Viscosity and stickiness of dental resin composites at elevated temperatures

ObjectiveTo investigate the influence of pre-heating different classes of dental resin composites on viscosity and stickiness at five different temperatures.MethodsSix flowable, five conventional packable, and one thermo-viscous bulk-fill resin composites were heated up to 54 °C in a plate-plate rheometer to determine their complex viscosity. Normal force measurements were carried out for the six packable materials to determine the unplugging force and unplugging work (stickiness) over the same temperature range. Data were analyzed using Kolmogorov–Smirnoff test, one-way ANOVA and Tukey Post Hoc test with α = 0.05 as level of significance.ResultsAt 23 °C packable composites showed viscosity between 6.75 and 19.14 kPa s, while flowable composites presented significantly lower viscosities between 1.31 and 2.20 kPa s. Pre-heating led to a drop of 30–82% in the viscosity of packable materials. The thermo-viscous material dropped to the level of flowables at 45 and 54 °C thus behaving as a packable composite at room temperature with flowable-like viscosity at higher temperatures. No statistically significant differences for viscosity were observed among flowable composites at any temperature.The unplugging force decreased for packable composites, while their unplugging work generally increased at elevated temperature. At 23 °C unplugging force was measured between 7.50 and 19.18 N, while pre-heating up to 54 °C led to values between 2.9 and 6.2 N. Regarding unplugging work at 23 °C the calculated values were between 3.0 and 8.9 × 10^?3 J and at 54 °C between 8.8 and 13.0 × 10^?3 J.SignificancePre-heating significantly reduced viscosity of highly viscous resin composites, while no influence was shown for flowable composites. In general stickiness, measured as unplugging work, increased at elevated temperatures. The thermo-viscous material showed low viscosity comparable to flowable composites at 45 and 54 °C, yet its stickiness did not increase significantly compared to the values at 23 °C.     

A method for assessing force/work parameters for stickiness of unset resin-composites

Objectives

To evaluate the stickiness of unset resin-composites, at different speeds and temperatures, in terms of maximum probe separation-force (F_max) and work-of-separation (W_s).

Materials and methods

Eight commercial light-cured resin-composites were selected. Each material was placed in a cylindrical mold (φ = 7 mm × 5 mm depth) held at 25 °C or 37 °C. The maximum force (F_max, N) and work probe separation (W_s, N mm) were measured by using a texture analyzer to register force/displacement. A flat-ended stainless-steel probe (φ = 6 mm) was mechanically lowered onto and into the surface of the unset sample. When a ‘trigger’ compressive force of 0.05 N was registered, data-acquisition commenced. Descent continued until a compressive force of 1 N was reached, which was held constant for 1 s. Then the probe was moved vertically upward at constant speed. This was varied over the range 2, 4, 6 and 8 mm/s. The tensile force produced on the probe by the sticky resin-composite was plotted against displacement and the maximum value was identified (F_max). W_s was obtained as the integrated area. Data was analyzed by multivariate ANOVA and multiple pair wise comparisons was done by using a Tukey post hoc test to establish homogenous subsets (at p = 0.05).

Results

F_max and W_s were taken as potential measures of stickiness. They ranged from 0.47 to 3.68 N and from 0.11 to 2.84 N mm, respectively. Multivariate ANOVA showed a strong interaction of withdrawal speed, temperature and materials on both F_max and W_s (p < 0.001).

Conclusion

F_max and W_s are useful parameters for characterizing the handling-stickiness of resin-composite materials, additional to previously reported stickiness-strain or ‘peak-height’. The resin-composites investigated could be differentiated, mostly showing increases in F_max and W_s stickiness with increased temperature and probe-withdrawal speed.     

Post-curing in dental resin-based composites

Objective

To determine the post-curing in six commercial contemporary resin-based composites (RBCs) using axial shrinkage, the degree of conversion, and Vickers hardness.

