Influence of bioactive particles and onium salt on the physicochemical properties of experimental infiltrants

Abstract This study evaluated physicochemical properties of experimental infiltrants after addition of hydroxyapatite nanoparticles (HAp) or 58S bioactive glass (BAG) and diphenyliodonium hexafluorophosphate (DPI). The resin matrix was composed of TEGDMA/Bis-EMA (3:1), 0.5 mol% CQ, and 1 mol% EDAB. The blends received or not 0.5 mol% DPI and 10% wt BAG or HAp. Icon was used as commercial control. The groups were characterized by XRD, FT-IR spectrometry, and SEM before and after simulated body fluid (SBF) immersion for up to 7 days. Polymerization kinetics (n =3 ), water sorption and solubility (n=10), and viscosity (n = 3) were surveyed. For polymerization kinetics, the samples were polymerized for 5 min and the data were obtained from 40 s and 5 min. Statistical analysis was made using ANOVA and Tukey's test (a = 0.05). After 7 days of SBF immersion, XRD and FT-IR showed that the HAp crystalline phase was present only in the HAp groups. A lower degree of conversion (DC) and polymerization rate were observed for the Icon and BAG groups, whereas HAp showed higher values. For the BAG group, DPI increased polymerization rate and DC in 40 s. After 5 min, all groups presented DC above 80%. In groups with particles, the HAp groups exhibited higher viscosity, whereas DPI groups showed a decrease in viscosity. Icon had the highest water sorption. To conclude, BAG neither improved the physicochemical properties studied, nor did it show bioactive properties. The addition of DPI reduced viscosity caused by particle addition and also attenuated the DC decrease caused by BAG addition. The addition of bioactive particles to infiltrants should be seen with caution because they increase viscosity and may not bring major clinical improvements that justify their use. DPI might be indicated only if any component is added to the infiltrant to act as a compensation mechanism

