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AIMS: The effect of reinforcement and cyclic loading on the resistance to impact (RI) of denture base biopolymer materials was evaluated using Charpy (C) and falling-weight (FW) impact tests. METHODS: Bar-shaped (60×6×2mm(3)) and denture-shaped specimens (2mm) for the C and FD tests, respectively, were prepared with Lucitone 550 (L) and Vipi Wave (V) and relined (2mm) using the same material or the autopolymerizing relining resins Tokuyama Rebase II (T) and Ufi Gel Hard (U). Bulk specimens (60×6×4mm(3)) of all materials (L, V, T and U) were also prepared and tested. To evaluate the effect of reinforcement, glass flakes were added to the powder of the relining resins T and U (5% by weight). Half of bar-shaped (n=320) and half of the denture-shaped specimens (n=480) were subjected to cyclic loading (10,000 cycles) before the impact tests. RESULTS: Data were analyzed by one-way ANOVAs (α=0.05) and revealed that the RI of L and V were comparable and higher than those of U and T. Compared to L and V, the RI was increased by relining with T and decreased by relining with U. When relining was made using the same material (L and V) the RI was maintained. Flexural cyclic loading and the incorporation of glass flakes into the resins T and U did not cause any significant alteration in the RI. A high correlation between results from C and FW tests was observed (r=0.8854). CONCLUSION: Relining may exert effects on the RI of L and V denture base resins, which vary according to the relining material used. The high correlation between C and FW, suggests that the Charpy test, using bar-shaped specimens, can be a simple and reliable method for evaluating factors that may influence the RI of denture base polymers.

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RESUMO

This study evaluated the in vitro susceptibility of C. albicans, C. dubliniensis, C. tropicalis and C. krusei to photodynamic therapy (PDT) induced by Photogem® and light emitting diode (LED). Suspensions of each Candida strain were treated with three photosensitizer (PS) concentrations (10, 25 and 50 mg/L) and exposed to 18.0, 25.5 and 37.5 J/cm² LED light fluences ( ~ 455 nm). Control suspensions were treated only with PS concentrations, only exposed to the LED light fluences or not exposed to LED light or PS. Sixteen experimental conditions were obtained and each condition was repeated three times. From each sample, serial dilutions were obtained and aliquots were plated on Sabouraud Dextrose Agar. After incubation of plates (37 ºC for 48 hours), colonies were counted (cfu/mL) and the data were statistically analyzed by ANOVA and the Tukey test (=0.05). Complete killing of C. albicans was observed after 18.0 J/cm² in association with 50 mg/L of PS. C. dubliniensis were inactivated after 18.0 J/cm² using 25 mg/L of PS. The inactivation of C. tropicalis was observed after photosensitization with 25 mg/L and subsequent illumination at 25.5 J/cm². For C. krusei, none of the associations between PS and light resulted in complete killing of this species. PDT proved to be effective for the inactivation of C. albicans, C. dubliniensis and C. tropicalis. In addition, reduction in the viability of C. krusei was achieved with some of the PS and light associations.