Investigating the limits of resin-based luting composite photopolymerization through various thicknesses of indirect restorative materials

Objective

To determine the limitations of using light-curable resin-based luting composites (RBLCs) to bond indirect ceramic/resin-composite restorations by measuring light transmittance through indirect restorative materials and the resulting degree of conversion (DC) of the luting-composites placed underneath.

Effect of exposure time and pre-heating on the conversion degree of conventional,bulk-fill,fiber reinforced and polyacid-modified resin composites

Objective

To determine the degree of conversion (DC) of different type of resin-based composites (RBC) in eight-millimeter-deep clinically relevant molds, and investigate the influence of exposure time and pre-heating on DC.

Degree of conversion and in vitro temperature rise of pulp chamber during polymerization of flowable and sculptable conventional,bulk-fill and short-fibre reinforced resin composites

ObjectiveDetermine the degree of conversion (DC) and in vitro pulpal temperature (PT) rise of low-viscosity (LV) and high-viscosity (HV) conventional resin-based composites (RBC), bulk-fill and short-fibre reinforced composites (SFRC).MethodsThe occlusal surface of a mandibular molar was removed to obtain dentine thickness of 2 mm above the roof of the pulp chamber. LV and HV conventional (2 mm), bulk-fill RBCs (2–4 mm) and SFRCs (2–4 mm) were applied in a mold (6 mm inner diameter) placed on the occlusal surface. PT changes during the photo-polymerization were recorded with a thermocouple positioned in the pulp chamber. The DC at the top and bottom of the samples was measured with micro-Raman spectroscopy. ANOVA and Tukey’s post-hoc test, multivariate analysis and partial eta-squared statistics were used to analyze the data (p < 0.05).ResultsThe PT changes ranged between 5.5–11.2 °C. All LV and 4 mm RBCs exhibited higher temperature changes. Higher DC were measured at the top (63–76%) of the samples as compared to the bottom (52–72.6%) in the 2 mm HV conventional and bulk-fill RBCs and in each 4 mm LV and HV materials. The SFRCs showed higher temperature changes and DC% as compared to the other investigated RBCs. The temperature and DC were influenced by the composition of the material followed by the thickness.SignificanceExothermic temperature rise and DC are mainly material dependent. Higher DC values are associated with a significant increase in PT. LV RBCs, 4 mm bulk-fills and SFRCs exhibited higher PTs. Bulk-fills and SFRCs applied in 4 mm showed lower DCs at the bottom.     

Degree of conversion of bulk-fill compared to conventional resin-composites at two time intervals

Objective

The purpose of this study was to assess the degree of conversion (DC) over time, using FTIR spectroscopy for bulk-fill flowable resin composite materials compared to conventional flowable and regular resin composite materials.

Methods

Eight resin composites were investigated including flowable bulk-fill materials SureFil SDR (SDR), Venus bulk-fill (VBF), x-tra base (XB), and Filtek Bulk Fill (FBF). Conventional flowable and regular composite materials included: Venus Diamond flow (VDF), Grandioso flow (GRF), Venus Diamond (VD), and Grandioso (GR). Degree of conversion (DC) was assessed by Fourier transform infrared spectroscopy using attenuated total reflectance technique. DC was measured for samples immediately post-cure (n = 3), and after 24 h storage period at 37 °C (n = 3). Results were analysed using one-way analysis of variance (ANOVA), Bonferroni post hoc test, and independent-samples t-test at α = 0.05 significance level.

Results

Immediately post-cure, the mean DC values of the different materials were in the following order: GRF > VDF > SDR > VBF > XB > GR > FBF < VD and ranged from 34.7 to 77.1%. 24 h post-cure, DC values were in the following order: GRF > VBF > VD > SDR > VDF > GR > XB < FBF and ranged from 50.9 to 93.1%. GRF showed significantly higher DC values than all other materials at both time intervals while XB and FBF showed significantly lower values at 24 h post-cure.

Significance

The 24 h post-cure DC values of the bulk-fill composites SDR and VBF are generally comparable to those of conventional composites studied; however, the 24 h post-cure DC values of XB and FBF were lower compared to the other materials.     

