Search

The purpose of this study was to explore the influence of Er:YAG laser irradiation with different pulse durations on the organic matrix, micromorphology of the hybrid layer (HL), and bond strength over time. Sixty caries-free human molars were cut to obtain flat dentin surfaces which were randomly divided into 4 groups: control (not irradiated-G1) and laser groups (80 mJ/2 Hz) with pulse duration ranging between 50 (G2), 300 (G3), and 600 μs (G4). A self-etch adhesive system (Universal 3M ESPE) was applied on pre-treated dentin surfaces and cylinders of resin composite were built up and stressed in a universal testing machine (μSBS) at 24 h and after12 months (n = 12). In addition, 3 other dentin-bonded specimens were prepared as previously described for each group with the adhesive doped with 0.1 wt% Rhodamine B to analyze hybrid layer morphology under Confocal Laser Microscope Scanning (CLMS). Organic matrix and collagen fibrils were analyzed by second harmonic generation (SGH). Two-way ANOVA and Tukey's test detected significantly higher μSBS values for the control group, whereas the lower values were observed in all laser groups at 24 h (p < 0.05). Storage in artificial saliva did not reduce μSBS in all groups. The low signal emitted by SHG images below the irradiated area demonstrated thermal damage of the collagen matrix. CLMS images of laser groups exhibited thicker and irregular resin-dentin interfaces than the control group. Regardless of the pulse duration, Er:YAG laser pre-treatment altered the organic matrix and HL formation which resulted in low μSBS values at 24 h. The alterations on dentin's organic structure did not jeopardize the μSBS after 1 year of saliva storage.

Research on the incorporation of cutting-edge nano-antibacterial agent for designing dental materials with potent and long-lasting antibacterial property is demanding and provoking work. In this study, a novel resin-based dental material containing photocurable core-shell AgBr/cationic polymer nanocomposite (AgBr/BHPVP) was designed and developed. The shell of polymerizable cationic polymer not only provided non-releasing antibacterial capability for dental resins, but also had the potential to polymerize with other methacrylate monomers and prevented nanoparticles from aggregating in the resin matrix. As a result, incorporation of AgBr/BHPVP nanocomposites did not adversely affect the flexural strength and modulus but greatly increased the Vicker's hardness of resin disks. By continuing to release Ag + ions without the impact of anaerobic environment, resins containing AgBr/BHPVP nanoparticles are particularly suitable to combat anaerobic cariogenic bacteria. By reason of the combined bactericidal effect of the contact-killing cationic polymers and the releasing-killing Ag + ions, AgBr/BHPVP-containing resin disks had potent bactericidal activity against S. mutans. The long-lasting antibacterial activity was also achieved through the sustained release of Ag + ions due to the core-shell structure of the nanocomposites. The results of macrophage cytotoxicity showed that the cell viability of dental resins loading less than 1.0 wt% AgBr/BHPVP was close to that of neat resins. The AgBr/BHPVP-containing dental resin with dual bactericidal capability and long term antimicrobial effect is a promising material aimed at preventing second caries and prolonging the longevity of resin composite restorations.

Literature regarding the influence of Er,Cr:YSGG laser pulse frequency with different output power levels on adhesion properties of adhesive resin to lased enamel is limited. Therefore, the aim of the present study was to evaluate the effects of laser pulse frequency (20, 35, and 50 Hz) at two different output power settings (3 and 6 W) of Er,Cr:YSGG on the microtensile bond strength (μTBS) of adhesive resin to enamel. Crowns of 35 intact bovine incisors were embedded into self-cure acrylic resin individually, and then flat enamel surfaces were prepared with 600-grit silicon carbide papers under water cooling. Teeth were divided randomly into seven groups. Enamel surfaces were irradiated with Er,Cr:YSGG laser operated at one of six output power-pulse frequency combinations (6 W20 Hz, 6 W-35 Hz, 6 W-50 Hz, 3 W-20 Hz, 3 W-35 Hz, and 3 W-50 Hz) in groups 1-6, respectively. Bur-treated surfaces served as a control in group 7. After surface treatments and bonding procedures, composite build-ups were done in three layers up to a height of 4 mm. Next, all bonded teeth were sectioned into the resin-enamel sticks to be tested in a μTBS testing machine. The μTBS data were analyzed with univariate analysis of variance under a general linear model with the factor 'tooth' added as a random effect to the design. Resin-enamel interfaces were evaluated with scanning electron microscopy (SEM). The μTBS to laser-irradiated enamel in group 1 (6 W-20 Hz) was significantly lower than those of bur-treated enamel (p<0.05). However, group 6 (3 W-50 Hz) showed significantly higher μTBS values than did bur-treated teeth (p<0.05). SEM evaluation revealed enormous morphological alterations of laser-irradiated specimens, such as extensive vertical and horizontal microcracks and gaps, with the exception of group 6. The bonding effectiveness of adhesive resin to laser-irradiated enamel was affected by the pulse frequency of the Er,Cr:YSGG laser. Although the parameters recommended by the manufacturer lowered μTBS, increasing the pulse rate may maintain optimum μTBS.

Objective: To assess the effects of different modes of a third-generation light-curing unit (LCU) (VALO) on the microhardness of restorative materials., Design: A microhybrid composite resin (Filtek(™) Z550), a giomer (Beautifil II), a compomer (Dyract eXtra) and a RMGIC (Photac(™) Fil) were used in the study. Three different modes of VALO were tested and a second-generation LCU (Elipar S10) was used as a control. The microhardness (VHN) was measured using a Vickers Hardness tester. Data were analyzed using two-way anova and post hoc Tukey's test (P < 0.05)., Results: The Filtek Z550 group had the highest VHN values followed by Photac Fil, Beautifil II and the Dyract eXtra at both top and bottom surfaces, however the difference between Filtek Z550 and Photac Fil was not statistically significant for the bottom surfaces (P > 0.05). Of the different curing protocols tested, the VALO LCU in Mode 3 resulted in the lowest VHN values at both top and bottom surfaces (P < 0.05)., Conclusion: Based on the results of this study, it can be concluded that the high-power mode of the VALO LCU can be recommended for clinical applications especially in pediatric patients, as it can shorten the time required to adequately polymerize resin-based tooth-colored restorative materials., (© 2015 BSPD, IAPD and John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

The aim of this study was to evaluate the radiopacity of silorane and methacrylate resin composites, comparing them to the enamel, dentin, and aluminum penetrometer using a digital image. From six resin composites (Filtek ™ P90, Filtek Z350, Filtek Z350 XT flow, Tetric Ceram, TPH Spectrum, and SureFil SDR flow) cylindrical disks (5 × 1 mm) were made and radiographed by a digital method, together with a 15-step aluminum step-wedge and a 1 mm slice of human tooth. The degree of radiopacity of each image was quantified using digital image processing. The mean values of the shades of gray of the tested materials were measured and the equivalent width of aluminum was calculated for each resin. The results of our work yielded the following radiopacity values, given here in descending order: Tetric Ceram > TPH > SDR > Z350 > Z350 flow > P90 > enamel > dentin. The radiopacity of the materials was different both for the enamel and for the dentin, except for resin P90, which was no different than enamel. In conclusion, silorane-based resin exhibited a radiopacity higher than dentin and closest to the enamel; a large portion of the methacrylate-based flow and conventional resins demonstrated greater radiopacity in comparison to dentin and enamel., Competing Interests: The authors declare that they have no competing interests.