PARAMETERS RELATED TO REACTION KINETICS AND POLYMERIZATION STRESS OF RESTORATIVE COMPOSITES

Proposição: O objetivo deste estudo foi avaliar como a contração volumétrica (CV), o grau de conversão (GC), a taxa máxima de polimerização (RPmax) e a tensão de polimerização (TPmax) de dois compósitos experimentais são influenciados pela concentração de fotoiniciadores na matriz e pela irradiância aplicada na fotopolimerização. Material e métodos: Duas séries de monômeros foram formuladas, com partes iguais em peso dos seguintes monômeros: série B= Bis-GMA/ TEGDMA; série U= Bis-GMA/ UDMA / TEGDMA. Essas séries foram combinadas a três níveis de fotoiniciadores, num total de seis materiais experimentais, com a concentração em porcentagem de peso de uma amina terciária (EDMAB) e canforoquinona (CQ), respectivamente: alta (H)= 0,8 / 1,6; intermediária (M)= 0,4 / 0,8 e baixa (L)= 0,2 / 0,4. A todas as misturas, 75% e peso de vidro de estrôncio e 5% em peso de OX-50 (sílica coloidal) foram adicionados. O estudo foi dividido em três módulos: no primeiro, os seis compósitos foram testados quanto aos parâmetros descritos acima para a mesma dose de energia aplicada. No segundo, os mesmos materiais foram testados com a dose de energia ajustada de acordo com a concentração de fotoiniciadores de modo que todos os níveis atingissem graus de conversão semelhantes. No terceiro módulo, os materiais com a concentração \"M\" de fotoiniciadores foram submetidos a uma de três irradiâncias: 200, 400 ou 600 mW/cm2, com o tempo de exposição ajustado para que a dose de energia fosse mantida constante. CV foi registrada em um dilatômetro de mercúrio, GC foi avaliado através de FTIR, RPmax foi obtida através de um DSC 7 e a TP foi avaliada em um aparato de compliance controlado, descrito por Sakaguchi et al., 2004. Resultados: Em todos os módulos, não houve interação entre os fatores e assim, as médias foram agrupadas por série de monômeros e nível de fotoiniciadores (módulos 1 e 2) ou nível de irradiância (módulo 3). No módulo 1, as concentrações \"H\" e \"M\" apresentaram GC semelhante, ambas estatisticamente superiores à apresentada pelo grupo com o menor conteúdo de CQ/amina. A série U apresentou GC superior à da série B. RPmax aumentou significantemente com a concentração de fotoiniciadores entre cada um dos níveis estudados (p0,05). CV foi maior para \"L\", estatisticamente diferente das outras duas. A série B apresentou maior CV (p0,05). A série U apresentou maior GC comparado com a série B (p0,05). A série B apresentou maior TPmax comparado com a série U (p<0,001). CV foi maior para \"L\", estatisticamente diferente das outras duas. A série B apresentou maiores valores de CV (p<0,001 para ambos os fatores). No módulo 3, GC variou significantemente apenas com a irradiância (p<0,001), sendo que os grupos de alta irradiância apresentaram valores estatisticamente mais baixos comparados aos níveis de irradiância médio e baixo. RPmax, aumentou com a irradiância e foi maior para a série U (p<0,001 para ambos). A série B apresentou valores de TPmax do que os da série U. CV não foi influenciada pela irradiância (p=0,442). A série B apresentou CV estatisticamente maior que a série U (p<0,001). Conclusões: De maneira geral, podemos dizer que CV, GC e RPmax mostraram uma interação bastante complexa e, nas condições deste estudo, não foi possível determinar a contribuição relativa de cada um destes fatores no desenvolvimento da tensão de polimerização. No entanto, parece haver uma tendência de TPmax ser influenciada mais pronunciadamente pelo GC ou CV do que pela RPmax, como demonstrado nos módulos 2 e 3.Proposition: The objective of this study was to evaluate how the volumetric shrinkage (VS), degree of conversion (DC), maximum rate of reaction (RPmax), polymerization stress (PSmax) and maximum rate of stress development (RSmax) of two experimental composites are influenced by the photoinitiator concentration ([photo]) and by the irradiance. Methods and materials: Bis-GMA/TEGDMA (B series) and Bis GMA/UDMA/TEGDMA (U series) were mixed in equal parts in weight. A tertiary amine (EDMAB) and camphoroquinone (CQ), respectively, were added in three concentrations: high (H)= 0.8/1.6; intermediate (M)= 0.4/0.8 and low (L)= 0.2/0.4 (in wt%). In all mixtures, 80 wt% filler was added. The study was divided in three sections: I) composites were photoactivated with 13 J/cm2. II) radiant exposure was adjusted so that all [photo] would achieve similar DC. III) [photo] \"M\" materials were submitted to three irradiances: 200 (L), 400 (I) or 600 (H) mW/cm2, with exposure time adjusted to convey the same radiant exposure. VS was registered in a mercury dilatometer, DC was evaluated by FTIR spectroscopy, RPmax was obtained in a DSC 7 and PSmax was evaluated in a controlled compliance device, described previously (SAKAGUCHI; WILTBANK; MURCHISON, 2004a). Results: Because no interaction between the factors was observed (except for RSmax in sections I and III), means were pooled for monomer series and [photo] (sections I and II) or irradiance (section III). I) concentrations \"H\" and \"M\" presented similar DC, both statistically superior to \"L\" (p<0.001). U series presented higher DC compared to B series. RPmax increased significantly with photoinitiator concentration between each of the studied levels (p<0.001), and was higher for U series (p<0.05). VS was higher for \"L\", statistically different than the other two (p<0.05). B series presented higher VS (p<0.05). The group with \"H\" concentration presented PSmax higher than \"L\", while \"M\" presented values similar to both (p<0.001). B and U series presented equivalent PSmax (p=0.284). For B series, RSmax increased 100% between the lower e intermediate [photo]. For U series, this increase was only around 50%. II) DC was not influenced by [photo] (p=0.388). U series presented higher DC compared to B series (p<0.001). RPmax increased with [photo] between all studied levels and was higher for U series (p<0.001 for both). VS was higher for \"L\", statistically different from the other two (p<0.001). B series presented higher VS (p<0.001). PSmax was not influenced by the photoinitiator concentration (p=0119). B series presented higher PSmax compared to U series (p<0.001). RSmax increased with [photo] and was higher for U series (p<0.001). III) High irradiance groups presented statistically lower DC compared to the other irradiance levels (p<0.001). Monomer series did not influence DC (p=0.793). RPmax increased with the irradiance and was higher for U series (p<0.001 for both). VS was not influenced by the irradiance (p=0.442). B series presented VS statistically higher than U series (p<0.001). \"H\" groups presented higher PSmax compared to \"L\". \"M\" presented PSmax similar to both (p<0.001). B series presented PSmax higher than U series. While no difference in RSmax between irradiance leves was observed for B series, RSmax increased with the irradiance for U series. Conclusions: There seems to be a trend for PSmax to be influenced more markedly by DC or VS than by RPmax. However, VS, DC and RPmax showed a quite complex interaction and, in the conditions of the present study, it was not possible to determine the relative contribution of each of these factors on stress development

