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Dental Composites (dental + composite)
Selected AbstractsHyperbranched polyesters and their application in dental composites: monomers for low shrinking compositesPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 6 2001J. E. Klee Abstract Using trimethylolpropane (TMP) and 2,2-bishydroxymethylpropionic acid (Bis-MPA), aliphatic hyperbranched polyesters (HBP) were synthesized, with a degree of branching of DB,=,0.47 and a degree of polymerization of Pn,=,16.5. Aromatic HBPs with repetitive units of 2,2-bis(4-hydroxyphenyl)pivalonic acid (Bis-PVA) lead to a higher DB,=,0.48 and Pn,=,30.5 compared to the aliphatic HBP. Reactive functionalization of the hyperbranched polymers was achieved via esterification of mixtures of methacrylic acid and carboxylic acids. In this manner, i -butyric acid and methacryloyl terminated HBPs were obtained. They have a low viscosity ranging from 200 to 364,Pa*s and exhibit relatively low volume shrinkage (1.9 to 3.6%) during photoinitiated cure. Dental composites with volume shrinkage of 0.5 to 1.5% have been prepared using these methacryloyl terminated HBPs in combination with a Ba/alumosilicate glass filler. Copyright © 2001 John Wiley & Sons, Ltd. [source] Dentin surface treatment using a non-thermal argon plasma brush for interfacial bonding improvement in composite restorationEUROPEAN JOURNAL OF ORAL SCIENCES, Issue 5 2010Andy C. Ritts Ritts AC, Li H, Yu Q, Xu C, Yao X, Hong L, Wang Y. Dentin surface treatment using a non-thermal argon plasma brush for interfacial bonding improvement in composite restoration. Eur J Oral Sci 2010; 118: 510,516. © 2010 Eur J Oral Sci The objective of this study was to investigate the treatment effects of non-thermal atmospheric gas plasmas on dentin surfaces used for composite restoration. Extracted unerupted human third molars were prepared by removing the crowns and etching the exposed dentin surfaces with 35% phosphoric acid gel. The dentin surfaces were treated using a non-thermal atmospheric argon plasma brush for various periods of time. The molecular changes of the dentin surfaces were analyzed using Fourier transform infrared spectrophotometry/attenuated total reflectance (FTIR/ATR), and an increase in the amount of carbonyl groups was detected on plasma-treated dentin surfaces. Adper Single Bond Plus adhesive and Filtek Z250 dental composite were applied as directed. To evaluate the dentin/composite interfacial bonding, the teeth thus prepared were sectioned into micro-bars and analyzed using tensile testing. Student,Newman,Keuls tests showed that the bonding strength of the composite restoration to peripheral dentin was significantly increased (by 64%) after 30 s of plasma treatment. However, the bonding strength to plasma-treated inner dentin did not show any improvement. It was found that plasma treatment of the peripheral dentin surface for up to 100 s resulted in an increase in the interfacial bonding strength, while prolonged plasma treatment of dentin surfaces (e.g. 5 min) resulted in a decrease in the interfacial bonding strength. [source] Fixed partial dentures: all-ceramics, fibre-reinforced composites and experimental systemsJOURNAL OF ORAL REHABILITATION, Issue 9 2003M. Rosentritt Summary, The aim of this in vitro study was to compare the fracture strength of three-unit FPDs (fixed partial dentures) and three-unit inlay FPDs after a simulated 5-year oral wearing period. The restorations were made of a pressable all-ceramic (Empress 2) and two specially designed, experimentally fixed partial dentures combining ceramics with dental composite. Three-unit FPDs and inlay FPDs were manufactured and were adhesively luted onto human molars. After thermal cycling and mechanical loading in an artificial environment, the fracture strength was determined. Zircon-based milled ceramic (Lava) three-unit FPDs were used as a control. The zircon ceramic and the fibre-based ceramic three-unit FPDs showed median fracture values between 1000 and 1400 N. For composite veneered zircon FPDs a fracture strength of about 800 N and for all-ceramic Empress 2 of about 350 N could be determined. The results for the inlay FPDs were between 1300 N and 1400 N for FRC/ceramic, 1000 N for zircon/composite and 500 N for all-ceramic restorations. The all-ceramic showed higher fracture resistance applied as inlay FPDs. The described hybrid techniques combining ceramics and composites could represent an interesting procedure for further investigations and, eventually, clinical implication. [source] Influence of fibre position on the flexural properties and strain energy of a fibre-reinforced compositeJOURNAL OF ORAL REHABILITATION, Issue 7 2003A. Ellakwa summary, The introduction of laboratory-processed composite systems and fibre reinforcement techniques have increased the possibilities for the prosthetic replacement of missing tooth