Previous studies have shown the effects of Er,Cr:YSGG laser irradiation on the dentin bond strength; but there are few reports that show the significance of the irradiation with different laser parameters on dentin bond strength and interface morphology. This in-vitro study attempted to evaluate the microtensile bond strength (μTBS) and interface morphology of resin-dentin interfaces, either followed by treatment with Er,Cr:YSGG laser irradiation with different parameters or not. The flattened dentin samples of 35 bovine teeth were embedded into acrylic blocks and randomly divided into seven groups according to surface treatments using Er,Cr:YSGG lasers with different parameters: 3 W/20 Hz, 3 W/35 Hz, 3 W/50 Hz, 1.5 W/20 Hz, 1.5 W/35 Hz, 1.5 W/50 Hz, or no laser treatment (n = 5). Composite buildups were done over bonded surfaces and stored in water (24 hours at 37°C). Specimens were sectioned into sticks that were subjected to μTBS testing and observed under FE-SEM. Control groups (27.70 ± 7.0) showed statistically higher values than laser-irradiated groups. There were no significant differences among laser groups. Despite that, increasing the pulse frequency yielded slightly higher bond strength. Depending on laser settings, Er,Cr:YSGG laser irradiation caused interfacial gaps and resin tags with wings morphology. With the parameters used in this study, Er,Cr:YSGG laser irradiation promoted morphological changes within resin-dentin interfaces and negatively influenced the bond strength of adhesive systems., (© 2015 Wiley Periodicals, Inc.)

The effect of polymerization cycles on flexural properties of conventional (Vipi Cril(®)-VC) or microwave-processed (Vipi Wave(®)-VW) denture base acrylic resins was evaluated. Specimens (n=10) were submitted to the cycles: WB=65ºC for 1 h+1 h boiling water (VC cycle); M630/25=10 min at 270 W+5 min at 0 W+10 min at 360 W (VW cycle); M650/5=5 min at 650 W; M700/4=4 min at 700 W; and M550/3=3 min at 550 W. Specimens were submitted to a three-point bending test at 5 mm/min until fracture. Flexural strength (MPa) and elastic modulus (GPa) data were analyzed by 2-way ANOVA/Tukey HSD (α=0.05). Overall, VC showed higher values than VW. The results obtained with microwave polymerization did not differ from those obtained with water-bath for both acrylic resins. The results observed when polymerization cycles using medium power and shorter time were used did not differ from those when manufacturer's recommended microwave cycle was applied. Conventional VC might be microwave-processed without compromising its flexural properties.

Objective: We examined the influence of light intensity on surface free energy characteristics and dentin bond strength of dual-cure direct core build-up resin systems., Methods: Two commercially available dual-cure direct core build-up resin systems, Clearfil DC Core Automix with Clearfil Bond SE One and UniFil Core EM with Self-Etching Bond, were studied. Bovine mandibular incisors were mounted in acrylic resin and the facial dentin surfaces were wet ground on 600-grit silicon carbide paper. Adhesives were applied to dentin surfaces and cured with light intensities of 0 (no irradiation), 200, 400, and 600 mW/cm(2). The surface free energy of the adhesives (five samples per group) was determined by measuring the contact angles of three test liquids placed on the cured adhesives. To determine the strength of the dentin bond, the core build-up resin pastes were condensed into the mold on the adhesive-treated dentin surfaces according to the methods described for the surface free energy measurement. The resin pastes were cured with the same light intensities as those used for the adhesives. Ten specimens per group were stored in water maintained at 37°C for 24 hours, after which they were shear tested at a crosshead speed of 1.0 mm/minute in a universal testing machine. Two-way analysis of variance (ANOVA) and a Tukey-Kramer test were performed, with the significance level set at 0.05., Results: The surface free energies of the adhesive-treated dentin surfaces decreased with an increase in the light intensity of the curing unit. Two-way ANOVA revealed that the type of core build-up system and the light intensity significantly influence the bond strength, although there was no significant interaction between the two factors. The highest bond strengths were achieved when the resin pastes were cured with the strongest light intensity for all the core build-up systems. When polymerized with a light intensity of 200 mW/cm(2) or less, significantly lower bond strengths were observed. CONClUSIONS: The data suggest that the dentin bond strength of core build-up systems are still affected by the light intensity of the curing unit, which is based on the surface free energy of the adhesives. On the basis of the results and limitations of the test conditions used in this study, it appears that a light intensity of >400 mW/cm(2) may be required for achieving the optimal dentin bond strength.

The purpose of this study was to evaluate the ability of two dentin adhesive systems to induce remineralization in the bonded dentin interface after in vitro thermo-cycling. Dentin surfaces were treated with two different adhesive approaches: (1) 37% phosphoric acid (PA) plus an "etch-and-rinse" dentin adhesive (single bond, SB) (PA+SB) or (2) application of a "self-etch" dentin adhesive (Clearfil SE bond, SEB). Three groups were established: (i) 24 h or (ii) 3 m storage, and (iii) specimens submitted to thermal cycling (100,000 cy/5 and 55ºC). Atomic force microscopy imaging/nanoindentation, Raman spectroscopy/cluster analysis with dye-assisted confocal laser scanning microscopy (CLSM) evaluation and Masson's trichrome staining assessments were implemented for characterization. Thermo-cycling increased nanohardness in PA+SB at the hybrid layer (HL) and in SEB at the bottom of the HL (BHL). Young's modulus increased at both the HL and BHL in SEB and at the HL in PA+SB, after thermal stress. Cluster analysis demonstrated an augmentation of the mineral-matrix ratio in thermo-cycled specimens. CLSM showed a decrease of both micropermeability and nanoleakage after thermo-cycling in PA+SB, and were completely absent in SEB. Trichrome staining reflected a scarce demineralized front in PA+SB after thermo-cycling and total remineralization in SEB.

