Does the initial surface roughness of different CuNiTi wires affect the frictional resistance?

This study aimed to assess and correlate initial surface roughness and frictional resistance of rectangular CuNiTi wires inserted in different self-ligating brackets. The sample consisted of 40 bracket-wire sets (rectangular CuNiTi wires of 0.017" x 0.025" and passive self-ligating brackets) divided into four groups (n=10): metallic self-ligating bracket and metallic CuNiTi wire (G1); metallic self-ligating bracket and rhodium-coated CuNiTi wire (G2); esthetic self-ligating bracket and metallic wire (G3); esthetic self-ligating bracket and rhodium-coated CuNiTi wire (G4). The initial surface roughness of the wires was examined with a Surfcorder roughness meter, model SE1700. Later, frictional resistance was assessed in an Instron 4411 universal testing machine at a speed of 5 mm/min, in an aqueous medium at 35°C. Microscopic analyses of surface morphology were performed with scanning electron microscopy, using an LEO 1430, with magnifications of 1000X. Generalized linear models were applied, considering the 2 x 2 factorial (bracket type x wire type), at a 5% significance level. Regardless of bracket type, the groups with esthetic wires presented higher initial surface roughness than the groups with metallic wires (p<0.05). There was no significant difference between the different bracket-wire sets for frictional resistance and no significant correlation between frictional resistance and initial surface roughness in the environment studied. It is concluded that esthetic wires presented higher initial surface roughness but did not interfere with the frictional resistance between brackets and wires.

Does the initial surface roughness of different CuNiTi wires affect the frictional resistance?

Abstract This study aimed to assess and correlate initial surface roughness and frictional resistance of rectangular CuNiTi wires inserted in different self-ligating brackets. The sample consisted of 40 bracket-wire sets (rectangular CuNiTi wires of 0.017" x 0.025" and passive self-ligating brackets) divided into four groups (n=10): metallic self-ligating bracket and metallic CuNiTi wire (G1); metallic self-ligating bracket and rhodium-coated CuNiTi wire (G2); esthetic self-ligating bracket and metallic wire (G3); esthetic self-ligating bracket and rhodium-coated CuNiTi wire (G4). The initial surface roughness of the wires was examined with a Surfcorder roughness meter, model SE1700. Later, frictional resistance was assessed in an Instron 4411 universal testing machine at a speed of 5 mm/min, in an aqueous medium at 35°C. Microscopic analyses of surface morphology were performed with scanning electron microscopy, using an LEO 1430, with magnifications of 1000X. Generalized linear models were applied, considering the 2 x 2 factorial (bracket type x wire type), at a 5% significance level. Regardless of bracket type, the groups with esthetic wires presented higher initial surface roughness than the groups with metallic wires (p<0.05). There was no significant difference between the different bracket-wire sets for frictional resistance and no significant correlation between frictional resistance and initial surface roughness in the environment studied. It is concluded that esthetic wires presented higher initial surface roughness but did not interfere with the frictional resistance between brackets and wires.

Resumo O objetivo deste estudo foi avaliar e correlacionar a rugosidade superficial inicial e a resistência a fricção dos fios CuNiTi retangulares inseridos em diferentes bráquetes autoligados. A amostra foi composta por 40 conjuntos bráquetes-fios (fios retangulares CuNiTi de 0.017" x 0.025" e braquetes autoligados passivos), divididos em 4 grupos (n=10): bráquete autoligado metálico e fio CuNiti metálico (G1); braquete autoligado metálico e fio CuNiti com revestimento de rhodium (G2); bráquete autoligado estético e fio metálico (G3); bráquete autoligado estético e fio CuNiti com revestimento de rhodium (G4). A rugosidade superficial inicial do fio foi examinada com um rugosímetro Surfcorder modelo SE1700. Posteriormente, a resistência a fricção foi avaliada em uma máquina de ensaios universal Instron 4411, a uma velocidade de 5mm/min em meio aquoso à 35oC. Análises microscópicas da morfologia de superfície foram realizadas por microscopia eletrônica de varredura, utilizando um LEO 1430, com ampliações de 1000X. Foram aplicados modelos lineares generalizados, considerando o fatorial 2 x 2 (tipo de bráquete x tipo de fio), com o nível de significância de 5%. Independentemente do tipo de bráquete, os grupos com fios estéticos apresentaram maior rugosidade superficial inicial que os grupos com fios metálicos (p<0,05). Não houve diferença significativa entre os diferentes conjuntos bráquetes-fios quanto a resistência à fricção e não houve correlação significativa entre a resistência a fricção e a rugosidade superficial inicial no ambiente estudado. Conclui-se que os fios estéticos apresentaram maior rugosidade superficial inicial porém não interferiram na resistência a fricção entre os braquetes e os fios.