tissues. Laboratory fabrication variables may significantly influence the properties of the final prosthesis. During the construction of a fibre-reinforced bridge it is necessary to place the fibre at some distance from the fitting surface of the restoration in the pontic region. No guidelines are available for optimal fibre placement in this respect. The purpose of this study was to assess the influence of placing ultra high molecular weight polyethylene (UHMWPE) fibre at five different distances from the tensile side of test samples on flexural properties and the strain energy stored within the dental composite. The results of this investigation showed that whilst moving the fibre reinforcement away from the tensile side by up to 1·5 mm led to a significant reduction in flexural strength, there was no significant decline in the increase in strain energy stored within the tested composite until this distance was exceeded. [source] The influence of fibre placement and position on the efficiency of reinforcement of fibre reinforced composite bridgeworkJOURNAL OF ORAL REHABILITATION, Issue 8 2001A. E. Ellakwa The effect of placement of ultra-high molecular weight polyethylene (UHMWPE) fibres on the flexural properties and fracture resistance of a direct dental composite was investigated. The UHMWPE fibres are increasingly being used for the reinforcement of laboratory fabricated resin composite crown and bridgework. The aim of this study was to assess the effect of a commonly used laboratory fabrication variable on the in vitro strength of beam shaped specimen simulating a three-unit fixed bridge. Four groups (10 specimens per group) of Herculite XRV were prepared for flexural modulus and strength testing after reinforcement with UHMWPE fibres. Two groups of control specimens were prepared without any fibre reinforcement. Half the specimen groups were stored in distilled water and the other groups were stored dry, both at 37 °C for 2 weeks before testing. The results of this study showed that placement of fibre at or slightly away from the tensile side improved the flexural properties of the composite in comparison with the unreinforced control specimen groups whilst the mode of failure differed according to fibre position. Scanning electron microscope (SEM) investigation revealed that placement of the fibre slightly away from the tensile side favoured crack development and propagation within the resin bridging the interfibre spaces in addition to debonding parallel to the direction of fibre placement. Laboratory fabrication variables may effect the strength of fibre reinforced bridgework significantly. [source] Correlation of Ultrastructure with Mechanical Properties of Nano-Hybrid Dental Composites,ADVANCED ENGINEERING MATERIALS, Issue 10 2009Lena Schmitt Determination of mechanical properties of nano-hybrid dental composites leads to strong correlation to material's ultrastructure. Not only does total filler content in percentage of weight affect the mechanical properties, but the combination of optimal filler size and shape with homogeneous distribution of filler particles and an optimal amount of different sized fillers in finally cured dental composites lead to desired mechanical and thermo-mechanical properties. [source] Effect of the structure of silane-coupling agent on dynamic mechanical properties of dental resin-nanocompositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008Irini D. Sideridou Abstract This work was aimed at the study by dynamic mechanical analysis (DMA) of dental composites consisted of a Bis-GMA/TEGDMA (50/50 wt/wt) matrix and silica nanoparticles (Aerosil OX50) as filler, silanized with various silanes. The silanes used were 3-[(1,3(2)-dimethacryloyloxypropyl)-2 (3)-oxycarbonylamido] propyltriethoxy-silane (UDMS), 3-methacryloxypropyl-trimethoxysilane (MPS), octyltrimethoxysilane (OTMS), blends of UDMS/OTMS (50/50 wt/wt), or MPS/OTMS (50/50 wt/wt). The total amount of silane was kept constant at 10% by weight fraction relative to the filler weight. The silanized nanoparticles were mixed with the dimethacrylate matrix (60% filler by weight fraction). The composites were light cured and tested by DMA for the determination of storage modulus (E,), loss modulus (E,), tangent delta (tan ,), and glass transition temperature (Tg). Measurements were performed in samples immediately after curing and samples stored in water at 37°C for 1, 7, 30, or 120 days. OTMS-composite in which OTMS does not form covalent bond with the dimethacrylate matrix showed lower elastic modulus both in dry and wet conditions. The ability of bifunctional UDMS for crosslinking was found not to increase the elastic behavior of the composite, as it was expected, compared with that of MPS-composite, because of the high amount of the silane used. After immersion in water the elastic modulus of OTMS-composite remained constant, while that of the other composites increased after 1 day and then remained constant up to 120 days. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Synthesis, characterization, and cure reaction of methacrylate-based multifunctional monomers for dental compositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2007Mousa Ghaemy Abstract The synthesis of 2,2-bis[(4-(2-hydroxy-3-methacryloxyethoxy)phenyl]propane (BHEP) and (1-methacryloxy-3-ethoxymethacryloxy-2-hydroxy)propane (MEHP) for use as the monomer phase in dental composites are reported. The monomers were prepared by the reaction of 2-hydroxyethyl methacrylate (HEMA) with diglycidyl-ether of bisphenol A (DGEBA) and with glycidyl methacrylate (GMA), respectively. The progress of the reaction was followed by measuring the disappearance of the epoxide group peak using FTIR and the structure of the monomers was characterized by 1H-NMR. BHEP and MEHP have lower viscosity because of the presence of long aliphatic spacer on both sides of the aromatic ring in BHEP and the absence of aromatic rings and the presence of only one hydroxyl group in each molecule of MEHP. Thermal curing of the monomers was conducted in a DSC using benzoyl peroxide as an initiator. Photopolymerization of the monomers was also conducted with the visible light using camphorquinone and N,N -dimethylaminoethyl methacrylate as the photoinitiating system. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source] Antibacterial activity of dental composites containing zinc oxide nanoparticles,JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2010Berdan Aydin Sevinē Abstract The resin-based dental composites commonly used in restorations result in more plaque accumulation than other materials. Bacterial biofilm growth contributes to secondary caries and failure of resin-based dental composites. Methods to inhibit biofilm growth on dental composites have been sought for several decades. It is demonstrated here that zinc oxide nanoparticles (ZnO-NPs) blended at 10% (w/w) fraction into dental composites display antimicrobial activity and reduce growth of bacterial biofilms by roughly 80% for a single-species model dental biofilm. Antibacterial effectiveness of ZnO-NPs was assessed against Streptococcus sobrinus ATCC 27352 grown both planktonically and as biofilms on composites. Direct contact inhibition was observed by scanning electron microscopy and confocal laser scanning microscopy while biofilm formation was quantified by viable counts. An 80% reduction in bacterial counts was observed with 10% ZnO-NP-containing composites compared with their unmodified counterpart, indicating a statistically significant suppression of biofilm growth. Although, 20% of the bacterial population survived and could form a biofilm layer again, 10% ZnO-NP-containing composites maintained at least some inhibitory activity even after the third generation of biofilm growth. Microscopy demonstrated continuous biofilm formation for unmodified composites after 1-day growth, but only sparsely distributed biofilms formed on 10% ZnO-NP-containing composites. The minimum inhibitory concentration of ZnO-NPs suspended in S. sobrinus planktonic culture was 50 ,g mL,1. ZnO-NP-containing composites (10%) qualitatively showed less biofilm after 1-day-anaerobic growth of a three-species initial colonizer biofilm after being compared with unmodified composites, but did not significantly reduce growth after 3 days. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2010. [source] In vitro cytotoxicity of dental composites based on new and traditional polymerization chemistries,JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 2 2007M. Goėl Brackett Abstract The biological response to dental restorative polymer composites is mediated by the release of unpolymerized residual monomers. Several new composite formulations claim to reduce unpolymerized residual mass. The current study assessed the cytotoxic responses to several of these new formations and compared them with more traditional formulations. Our hypothesis predicted that if these new polymerization chemistries reduce unpolymerized residual mass, the cytotoxicity of these materials also should be reduced relative to traditional formulations. Methods: Materials (HerculiteXRV, Premise, Filtek Supreme, CeramxDuo, Hermes, and Quixfil) were tested in vitro in direct contact with Balb mouse fibroblasts, initially, then after aging in artificial saliva for 0, 1, 3, 5, or 8 weeks. The toxicity was determined by using the MTT assay to the estimate SDH activity. Knoop hardness of the materials also was measured at 0 and 8 weeks to determine whether surface breakdown of the materials in artificial saliva contributed to cytotoxic responses. Results: Materials with traditional methacrylate chemistries (Herculite, Premise, Filtek Supreme) were severely (>50%) cytotoxic throughout the 8-week interval, but materials with newer chemistries or filling strategies (Hermes, CeramXDuo, and Quixfil) improved over time of aging in artificial saliva. Hermes showed the least cytotoxicity at 8 weeks, and was statistically equivalent to Teflon® negative controls. Hardness of the materials was unaffected by exposure to artificial saliva. Conclusions: Newer polymerization and filling strategies for dental composites show promise for reducing the release of unpolymerized components and cytotoxicity. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006 [source] Effects of incorporating nanosized calcium phosphate particles on properties of whisker-reinforced dental composites,,JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2007Hockin H. K. Xu Abstract Clinical data indicate that secondary caries and restoration fracture are the most common problems facing tooth restorations. Our ultimate goal was to develop mechanically-strong and caries-inhibiting dental composites. The specific goal of this pilot study was to understand the relationships between composite properties and the ratio of reinforcement filler/releasing filler. Nanoparticles of monocalcium phosphate monohydrate (MCPM) were synthesized and incorporated into a dental resin for the first time. Silicon carbide whiskers were fused with silica nanoparticles and mixed with the MCPM particles at MCPM/whisker mass ratios of 1:0, 2:1, 1:1, 1:2, and 0:1. The composites were immersed for 1,56 days to measure Ca and PO4 release. When the MCPM/whisker ratio was changed from 0:1 to 1:2, the composite flexural strength (mean ± SD; n = 5) decreased from 174 ± 26 MPa to 138 ± 9 MPa (p < 0.05). A commercial nonreleasing composite had a strength of 112 ± 14 MPa. When the MCPM/whisker ratio was changed from 1:2 to 1:1, the Ca concentration at 56 days increased from 0.77 ± 0.04 mmol/L to 1.74 ± 0.06 mmol/L (p < 0.05). The corresponding PO4 concentration increased from 3.88 ± 0.21 mmol/L to 9.95 ± 0.69 mmol/L (p < 0.05). Relationships were established between the amount of release and the MCPM volume fraction vMCPM in the resin: [Ca]= 42.9 v, and [PO4] = 48.7 v. In summary, the method of combining nanosized releasing fillers with reinforcing fillers yielded Ca- and PO4 -releasing composites with mechanical properties matching or exceeding a commercial stress-bearing, nonreleasing composite. This method may be applicable to the use of other Ca,PO4 fillers in developing composites with high stress-bearing and caries-preventing capabilities, a combination not yet available in any dental materials. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006 [source] Subcritical crack growth behavior of Al2O3 -glass dental compositesJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 2 2003Qingshan Zhu Abstract The purpose of this study is to investigate the subcritical crack growth (SCG) behavior of alumina-glass dental composites. Alumina-glass composites were fabricated by infiltrating molten glass to porous alumina preforms. Rectangular bars of the composite were subject to dynamic loading in air, with stressing rates ranging from 0.01 MPa/s to 2 MPa/s. The SCG parameter n was determined to be 22.1 for the composite, which is substantially lower than those of high-purity dense alumina. Investigations showed that glass phases are responsible for the low n value as cracks propagate preferentially within glass phases or along the interface between glass phases and alumina phases, due to the fact that glasses are more vulnerable to chemical attacks by water molecules under stress corrosion conditions. The SCG behavior of the infiltration glass was also investigated and the SCG parameter n was determined to be 18.7. © 2003 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 65B: 233,238, 2003 [source] Hyperbranched polyesters and their application in dental composites: monomers for low shrinking compositesPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 6 2001J. E. Klee Abstract Using trimethylolpropane (TMP) and 2,2-bishydroxymethylpropionic acid (Bis-MPA), aliphatic hyperbranched polyesters (HBP) were synthesized, with a degree of branching of DB,=,0.47 and a degree of polymerization of Pn,=,16.5. Aromatic HBPs with repetitive units of 2,2-bis(4-hydroxyphenyl)pivalonic acid (Bis-PVA) lead to a higher DB,=,0.48 and Pn,=,30.5 compared to the aliphatic HBP. Reactive functionalization of the hyperbranched polymers was achieved via esterification of mixtures of methacrylic acid and carboxylic acids. In this manner, i -butyric acid and methacryloyl terminated HBPs were obtained. They have a low viscosity ranging from 200 to 364,Pa*s and exhibit relatively low volume shrinkage (1.9 to 3.6%) during photoinitiated cure. Dental composites with volume shrinkage of 0.5 to 1.5% have been prepared using these methacryloyl terminated HBPs in combination with a Ba/alumosilicate glass filler. Copyright © 2001 John Wiley & Sons, Ltd. [source] | |||||||||||||