Cross-linked resin-captured palladium (XL-QPPd) was readily prepared by simple physical adsorption onto the high loading QuadraPure macroporous resin and a subsequent reduction process. To enhance the mechanical stability, entrapped palladium nanocatalysts were cross-linked with succinyl chloride. Both transmission electron microscopy images and X-ray diffraction analysis revealed that the palladium nanoparticles were well dispersed with diameters ranging in 4-10 nm. The catalyst performed good catalytic activity in microwave-promoted Suzuki cross-coupling reactions in water under aerobic condition with mild condition by using various aryl halides and phenylboronic acid. In addition, the catalyst showed an excellent recyclability without significant loss of catalytic activity.

Photocatalysis induced by TiO2 and UV light constitutes a decontamination and antibacterial strategy utilized in many applications including self-cleaning environmental surfaces, water and air treatment. The present work reveals that antibacterial effects induced by photocatalysis can be maintained even after the cessation of UV irradiation. We show that resin-based composites containing 20% TiO2 nanoparticles continue to provide a pronounced antibacterial effect against the pathogens Escherichia coli, Staphylococcus epidermidis, Streptococcus pyogenes, Streptococcus mutans and Enterococcus faecalis for up to two hours post UV. For biomaterials or implant coatings, where direct UV illumination is not feasible, a prolonged antibacterial effect after the cessation of the illumination would offer new unexplored treatment possibilities.

The formation mechanism of space charges in polyimide (PI) which was exposed to dielectric barrier discharge (DBD) in SF6 medium and the effects of the space charges on interfacial and electrical properties of PI were investigated. The variation of normalized surface charge density on PI sample was calculated and illustrated for different DBD exposure times. The surface potential was measured to determine the effect of the space charges on the sample. Then, the contact angle values were measured to obtain the relation between the surface energy and the surface charge density. The expressions for the total charge and the concentration of trapped electrons were derived by using Poisson and continuity equations at stationary state. The space charges were determined experimentally by using thermally stimulated depolarization current (TSDC) method. Also, SEM image and FTIR spectrum of virgin and treated samples were presented to observe the structural variations. It was seen that the approach for the formation mechanism of the space charges agreed with the experimental data. However, it was concluded particularly for the short-time DBD treatments that the space charges accumulated in the sample should be considered besides the effects of surface functionalization in the determination of the surface energy.

Aim: This study evaluated the cytotoxicity of a dental bonding model resin (DBMR) submitted to different photo-activation distances., Methods: A monomer mixture based on Bis-GMA and HEMA was used to assess the cytotoxicity in a mouse fibroblast-cell line. To promote different photo-activation distances glass slides were interposed between DBMR surface and halogen light curing unit (LCU) tip. Afterwards, the specimens were immersed in RPMI culture medium for 24 h to obtain extracts. The extracts were incubated in contact with the cells for 24 h. Finally, an MTT colorimetric assay was used to assess the cytotoxicity. The cell viability data (absorbance) were analyzed by one way ANOVA followed by Tukey's test (P<0.05)., Results: The light output decreased according to the increase in the number of glass slides between the halogen LCU tip and DBMR surface. Yet, the distance between the tip of the curing light system and the specimens had significant influence on the cytotoxicity. All extracts produced by groups submitted to different photo-activation distances showed cytotoxic effect after 24h of incubation., Conclusion: The photo-activation distance and the interposition of glass slides between LCU tip and DBMR was shown to play an important role in the cytotoxic effect.

Delivering an inadequate amount of light to a light-cured resin will result in a resin that is inadequately cured. This study measured the radiant exposure that students delivered to a simulated restoration to determine if instruction with immediate feedback increased the amount of light they delivered. The amount of light (radiant exposure in J/cm(2)) delivered to a simulated restoration by sixty-three dental students using the same curing light for twenty seconds was recorded. The experiment was repeated after the students had been given detailed light-curing instructions together with immediate feedback using the MARCPS system. Initially, the students delivered between 1.4 and 17.5 J/cm(2) (mean±SD: 9.8±3.5 J/cm(2)). After receiving instructions and feedback on their light-curing technique, they delivered between 6.7 J/cm(2) and 17.8 J/cm(2) (mean±SD: 13.2±3.3 J/cm(2)). ANOVA and Fisher's post hoc multiple comparison tests showed that providing immediate feedback on the students' light-curing technique made a significant improvement in the radiant exposure they delivered (p<0.05). It was concluded that many dental students in this study were not using the curing light properly. After the students had received one session of additional instruction and immediate feedback using the MARC-PS, they delivered 35 percent more light energy to the same simulated restoration. Students who were closer to graduation showed a greater improvement in their light-curing technique (p=0.0091).

Objective: Recent studies confirmed that resin-modified glass ionomers (RMGIs) set on the basis of two competing mechanisms, an acid-base reaction and a light-activated resin polymerization. This study evaluated the effect of the setting mechanism on bond strength by measuring the shear bond strength of three RMGIs to dentin with and without light activation., Methods: Sixty human molars were ground to midcoronal dentin and randomly divided into six even groups: 1) Ketac Nano (KN), 2) KN without light cure (woLC), 3) Fuji Filling LC (FF), 4) FF woLC, 5) Fuji II LC (FII), and 6) FII woLC. The dentin surfaces of the specimens were conditioned/primed according to the manufacturers' instructions. A 1.54-mm diameter plastic tube was filled with RMGI material and affixed to the dentin surface. Groups 1, 3, and 5 were light cured for 20 seconds, and groups 2, 4, and 6 were immediately placed in a damp dark box with no light curing at 37°C for 24 hours. Shear bond strength testing was performed in an Instron device at 1 mm/min. Data were analyzed with a one-way analysis of variance (ANOVA) and Tukey/Kramer test (α=0.05)., Results: Mean ± standard deviation shear bond strength values (MPa) are: 7.1 ± 4.2 (KN), 11.7 ± 3.9 (FF), 10.2 ± 3.2 (FF woLC), 12.5 ± 5.1 (FII), and 0.3 ± 0.4 (FII woLC). Two KN, all KN woLC, and seven FII woLC specimens debonded before testing. Tukey/Kramer analysis revealed no significant differences in bond strength between the three light-cured RMGIs. KN and FII showed significantly lower bond strength without light cure, but no significant difference was observed between FF and FF woLC., Conclusions: The results of this study strongly suggest that light activation is necessary to obtain optimal bond strength between RMGI and dentin. FF may contain components that chemically activate resin polymerization. Clinically, KN and FII need to be light cured after placement of these RMGIs.

