Impact of the distance of light curing on the degree of conversion and microhardness of a composite resin.

OBJECTIVE: This study evaluated the impact of the distance between the light guide tip of the curing unit and material surface on the degree of conversion and Knoop microhardness of a composite resin. MATERIALS AND METHODS: Circular samples were carried out of a methacrylate micro-hybrid resin-based composite and light cured at 0, 2 and 4 mm distance. Monomer conversion rate was measured using a Fourier-transform Raman spectrometer and Knoop hardness number was obtained using a microhardness tester on the top and bottom surfaces. Data were statistically analyzed by analysis of variance and Tukey's test (α=0.05). RESULTS: Overall, the increase of curing distance reduced the microhardness (p≤0.05), but did not influence the carbon double bond conversion rate (p>0.05) of the composite resin tested; and the top surface showed better properties compared to the bottom (p≤0.05). CONCLUSIONS: The light curing at distance can reduce mechanical properties and could affect long-term durability of the composite restorations. Thus, the use of a curing device with high irradiance is recommended.

Influence of BisGMA, TEGDMA, and BisEMA contents on viscosity, conversion, and flexural strength of experimental resins and composites.

Different monomer structures lead to different physical and mechanical properties for both the monomers and the polymers. The objective of this study was to determine the influence of the bisphenylglycidyl dimethacrylate (BisGMA) concentration (33, 50 or 66 mol%) and the co-monomer content [triethylene glycol dimethacrylate (TEGDMA), ethoxylated bisphenol-A dimethacrylate (BisEMA), or both in equal parts] on viscosity (eta), degree of conversion (DC), and flexural strength (FS). Eta was measured using a viscometer, DC was obtained by Fourier transfer Raman (FT-Raman) spectroscopy, and FS was determined by three-point bending. At 50 and 66% BisGMA, increases in eta were observed following the partial and total substitution of TEGDMA by BisEMA. For 33% BisGMA, eta increased significantly only when no TEGDMA was present. The DC was influenced by BisGMA content and co-monomer type. Mixtures containing 66% BisGMA showed a lower DC compared with mixtures containing other concentrations of BisGMA. The BisEMA mixtures had a lower DC compared with the TEGDMA mixtures. The FS was influenced by co-monomer content only. BisEMA mixtures presented a statistically lower FS, followed by TEGDMA + BisEMA mixtures, and then by TEGDMA mixtures. Partial or total replacement of TEGDMA by BisEMA increased eta, which was associated with the observed decreases in DC and FS. Although the BisGMA content influenced the DC, it did not affect the FS results.

Hybrid materials from intermolecular associations between cationic lipid and polymers.

Intermolecular associations between a cationic lipid and two model polymers were evaluated from preparation and characterization of hybrid thin films cast on silicon wafers. The novel materials were prepared by spin-coating of a chloroformic solution of lipid and polymer on silicon wafer. Polymers tested for miscibility with the cationic lipid dioctadecyldimethylammonium bromide (DODAB) were polystyrene (PS) and poly(methyl methacrylate) (PMMA). The films thus obtained were characterized by ellipsometry, wettability, optical and atomic force microscopy, Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and activity against Escherichia coli. Whereas intermolecular ion-dipole interactions were available for the PMMA-DODAB interacting pair producing smooth PMMA-DODAB films, the absence of such interactions for PS-DODAB films caused lipid segregation, poor film stability (detachment from the silicon wafer) and large rugosity. In addition, the well-established but still remarkable antimicrobial DODAB properties were transferred to the novel hybrid PMMA/DODAB coating, which is demonstrated to be highly effective against E. coli.

Early and 24-hour bond strength and degree of conversion of etch-and-rinse and self-etch adhesives.