High irradiance curing and anomalies of exposure reciprocity law in resin-based materials

Objectives

The aim of this work was to investigate the effect of high irradiance curing on resultant degree of conversion of ‘flowable’ resin composites and their counterpart higher viscosity paste materials.

Methods

Five commercial flowable materials (Venus; Heraeus Kulzer, Synergy D6; Coltene, Premise; Kerr, Grandio; Voco and Gradia; GC Corp) and their counterpart higher viscosity restorative versions were tested. Specimens were cured with a halogen Swiss Master Light (EMS, Switzerland) using five different curing protocols with similar radiant exposure (18 J/cm²): 400 mW/cm² for 45 s, 900 mW/cm² for 20 s, 1500 mW/cm² for 12 s, 2000 mW/cm² for 9 s and 3000 mW/cm² for 6 s. Degree of conversion (DC) was measured in real time by Fourier transform near infrared spectroscopy (FT-NIRS).

Results

Three- and subsequent two way ANOVA testing revealed significant differences (p ≤ 0.02) with respect to “composite type” and “cure protocol” for DC for all 5 product comparisons. Supplementary one-way ANOVA also revealed significant differences between curing protocols (p < 0.05). The majority of higher viscosity resin composite paste materials exhibited similar DC regardless of curing protocol. However, a significant decrease in DC for specimens cured at 3000 mW/cm² for 6 s compared with 400 mW/cm² for 45 s was observed for the flowable materials, Grandio (41 ± 0.36 and 62 ± 1.15%, respectively) and Venus (44 ± 0.44 and 67 ± 0.44%, respectively). Conversely, other flowable materials exhibited little or no significant differences between curing modes. Generally, a higher degree of conversion was observed for flowables compared with their more viscous counterpart, except at high irradiance for those materials where a reciprocal relationship with exposure time was not observed.

Conclusions

The validity of exposure reciprocity law and final degree of conversion depends on several factors, amongst which resin viscosity and filler content were important. Practitioners should be aware of the importance of resin composite constituents and irradiation protocols. Information on material composition and appropriate radiation sources by manufacturers may assist practitioners with the selection of appropriate curing protocols for specific material/light curing unit combinations with the aim of reducing the incidence of under-cured restorations and the clinical impact thereof.     

Pre-heating time and exposure duration: Effects on post-irradiation properties of a thermo-viscous resin-composite

ObjectiveTo evaluate the effects of pre-heating time and exposure duration on the degree of conversion (DC), maximum rate of polymerization (RP_max), polymerization shrinkage strain (PS) and surface micro-hardness (VHN) of Viscalor.MethodsViscalor syringes were pre-heated using a Caps Warmer (VOCO, Germany) in T3 mode (at 68 °C) for 30 s (T3-30s) and 3 min (T3-3min) and then the composite paste was extruded into appropriately sized molds. Light irradiation was applied at zero distance from the upper surface with a LED-LCU of mean irradiance 1200 mW/cm² for either 20 or 40 s. The real-time polymerization kinetics and DC at 5 min and 24 h post-irradiation (DC_5min and DC_24h) were measured using ATR-FTIR (n = 3). PS was obtained with the bonded-disk technique (n = 3). Top and bottom Vickers micro-hardness (VHN_top and VHN_bottom) were measured at 5 min post-irradiation and after 24 h dry storage (n = 5). Data were analysed using one-way ANOVA, two-way ANOVA, independent t-test and Tukey post hoc tests (p < 0.05).ResultsPolymerization kinetic curves of Viscalor from 0 to 15 min were similar for different pre-heating times and exposure durations. Pre-heated Viscalor (T3-30s and T3-3min) with 40 s exposure had greater VHN_top and VHN_bottom than for Viscalor (no heat) (p < 0.05). Exposure duration did not significantly affect DC, RP_max and PS (p > 0.05). After 24 h storage, DC and VHN increased. Pre-heating did not increase the DC_24h, relative to no pre-heating (p > 0.05). Two-way ANOVA showed that there was no significant interaction between pre-heating time and exposure duration (p > 0.05).SignificanceIncreasing irradiation time from 20 to 40 s did not affect DC, RP_max or PS, but increased VHN_top. Composite pre-heating had no adverse effect through any premature polymerization. For Viscalor, 3 min pre-heating and 20 s irradiation were sufficient to provide adequate hardness, without increasing PS or compromising polymerization kinetics.     

