This study evaluated the effect of the photoinitiator type on the maximum rate of polymerization , stress development (final stress and maximum rate, ), degree of conversion (DC) and cross-link density (CLD) of materials containing camphorquinone (CQ), phenylpropanedione (PPD) or CQ/PPD. Materials and methods: was evaluated via differential scanning calorimetry (DSC). Contraction force measurement was assessed with a single cantilever device for 5min. The samples were subsequently tested by infrared spectroscopy (FTIR) to evaluate the DC. After, samples were soaked in ethanol to evaluate the swelling coefficient (α) as a way to estimate the CLD. The results were analyzed by one-way ANOVA and Tukey''s test (p =0.05). Results: CQ showed the highest and . PPD produced the lowest DC and the highest α. The mixture CQ/PPD produced statistically lower and than CQ alone, but similar DC and CLD. Conclusion: CQ/PPD reduced the and without a reduction in DC and CLD. Therefore, the use of alternative photoinitiator systems could be a promising way to reduce the stress developed during the composite''s polymerization without affecting the final properties. [Copyright &y& Elsevier]

Abstract: Objectives: To evaluate the effect of amine ratio (ethyl 4-dimethylaminobenzoate, EDMAB) on the maximum rate of polymerization (), degree of conversion (DC), Knoop hardness (KH), water sorption (Wsp), water solubility (Wsl) and color changes (ΔE) over time of resin composites formulated with the photoinitiators camphorquinone (CQ), phenylpropanedione (PPD) and CQ-PPD in combination. Materials and methods: Experimental resin composites were made with photoinitiator:amine ratios of 2:1, 1:1, 1:1.5 and 1:2 by weight. was evaluated with differential scanning calorimetry (DSC), DC with DSC and Fourier transformed infrared (FTIR) spectroscopy, KH with Knoop indentation, Wsp and Wsl adapted from ISO 4049; and color with a chromameter. The results were analyzed with two-way ANOVA/Tukey’s multiple comparison test (p <0.05). Results: The higher the amine ratio in the composite, the higher was DC, , and KH, and the lower was Wsl, regardless of the photoinitiator type. The use of PPD alone resulted in poorer properties than CQ and CQ-PPD. Many factors seem to affect the color changes and the b-axis data revealed that the higher the amine ratio, the higher was the +b value (yellowing) for CQ and CQ-PPD formulations. Conclusions: Higher amine ratios led to improved polymer properties, but also produced more yellowing in resin composites with CQ and CQ-PPD. The use of PPD alone was not advantageous for producing good final properties when compared to CQ and CQ-PPD. [Copyright &y& Elsevier]

Abstract: Objectives: To evaluate the degree of conversion (DC), maximum rate of polymerization (), Knoop hardness (KHN) and yellowing (b-value) of resin composites formulated with phenylpropanedione (PPD), camphorquinone (CQ), or CQ/PPD at different concentrations. The hypotheses tested were (i) PPD or CQ/PPD would produce less and yellowing than CQ alone without affecting DC and KHN, and (ii) , DC, and KHN would be directly related to the absorbed power density (PDabs). Methods: CQ/amine, PPD/amine and CQ/PPD/amine were used at low, intermediate and high concentrations in experimental composites. Photoinitiator absorption and halogen-light emission were measured using a spectrophotometer, R p with differential scanning calorimetry (DSC), DC with DSC and FTIR, KHN with Knoop indentation; and color with a chromameter. The results were analyzed with two-way analysis of variance (ANOVA)/Student–Newman–Keul''s test (p <0.05). Correlation tests were carried out between PDabs and each of DC, and KHN. Results: The PDabs increased with photoinitiator concentration and PPD samples had the lowest values. In general, maximum DC was comparable at intermediate concentration, while and KHN required higher concentrations. DC was similar for all photoinitiators, but was lower with PPD and CQ/PPD. PPD produced the lowest KHN. Yellowing increased with photoinitiator concentration. PPD did not reduce yellowing at intermediate and/or high concentrations, compared to CQ-formulations. PDabs showed significant correlations with DC, and KHN. Conclusion: PPD or CQ/PPD reduced in experimental composites without affecting the DC. The use of PPD did not reduce yellowing, but reduced KHN. DC, and KHN were dependent on PDabs. [Copyright &y& Elsevier]