PURPOSE: To evaluate early and 24-hour microtensile bond strength (microTBS) and the degree of conversion (DC) of one representative adhesive system from each of the four current bonding approaches. METHODS: 40 human molars were sectioned occluso-gingivally into two halves. Resin composite was bonded incrementally to flat, mid-coronal dentin, using the adhesives Adper Scotchbond MP (MP); Adper Scotchbond 2 (SB); Clearfil SE Bond (SE); and Adper Prompt L-Pop (LP) according to the respective manufacturer's instructions (n = 10). One half was immediately sectioned into sticks and subjected to muTBS test. As the sectioning process took approximately 1 hour, the results were designated as 1-hour bond strengths. The other half was stored in distilled water at 37 degrees C for 24 hours before being sectioned and tested. The DC of these systems was measured using Fourier Transform-Raman spectroscopy in three periods: immediately, 1 and 24 hours after polymerization. Data were analyzed with ANOVA and Tukey's tests. RESULTS: There were no significant differences between the 1-hour and 24-hour bond strengths (P > 0.05), or among the DC measured immediately, 1 hour and 24 hours after polymerization (P > 0.05). However, significant differences were observed among adhesives (P < 0.05). microTBS values obtained, in MPa (1 hour/24 hour), were: SB (48.6 + 1.3/48.4 + 3.5) = SE (51.9 + 4.7/53.3 +/- 2.9) > MP (35.3 +/- 10.9/38.6 + 6.7) > LP (25.5 + 1.1/26.0 + 1.5). The DC, in percentage (immediately/1 hour/24 hour), were: SE (81/82/87) > MP (79/77/81) > SB (60/63/65) > LP (39/37/42).

Evaluation of curing light distance on resin composite microhardness and polymerization.

This study evaluated the influence of the curing tip distance on cure depth of a resin composite by measuring Vickers microhardness and determining the degree of conversion by using FT-Raman spectroscopy. The light curing units used were halogen (500mW/cm2) and LED (900mW/cm2) at a conventional intensity and an Argon laser at 250mW. The exposure time was 40 seconds for the halogen light, 20 seconds for the LED and 20 and 30 seconds for the Argon laser. The curing tip distances of 0, 3, 6 and 9 mm were used and controlled via the use of metal rings. The composite was placed in a black matrix in one increment at a thickness of 1 mm to 4 mm. The values of microhardness and the degree of conversion were analyzed separately by ANOVA (Analysis of Variance) and Tukey test, with a significance level set at 5%. Correlations were analyzed using the Pearson test. The results obtained conclude that greater tip distances produced a decrease in microhardness and degree of conversion values, while increasing the resin thickness decreased the microhardness and degree of conversion values. A higher correlation between microhardness and the degree of conversion was shown. This study suggests that the current light curing units promote a similar degree of conversion and microhardness, provided that the resin is not thicker than 1 mm and the light source is at a maximum distance of 3 mm from the resin surface.

Influence of radiant exposure on contraction stress, degree of conversion and mechanical properties of resin composites.

OBJECTIVE: To verify the influence of radiant exposure (H) on contraction stress (CS), degree of conversion (DC) and mechanical properties of two restorative composites. METHODS: Filtek Z250 (3M ESPE) and Heliomolar (Ivoclar) were photoactivated with 6, 12, 24, or 36 J/cm2 at continuous irradiance of 600 mW/cm2. CS at 10 min was determined in a low compliance testing system. DC, flexural strength (FS), flexural modulus (FM) and Knoop microhardness (KHN) were measured after 24 h storage at 37 degrees C. KHN and DC measurements were conducted on the irradiated surface of 1mm thick disk-shaped specimens. Bar-shaped specimens were submitted to three-point bending to determine FS and FM. Data were analyzed by one-way ANOVA/Tukey's test (alpha = 0.05) separately for each composite. RESULTS: For Filtek Z250, no significant increase in CS was observed above 12 J/cm2. DC and FM were similar at all H values, while FS increased significantly between 6 and 24 J/cm2. KHN was significantly different among all H levels, except between 12 and 24 J/cm2. For Heliomolar, CS and KHN increased significantly with H, except between 24 and 36 J/cm2. DC, FM and FS did not vary, regardless of the radiant exposure. SIGNIFICANCE: Variables tested behaved differently. CS and KHN were more sensitive to increasing radiant exposures than the other properties evaluated. FS varied only for Filtek Z250, while, for both composites, DC and FM were not affected by different H values.

Influence of photoactivation method on conversion, mechanical properties, degradation in ethanol and contraction stress of resin-based materials.