Effect of filler particle size and morphology on force/work parameters for stickiness of unset resin-composites

ObjectivesTo investigate the effect of variation in filler particle size and morphology within an unset model series of resin-composites on two stickiness parameters: (1) maximum probe separation-force and (2) work-of-separation. This study was to complement previously reported measurements of composite stickiness in terms of a strain-parameter, ‘peak-height’.Materials and methodsEleven experimental light cured resin-composites were selected. All had the same matrix (Bis-GMA, UDMA and TEGDMA, with 0.33% camphoroquinone) and the same filler volume fraction—56.7%, however filler particles varied in size and shape and were either unimodal or multimodal in size-distribution. Each material was placed in a cylindrical mould (φ = 7 mm × 5 mm depth) held at 26 or 37 °C. The maximum force (F_max, N) and work of probe-separation (W_s, N mm) were measured. A flat-ended stainless-steel probe (φ = 6 mm) was mechanically lowered onto and into the surface of the unset sample, until a compressive force of 1 N was reached, which was held constant for 1 s. Then the probe was moved vertically upward at a constant speed; either 2 or 8 mm/s. The tensile force produced on the probe by the sticky composite was plotted against displacement and the maximum value was identified (F_max). W_s was obtained as the integrated area. Data was analyzed by multivariate ANOVA and multiple pair-wise comparisons using a Tukey post hoc test to establish homogenous subsets (at p = 0.05) for F_max and a Games–Howell was used for W_s.ResultsAs potential measures of stickiness, F_max and W_s showed more coherent trends with fillersize when measured at the lower of the two probe speeds, 2 mm/s. For unimodal resin-composite F_max ranged from 1.04 to 5.11 N and W_s from 0.48 to 11.12 N mm. For the multimodal resin-composite they ranged from 1.64 to 4.13 N and from 2.32 to 8.34 N mm respectively. Temperature increase tended to slightly reduce F_max, although this trend was not consistent. W_s generally increased with temperature.ConclusionFiller particle size and morphology influences F_max and W_s of uncured resin-composite which partly express the handling behaviors of resin-composites.     

Influence of resin matrix on the rheology,translucency, and curing potential of experimental flowable composites for bulk-fill applications

ObjectiveTo propose monomer formulations that show an optimal degree of conversion as a function of depth for bulk-fill applications.MethodsFour 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 CC 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.ResultsThe 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%).SignificanceThe 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.     

大块充填树脂在牙体修复中的应用与研究进展

传统复合树脂在临床应用中分层充填,步骤较多,树脂的聚合收缩可导致修复体边缘微渗漏、术后敏感等,导致修复失败.2009年,大块充填树脂(bulk-fill resin-based composite)应运而生,改良的基质单体、改性强化的纳米混合填料以及独特的光引发剂,使得大块充填树脂能够一层充填4 mm,其简化操作步骤、节约椅旁时间、并能显著降低聚合收缩和聚合应力.本文就大块充填树脂的分类、固化原理、性能等方面进行阐述和讨论,并提出大块充填树脂的应用发展方向.     

Effect of temperature on post-cure polymerization of bulk-fill composites

Objectives

To investigate the 24 h post-cure polymerization and the effect of temperature on the post-cure polymerization of one conventional and three bulk-fill composite materials.

