Diametral tensile strength and film thickness of an experimental dental luting agent derived from castor oil.

UNLABELLED: The need to develop new dental luting agents in order to improve the success of treatments has greatly motivated research. OBJECTIVE: The aim of this study was to evaluate the diametral tensile strength (DTS) and film thickness (FT) of an experimental dental luting agent derived from castor oil (COP) with or without addition of different quantities of filler (calcium carbonate - CaCO3). MATERIAL AND METHODS: Eighty specimens were manufactured (DTS N=40; FT N=40) and divided into 4 groups: Pure COP; COP 10%; COP 50% and zinc phosphate (control). The cements were mixed according to the manufacturers' recommendations and submitted to the tests. The DTS test was performed in the MTS 810 testing machine (10 KN, 0.5 mm/min). For FT test, the cements were sandwiched between two glass plates (2 cm²) and a load of 15 kg was applied vertically on the top of the specimen for 10 min. The data were analyzed by means of one-way ANOVA and Tukey's test (α=0.05). RESULTS: The values of DTS (MPa) were: Pure COP- 10.94 ± 1.30; COP 10%- 30.06 ± 0.64; COP 50%- 29.87 ± 0.27; zinc phosphate- 4.88 ± 0.96. The values of FT (µm) were: Pure COP- 31.09 ± 3.16; COP 10%- 17.05 ± 4.83; COP 50%- 13.03 ± 4.83; Zinc Phosphate- 20.00 ± 0.12. One-way ANOVA showed statistically significant differences among the groups (DTS - p=1.01E-40; FT - p=2.4E-10). CONCLUSION: The experimental dental luting agent with 50% of filler showed the best diametral tensile strength and film thickness.

Diametral tensile strength and film thickness of an experimental dental luting agent derived from castor oil

The need to develop new dental luting agents in order to improve the success of treatments has greatly motivated research. OBJECTIVE: The aim of this study was to evaluate the diametral tensile strength (DTS) and film thickness (FT) of an experimental dental luting agent derived from castor oil (COP) with or without addition of different quantities of filler (calcium carbonate - CaCO3). MATERIAL AND METHODS: Eighty specimens were manufactured (DTS N=40; FT N=40) and divided into 4 groups: Pure COP; COP 10 percent; COP 50 percent and zinc phosphate (control). The cements were mixed according to the manufacturers' recommendations and submitted to the tests. The DTS test was performed in the MTS 810 testing machine (10 KN, 0.5 mm/min). For FT test, the cements were sandwiched between two glass plates (2 cm²) and a load of 15 kg was applied vertically on the top of the specimen for 10 min. The data were analyzed by means of one-way ANOVA and Tukey's test (α=0.05). RESULTS: The values of DTS (MPa) were: Pure COP- 10.94±1.30; COP 10 percent- 30.06±0.64; COP 50 percent- 29.87±0.27; zinc phosphate- 4.88±0.96. The values of FT (µm) were: Pure COP- 31.09±3.16; COP 10 percent- 17.05±4.83; COP 50 percent- 13.03±4.83; Zinc Phosphate- 20.00±0.12. One-way ANOVA showed statistically significant differences among the groups (DTS - p=1.01E-40; FT - p=2.4E-10). CONCLUSION: The experimental dental luting agent with 50 percent of filler showed the best diametral tensile strength and film thickness.

Experimental use of a castor bean (Ricinus communis L. ) oil derived polymer on lamellar, interlamellar and penetrating implahts in rabbit's cornea

Há muito que se estudam métodos e materiais reparadores de córnea, em busca de uma melhor reposição tecidual e, principalmente, manutenção ou recuperação da visão. A pesquisa de novos biomateriais tem permitido produzir próteses capazes de desempenhar a função requerida, sem reação importante. Conhecendo-se os bons resultados obtidos com a utilização da poliuretana vegetal derivada de óleo de mamona (Ricinus communis L ) em vários procedimentos, estudou-se sua implantação, em forma de membrana, na córnea, objetivando oferecer novo material para a reparação de lesões corneanas e a confecção de ceratopróteses biologicamente inertes. Utilizaram-se 28 coelhos, divididos em dois grupos (G 1 e G2) e estes em subgrupos para avaliações de implantes lamelares e interlamelares aos 2, 7, 15, 30, 60 e 120 dias, e implantes penetrantes, aos 2, 7,15, 30 e 60 dias de pós-operatório. Estudaram-se parâmetros como neovascularização, inflamação, transparência de córneas e implantes, bem como a aderência e viabilidade destes, através de exames oculares, e histopatológicos à microscopia óptica. Observou-se reação inflamatória branda em todos os períodos. Os implantes lamelares e penetrantes permitiram reparação da córnea e manutenção da integridade dos globos oculares, embora sofressem deiscência entre 5 e 28 dias de pós-operatório. Concluiu-se pela boa biocompatibilidade do material e pela possibilidade de empregar-se o polímero na reparação corneana e, possivelmente, em ceratopróteses.