The aim of this work is to evaluate the effect of surface treatment with Er:YAG and Nd:YAG lasers on resin composite bond strength to recently bleached enamel. In this study, 120 bovine incisors were distributed into two groups: group C: without bleaching treatment; group B: bleached with 35% hydrogen peroxide. Each group was divided into three subgroups: subgroup N: without laser treatment; subgroup Nd: irradiation with Nd:YAG laser; subgroup Er: irradiation with Er:YAG laser. The adhesive system (Adper Single Bond 2) was then applied and composite buildups were constructed with Filtek Supreme composite. The teeth were sectioned to obtain enamel-resin sticks (1 × 1 mm) and submitted to microtensile bond testing. The data were statistically analyzed by the ANOVA and Tukey tests. The bond strength values in the bleached control group (5.57 MPa) presented a significant difference in comparison to the group bleached and irradiated with Er:YAG laser (13.18 MPa) or Nd:YAG (25.67 MPa). The non-bleached control group presented mean values of 30.92 MPa, with statistical difference of all the others groups. The use of Nd:YAG and Er:YAG lasers on bleached specimens was able to improve the bond strengths of them.

The purpose of this study was to investigate the tensile strength of the bond between a silicone lining material and heat-cured polymethyl methacrylate (PMMA) denture base resin after Er:YAG laser treatment with different pulse durations and energy levels. PMMA test specimens were fabricated and each received one of six surface treatments: no treatment (control), and five Er:YAG laser treatments comprising (1) 100 mJ, 1 W, long pulse duration, (2) 200 mJ, 2 W, long pulse duration, (3) 200 mJ, 2 W, very short pulse duration, (4) 300 mJ, 3 W, long pulse duration, and (5) 400 mJ, 4 W, long pulse duration. The resilient liner specimens (n = 15) were processed between two PMMA blocks. The tensile strengths of the bonds between the liners and PMMA were determined using a universal testing machine at a crosshead speed of 5 mm/min. The mode of failure was characterized as cohesive, adhesive, or mixed modes. One-way ANOVA and the post hoc Tukey-Kramer multiple comparisons test were used to analyze the data (α = 0.05). There was a statistically significantly difference in tensile bond strength between laser-treated and untreated specimens (P < 0.05). The 300-mJ, 3 W, long pulse duration laser treatment produced the highest mean tensile bond strength. In addition, the long pulse duration treatments resulted in greater bond strength than very short pulse duration treatment (P < 0.05). Laser irradiation produced significant surface texture changes of the denture base material and improved the adhesion between denture base and soft lining material. In addition, different pulse durations and energy levels were found to effectively increase the strength of the bond.

The aim of this in vitro study was to assess the effect of Er:YAG laser surface treatment on the tensile bond strength of a sealant in permanent teeth. A total of 30 sound third molars were selected and embedded in cold-cure acrylic resin. The enamel surfaces were flattened by a grinding. The teeth were randomly divided into three groups and pretreated as follows: (1) 37% phosphoric acid; (2) Er:YAG laser (1.5 ml/min water spray, 100 mJ energy output, 10 Hz frequency, focal distance 17 mm); (3) Er:YAG laser + 37% phosphoric acid. The treated surfaces were isolated by double adhesive Sellotape and after insertion of a split Teflon matrix at an isolated site, sealant was applied. The specimens were thermocycled and stored at 37°C in distilled water for 72 h, then subjected to a tensile bond strength test (50 kgf at 0.5 mm/min). The mean tensile bond strengths (± SD, in megapascals) were: 18.51 ± 5.68 in group 1, 8.06 ± 2.69 in group 2, and 17.33 ± 5.04 in group 3. Data were submitted to analysis of variance and the Tukey test. No significant difference were found between groups 1 (37% phosphoric acid) and group 3 (Er:YAG laser + 37% phosphoric acid) but treatment with the Er:YAG laser alone (group 2) resulted in significantly lower tensile bond strength than seen in the other groups. In this setting, the Er:YAG laser prepared the enamel surface for sealing but did not eliminate the need for acid etching before sealant application.

The purpose of this study was to evaluate whether a Gallium Nitride (GaN) -based violet laser diode (VLM500) could be used as a light source for light-cured dental resins. Three experimental unfilled resins containing different photoinitiators (camphorquinone, CQ; phenyl propanedione, PPD; or mono acylphosphineoxide, MAPO) were evaluated. These resins were light-cured with a VLM500 laser diode, and their ultimate micro-tensile strengths (μTS) were compared to those cured with three different LED light sources (Curenos, G-Light Prima-normal mode and G-Light Prima-PL mode). The VLM500 produced high μTS values in all three resins, and we concluded that this violet laser diode can be used as a light source for light-cured dental resin materials.

A high temperature polyimide bearing anthracene moieties, poly(3,3'-di(9-anthracenemethoxy)-4,4'-biphenylene hexafluoroisopropylidenediphthalimide) (6F-HAB-AM PI) was synthesized. The polymer exhibits excellent thermal stability up to around 410 °C. This polymer is amorphous but orients preferentially in the plane of nanoscale thin films. In device fabrications of its nanoscale thin films with metal top and bottom electrodes, no diffusion of the metal atoms or ions between the polymer and electrodes was found; however, the aluminum bottom electrode had somewhat undergone oxide layer (about 1.2 nm thick) formation at the surface during the post polymer layer formation process, which was confirmed to have no significant influence on the device performance. The polymer thin film exhibited excellent unipolar and bipolar switching behaviors over a very small voltage range, less than ±2 V. Further, the PI films show repeatable writing, reading, and erasing ability with long reliability and high ON/OFF current ratio (up to 10(7)) in air ambient conditions as well as even at temperatures up to 200 °C.

Aim: This study compared the microleakage of light cure glass ionomer and flowable compomer as pit and fissure sealant, with and without tooth preparation., Materials and Methods: One hundred premolars that were extracted for orthodontic purpose were used. After adequate storage and surface debridement, the teeth were randomly divided into four groups. In Group I and III, the occlusal surfaces were left intact, while in Group II and Group IV, tooth surfaces were prepared. Teeth in Group I and Group II were sealed with Light cure glass ionomer, whereas flowable compomer was used to seal teeth in Group III and IV. The sealed teeth were then immersed in dye. Subsequently, buccolingual sections were made and each section was examined under stereomicroscope for microleakage followed by scoring., Results: In group I, microleakage score ranged from 2 to 4 with mean of 3.64 (±0.757), while in group II the range was observed to be 1-4 with mean of 2.88 (±1.236). Group III recorded a range of 0-4 with the mean of 2.20 (±1.443) while 0-2 and 0.60 (±0.707) being the range and mean observed, respectively, for group IV., Conclusion: Flowable compomer placed after tooth preparation showed better penetration and less marginal leakage than the light cure glass ionomer.