OBJECTIVES: To investigate the influence of photoactivation method on degree of conversion (DC), flexural strength (FS), flexural modulus (FM) and Knoop hardness (KHN) of a composite and an unfilled resin (Filtek Z250 and Scotchbond multi-purpose plus, 3M ESPE) after storage in water or ethanol, and on composite contraction stress (CS). METHODS: Specimens 1x2x10 mm were prepared for FS test, photoactivated by 600 mW/cm2 x 40 s (A), 200 mW/cm2 x 120 s (B), or 600 mW/cm2 x1 s +3 min delay +600 mW/cm2 x 39 s (C), and tested after 24 h in water or ethanol. Load and displacement values were used to calculate FM. Specimen fragments were used to measure KHN. DC was determined by FT-Raman spectroscopy. CS was determined by mechanical testing. Data were submitted to ANOVA/Tukey's test (alpha=0.05). RESULTS: Composite DC was not affected by photoactivation (A: 65+/-1.8%; B: 66+/-3.4%; C: 65+/-2.9%). Unfilled resin DC was statistically higher using method A (79+/-0.3%) than B (74+/-1.0%) and C (73+/-0.9%). Photoactivation did not influence composite properties, regardless of the storage medium (p>0.05). After ethanol storage, FS of the unfilled resin was lower for specimens irradiated by method B (p<0.001). Pulse-delay curing (C) significantly reduced CS (7.7+/-1.3 MPa), compared to A (10.7+/-1.2 MPa) and B (10.1+/-1.3 MPa). SIGNIFICANCE: Photoactivation method did not affect composite properties or susceptibility to ethanol degradation. For the unfilled resin, DC was lower with the use of low intensity and pulse-curing, while FS after ethanol storage was reduced by low intensity curing. Pulse-delay curing significantly reduced CS.

Influence of polymeric matrix on the physical and chemical properties of experimental composites.

Nowadays, the main reasons for replacement of resin-based composite restorations are fracture or problems with the integrity of their interface, such as marginal staining, microleakage, or secondary caries. The aim of the present study was to evaluate the influence of the organic matrix on polymerization stress (PS), degree of conversion (DC), elastic modulus (E), flexural strength (FS), Knoop hardness (KHN), sorption (SP), and solubility (SL). In order to obtain a material which combines better mechanical properties with lower PS, seven experimental composites were prepared using BisGMA to TEGDMA molar ratios of 2:8, 3:7, 4:6, 5:5, 6:4, 7:3 and 8:2 and 40% of silica. PS was obtained in a universal testing machine, using acrylic as bonding substrate. DC was determined using Fourier Transform Raman spectroscopy. E and FS were obtained by the three-point bending test. KHN was measured by a microindentation test using a load of 25 g for 30 s. SP and SL were assessed according to ISO 4049. The data were submitted to one-way ANOVA. The increase in BisGMA concentration resulted in the decrease of PS, DC, E, FS and KHN. However, it did not change the SP and SL values. FS, E and KHN showed a strong and direct relationship with the DC of the materials. The composite material with a BisGMA to TEGDMA molar ratio of 1:1 was the one with better mechanical properties and lower PS.

Relationship between contraction stress and degree of conversion in restorative composites.

OBJECTIVES: To verify the relationship between contraction stress and degree of conversion (DC) in different composites (Filtek Z250, Filtek A110, Tetric Ceram and Heliomolar). METHODS: For the contraction stress test, composite (2 mm thick) was applied between two 5-mm diameter glass rods, mounted in a tensilometer. DC was determined by Infrared Photoacoustic spectroscopy in specimens with similar dimensions and geometry, submitted to identical curing conditions. Specimens were exposed to different energy densities (4.5, 13.5, 27.0, 54.0 and 108.0 J/cm2) by varying exposure time. Contraction stress and DC were recorded 10 min after the beginning of photoactivation. Results were analyzed by ANOVA/Tukey's test and regression analysis. RESULTS: For contraction stress, the interaction between composite and energy density was significant. Stress values ranged between 0.6+/-0.2 and 2.0+/-0.3 MPa at 4.5 J/cm2, 2.3+/-0.5 and 4.3+/-0.4 MPa at 13.5 J/cm2, 3.8+/-0.5 and 5.8+/-0.9 MPa at 27.0 J/cm2, 4.2+/-0.8 and 7.9+/-0.9 MPa at 54.0 J/cm2 and 6.6+/-0.8 and 8.1+/-0.9 MPa at 108.0 J/cm2. Tetric Ceram (39+/-5.8%) showed a higher average DC than the other materials. Heliomolar (28+/-5.2%) showed an average DC similar to Filtek Z250 (32+/-6.6%) and to Filtek A110 (24+/-7.5%) regardless of the energy density level. No significant increase in DC was observed above 27 J/cm2. CONCLUSIONS: At high energy levels, DC had a tendency to level off earlier than contraction stress values. SIGNIFICANCE: Using high energy densities may cause a significant increase in stress values, without producing a significant increase in conversion.