Influence of Photoinitiator System on Physical-Chemical Properties of Experimental Self-Adhesive Composites.

The aim of this study was to determine the influence of photoinitiator systems on physical-chemical properties of flowable composites. Conventional (CFC), composed by bisphenol-glycidyl dimethacrylate (BisGMA)+triethyleneglycol dimethacrylate (TEGDMA), and self-adhesive (SAFC), composed by BisGMA+TEDGMA+bis{2-(methacryloyloxy) ethyl} phosphate (2MP), flowable composites were developed. Five photoinitiator systems were tested: camphorquinone (CQ), ethyl-4-dimethylaminobenzoate (EDMAB), diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO), phenylbis (2,4,6-trimethylbenzoyl)phosphine oxide (BAPO), CQ+EDMAB+TPO and CQ+EDMAB+BAPO. A two-peak LED was used; degree of conversion (DC) and the maximum polymerization rate (RPmax) were determined by near infrared spectroscopy. For the yellowing degree a spectrophotometer was used. Water sorption (Wsp) was obtained after 30 days of water storage (n=5). Data were submitted to two-way analysis of variance and Tukey's test (a=0.05). BAPO presented the highest DC and RPmax values for both series. SAFCs presented lower DC and RPmax for CQ+EDMAB-based materials. Greater yellowing was observed for SAFCs compared with CFCs, except for BAPO. Greater Wsp was observed for SAFCs compared with CFCs. The photoinitiator did not influence Wsp for CFCs, but TPO and BAPO presented the highest Wsp in SAFCs. The photoinitiator system affected differently the physical-chemical properties of CFCs and SAFCs.

Influence of Photoinitiator System on Physical-Chemical Properties of Experimental Self-Adhesive Composites

Abstract The aim of this study was to determine the influence of photoinitiator systems on physical-chemical properties of flowable composites. Conventional (CFC), composed by bisphenol-glycidyl dimethacrylate (BisGMA)+triethyleneglycol dimethacrylate (TEGDMA), and self-adhesive (SAFC), composed by BisGMA+TEDGMA+bis{2-(methacryloyloxy) ethyl} phosphate (2MP), flowable composites were developed. Five photoinitiator systems were tested: camphorquinone (CQ), ethyl-4-dimethylaminobenzoate (EDMAB), diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO), phenylbis (2,4,6-trimethylbenzoyl)phosphine oxide (BAPO), CQ+EDMAB+TPO and CQ+EDMAB+BAPO. A two-peak LED was used; degree of conversion (DC) and the maximum polymerization rate (RPmax) were determined by near infrared spectroscopy. For the yellowing degree a spectrophotometer was used. Water sorption (Wsp) was obtained after 30 days of water storage (n=5). Data were submitted to two-way analysis of variance and Tukey’s test (a=0.05). BAPO presented the highest DC and RPmax values for both series. SAFCs presented lower DC and RPmax for CQ+EDMAB-based materials. Greater yellowing was observed for SAFCs compared with CFCs, except for BAPO. Greater Wsp was observed for SAFCs compared with CFCs. The photoinitiator did not influence Wsp for CFCs, but TPO and BAPO presented the highest Wsp in SAFCs. The photoinitiator system affected differently the physical-chemical properties of CFCs and SAFCs.

