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1.
J. appl. oral sci ; 25(5): 523-532, Sept.-Oct. 2017. tab, graf
Artículo en Inglés | LILACS, BBO | ID: biblio-893652

RESUMEN

Abstract Objectives: This study investigated whether increasing the concentration of acidic monomers in one-step adhesives would allow reducing their application time without interfering with the bonding ability to primary enamel and dentin. Material and methods: Experimental one-step self-etch adhesives were formulated with 5 wt% (AD5), 20 wt% (AD20), or 35 wt% (AD35) acidic monomer. The adhesives were applied using rubbing motion for 5, 10, or 20 s. Bond strengths to primary enamel and dentin were tested under shear stress. A commercial etch-and-rinse adhesive (Single Bond 2; 3M ESPE) served as reference. Scanning electron microscopy was used to observe the morphology of bonded interfaces. Data were analysed at p<0.05. Results: In enamel, AD35 had higher bond strength when rubbed for at least 10 s, while application for 5 s generated lower bond strength. In dentin, increased acidic monomer improved bonding only for 20 s rubbing time. The etch-and-rinse adhesive yielded higher bond strength to enamel and similar bonding to dentin as compared with the self-etch adhesives. The adhesive layer was thicker and more irregular for the etch-and-rinse material, with no appreciable differences among the self-etch systems. Conclusion: Overall, increasing the acidic monomer concentration only led to an increase in bond strength to enamel when the rubbing time was at least 10 s. In dentin, despite the increase in bond strength with longer rubbing times, the results favoured the experimental adhesives compared to the conventional adhesive. Reduced rubbing time of self-etch adhesives should be avoided in the clinical setup.


Asunto(s)
Humanos , Recubrimiento Dental Adhesivo/métodos , Recubrimientos Dentinarios/química , Bisfenol A Glicidil Metacrilato/química , Esmalte Dental/efectos de los fármacos , Dentina/efectos de los fármacos , Metacrilatos/química , Solventes/química , Propiedades de Superficie/efectos de los fármacos , Factores de Tiempo , Ensayo de Materiales , Agua/química , Microscopía Electrónica de Rastreo , Reproducibilidad de los Resultados , Análisis de Varianza , Fracaso de la Restauración Dental , Resistencia al Corte , Glicerol/química
2.
Journal of Korean Medical Science ; : 8-14, 1999.
Artículo en Inglés | WPRIM | ID: wpr-96720

RESUMEN

Butylated hydroxytoluene (BHT) can inhibit experimental atherosclerosis in animals. Although the agent is an antioxidant, the exact mechanism of the reaction in atherosclerosis is still unknown. To investigate the effects of BHT on expression of P-selectin (PADGEM, GMP-140), intercellular adhesion molecule-1 (ICAM-1) and class II MHC (Ia) antigen, we proposed an experiment on rats. Male rats (n=18 per group) were fed either a normal cholesterol control diet, a normal cholesterol diet containing 0.5% BHT (BD), a high cholesterol diet containing 1.5% cholesterol and 0.1% sodium cholate (CD), or the CD diet containing 0.5% BHT (BCD). Rats were sacrificed after 3 days, and after 1, 2, 4, 10, and 17 weeks of dietary treatment. Although there was no gross or light microscopic atherosclerotic lesions, scanning electron microscopy revealed monocytic adhesion to aortic endothelium and mild endothelial injuries in CD and BCD groups. Immunohistochemically, the addition of BHT to a high cholesterol diet inhibited P-selectin expression but not in ICAM-1 and Ia antigen. These findings suggest that in rats, high cholesterol diets induce expression of ICAM-1, P-selectin and Ia antigen. In addition, the antiatherogenic effect of BHT may play a role in the inhibition of P-selectin.


Asunto(s)
Masculino , Ratas , Animales , Antioxidantes/farmacología , Antioxidantes/metabolismo , Aorta Abdominal/ultraestructura , Aorta Abdominal/patología , Aorta Torácica/ultraestructura , Aorta Torácica/patología , Hidroxitolueno Butilado/farmacología , Hidroxitolueno Butilado/metabolismo , Colesterol/metabolismo , Colesterol en la Dieta/metabolismo , Microscopía Electrónica de Rastreo , Selectina-P/biosíntesis , Ratas Sprague-Dawley
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