Knoop microhardness and FT-Raman evaluation of composite resins: influence of opacity and photoactivation source.

The aim of this study was to evaluate the degree of conversion by Knoop microhardness (KHN) and FT-Raman spectroscopy (FTIR) of one nanofilled (Filtek Supreme-3M-ESPE [FS]) and one microhybrid composite (Charisma-Heraeus-Kulzer [CH]), each with different opacities, namely enamel, dentin, and translucent, which were photo-activated by a quartz-tungsten-halogen lamp (QTH) and a light-emitting diode (LED). Resin was bulk inserted into a disc-shaped mold that was 2.0 mm thick and 4 mm in diameter, obtaining 10 samples per group. KHN and FTIR values were analyzed by two-way ANOVA and Tukey's tests (α = 0.05). Nanofilled resin activated by a LED presented higher microhardness values than samples activated by a QTH for dentin opacity (p < 0.05). The microhybrid resin showed no differences in KHN or FTIR values with different activation sources or opacity. The nanofilled dentin and enamel resins showed lower FTIR values than the translucent resin. The KHN values of the translucent resins were not influenced by the light source.

Composite pre-heating: effects on marginal adaptation, degree of conversion and mechanical properties.

OBJECTIVES: This study evaluated the effect of composite pre-polymerization temperature and energy density on the marginal adaptation (MA), degree of conversion (DC), flexural strength (FS), and polymer cross-linking (PCL) of a resin composite (Filtek Z350, 3M/ESPE). METHODS: For MA, class V cavities (4 mm x 2 mm x 2 mm) were prepared in 40 bovine incisors. The adhesive system Adper Single Bond 2 (3M/ESPE) was applied. Before being placed in the cavities, the resin composite was either kept at room-temperature (25 degrees C) or previously pre-heated to 68 degrees C in the Calset device (AdDent Inc., Danbury, CT, USA). The composite was then light polymerized for 20 or 40s at 600 mW/cm(2) (12 or 24 J/cm(2), respectively). The percentage of gaps was analyzed by scanning electron microscopy, after sectioning the restorations and preparing epoxy resin replicas. DC (n=3) was obtained by FT-Raman spectroscopy on irradiated and non-irradiated composite surfaces. FS (n=10) was measured by the three-point-bending test. KHN (n=6) was measured after 24 h dry storage and again after immersion in 100% ethanol solution for 24h, to calculate PCL density. Data were analyzed by appropriate statistical analyses. RESULTS: The pre-heated composite showed better MA than the room-temperature groups. A higher number of gaps were observed in the room-temperature groups, irrespective of the energy density, mainly in the axial wall (p<0.05). Composite pre-heating and energy density did not affect the DC, FS and PCL (p>0.05). SIGNIFICANCE: Pre-heating the composite prior to light polymerization similar in a clinical situation did not alter the mechanical properties and monomer conversion of the composite, but provided enhanced composite adaptation to cavity walls.

Influence of polymeric matrix on the physical and chemical properties of experimental composites

Nowadays, the main reasons for replacement of resin-based composite restorations are fracture or problems with the integrity of their interface, such as marginal staining, microleakage, or secondary caries. The aim of the present study was to evaluate the influence of the organic matrix on polymerization stress (PS), degree of conversion (DC), elastic modulus (E), flexural strength (FS), Knoop hardness (KHN), sorption (SP), and solubility (SL). In order to obtain a material which combines better mechanical properties with lower PS, seven experimental composites were prepared using BisGMA to TEGDMA molar ratios of 2:8, 3:7, 4:6, 5:5, 6:4, 7:3 and 8:2 and 40% of silica. PS was obtained in a universal testing machine, using acrylic as bonding substrate. DC was determined using Fourier Transform Raman spectroscopy. E and FS were obtained by the three-point bending test. KHN was measured by a microindentation test using a load of 25 g for 30 s. SP and SL were assessed according to ISO 4049. The data were submitted to one-way ANOVA. The increase in BisGMA concentration resulted in the decrease of PS, DC, E, FS and KHN. However, it did not change the SP and SL values. FS, E and KHN showed a strong and direct relationship with the DC of the materials. The composite material with a BisGMA to TEGDMA molar ratio of 1:1 was the one with better mechanical properties and lower PS.

