RESUMO
PURPOSE: The success of zirconia-reinforced all-ceramic crowns depends on the formation of a stable bond between the zirconia core and the veneering porcelain. The purpose of this study was to test the effects of liner application and airborne particle abrasion of a postsintered Y-TZP core on the bond strength between the zirconia core and veneering porcelain with or without cyclic loading. MATERIALS AND METHODS: Kavo Everest® Y-TZP blank disks were sintered and divided into three treatment groups: airborne particle abrasion, IPS e.max® Ceram Zirliner application, or no surface treatment. The disks were then veneered with IPS e.max® ZirPress veneering porcelain. Half the veneered disks from each group were cyclically loaded. This created six experimental groups: three surface treatment groups cyclically loaded and three not loaded. The disks were then sectioned into microbars for microtensile bond strength (MTBS) testing (40 specimens per group). Specimens were luted to a fixture mount and loaded to failure using a universal testing machine (MTS Insight). The maximum force was measured and bond strength computed. Data were analyzed with a two-way ANOVA and Tukey's HSD test (α= 0.05). RESULTS: Airborne particle abrasion significantly decreased MTBS values (p= 0.043), and ZirLiner application did not have a significant effect on MTBS values compared to control. Cyclic loading did not have a significant effect on MTBS values. The predominant failure mode in all groups was mixed. CONCLUSIONS: Airborne particle abrasion of the interfacial surface of the Everest® Y-TZP core significantly decreased the MTBS to ZirPress veneering porcelain when compared to no interfacial surface treatment. Application of ZirLiner to the interfacial surface of the Everest® Y-TZP core did not significantly increase or decrease the MTBS to ZirPress veneering porcelain, compared to the other surface treatments. Cyclic loading did not affect bond strengths in any of the groups, regardless of surface treatment. Neither cyclic loading nor surface treatment affected the failure mode of the specimens.
Assuntos
Colagem Dentária , Materiais Dentários/química , Porcelana Dentária/química , Facetas Dentárias , Ítrio/química , Zircônio/química , Óxido de Alumínio/química , Apatitas/química , Butileno Glicóis/química , Cerâmica/química , Corrosão Dentária/métodos , Análise do Estresse Dentário/instrumentação , Humanos , Teste de Materiais , Estresse Mecânico , Propriedades de Superfície , Temperatura , Resistência à Tração , Água/químicaRESUMO
As a part of the continuous pursuit to develop an ideal resinous dental restorative material for use in large posterior cavity restorations, this article reports the easy, high-yield synthesis and the incredibly low polymerization shrinkage property of a new bifunctional liquid crystal (LC) monomer. This new polymerizable nematic liquid crystal is the next higher homolog of the acrylate monomer reported in a previous work.1 It remains liquid crystalline between room and mouth temperatures and can be polymerized to isotropic polymer with the use of the same visible light inhibitor system as used with conventional monomers. The structure of this new monomer has been confirmed to be 2-(t-butyl), 1,4-bis-[4-(6-methacryloxy-hexan-1-oxy)-benzoyloxy]-benzene. Unlike the synthesis of its acrylate homolog, when the same procedure is adopted for the synthesis of this compound, the recovery of the product is not split by a sizable amount of the by-product. Therefore, the reaction is cleaner, with high yield and a less labor-intensive purification procedure. Thus, the synthetic methodology has the potential for easy commercial scale-up. The monomer (V) polymerizes at room temperature with a shrinkage of about 2 vol %, as compared to > 8 vol % for conventional control (GTE), at similar degrees of conversion.
Assuntos
Metacrilatos/química , Polímeros/síntese química , Polímeros/químicaRESUMO
Polymerization shrinkage remains a major barrier to the universal use of resin restorative in large posterior cavity preparations. A new bifunctional liquid crystal (LC) monomer, 2-(t-butyl), 1,4-bis-[4-(6-acryloxy-hexane-1-oxy)-benzoyloxy] benzene, with exceptionally low polymerization shrinkage, has recently been discovered. The purpose of this communication is to report a new, easy, high-yield synthetic route to synthesize this compound in comfortable larger batches. Synthetic and isolation details, chemical characteristics, and the polymerizable properties of a new structurally related by-product monomer, namely, 2-(t-butyl),1-[4-(6-acryloxy-hexane-1-oxy)-benzoyloxy], 4-[4-[6-(3-acryl oxy-propionoxy)-hexane-1-oxy]-benzoyloxy]-benzene, is also reported. The structural confirmation of this by-product indicates that it resulted from the Michael-type addition of acrylate ion on one of the terminal acryloxy groups of 2-(t-butyl), 1,4-bis-[4-(6-acryloxy-hexane-1-oxy)-benzoyloxy] benzene. The by-product itself, as well as the natural blend of the aforesaid both products as formed in the reaction mixture, also polymerized at room temperature with lesser volume shrinkage as compared to the conventional control (GTE) at similar degrees of conversion.
Assuntos
Biopolímeros/química , Varredura Diferencial de Calorimetria , Cristalização , Espectroscopia de Ressonância Magnética , Teste de MateriaisRESUMO
OBJECTIVES: To demonstrate that silver nanoparticles (AgNPs) could be synthesized in situ in acrylic dental resins. METHODS: Light-cure (LC; bisphenol A glycidyl methacrylate, tetraethyleneglycol dimethacrylate, bisphenol A ethoxylate dimethacrylate blend) and chemical-cure systems (CC; orthodontic denture resin) were used to synthesize AgNPs using different concentrations of Ag benzoate (AgBz). RESULTS: Rockwell hardness for LC resins showed that resins could be cured with up to 0.15% AgBz, while the hardness of CC resins were unaffected in the concentrations tested. UV-Vis spectroscopy and transmission electron microscopy confirmed the presence of AgNPs in both LC and CC resins. Generally, CC resins had better distribution of and much smaller AgNPs as compared to LC resins overall. In some samples, especially in LC resins, nanoclusters were visible. An in vitro release study over four-weeks showed that CC resins released the most Ag(+) ions, with release detected in all samples. However, LC resins only released Ag(+) ions when AgBz concentration was greater than 0.1% (w/w). AgNP-loaded CC resins made with 0.2 and 0.5% (w/w) AgBz were tested for antibacterial activity in vitro against Streptococcus mutans, and results showed 52.4% and a 97.5% bacterial inhibition, respectively. Further work is now warranted to test mechanical properties and to optimize the initiator system to produce commercially useful dental and medical resins. SIGNIFICANCE: Success in this work could lead to a series of antimicrobial medical and dental biomaterials that can prevent secondary caries and infection of implants.