Introduction: Electron-beam irradiation can be used to influence the properties of polymers. Electron beams cause cross-linking that enhances the molecular mass of the polymer; this leads to branched chains until, ultimately, a 3-dimensional network is formed. The aim of this study was to evaluate the effect of electron-beam irradiation on polymer bracket materials., Methods: Since polymers are commonly used materials for brackets, polyoxymethylene, polycarbonate, and polyurethane were chosen for this study. The acceleration voltage of the electron-beam device was 10 MeV, and the energy dose was 100 kGy with an electron accelerator (BGS beta gamma service, Rhodotron, Bruchsal, Germany). Three-medium wear, fracture toughness, and Vickers hardness tests were performed. The irradiated samples were compared with untreated control groups., Results: Polycarbonate and polyurethane bracket materials have enhanced fracture toughness and Vickers hardness after electron-beam irradiation of 100 kGy and 10 MeV. Polyoxymethylene bracket materials showed significantly lower fracture toughness values after irradiation compared with the untreated control group. Polyoxymethylene had the best mechanical properties, followed by polycarbonate and polyurethane. Almost the same effects could be measured during the 3-medium wear test., Conclusions: Electron-beam postcuring improved Vickers hardness and fracture toughness of polymers with lower mechanical properties (polycarbonate and polyurethane). Polyoxymethylene, with sufficient hardness and fracture toughness, could not be improved with electron-beam postcuring., (Copyright © 2011 American Association of Orthodontists. Published by Mosby, Inc. All rights reserved.)

Camphorquinone (CQ) derivatives having acylphosphine oxide (APO) group are unknown. This study synthesized such a novel 7,7dimethyl-2,3-dioxobicyclo[2.2.1]heptane-1-carbonyldiphenyl phosphine oxide (DOHC-DPPO = CQ-APO). Ultraviolet and visible (UVVIS) spectra of CQ-APO, CQ, and APO were measured. Photopolymerization performances of experimental light-cured resins comprising these photoinitiators were investigated. Newly synthesized CQ-APO showed as a pale yellow crystal (mp 365K). UV-VIS spectrum of CQ-APO showed two maximum absorption wavelengths (lambda(max)) [372 nm (from APO group) and 475 nm (from CQ moiety)] within 350-500 nm. Unfilled resin containing CQ-APO exhibited good photopolymerization time (9.6 sec) and relaxed operation time (50 sec), as well as a pronouncedly lower b value (4.0) in the CIELab color specification system than that containing CQ (84.0). Resin composites containing CQ-APO, exhibited high flexural strength (114.3-133.8 MPa). It was concluded that CQ-APO possessed two lambda(max )peaks within 350-500 nm, and that CQ-APO-containing resins exhibited excellent color tone, good photopolymerization reactivity, relaxed operation time, and high mechanical strength.

Purpose: To determine the effect of operator, curing light and preparation location, as well as any correlations among these variables, on the amount of light energy delivered to simulated cavity preparations., Materials and Methods: Each of 10 dentists and 10 fourth-year dental students light-cured a Class I preparation in tooth 26 and a Class V preparation in tooth 37 in a dental mannequin head. The operators exposed each preparation for 10 seconds with each of 3 LED-based curing lights (Bluephase G2 on high power, Demi and VALO on standard power). Each operator also used the VALO unit in the plasma mode for 2 sequential 3-second curing cycles. For each combination of operator, curing light and preparation, the irradiance (mW/cm(2)) received at the base of the preparation was measured with a laboratory-grade spectroradiometer, and software was used to calculate the energy density delivered in real time. The statistical analysis included 3-way analysis of variance (ANOVA) and the Fisher protected least significant difference (PLSD) test for post hoc pairwise comparisons., Results: There was a large qualitative and quantitative variation in the irradiance delivered to the preparations by each operator. Three-way ANOVA showed no statistically significant differences between dentists and dental students in terms of the amount of energy delivered (p = 0.90). However, there were statistically significant differences in energy delivered by the various curing lights (p < 0.001) and between the 2 preparation locations (p < 0.001). According to the Fisher PLSD test for post hoc pairwise comparison of means, the VALO unit used in the plasma mode for two 3-second curing cycles delivered the most energy (16.4 +/- 3.1 J/cm(2)) to the Class I preparation, and the same light used for 10 seconds in the standard mode delivered the least amount of energy (9.9 +/- 2.4 J/cm(2)) (p < 0.001). For the Class V preparation, the VALO unit used in the plasma mode for two 3-second curing cycles delivered the most energy (12.5 +/- 4.0 J/cm(2)), and the Demi unit, used for 10 seconds, delivered the least energy (7.4 +/- 2.5 J/cm(2))., Conclusions: The energy delivered by a curing light to a preparation in a simulated clinical environment was affected by the operator's light-delivery technique, the choice of curing light and the location of the preparation.

A natural component, sesamin (SA), was used to replace conventional amine as co-initiator for dental composite. A combination of camphorquinone (CQ) and SA was employed to initiate the photopolymerization of 2-2-bis[4-(2-hydroxy-3-methacryloxyprop-1-oxy)phenyl] propane/triethylene glycol dimethacrylate (70/30wt.%). The kinetics was recorded by real-time Fourier transform infrared spectroscopy. The mechanical properties were measured by dynamic mechanical analysis, the cell toxicity was investigated by MTT assay and a mixture of CQ and ethyl 4-N,N-dimethylaminobenzoate (EDMAB) was used as control in the same photocuring condition. The results indicated that the addition of SA as co-initiator greatly improved the rate of polymerization and final double-bond conversion (DC) when compared with the system initiated by CQ alone. Compared with EDMAB, the final DC of the CQ/SA system (71%) was slightly lower than that of CQ/EDMAB (76%); SA resulted in approximately the same storage modulus at around 37 degrees C, but a slightly higher glass transition temperature. SA produced lower yellowing effect and good in vitro biocompatibility. The water sorption and solubility for two mixtures were very close and within the range of the ISO 4049 specification. These results suggest that SA is an effective alternative co-initiator to conventional amine. The natural compound characteristics of SA make it more promising than amine in dental resin formulations.

Objectives: To monitor the influence of the power density of the curing unit on the setting behaviour of light-cured glass-ionomer cements (LCGICs) using ultrasound measurements., Methods: The ultrasound equipment comprised a pulser-receiver, transducers and an oscilloscope. The LCGICs used were Fuji II LC, Fuji II LC EM and Fuji Filling LC. The cements were mixed according to the manufacturer's instructions and then inserted into a transparent mould. The specimens were placed on the sample stage and cured with power densities of 0 (no irradiation), 200 or 600 mW/cm(2). The transit time through the cement disk was divided by the specimen thickness and then the longitudinal ultrasound velocity (V) within the material was obtained. Analysis of variance and Tukey's Honestly Significantly Different test were used to compare the V values between the set cements., Results: When the LCGICs were light-irradiated, each curve displayed an initial plateau at approximately 1500 m/s and then rapidly increased to a second plateau at approximately 2600 m/s. The rate of increase of V was retarded when the cements were light-irradiated with a power density of 200 mW/cm(2) than with a power density of 600 mW/cm(2). Although sonic echoes were detected from the beginning of the measurements, the rates of increase of the sonic velocity were relatively slow when the cement was not light-irradiated., Conclusions: The ultrasound device monitored the setting processes of LCGICs accurately based on the longitudinal V. The polymerization behaviour of LCGICs was shown to be affected by the power density of the curing unit.