Optical properties and colorimetric evaluation of resin cements formulated with thio-urethane oligomers

The aim of this study was to evaluate the color parameters and optical properties of resin cements (RCs) formulated with thio-urethanes (TUs). Six TUs were synthesized by combining thiols (pentaerythritol tetra-3-mercaptopropionate [PETMP] or trimethylol-tris-3-mercaptopropionate [TMP]) with di-functional isocyanates (1,6-Hexanediol-diissocyante [HDDI] [aliphatic-AL] or 1,3-bis(1-isocyanato-1-methylethyl) benzene [BDI] [aromatic-AR] or Dicyclohexylmethane 4,4 '-Diisocyanate [HMDI] [cyclic-CC]). TUs (20 wt%) were added to a BisGMA/UDMA/TEGDMA matrix. Filler was introduced at 60 wt%. Fluorescence was evaluated through an UV-light emitting equipment. Coordinates L*, a*, and b* were obtained in the black and white reflectance to evaluate the contrast ratio (CR) and translucency parameter (TP00). The coordinates obtained from transmittance were used to evaluate lightness (L*), chroma (C*), color difference (Delta E-00) after 6 month, and whiteness index for Dentistry (WID). RCs formulated with TUs presented significantly higher CR, and fluorescence (with T_AR). Significantly lower C*, L*, and TP00 (except for P_AR and T_AL) were also observed in RCs containing TUs. Delta E-00 were not significant among the materials. WID was not influenced. RCs composed by TU oligomers present higher CR and lower translucency. The material also present higher fluorescence depending on the oligomer used. The use of thio-urethanes to formulate resin cements can ensure a luting material with improved potential to mask colored substrates due to the higher contrast ratio and lower translucency obtained. A final higher fluorescence of restoration is also expected with the use of specific oligomer312153159FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESP2017-11913-8The authors thank NIH‐NIDCR (1R15‐DE023211‐01A1 and 1U01‐DE02756‐01) and FAPESP 2017‐11913‐8 for financial support. The donation of methacrylate monomers by Esstech is also greatly appreciate

Modulated Photoactivation Methods: Influence On Contraction Stress, Degree Of Conversion And Push-out Bond Strength Of Composite Restoratives.

Verify the influence of curing methods on contraction stress, stress rate, and degree of conversion (DC) of a restorative composite and on bond strength of composite restoratives. For the stress test, composite (0.84 mm thick) was applied between two 5-mm diameter glass rods, mounted in a servohydraulic machine. Stress rate was taken by the value of stress/time at each second. DC was measured by micro-FTIR. Bond strength testing was performed using a push-out test. The C-factor in all tests was 3.0. Four curing methods were tested: continuous light (CL), soft-start (SS), and two pulse delay methods using different initial irradiances--150 mW/cm(2) (PD150) and 80 mW/cm(2) (PD80). Results were analyzed by ANOVA and Tukey's test (alpha=0.05). Stress values ranged from 7.9 MPa (PD80) to 10.3 MPa (CL). No statistical difference was verified among CL, SS, and PD150. PD80 presented statistically lower stress values compared to CL and SS. CL presented the highest maximum stress rate, followed by SS, PD150 and PD80. Mean DC values ranged from 54.2% (PD150) to 55.9% (PD80), with no difference observed among the methods. For the bond strength test, values ranged from 26.4 MPa (CL) to 35.5 MPa (PD150). PD150 and PD80 were both statistically superior to SS and CL. SS presented statistically higher bond strength compared to CL. Modulated curing methods were shown to be effective in reducing contraction stress rate and improving the strength of the bonded interface, and without compromising the DC of the restorative composite.35318-2

Effect of irradiance and light source on contraction stress, degree of conversion and push-out bond strength of composite restoratives