Resumo O objetivo do estudo foi determinar a influência do sistema fotoiniciador sobre as propriedades físico-químicas de compósitos fluidos. Os compósitos convencionais foram compostos por bisfenol-glicidil dimetacrilato (BisGMA) + trietilenoglicol dimetacrilato (TEGDMA), e os autoadesivos, apresentavam BisGMA +TEGDMA+ Bis2(metacriloiloxi)etil fosfato (2 MP). Cinco sistemas fotoiniciadores foram testados: canforquinona + etil-4- dimetilamino benzoato (CQ+EDMAB), óxido mono-alquil fosfínico (TPO) e óxido bis-alquil fosfínico (BAPO), CQ+EDMAB+TPO e CQ+EDMAB+BAPO. LED de amplo espectro foi usado; o grau de conversão (GC) e a taxa de polimerização (TP) foram determinados por espectroscopia próximo ao infravermelho; o grau de amarelo foi mensurado por um espectrofotômetro e absorção de água foi obtida após 30 dias de armazenamento em água (n=5). Os dados foram submetidos a análise de variância de dois fatores e teste de Tukey (?=0,05). BAPO apresentou os maiores valores de GC e TP nos compósitos convencionais e autoadesivos. Compósitos autoadesivos apresentaram menor GC e TP quando CQ+EDMAB foi usado. Maior amarelecimento foi observado nos compósitos autoadesivos em relação aos convencionais, exceto para BAPO. Compósitos autoadesivos promoveram maior absorção de água. Não houve influência dos fotoiniciadores nos compósitos convencionais, no entanto TPO e BAPO apresentaram os maiores valores de absorção de água nos compósitos autoadesivos. Os sistemas fotoiniciadores influenciaram de maneira diferente as propriedades físico-químicas dos compósitos convencionais e autoadesivos.

Evaluation of phenyl-propanedione on yellowing and chemical-mechanical properties of experimental dental resin-based materials

ABSTRACT Objective To evaluate the influence of phenyl-propanedione on yellowing and chemical-mechanical properties of experimental resin-based materials photoactivated using different light curing units (LCUs). Material and Methods Experimental resin-based materials with the same organic matrix (60:40 wt% BisGMA:TEGDMA) were mechanically blended using a centrifugal mixing device. To this blend, different photoinitiator systems were added in equimolar concentrations with aliphatic amine doubled by wt%: 0.4 wt% CQ; 0.38 wt% PPD; or 0.2 wt% CQ and 0.19 wt% PPD. The degree of conversion (DC), flexural strength (FS), Young’s modulus (YM), Knoop hardness (KNH), crosslinking density (CLD), and yellowing (Y) were evaluated (n=10). All samples were light cured with the following LCUs: a halogen lamp (XL 2500), a monowave LED (Radii), or a polywave LED (Valo) with 16 J/cm2. The results were analysed by two-way ANOVA and Tukey’s test (α=0.05). Results No statistical differences were found between the different photoinitiator systems to KNH, CLS, FS, and YM properties (p≥0.05). PPD/CQ association showed the higher DC values compared with CQ and PPD isolated systems when photoactivated by a polywave LED (p≤0.05). Y values were highest for the CQ compared with the PPD systems (p≤0.05). Conclusion PPD isolated system promoted similar chemical and mechanical properties and less yellowing compared with the CQ isolated system, regardless of the LCU used.

Evaluation of phenyl-propanedione on yellowing and chemical-mechanical properties of experimental dental resin-based materials.

OBJECTIVE: To evaluate the influence of phenyl-propanedione on yellowing and chemical-mechanical properties of experimental resin-based materials photoactivated using different light curing units (LCUs). MATERIAL AND METHODS: Experimental resin-based materials with the same organic matrix (60:40 wt% BisGMA:TEGDMA) were mechanically blended using a centrifugal mixing device. To this blend, different photoinitiator systems were added in equimolar concentrations with aliphatic amine doubled by wt%: 0.4 wt% CQ; 0.38 wt% PPD; or 0.2 wt% CQ and 0.19 wt% PPD. The degree of conversion (DC), flexural strength (FS), Young's modulus (YM), Knoop hardness (KNH), crosslinking density (CLD), and yellowing (Y) were evaluated (n=10). All samples were light cured with the following LCUs: a halogen lamp (XL 2500), a monowave LED (Radii), or a polywave LED (Valo) with 16 J/cm2. The results were analysed by two-way ANOVA and Tukey's test (α=0.05). RESULTS: No statistical differences were found between the different photoinitiator systems to KNH, CLS, FS, and YM properties (p≥0.05). PPD/CQ association showed the higher DC values compared with CQ and PPD isolated systems when photoactivated by a polywave LED (p≤0.05). Y values were highest for the CQ compared with the PPD systems (p≤0.05). CONCLUSION: PPD isolated system promoted similar chemical and mechanical properties and less yellowing compared with the CQ isolated system, regardless of the LCU used.