Bis-GMA co-polymerizations: influence on conversion, flexural properties, fracture toughness and susceptibility to ethanol degradation of experimental composites.

OBJECTIVES: The aim of this study was to evaluate the influence of monomer content on fracture toughness (K(Ic)) before and after ethanol solution storage, flexural properties and degree of conversion (DC) of bisphenol A glycidyl methacrylate (Bis-GMA) co-polymers. METHODS: Five formulations were tested, containing Bis-GMA (B) combined with TEGDMA (T), UDMA (U) or Bis-EMA (E), as follows (in mol%): 30B:70T; 30B:35T:35U; 30B:70U; 30B:35T:35E; 30B:70E. Bimodal filler was introduced at 80 wt%. Single-edge notched beams for fracture toughness (FT, 25 mm x 5 mm x 2.5 mm, a/w=0.5, n=20) and 10 mm x 2 mm x 1 mm beams for flexural strength (FS) and modulus (FM) determination (10 mm x 2 mm x 1 mm, n=10) were built and then stored in distilled water for 24 h at 37 degrees C. All FS/FM beams and half of the FT specimens were immediately submitted to three-point bending test. The remaining FT specimens were stored in a 75%ethanol/25%water (v/v) solution for 3 months prior to testing. DC was determined with FT-Raman spectroscopy in fragments of both FT and FS/FM specimens at 24 h. Data were submitted to one-way ANOVA/Tukey test (alpha=5%). RESULTS: The 30B:70T composite presented the highest K(Ic) value (in MPa m(1/2)) at 24 h (1.3+/-0.4), statistically similar to 30B:35T:35U and 30B:70U, while 30B:70E presented the lowest value (0.5+/-0.1). After ethanol storage, reductions in K(Ic) ranged from 33 to 72%. The 30B:70E material presented the lowest reduction in FT and 30B:70U, the highest. DC was similar among groups (69-73%), except for 30B:70U (52+/-4%, p<0.001). 30B:70U and 30B:35T:35U presented the highest FS (125+/-21 and 122+/-14 MPa, respectively), statistically different from 30B:70T or 30B:70E (92+/-20 and 94+/-16 MPa, respectively). Composites containing UDMA or Bis-EMA associated with Bis-GMA presented similar FM, statistically lower than 30B:35T:35U. SIGNIFICANCE: Composites formulated with Bis-GMA:TEGDMA:UDMA presented the best compromise between conversion and mechanical properties.

Radiant exposure effects on physical properties of methacrylate - and silorane-composites

AIM: To evaluate the effect of different radiant exposures on the degree of conversion (DC), Knoop hardness number (KHN), plasticization (P), water sorption (WS), and solubility (S) of different monomer resin-based composites. METHODS: Circular specimens (5 x 2 mm) were manufactured from methacrylate and silorane composite resins, and light-cured at 19.8, 27.8, 39.6, and 55.6 J/cm2, using second-generation LED at 1,390 mW/cm2. After 24 h, DC was obtained using a FT-Raman spectrometer equipped with a Nd:YAG laser, KHN was measured with 50-g load for 15 s, and P was evaluated on the top and bottom surfaces by the percentage of hardness reduction after 24 h immersed in absolute alcohol. WS and S were determined according to ISO 4049. Data were subjected to statistical analysis (α=0.05). RESULTS: Methacrylate material presented higher DC, KHN, P, and WS than silorane (p<0.05). There was no difference in the S values (p>0.05). The increased radiant exposures improved only the KHN (p<0.05). In general, top surfaces showed higher DC and KHN than bottom, for both materials (p<0.05). The increase of the radiant exposure did not improve most physical properties of the composites and were monomer-base dependent. CONCLUSIONS: Chemical composition of the composite resins resulted in different physical properties behavior and could affect the clinical longevity of dental restorations, but overall these properties were not influenced by the different radiant exposures evaluated in the study...

Knoop microhardness and FT-Raman spectroscopic evaluation of a resin-based dental material light-cured by an argon ion laser and halogen lamp: an in vitro study.