Purpose: To evaluate in vitro the solubility of the Epiphany endodontic filling material Epiphany (Pentron Clinical Technologies, Wallingford, CT) prepared with its resinous solvent., Methods: The specimens were prepared in the following experimental conditions: (1) GI, epiphany without photoactivation; (2) GII, Epiphany prepared with resinous solvent without photoactivation; (3) GIII, Epiphany followed by photoactivation; and (4) GIV, Epiphany prepared with resinous solvent followed by photoactivation. Ten specimens of each group were obtained from Teflon molds with 80% reduction in volume of the specimen's dimensions based on American National Standard Institute/American Dental Association (ANSI/ADA) Specification No. 57. The samples were weighted and immersed in distilled water for 7 days. After this period, they were removed, dried, and weighed again. Solubility was calculated by using samples weight loss (%). The immersion liquid was evaluated through atomic absorption spectrometry., Results: The sealers without photoactivation were statistically similar (p > 0.05) between themselves (GI = 6.93% and GII = 6.39%) and different from the uncured sealers, which were statistically different between themselves (p < 0.05) (GIII = 3.56% and GIV = 0.47%). Only the Epiphany sealer prepared with resinous solvent followed by photoactivation presented solubility values within ANSI/ADA requirements, liberating the following amounts of ions: 114.43 microg of Ca(2+)/mL, 2.4 microg of Mg(2+)/mL, 0.33 microg of Fe(2+)/mL, 0.11 microg of Zn(2+)/mL, 1.31 microg of Ni(2+)/mL, and 7.1 microg of Na(+)/mL., Conclusion: The association of resinous solvent to the Epiphany sealer followed by photoactivation resulted in a filling material with low solubility and expressive liberation of calcium ions.

Objective: To evaluate the microhardness of resin-modified glass-ionomer cements (RMGICs) photoactivated with a blue light-emitting diode (LED) curing light., Material and Methods: Thirty specimens were distributed in 3 groups: Fuji II LC Improved/GC (RM1), Vitremer/3M ESPE (RM2) and Filtek Z250/3M ESPE (RM3). Two commercial light-curing units were used to polymerize the materials: LED/Ultrablue IS and a halogen light/XL3000 (QTH). After 24 h, Knoop microhardness test was performed. Data were submitted to three-way ANOVA and Tukey's test at a pre-set alpha of 0.05., Results: At the top surface, no statistically significant difference (p>0.05) in the microhardness was seen when the LED and QTH lights were used for all materials. At the bottom surface, microhardness mean value of RM2 was significantly higher when the QTH light was used (p<0.05). For RM1, statistically significant higher values (p<0.05) were seen when the LED light was used. No statistically significant difference (p>0.05) was seen at the bottom surface for RM3, irrespective of the light used. Top-to-bottom surface comparison showed no statistically significant difference (p>0.05) for both RMGICs, regardless of the light used. For RM3, microhardness mean value at the top was significantly higher (p<0.05) than bottom microhardness when both curing units were used., Conclusion: The microhardness values seen when a LED light was used varied depending on the restorative material tested.

Objectives: To investigate if and why a plasma arc curing (PAC) light tends to undercure methacrylate-based resins or resin composites., Methods: Model dimethacrylate resins, commercial dental adhesives, and commercial resin composites were cured using a PAC light and a halogen light with the similar radiant exposures but different combinations of irradiance and irradiation time. The degree of double bond conversion (DC) was measured with FTIR spectroscopy and analyzed as a function of radiant exposure., Results: The PAC light produced a lower DC than the halogen light for the model resin with the lowest viscosity and for three of the four adhesives. With a high irradiance, the PAC light could cure three of the four composites as thoroughly as its halogen counterpart. When the irradiance was reduced, however, three composites yielded a lower DC., Conclusions: Insufficient cure by PAC lights or any curing lights with very high irradiance is likely to happen when too short an irradiation time is used. It is because under higher irradiance, the lifetime of free radicals is shorter.

This study evaluated the effect of gamma irradiation on fluoride release and antibacterial activity of FluroShield (FS) and Clearfil Protect Bond (CPB). Four groups were formed: G1-FS + gamma; G2-FS without gamma; G3-CPB + gamma; G4-CPB without gamma. For fluoride release analysis, 12 disks of each material were prepared and covered with nail polish, except for one side (50.4 mm(2) area). G1 and G3 were sterilized with a 14.5 KGy dose at 27 degrees C for 24 h, while G2 and G4 (controls) were not sterilized and were maintained under the same time and temperature conditions. Fluoride release measurements were made in duplicate (n=6) by an ion specific electrode. The antibacterial activity of the CPB and FS against Streptococcus mutans after gamma sterilization was evaluated by the agar-disc diffusion method. The diameter of the zones of microbial growth inhibition was recorded after 48 h. Data were analyzed statistically by ANOVA and Tukey's test (alpha=5%). Gamma sterilization decreased the fluoride release of FS by approximately 50%, while CPB was not affected. There was no statistically significant difference (p>0.05) in the antibacterial effect of CPB between gamma and non-gamma sterilization groups. FS presented no antibacterial activity. Gamma irradiation decreased the fluoride release of FS, but did not affect the antibacterial activity of the studied materials.

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.

The effect of the 488-nm wavelength of argon laser at different power densities and irradiation times on the degree of conversion (DC), temperature rise, water sorption, solubility, flexural strength, flexural modulus, and microhardness of bisphenole A glycol dimethacrylate and triethylen glycol dimethacrylate with a mass ratio of 75:25 was studied. Camphorquinone and N,N'-dimethyl aminoethyl methacrylate were added to the monomer as a photo initiator system. The DC% of the resin was measured using Fourier transform infrared spectroscopy. The maximum DC% (50%), which was reached in 20 s, and temperature rise because of the reaction (13.5 degrees C) were both higher at 1075 than 700 mW/cm(2). Water sorption and solubility were measured according to ISO4049, which in our case were 23.7 and 2.20 microg/mm(3) at 1075 mW/cm(2), respectively. A flexural modulus of 1.1 GPa and microhardness of 19.6 kg/mm(2) were achieved above the power density. No significant difference was observed (i.e., p>0.05) for water sorption and flexural strength at 700 and 1075 mW/cm(2).