Abstract: Objectives: The aim of this study was to investigate whether the ethanol concentration used would influence the outcomes obtained through softening tests when comparing light-activation modes. Methods: Disc specimens (n =20) of Filtek Z250 and Filtek Z100 (3M ESPE) were light activated by standard (S) and pulse-delay (PD) modes. Initial Knoop hardness (KHN) measurements were performed 24h after dry storage at 37°C. Half of the specimens (n =10) of each resin-composite were stored in absolute ethanol (100%) and the other half in 75% ethanol solution, for 24h at room temperature, and KHN was determined anew. Initial hardness data were submitted to Student''s t-test (p =0.05). Percentages of hardness decrease were analyzed by two-way ANOVA followed by pairwise Tukey''s test (p =0.05). The statistical analyses were performed separately for each resin-composite. Results: No statistically significant differences were observed between standard and pulse-delay modes for initial Knoop hardness values. After storage in 75% ethanol solution, KHN was decreased in all cases but no significant differences were detected between light-activation modes (Filtek Z250: PD=12.6%, S =13.5%; Filtek Z100: PD=13.5%, S =11.8%) regardless of the resin-composite tested. After absolute ethanol storage, higher decrease in KHN were observed. Samples light-activated by the PD mode (Filtek Z250=20.4% and Filtek Z100=16.9%) exhibited significantly higher percentage decrease of KHN than specimens light-activated by the standard mode (Filtek Z250=14.1% and Filtek Z100=8.8%), regardless of the resin-composite tested. Conclusion: The ethanol concentration affected the outcomes of the softening test. [Copyright &y& Elsevier]

Regular composites could produce less polymerization stress than resin cements when luting laminate veneers but there is no proper evidence to support this theory. The current study aimed to determine the degree of conversion, volumetric shrinkage, polymerization stress and the resultant elastic moduli of materials currently used for adhesive cementation and to determine possible correlations. The study considered (i) regular resin composites (Admira Fusion, Gradia, Grandioso, Palfique, Sirius Z, Viscalor and Z100) at room and pre-warmed (PW) at 69ºC, (ii) flowable composites (Sigma Flow and Grandioso Flow); (iii) solely light-activated cements (AllCem Veneer, Variolink Esthetic and RelyX Veneer); and (iv) one dual-activated resin cement (SpeedCEM). Degree of conversion (DC, n = 3) was accessed with FTIR 1 h after irradiation. Bonded-disk and Bioman II instruments were used to access polymerization shrinkage strain and shrinkage stress, respectively, for 60 min at 23 ± 1◦C (n = 3). The elastic modulus was determined by 3-point bending flexural test (n = 6). The results were submitted to analyse s of variance, Tukey's, and correlation tests. For regular composites, the pre-warming did not affect DC, shrinkage and modulus but significantly increased the stress magnitude. Correlation tests indicated a significant relationship only between stress and polymerization shrinkage (r = 0.811343). Regular composites can produce less polymerization stress than resin cements when luting laminate veneers. Polymerization stress was dependent on the shrinkage magnitude, but not on the degree of conversion nor the elastic modulus. [ABSTRACT FROM AUTHOR]

Abstract: Objectives: To evaluate (1) the influence of fluoride-containing adhesive on microtensile bond strength (μTBS) and (2) in vitro secondary caries inhibition at the resin–dentin interface after 24h and 3 months water-storage and (3) the degree of conversion of different adhesives after 24h 1 month. Methods: Flat surfaces of human teeth were ground and randomly assigned to six groups: (SBMP-24) Scotchbond Multi-Purpose control [SBMP], 24h; (SE-24) SBMP etch and primer+Clearfil SE Bond adhesive [SE], 24h; (PB-24) SBMP etch and primer+Clearfil Protect Bond adhesive [PB], 24h; (SBMP-3) SBMP, 3 months; (SE-3) SBMP+SE, 3 months; and (PB-3) SBMP+PB, 3 months. To evaluate the effect of the adhesive resin alone, all teeth were etched with 35% phosphoric acid and primed with SBMP primer prior to applying the adhesive resin. Bonded assemblies were prepared for μTBS and stored in distilled water at 37°C for 24h and 3 months. Sections of restored teeth of each group were exposed to an acid challenge. The specimens were sectioned, polished, and then observed with polarized light microscopy (PLM). Also, the degree of conversion (DC) of the adhesives was measured using Fourier Transform-Infrared spectroscopy (FTIR) at 24h and 1 month, after polymerization. Results: μTBS values obtained in MPa (24h/3m) were: (MP) 61.5±10.5/52.9±8.9, (SE) 55.5±11.8/55.6±13, and (PB) 50.3±9.9/61.0±13.6. For interface analysis by PLM, an inhibition zone (IZ) adjacent to the hybrid layer was created only when the fluoride-containing adhesive (PB) was used. The DC in percentage (24h, 1 month) were: (MP) 60.5±2.8/61.3±0.6, (SE) 69.6±1.3/70.7±0.05, and (PB) 53.1±0.4/58.3±1.6. Significance: The fluoride-containing adhesive demonstrated significant increase of bond strength values after water-storage. This material was also able to create an acid inhibition zone in dentin. There was a significant increase of degree of conversion after 1 month only for PB. [Copyright &y& Elsevier]