Methods

A conventional composite GrandioSO (GR) and three bulk-fill composites: Tetric EvoCeram Bulk Fill (TECBF), Quixfil (QF) and X-tra fil (XF) were investigated. The samples were cured for 20 s with irradiance of 1090 mW/cm². Composite samples were divided into two groups: the “room-temperature” group (RT, n = 5) and the “body-temperature” group (BT, n = 5) and they were stored in dark at 20 °C and 37 °C, respectively. Measurements of degree of conversion (DC) were made immediately after curing (0 h) and 24 h post-cure (24 h). To analyse the extent of post-cure DC increase, the DC values of 0 h-RT/24 h-RT and 0 h-BT/24 h-BT were compared. To analyse the difference in DC between RT and BT, the DC values of 0 h-RT/0 h-BT and 24 h-RT/24 h-BT were compared.

Results

DC increase 24 h post-cure was significant for all composites and ranged between 6.3% and 8.2% in RT and between 12.5% and 15.7% in BT. All composites demonstrated a higher DC in 24 h-BT compared to 24 h-RT. The difference was statistically significant for GR, TECBF and QF.

Conclusions

All composites demonstrated a significant post-cure effect after 24 h. Post-cure temperature increase from 20 °C to 37 °C yielded a higher post-cure DC increase.

Clinical significance

Due to the temperature effect on the final DC, studies performed at composite samples at room temperature may record more inferior properties than these attained in the oral cavity.     

Effect of the degree of conversion of resin-based composites on cytotoxicity,cell attachment,and gene expression

ObjectiveThis study investigated the influence of the degree of conversion (DC), resin-based composites (RBC) composition, and the effect of additional violet light from one light curing unit (LCU) on cell attachment/growth, eluate cytotoxicity, and gene expression.MethodsThe effect of different DC of RBCs on human gingival fibroblasts (HGFs) when cultured directly onto cured RBCs, and when exposed afterwards to eluates in cell culture medium was examined. Venus^® (RBC-V; Bis-GMA-based) and Venus Pearl^® (RBC-P; TCD-DI-HEA and UDMA-based) were cured using a single emission peak (blue) light, Translux Wave^®; TW and a dual emission peak (blue-violet) light, Translux 2 Wave^®; T2W. To determine the value of the additional violet light from the T2W, exposure times and distances were adjusted to deliver similar radiant exposures (RE) from the blue region of both lights at five different RE levels from 1.5 J/cm² to 28.9 J/cm².ResultsBoth RBCs light-cured with the T2W at higher REs resulted in higher DC, increased cell adhesion and decreased eluate cytotoxicity. RBC-V induced greater cell adhesion, lower mRNA levels of pro-inflammatory markers, and higher mRNA levels of a proliferation marker than RBC-P. Wettability was the same for both RBCs. Toxicity decreased with increasing number of elution cycles. The initial eluates from RBC-P had a lower toxicity than from RBC-V.SignificanceRBCs cured with T2W (delivering both blue and violet light) at higher RE had greater DCs. The greatest DC and the least cell reactions were observed when the RE was >25 J/cm².     

Rheological properties of resin composites according to variations in composition and temperature

Objective

To study the effect of compositional variables and temperature (25 °C and 37 °C) on the rheological properties of contemporary resin composites.

Methods

Fourteen commercial resin composites with different resin matrices of Bis-GMA and TEGDMA, different filler loading (41–65, v/v) and particle sizes (ranging 5 nm to 20 μm) were studied using a parallel plate rheometer. Shear sweep measurements were made to determine each composite's viscosity over the angular frequency range of ω = 10⁻⁴–10² rad/s. Data were analyzed using one way ANOVA, Bonferroni post hoc and t-independent tests (p < 0.05).

Results

All composites exhibited viscosity reducing with shear rate (pseudoplasticity). Viscosity averages were calculated over the shear rate range. These viscosities increased as the percentage of filler loading (by volume) increased ranging between 0.05–349.33 kPa s at 25 °C and 0.03–132.00 kPa s at 37 °C. Filtek Supreme XTE exhibited the highest viscosity at both temperatures (p < 0.05). Filtek Bulk Fill on the other hand, showed the lowest viscosity at both temperatures (p < 0.05). Viscosity significantly decreased with the increase in the temperatures for all materials (p < 0.05). The reduction ranged from 40.8% (for Venus Diamond Flow) to 92.2% (for Spectrum TPH3).