Unlabelled: Attempts have been made to improve the mechanical properties and convenience of use of glass-ionomer cement (GIC) by various modifications, in particular by including a free radical-polymerizable component ("resin-modified" GIC, RMGIC). Necessarily, the one replaces part of the other, but the chemistry suggests that the formation of each network separately would inhibit diffusion and thus the other reaction., Objective: To ascertain whether interference occurs between the components of an RMGIC by variation of the irradiation regime., Materials and Methods: Cylindrical specimens (6 mm x 3 mm diameter) of one brand of RMGIC (Shades A3, D2; Fuji II LC, GC; capsules) were prepared in ptfe moulds. After machine-mixing for 10s, each of the three increments was irradiated from the top for various times (0-60s). In addition, extra irradiation from the bottom; from the bottom before, and from the side after, ejection from the mould; the same using two curing lamps; and at various delays after mixing (0-18 h), with four replicates of each. After exposure, or as appropriate, specimens were wrapped tightly in aluminium foil for dry storage in the dark at 37 degrees C for testing at 24h after mixing. Specimens with evident defects were replaced before testing., Results: No increase in strength was found beyond the recommended 20-s irradiation, indeed further exposure reduced the strength. For top-only irradiation, strength rose from the unirradiated value (66+/-9 MPa) to a peak at 20s (215+/-25 MPa), after which it declined steadily. Adding bottom irradiation gave a small decrease in peak value (194+/-36 MPa); adding side irradiation reduced it substantially (113+/-7 MPa). Delay for 2 min gave a marked reduction (155+/-15 MPa), declining to the unirradiated value at 18 h (70+/-15 MPa). No effect due to shade was detected., Significance: Competition between network-forming reactions leads to a sensitive balance between the two, and a critical optimum irradiation: too much may be detrimental, as is delay. The essential compromise involved in such mixed chemistry jeopardizes reliability. It is advisable to follow the duration of exposure prescribed by the manufacturer to achieve optimal performance.

To develop practical and inexpensive multichannel neural electrodes, we designed and fabricated photosensitive polyimide based flexible multichannel neural electrodes using MEMS technologies. Compared to a conventional micromachining with non-photosensitive materials, the advantage of applying photosensitive polyimide is the elimination of the dry etching, which involves the complex multilevel processes for controlling the etching conditions to define the outline of the neural electrodes and expose the microelectrodes. Thus, photosensitive polyimide allows more options in optimization of the configuration and size of neural electrodes depending on experimental purposes, and enables fabrication at a lower cost with improvement of process yields.

Stereolithography using photo-cross-linkable polymeric biomaterials is an effective technique for fabricating highly complex three-dimensional (3D) scaffolds with controlled microstructures for tissue engineering applications. In this study, we have optimized the UV curable polymer solution composition and laser parameters for the stereolithography machine. Poly(propylene fumarate) (PPF) was used as the biomaterial, diethyl fumarate (DEF) was used as the solvent, and bisacrylphosphrine oxide (BAPO) was used as the photoinitiator. Three different weight ratios of PPF/DEF and BAPO contents were characterized by measuring the viscosities and thermal properties of the un-cross-linked solutions and the mechanical properties of the formed scaffolds. After optimizing the resin composition by satisfying both the viscosity limitation and the mechanical requirement, laser parameters such as critical exposure (Ec) and penetration depth (Dp) were determined from the working curve and the relationship between laser speed and energy by measuring the thickness of predesigned windows fabricated in stereolithography with different ranges of Ec and Dp. Three-dimensional scaffolds with various pore sizes, pore shapes, and porosities were designed in computer-aided design (CAD) software and were fabricated in stereolithography. The fabricated scaffolds were characterized by measuring external dimensions, porosities, mean pore sizes, and compressive moduli and were compared to the CAD models. Feature accuracy in the xy-plane was achieved and overcuring of the resin in z-axis was minimized. The stereolithographically fabricated scaffolds with controlled microstructures can be useful in diverse tissue engineering applications.

In chronic recording experiments, self-curing dental acrylic resins have been used as a mounting base of electrodes or microdialysis-probes. Since these acrylics do not bond to the bone, screws have been used as anchors. However, in small experimental animals like finches or mouse, their craniums are very fragile and can not successfully hold the anchors. In this report, we propose a new application of light-curing dental resins for mounting base of electrodes or microdialysis probes in chronic experiments. This material allows direct bonding to the cranium. Therefore, anchor screws are not required and surgical field can be reduced considerably. Past experiences show that the bonding effect maintains more than 2 months. Conventional resin's window of time when the materials are pliable and workable is a few minutes. However, the window of working time for these dental adhesives is significantly wider and adjustable.

Solid-phase synthesis of diketopiperazines (DKPs) was preformed using various combinations of resins (polystyrene, TentaGel, ArgoGel, and PEGA) and solvents (toluene, tert-butyl alcohol, water, and toluene/2-butanol (1:4, v/v). The DKPs were synthesized from solid-phase bound dipeptides via intramolecular aminolysis. Both thermal and microwave-assisted solid-phase synthesis of DKPs gave high yields of products independently of resin and organic solvent used; however, only the PEGA resin resulted in high yields of DKPs in water independent of heating method. The short reaction times, high yields, and the possibility to run reactions in water when an appropriate resin is used makes the microwave-assisted solid-phase synthesis the method of choice. The method should be suitable for solid-phase synthesis of diketopiperazine-based libraries.

Objective: The aim of this in vitro study was to evaluate the cytotoxicity of resin-modified glass-ionomer lining cements submitted to different curing regimes and applied to an immortalized odontoblast-cell line (MDPC-23)., Methods: Forty round-shaped specimens of each experimental material (Fuji Lining LC and Vitrebond) were prepared. They were light-cured for the manufacturers' recommended time (MRT = 30 s), under-cured (0.5 MRT = 15 s), over-cured (1.5 MRT = 45 s) or allowed to dark cure (0 MRT). Sterilized filter papers soaked with either 5 microL of PBS or HEMA were used as negative and positive control, respectively. After placing the specimens individually in wells of 24-well dishes, odontoblast-like cells MDPC-23 (30,000 cells/cm2) were plated in each well and incubated for 72 h in a humidified incubator at 37 degrees C with 5% CO2 and 95% air. The cytotoxicity was evaluated by the cell metabolism (MTT assay) and cell morphology (SEM)., Results: Fuji Lining LC was less cytotoxic than Vitrebond (p < 0.05) in all the experimental conditions. However, the cytotoxicity of Fuji Lining LC was noticeably increased in the absence of light-curing while the same was not observed for Vitrebond. The length of light-curing (15, 30 or 45 s) did not influence the toxicity of both lining materials when they were applied on the odontoblast-cell line MDPC-23., Significance: The light-activation plays an important role in reducing the cytotoxicity of Fuji Lining LC. Following the manufacturer' recommendation regarding the light-curing regime may prevent toxic effect to the pulp cells.