• Bulkfills is considered the most recent approach by the industry and have impacted the possibilities of clinical use. • Manufacturers have claimed to introduce novel technologies to achieve proper depth of cure. • The current scientific investigation demonstrated that bulkfills can be formulated by proper recombination of monomers traditionally used in the manufacture of conventional resin composites. To propose monomer formulations that show an optimal degree of conversion as a function of depth for bulk-fill applications. Four resin blends were formulated with methacrylate-based monomers: BisGMA + TEGDMA (control); BisEMA + BisGMA + TEGDMA (BisEMA-based); UDMA + BisGMA + TEGDMA (UDMA-based) and BisEMA + UDMA + BisGMA + TEGDMA (BisEMA + UDMA-based). For each material, a photoinitiating system and silanized filler particles were added. The rheological analyses were performed with a rotational rheometer using the cone/plate geometry. CIELab coordinates were assessed over black and white backgrounds using a bench spectrophotometer (SP60, X-Rite) to calculate the translucency parameter (TP) for samples with 0.5, 4, and 6 mm thickness. The degree of C C conversion (DC) was determined by infrared spectroscopy (FTIR/ATR) at 0.05 mm (top), 4, and 6 mm depths (bottom), and the bottom-to-top ratio was considered. A broad spectrum–based LED was used for light activation. Analysis of variance and Tukey's test (95%) were performed on the results. The materials tested showed pseudoplastic and thixotropic behavior and a predominance of viscous effects over elastics. The control resin yielded the lowest viscosity for the entire shear rate investigated, followed by the BisEMA-based, BisEMA + UDMA-based, and UDMA-based group, which had the highest viscosity. The UDMA-based material showed the lowest TP as a function of thickness. Both the materials' formulations and depths significantly influenced the DC. The UDMA-based group promoted the highest DC ​​on the top (71 ± 1%) and 4 mm depth (68 ± 1%) but exhibited lower bottom-to-top DC ratio. The BisEMA + UDMA-based material promoted the highest bottom-to-top DC ratio at 4 mm (99%) and 6 mm (97%). The resin matrix interferes in the rheological behavior, translucency parameter, and polymerization capacity as a function of depth. The material formulated with the addition of UDMA and BisEMA demonstrated the highest curing potential as a function of depth and can be useful for bulk-fill applications. [ABSTRACT FROM AUTHOR]

Abstract The aim of this study was to determine the influence of the monomer type and photoinitiator systems on the degree of C=C conversion and color stability of model self-adhesive flowable composites (SAFCs). Three sets of flowable composites were formulated varying the monomer type: set 1 (control), with bisphenol-A glycidyl methacrylate and triethylene glycol dimethacrylate (BisGMA/TEGDMA) at 50/50 wt%; set 2, with BisGMA/TEGDMA/bis[2(methacryloyloxy)ethyl]phosphate (2MP) at 30/30/40 wt%; and set 3, with BisGMA/TEGDMA/4-ethyl-methacryloxy-trimetilato anhydride (4-META) at 30/30/40 wt%. For each set, different initiator systems were added: camphorquinone (CQ) + ethyl-4-dimethylamino benzoate (EDMAB); diphenyl(2,4,6-trimethylbenzoyl)-phosphine oxide (TPO); phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (BAPO); and the combinations CQ + EDMAB + TPO and CQ + EDMAB + BAPO. Degree of C=C conversion was determined by Fourier-transformed infrared spectroscopy with an attenuated total reflectance device (ATR-FTIR). The color stability was determined by CIE 00 color difference formula (∆ E * 00), after water (T 1) and coffee (T 2) storages for 30 days. Data was submitted to two-way analysis of variance (ANOVA) followed by Student-Newman-Keuls test (α = 0.05). Degree of conversion and color stability were dependent on the resin matrix composition and the photoinitiator system. The 2MP-based set showed the highest DC, but also the poorest color stability. For the 4-META-base set, TPO and BAPO produced the highest degree of C=C conversion. The use of BAPO produced the best color stability for the acidic-monomer-based sets. [ABSTRACT FROM AUTHOR]