Significances

There was a considerable variation in the resin composite viscosities measured at 25 °C as an average value for shear-rate sweep. The factor between the least and highest viscosities was about 7000.The formulation differences that led to such a great variation were primarily: (i) volume fraction of fillers and (ii) particle size, the latter influencing total particle surface area.Rheological properties such as viscosity are key parameters influencing perceived differences in handling behavior of resin composites.     

Effect of calcium orthophosphate particle size and CaP:glass ratio on optical,mechanical and physicochemical characteristics of experimental composites

ObjectiveEvaluate light transmittance (%T), color change (ΔE), degree of conversion (DC), bottom-to-top Knoop microhardness (KHN), flexural strength (BFS) and modulus (FM), water sorption/solubility (WS/SL) and calcium release of resin composites containing different dicalcium phosphate dihydrate (DCPD)-to-barium glass ratios (DCPD:BG) and DCPD particle sizes.MethodsTen resin-based composites (50 vol% inorganic fraction) were prepared using BG (0.4 µm) and DCPD particles (12 µm, 3 µm or mixture) with DCPD:BG of 1:3, 1:1 or 3:1. A composite without DCPD was used as a control. DC, KHN, %T and ΔE were determined in 2-mm thick specimens. BFS and FM were determined after 24 h. WS/SL was determined after 7 d. Calcium release was determined by coupled plasma optical emission spectroscopy. Data were analyzed by ANOVA/Tukey test (alpha: 0.05).Results%T was significantly reduced in composites with milled, compared to pristine DCPD (p < 0.001). ΔE > 3.3 were observed with DCPD:BG of 1:1 and 3:1 formulated with milled DCPD (p < 0.001). DC increased at 1:1 and 3:1 DCPD:BG (p < 0.001). All composites presented bottom-to-top KHN of at least 0.8. BFS was not affected by DCPD size but was strongly dependent on DCPD:BG (p < 0.001). Reductions in FM were observed with milled DCPD (p < 0.001). WS/SL increased with DCPD:BG (p < 0.001). At 3DCPD: 1BG, using small DCPD particles led to a 35 % increase in calcium release (p < 0.001).SignificanceA trade-off between strength and Ca²⁺ release was observed. In spite of its low strength, the formulation containing 3 DCPD: 1 glass and milled DCPD particles is preferred due to its superior Ca²⁺ release.     

Conversion kinetics of rapid photo-polymerized resin composites

ObjectiveTo measure the degrees of conversion (DC), conversion kinetics, and the effect of post-irradiation time on rapid photo-polymerized bulk-fill resin composites under conditions equivalent to clinical depths of 1 and 4 mm.Methods36 specimens (n = 3), based on two resin composites incorporating PowerCure rapid-polymerization technology in two consistencies (PFill; PFlow) and two comparators with matching consistencies (Eceram; EFlow), were investigated from the same manufacturer (Ivoclar AG, Liechtenstein). Specimens were prepared within 4 mm diameter cylindrical molds, of either 1 mm or 4 mm depths respectively, to simulate near-surface and deep locations in a bulk-fill restoration. The independent variables in this study were: materials, thickness and time. Two high irradiance polymerization protocols were utilized for PowerCure materials: 2000 and 3050 mW/cm² for 5 and 3 s, respectively. A standard (1200 mW/cm²) polymerization protocol was used with control materials. FTIR was utilized to measure DC in real-time for 24 h post-irradiation. The data were analyzed using Welch’s-ANOVA, Games-Howell post-hoc test, kinetic dual-exponential sum function and independent sample t-tests (p = 0.05).ResultsThe DC of the materials ranged between 44.7–59.0 % after 5 min, which increased after 24 h reaching 55.7–71.0 % (p < 0.05). Specimen thickness did not influence the overall DC. At 5 min, the highest DC was shown in EFlow. But PFlow, irradiated for 3 s and 5 s exhibited comparable results (p > 0.05). PFill composite irradiated with the 3 s and 5 s protocols did not differ from ECeram (p > 0.05). Specimen thickness and material viscosity affected polymerization kinetics and rate of polymerization (RP_max). Faster polymerization occurred in 1 mm specimens (except PFill-5 s and ECeram). PFill and PFlow exhibited faster conversion than the controls. RP_max varied across the specimen groups between 4.3–8.8 %/s with corresponding DC _RPmax between 22.2–45.3 %.SignificancePolymerization kinetics and RP_max were influenced by specimen thickness and material viscosity. PFill and PFlow materials produced an overall comparable conversion at 5 min and 24 h post-irradiation, despite the ultra-short irradiation times, throughout the 4 mm specimen thickness.     