Objectives: To evaluate the efficiency of the photopolymerization of dental resins it is necessary to know to what extent the light emitted by the light curing units is absorbed by the photoinitiators. On the other hand, the efficiency of the absorbed photons to produce species that launch the polymerization process is also of paramount importance. Therefore, the previously determined PAE (photon absorption efficiency) is used in conjunction with the polymerization quantum yields for the photoinitiators, in order to be able to compare the total process on an equivalent basis. This parameter can be used to identify the best performance for the photochemical process with specific photoinitiators., Methods: The efficiency of LED (Ultrablue IS) and QTH (Optilux 401) lamps were tested comparing their performances with the photoinitiators camphorquinone (CQ); phenylpropanedione (PPD); monoacylphosphine oxide (Lucirin TPO); and bisacylphosphine oxide (Irgacure 819). The extent of photopolymerization per absorbed photon was determined from the polymerization quantum yields obtained by using the photoinitiators to polymerize methyl methacrylate, and afterwards combined with the previously determined PAEs., Results: Although CQ presents a rather low polymerization quantum yield, its photopolymerization efficiency is practically the highest when irradiated with the Ultrablue LED. On the other hand, Lucirin is much more efficient than the other photoinitiators when irradiated with a QTH lamp, due to its high quantum yield and the overlap between its absorption spectrum and the output of the visible lamp light., Significance: Difference in photopolymerization efficiencies arise when combinations of photoinitiators are used, and when LED sources are used in preference to QTH. Mechanistic understanding is essential to optimal initiator formulation.

Merrifield resin was functionalised with hydroxybenzaldehyde under microwave irradiation. The resultant resin was used as a means for immobilisation and activation of alpha-amino acid esters for alkylation reactions. Alpha,alpha-disubstituted and cyclic amino acid esters were prepared in good yields.

This article describes a technique for fabricating an obturator prosthesis using new visible light-polymerized resin denture base material. This technique incorporates the advantages of a processed record base that allows a more stable record base to assist with making maxillomandibular relationship records.

Making an incorrect selection of polymeric materials, formulations and compounding can result in a compromised design and impaired functionality of the end product. Part I of this article provides guidance on how to simplify and expedite materials selection.

The solution-phase preparation of the 3',5'-dialkoxybenzoin photolabile safety-catch linker 16 is described. Pivotal to this convenient synthesis is the selection of appropriate orthogonal protecting groups for the alkoxy functionalities present. The new linker can be readily loaded onto any standard amine-terminating resin under peptide-coupling conditions, without the need to protect the secondary alcohol functionality, and subsequently loaded with substrate. Alternatively, the loading efficiency of sterically hindered substrates can be enhanced by preloading the semiprotected linker variant 10 in solution prior to immobilization onto the resin. This second generation of benzoin photolabile safety-catch linkers provides greater control of both linker loading and resin attachment and should prove to be a more versatile and convenient form of the linker.

To develop materials for shielding astronauts from the hazards of GCR, natural Martian surface materials are considered for their potential as radiation shielding for manned Mars missions. The modified radiation fluences behind various kinds of Martian rocks and regolith are determined by solving the Boltzmann equation using NASA Langley's HZETRN code along with the 1977 Solar Minimum galactic cosmic ray environmental model. To develop structural shielding composite materials for Martian surface habitats, theoretical predictions of the shielding properties of Martian regolith/polyimide composites has been computed to assess their shielding effectiveness. Adding high-performance polymer binders to Martian regolith to enhance structural properties also enhances the shielding properties of these composites because of the added hydrogenous constituents. Heavy ion beam testing of regolith simulant/polyimide composites is planned to validate this prediction. Characterization and proton beam tests are performed to measure structural properties and to compare the shielding effects on microelectronic devices, respectively.

Unlabelled: The development and continued evolution of photopolymerizable dental materials, particularly dental composite restoratives, represent a significant, practical advance for dentistry. The highly successful integration of the light-activated curing process for dental applications is described in this review. The basic mechanisms by which the photoinitiators efficiently convert monomers into polymers are discussed along with the variety of factors that influence the photopolymerization process. The conventional camphorquinone-amine visible light photoinitiator system used in most dental restorative materials is illustrated in addition to some alternative initiator systems that have been studied for dental materials applications., Clinical Significance: Photopolymerization has become an integral component of the practice of dentistry. A better appreciation of the photopolymerization process as well as its potential and limitations may aid the dentist in the delivery of both esthetic and restorative dental care.

Background and Objective: The argon laser has been promoted as a competing technology to multi-wavelength visible light as a curing source for dental restorative resins. However, the comparative thermal risk to the pulp between these two sources of light energy requires determination. The objective of this study is to compare the temperature induced at the dentin-pulpal interface between the argon laser and visible light curing unit at a variety of exposure regimens and conditions., Study Design/materials and Methods: In vitro temperatures were measured and recorded at the dentin-pulpal interface upon external light exposure. Independent variables included the dentin thickness, duration and waveform of exposure, and presence of composite resin., Results: In most instances, the argon laser resulted in less temperature rise on the pulpal-dentin interface., Conclusion: The argon laser should not pose a serious thermal risk to the pulp if used at recommended energies., (Copyright 2000 Wiley-Liss, Inc.)

Objectives: Recently, a new restorative material called a 'compomer', which is classified as a polyacid-modified resin composite, has become available. The volumetric shrinkage of compomers may create marginal gaps that influence the bonding ability and longevity of a restoration. Since compomers have been introduced recently, their volumetric change during curing is not fully understood. The purpose of this study was to evaluate the volumetric change of compomers., Methods: Three compomers, Compoglass (Vivadent), Dyract (Dentsply), and Ionosit Fil (DMG) were employed. The material was placed into a Teflon mould, 4 mm in diameter and 2 mm height, and extruded into the dilatometer. Then the specimens were light activated and the change in the height of the meniscus of water was recorded using a CCD camera and VRC., Results: The average volumetric shrinkages of the compomers after 160 s were 2.4% for Compoglass, 2.7% for Dyract, and 2.1% for Ionosit-Fil. For all materials tested, there was a tendency of increasing volumetric shrinkage with increased irradiation time., Conclusions: The results of this study indicate that the volumetric change of compomer is influenced by the duration of light exposure, light intensity, and environmental conditions to which the materials are exposed.