Objective This study has investigated the influence of BisGMA, BisEMA, BisEMA 30, and two UDMA-based monomers (UDMA and Fit 852), with TEGDMA as co-monomer, on the degree of conversion, water sorption, water solubility, and optical properties of experimental dental composites. Methods Materials were formulated at 70/30 molar rations using BisGMA, BisEMA, BisEMA 30, UDMA or FIT 852, as base monomers, combined with TEGDMA. 60 wt% of silanated-glass particles was added. Degree of conversion (DC) and polymerization kinetics were monitored using Fourier-transformed infrared spectroscopy in the near-IR range. Water sorption (Wsp) and solubility (Wsl) were assessed using mass variation after 60 days water storage. Color was evaluated using a digital spectrophotometer, applying the CIELab parameters 24 h after dry storage and 60 days after water immersion to calculate ΔE values. All data were analyzed using ANOVA and Tukey’s test (pre-set alpha = 0.05). Results The BisGMA-based co-monomer mixture presented the lowest DC (62 ± 1%), whereas BisEMA 30 had the highest DC value (95 ± 2%). The highest Wsp was observed for BisEMA 30 (12.2 ± 0.8%), and the lowest for BisEMA (0.4 ± 0.1%). BisEMA has shown the lowest Wsl (0.03 ± 0.01%) and BisEMA 30 the highest one (0.97 ± 0.1%). The ΔE values showed that BisEMA 30 (7.3 color units) and Fit 852 (3.8 color units) altered the color stability providing ΔE > 3.3, which is considered clinically unacceptable. Conclusions The chemical composition and structure of the base monomer influenced the degree of conversion, water sorption, water solubility, and color stability. Considering the overall results, it is possible to state that the base monomer BisEMA mixed with the co-monomer TEGDMA presented the best performance in terms of all the parameters tested. Significance The resin matrix composition might influence physical property degradation processes and color stability of dental resin composites. Formulations based on BisEMA seem most promising for materials’ development. [ABSTRACT FROM AUTHOR]

Objectives: To investigate the influence of nanoscale inorganic content over optical and surface properties of model composites before and after ageing. Methods: Three model composites were formulated with silica fillers in nanoscale of 7 nm (G1), 12 nm (G2) and 16 nm (G3), at 45.5% by weight in a matrix of BisGMA/TEGDMA 1:1. Color coordinates (CIE L*a*b* parameters), color difference (ΔE*), translucency parameter (TP), surface gloss (SG) and surface roughness (SR) were measured before and after ageing procedures of immersion in water and toothbrush abrasion. Surface hardness (SH) were evaluated before and after immersion in absolute ethanol. Results were submitted to twoway ANOVA followed by Tukey's post hoc test performed at a pre-set alpha of 0.05. Results: Regarding CIE L*a*b* parameters, a darkening, a redness and a blueness effect, were respectively detected after water storage for all groups. Smaller filler sizes (G1) had the highest CIE b* values, whereas medium (G2) ( p < 0.05) had higher values than larger fillers (G3) ( p < 0.05) either before or after water immersion. Toothbrush abrasion did not produce any significant effect on CIE a* and CIE b* values, however increased CIE L*, decreased TP in addition to produce rougher and matte surfaces in all groups. Filler size did not influence ΔE* ( p > 0.05), although a tendency towards lower values in smaller filler materials was observed. Ageing after immersion in absolute ethanol decreased SH for all model composites. Conclusions: Filler sizes and ageing procedures influenced the optical and surface properties of the nanostructured composites evaluated in this study. Clinical significance: Filler size influenced optical and surface properties of resin composites. Materials containing smaller filler size offered improved optical stability and surface properties that can lead to longer maintenance of the restoration's appearance in the oral environment. [ABSTRACT FROM AUTHOR]