Made available in DSpace on 2019-09-12T16:57:14Z (GMT). No. of bitstreams: 0 Previous issue date: 2009Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Purpose: To evaluate the influence of five curing methods on contraction stress, stress rate, and degree of conversion (DC) of a composite and on bond strength of composite restoratives. Methods: For the stress test, composite was applied between two 5-mm diameter glass rods, mounted in a servohydraulic machine. Stress rates were calculated as the change in stress vs. time. DC was measured by FTIR. Bond strength testing was performed using a push-out test in bovine incisors. The C-factor was 3.0 for all tests. Five methods were evaluated: High Intensity LED (LED HI), Continuous Halogen Light (QTH CL), Medium Intensity LED (LED MI), Low Intensity LED (LED LI), and Pulse Delay Halogen Light (QTH PD). Results were analyzed by ANOVA and Tukey's test (alpha = 0.05). Results: Stress values ranged from 9.25 MPa (QTH PD) to 10.46 MPa (LED MI). No statistical difference was observed among the methods. Bond strength values ranged from 24.6 MPa (LED HI) to 35.4 MPa (QTH PD), with the QTH PD presenting a statistically higher value compared to the other methods. Stress rate and bond strength presented an inverse linear correlation ( = 0.79). LED HI presented the highest maximum stress rate, followed by LED MI, QTH CL, LED LI, and QTH PD. The reduction in stress rate observed for the low intensity groups was associated with a general increase in bond strength, with no adverse effect on the degree of conversion of the restorative composite. (Am J Dent 2009;22:165-170).[Cunha, Leonardo Goncalves] Universidade de Taubaté (Unitau), Dept Dent, Prosthodont Area, BR-12020330 Taubate, SP, Brazil[De Goes, Mario Fernando; Coelho Sinhoreti, Mario Alexandre] Univ Estadual Campinas, Sch Dent, Dent Mat Area, Dept Restorat Dent, Piracicaba, SP, Brazil[Ferracane, Jack Liborio] Oregon Hlth & Sci Univ, Dept Restorat Dent, Div Biomat & Biomech, Portland, OR 97201 US

Heat treatment-improved bond strength of resin cement to lithium disilicate dental glass-ceramic

This study investigated the influence of different hydrofluoric acid (HF) concentrations and heat treatments applied to a lithium disilicate dental glass-ceramic (EMX) on surface morphology and micro-shear bond strength (mu SBS) to resin cement. Five HF concentrations (1%, 2.5%, 5%, 7.5% and 10%) and four different heat treatments applied before etching were assessed: I. etching at room temperature with no previous heat treatment (control group); 2. HF stored at 70 degrees C for 1 min applied to the ceramic surface at room temperature; 3. HF at room temperature applied after a hot air stream is applied perpendicularly to the ceramic surface for 1 min; 4. the combination of previously heated HF and heated EMX surface. The etching time was fixed for 20 s for all groups. Etched EMX specimens were analyzed on field-emission scanning electron microscope (FE-SEM) and the mu SBS was carried out on a universal testing machine at a crosshead speed of 1 mm/min until fracture. For the control groups, FE-SEM images showed greater glassy matrix dissolution and higher mu SBS for 7.5% and 10% HF concentrations. The previous heat treatments enhanced the glassy matrix dissolution more evidently for 1%, 2.5% and 5% and yielded increased mu SBS values, which were not statistically different for 7.5% and 10% HF concentrations (control group). HF concentrations and previous heat treatments did show to have an influence on the etching/ bonding characteristics to lithium disilicate dental glass-ceramic4281007110078CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQFUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESP140696/2013-0; 304493/2014-72013/26573-7; 2014/23320-

Polymerization shrinkage stress of composite resins and resin cements – What do we need to know?

Abstract Polymerization shrinkage stress of resin-based materials have been related to several unwanted clinical consequences, such as enamel crack propagation, cusp deflection, marginal and internal gaps, and decreased bond strength. Despite the absence of strong evidence relating polymerization shrinkage to secondary caries or fracture of posterior teeth, shrinkage stress has been associated with post-operative sensitivity and marginal stain. The latter is often erroneously used as a criterion for replacement of composite restorations. Therefore, an indirect correlation can emerge between shrinkage stress and the longevity of composite restorations or resin-bonded ceramic restorations. The relationship between shrinkage and stress can be best studied in laboratory experiments and a combination of various methodologies. The objective of this review article is to discuss the concept and consequences of polymerization shrinkage and shrinkage stress of composite resins and resin cements. Literature relating to polymerization shrinkage and shrinkage stress generation, research methodologies, and contributing factors are selected and reviewed. Clinical techniques that could reduce shrinkage stress and new developments on low-shrink dental materials are also discussed