OBJECTIVE: The purpose of this study was to evaluate in vitro the Knoop microhardness (Knoop hardness number [KHN]) and the degree of conversion using FT-Raman spectroscopy of a light-cured microhybrid resin composite (Z350-3M-ESPE) Vita shade A3 photopolymerized with a halogen lamp or an argon ion laser. BACKGROUND DATA: Optimal polymerization of resin-based dental materials is important for longevity of restorations in dentistry. MATERIALS AND METHODS: Thirty specimens were prepared and inserted into a disc-shaped polytetrafluoroethylene mold that was 2.0 mm thick and 3 mm in diameter. The specimens were divided into three groups (n = 10 each). Group 1 (G1) was light-cured for 20 sec with an Optilux 501 halogen light with an intensity of 1000 mW/cm(2). Group 2 (G2) was photopolymerized with an argon laser with a power of 150 mW for 10 sec, and group 3 (G3) was photopolymerized with an argon laser at 200 mW of power for 10 sec. All specimens were stored in distilled water for 24 h at 37 degrees C and kept in lightproof containers. For the KHN test five indentations were made and a depth of 100 microm was maintained in each specimen. One hundred and fifty readings were obtained using a 25-g load for 45 sec. The degree of conversion values were measured by Raman spectroscopy. KHN and degree of conversion values were obtained on opposite sides of the irradiated surface. KHN and degree of conversion data were analyzed by one-way ANOVA and Tukey tests with statistical significance set at p < 0.05. RESULTS: The results of KHN testing were G1 = 37.428 +/- 4.765; G2 = 23.588 +/- 6.269; and G3 = 21.652 +/- 4.393. The calculated degrees of conversion (DC%) were G1 = 48.57 +/- 2.11; G2 = 43.71 +/- 3 .93; and G3 = 44.19 +/- 2.71. CONCLUSIONS: Polymerization with the halogen lamp (G1) attained higher microhardness values than polymerization with the argon laser at power levels of 150 and 200 mW; there was no difference in hardness between the two argon laser groups. The results showed no statistically significant different degrees of conversion for the polymerization of composite samples with the two light sources tested.

Flexural properties, microleakage, and degree of conversion of a resin polymerized with conventional light and argon laser.

OBJECTIVE: To evaluate the flexural strength, microleakage, and degree of conversion of a microhybrid resin polymerized with argon laser and halogen lamp. METHOD AND MATERIALS: For both flexural test and degree of conversion analysis, 5 bar samples of composite resin were prepared and polymerized according to ISO 4049. The halogen light-curing unit was used with 500 mW/cm(2) for 20 seconds and the argon laser with 250 mW for 10 and 20 seconds. Samples were stored in distilled water in a dark environment at 37 degrees C for 24 hours. The flexural property was quantified by a 3-point loading test. For the microleakage evaluation, 60 bovine incisors were used to prepare standardized Class 5 cavities, which were restored and polished. Specimens were stored in distilled water for 24 hours at 37 degrees C and thermocycled 500 times (6 degrees C to 60 degrees C). Specimens were then immersed in an aqueous solution of basic fuchsin for 24 hours. Longitudinal sections of each restoration were obtained and examined with a stereomicroscope for qualitative evaluation of microleakage. Fourier transform (FT)-Raman RFS 100/S spectrometer (Bruker) was used to analyze the degree of conversion. RESULTS: ANOVA showed no statistically significant differences of flexural strength between the photoactivation types evaluated in the flexural study. Microleakage data were statistically analyzed by Mann-Whitney and Kruskal-Wallis tests. Enamel margins resulted in a statistically lower degree of leakage than dentin margins. No statistically significant difference was found among the 3 types of photocuring studied. ANOVA also showed no statistically significant difference in the degree of conversion among the studied groups. CONCLUSION: According to the methodology used in this research, the argon laser is a possible alternative for photocuring, providing the same quality of polymerization as the halogen lamp. None of the photocured units tested in this study completely eliminated microleakage.

Knoop microhardness and FT-Raman evaluation of composite resins: influence of opacity and photoactivation source

The aim of this study was to evaluate the degree of conversion by Knoop microhardness (KHN) and FT-Raman spectroscopy (FTIR) of one nanofilled (Filtek Supreme-3M-ESPE [FS]) and one microhybrid composite (Charisma-Heraeus-Kulzer [CH]), each with different opacities, namely enamel, dentin, and translucent, which were photo-activated by a quartz-tungsten-halogen lamp (QTH) and a light-emitting diode (LED). Resin was bulk inserted into a disc-shaped mold that was 2.0 mm thick and 4 mm in diameter, obtaining 10 samples per group. KHN and FTIR values were analyzed by two-way ANOVA and Tukey's tests (α = 0.05). Nanofilled resin activated by a LED presented higher microhardness values than samples activated by a QTH for dentin opacity (p < 0.05). The microhybrid resin showed no differences in KHN or FTIR values with different activation sources or opacity. The nanofilled dentin and enamel resins showed lower FTIR values than the translucent resin. The KHN values of the translucent resins were not influenced by the light source.