Influence of extended light exposure curing times on the degree of conversion of resin-based pit and fissure sealant materials

Purpose

The aim of present study was to evaluate extended curing times on the degree of conversion (DC) of filled and unfilled resin-based materials used as pit and fissure sealants.

Materials and methods

The materials examined were a flowable composite (Filtek™ Z350 XT Flowable) and a pit and fissure sealant (Clinpro™ Sealant). Thirty disks of each material were prepared. The 30 made of the flowable composite were divided into three groups (n = 10 each) according to the three different curing times studied: 20 s (group 1), 40 s (group 2), and 60 s (group 3). Similarly, the 30 disks made of the pit and fissure sealant were divided into three groups (n = 10 each) according to the three different curing times: 20 s (group 4), 40 s (group 5), and 60 s (group 6). After polymerization, the disks were removed from the mold and stored in dry, lightproof containers in an incubator at 37 °C for 24 h. The DC was obtained using an Avatar 320 FTIR spectrometer. Then the data were analyzed using the Kruskal–Wallis test and the Fisher’s least significant difference post hoc test for multiple comparisons (alpha = 0.05).

Results

DC values for the flowable composite (Filtek™ Z350 XT) were higher (p = 0.002) than those for the pit and fissure sealant (Clinpro™ Sealant). Group 2 and group 5 showed significantly higher DC values than group 1 and group 4, respectively. There was no difference between groups 2 and 3 or between groups 5 and 6 (p = 2.93).

Conclusion

An extended curing time improves the DC to some extent for both materials.     

3种抛光方法对树脂表面粗糙度影响的比较

目的通过定性与定量分析比较3种抛光方法对3种不同树脂表面粗糙度的影响。方法将3种不同类型的树脂制作成15个直径为5mm,厚度为3mm的圆柱本样本,随机分为3组：Sof—Lex抛光碟组．Brilliant Gloss橡皮抛光尖组,One Gloss橡皮抛光尖组。抛光后用轮廓测定仪在样本测试面中心区测表面粗糙度（Ra）,然后每个小组中随机选取1个样本,采用原子力显微镜观察其表面微观形貌。结果Sof-Lex、One Gloss抛光后,3种不同树脂的Ra均值差异有统计学意义（P〈0．05）、单因素方差分析结果显示材料组之间、抛光方法组之间Ra均值差异均有统计学意义（P〈0．05）,且组内两两比较结果显示同种树脂3种抛光方法之间Ra均值差异有统计学意义（P〈0．05）：多因素方差分析结果显示材料类型和抛光方法均会影响树脂表面粗糙度,二者具有明显交互作用（P〈0．01）原子力显微镜观察结果显示Sof-Lex和BrilliantGloss抛光后树脂表面相对均一,OneGloss抛光后树脂表面有划痕、空穴、填料颗粒突出等结构。结论3种树脂之间、3种不同抛光方法之间Ra均值差异均存在统计学患义,抛光效果具有材料依赖性。     

The effect of adding a new monomer “Phene” on the polymerization shrinkage reduction of a dental resin composite

Objective

A new photocurable monomer, “Phene” (N-methyl-bis(ethyl-carbamate-isoproply-α-methylstyryl)amine) was synthesized and incorporated into Bis-GMA/TEGDMA with the aim of reducing polymerization shrinkage swithout detriment to the physical properties and wearing of the resin composites.