Objectives: The aim of this study was to formulate materials with high color stability and reduced degradation by using photoinitiator systems derived from phosphine oxides alternative to the traditional camphorquinone (CQ)/amine system. Methods: Materials were formulated with the monomers BisGMA and TEGDMA as organic matrix. The photoinitiators tested were CQ+ amine (EDMAB), phenylbis(2,4,6-trimethylben-zoyl)phosphine oxide (BAPO), BAPO + EDMAB, diphenyl(2,4,6-trimethylbenzoyl)-phosphine oxide (TPO) and TPO + EDMAB. A 60% mass of silanated glass filler particles was added. Degree of CC conversion was evaluated by Fourier-transformed infrared spectroscopy 10 min after photopolymerization. The color properties were evaluated by a digital spectrophotometer, applying the CIELab parameters, either before photoactivation, immediately after photoacti-vation, 24 h after dry storage, and one month after water immersion. Water sorption and solubility were assessed by mass gain or loss after storage in water for 30 days. Data were analyzed using ANOVA and Tukey's test (5%). Results: Degree of conversion did not differ statistically among all the tested formulations. Regarding color, only groups with TPO presented satisfactory color stability after one month of water storage (ΔE < 3.3). Water sorption and water stability did not differ among the groups. Conclusions: Degree of conversion, water sorption and water solubility did not differ among all the tested groups. The TPO-based groups were the only materials with satisfactory color stability after one month of water storage. [ABSTRACT FROM AUTHOR]

Abstract: Objective: To evaluate the influence of tetrahydrofuran (THF) on the resin-to-dentin microtensile bond strength (μTBS) after water storage, for 24h and 6 months, and to compare its behavior with that of traditional solvents. Methods: Seven versions of monomer/solvent mixtures (primers) were prepared using the following solvent and water combinations: (1) THF, (2) acetone, (3) ethanol, (4) water, (5) THF/water, (6) acetone/water and (7) ethanol/water. An experimental adhesive resin was also synthesized to compare adhesive systems with the different primers. Forty-two bovine incisors, randomly separated into seven groups, had their superficial coronal dentin exposed. After acid-etching and rinsing, the excess water was removed from the surface with absorbent paper. Each experimental primer was applied with agitation (30s) followed by a mild air stream (10s). The experimental adhesive resin was applied and light-activated (20s). Resin composite restorations were constructed incrementally. Restored teeth were stored in distilled water at 37°C (24h) and sectioned to obtain sticks with an area of 0.5mm2. Half the specimens were subjected to the μTBS test immediately after being cut and the other half were tested after 6 months of water storage. Data (MPa) were analyzed by two-way ANOVA (solvent type and storage time as factors) and Tukey–Kramer''s test at α =0.05. Results: Factors and interaction showed a statistical effect. After 6 months storage, acetone groups and primers containing THF showed similar μTBS to initial means. Significance: THF seems to be a promising solvent for use in dental adhesive systems, maintaining bond strength on dentin substrate after storage. [Copyright &y& Elsevier]

Objective To establish the relationship between photoinitiator system and nanofiller size on the optical properties and cure efficiency of model composites. Methods Model composites based on BisGMA/TEGDMA (60:40 mol%) were loaded with 40 wt% of 7 nm or 16 nm-sized filler particles. One of the following photoinitiator systems was added: camphorquinone (CQ) associated with an amine (EDMAB), monoacylphosphine oxide (TPO), or bysacylphosphine oxide (BAPO). The optical properties of disk-shaped specimens were measured 24 h after curing and repeated after storage in water for 90 days and coffee for 15 days. A large spectrum LED unit (Bluephase G2, Ivoclar Vivadent) was used for photoactivation. CIE L * a * b * parameters, color difference (Δ E ), and translucency parameter (TP) were calculated. Knoop hardness readings were taken at top and bottom composite surfaces. Cure efficiency was determined by bottom/top hardness ratio. Data were statistically analyzed at α = 0.05 significance level. Results Composites formulated with 16 nm particles had higher CIE L * than those with 7 nm particles in all storage conditions. BAPO-based composites generally had lower CIE a * than the other composites. The group TPO + 16 nm before storage and all groups with 16 nm-sized particles after storage had lower CIE b * (i.e. lower degree of yellowing) than the other groups. TPO-based materials had higher color stability. The cure efficiency was not significantly affected by photoinitiator system or particle size. CQ + 7 nm had the lowest and BAPO + 16 nm the highest hardness values. Significance Combination of photoinitiator system and filler particle size might affect the optical properties of composites, with low influence on cure efficiency. [ABSTRACT FROM AUTHOR]