Influência de diferentes opacidades e fontes ativadoras na microdureza e no grau de conversão de resinas compostas diretas / Influence af different apacities and activatian saurce in microhardness and degree af canversian oi direct campasite resin

Objetivos: avaliar o grau de conversão por meio da microdureza (KHN) e espectroscopia FT-Raman (GC) de uma resina composta direta microhíbrida (Opallis-FGM) com opacidades distintas: esmalte, dentina e translúcida fotoativadas com luz halógena (OTH, 700mW/cm2) ou luz emitida por diodo (LED, 1200mW/ em']. Materiais e métodos: sessenta corpos-de-prova foram preparados através da inserção da resina composta em incremento único em matriz de teflon bipartida com orifício central cilíndrico (2mm de altura e 4mm de diâmetro) e foram divididos em seis grupos (n= 10). Para o teste de microdureza Knoop foram realizadas cinco identações no lado oposto da superfície irradiada. O grau de conversão foi mensurado através de espectroscopia FT-Raman no lado oposto da superfície irradiada (n=5). Os dados de KHN e GC foram analisados separadamente por meio da análise de variância two-way e teste de Tukey (a=0,05) e correlacionados pelo teste de Pearson-r. Resultados: independente da opacidade, o LED proporcionou um maior GC do que OTH. Para a opacidade de dentina maiores valores de KHN e GC foram observados após ativação com LED, entretanto a resina translúcida não apresentou diferenças de KHN. A opacidade de esmalte apresentou valores de GC intermediários entre as demais e KHN similar à dentina, quando ativada com LED ou com OTH. Houve uma boa correlação entre KHN e GC r=0,5671 (p=O,OOll). Conclusões: pode- se concluir que o uso do LED pode resultar em valores maiores de KHN e GC para resina composta mais opaca comparadas à fonte halógena, tal diferença não é observada na resina composta translúcida.

Objectives: to evaluate the degree of conversion by Knoop microhardness (KHN) and FT-Raman spectroscopy (DC) of one microhybrid composite resin (Opallis-FGM) with different opacities: enamel, dentin, and translucent; photo-activated by quartz-tungsten-halogen lamp (OTH; 700mW/cm2) or light emitting diode (LED; 1200mW/cm2). Materiais and Methods: sixty samples were prepared by the resin insertion in bulk in a disc-shaped mold (2.0mm-thick and 4mm in dia meter) according to 6 groups of samples (n= 10). To Knoop evaluation five indentations in the center of the opposite surfa- ce to the light irradiated surface of the specimen were performed. The DC of the side opposite to the irradiated surface of the specimens was determined bya FT-Raman spectroscopy (n=5). KHN and DC values were analyzed by two-way ANOVA and Tukey tests (a=0.05) and correlated by Pearson-r test. Results: independent of the composite resin opacity the use of LED resulted in the higher DC than OTH. To dentin opacity higher KHN and DC were observed when activated by LED, in the other hand the translucent resin did not showed differences in KHN. The enamel opacity showed intermediary results of DC amongs others and similar KHN to dentin groups activated by LED or with OTH. There was a good correlation between KHN and DC r=0.5671 (p=O.OOll). Conclusions: it can be concluded that LED use may result in higher KHN and DC to the composite resin more opaque compared to OTH, this difference may not be observed to translucent composite resin.

Estudo sobre a biocompatibilidade da polisulfona sob a forma de partículas e bastöes / Study of biocompatibility of particles and rods of polysulfone

Foi estudada comparativamente a resposta do músculo tríceps sural e reto do abdome de ratos Wistar à implantação da polisulfona (PSU) e do polietileno de ultra alto peso molecular (UHMWPE) sob a forma de bastões e partículas, por um período de até 52 semanas. Ao final, a PSU foi considerada como tendo a mesma biocompatibilidade do UHMWPE, segundo os critérios utilizados.