Abstract Objective: To compare the clinical effect of two desensitizing agents used before the application of a bleaching gel based on 35% hydrogen peroxide (HP). Material and Methods: 30 patients were selected, and two desensitizing agents with different mechanisms of action were applied: Fluorine Neutral 2% (FN), which acts by blocking dentinal canaliculi while Potassium Nitrate 5% with 2% Sodium Fluoride (PN/SF) that acts in nerve transmission and blockade. Desensitizers were used before the application of 35% HP. For whitening, three clinical sessions were performed, with an interval of seven days, with three applications of the bleaching gel for 15 minutes, totaling 45 minutes/session. Tooth sensitivity (TS) was assessed with the numerical analog scale, and a spectrophotometer was used to obtain the color variation (ΔE). ΔE were submitted to ANOVA and Tukey test (p<0.05), and TS data were submitted to a two-way ANOVA analysis. Results: For sensitivity experience, the Tukey test indicated differences between PN/SF and the placebo I, but there was no statistically significant difference between FN and the placebo II. The TS was lower when the desensitizing gel was used during the bleaching procedure compared to after treatment, regardless of the desensitizing agents. Conclusion: PN/SF before in-office tooth bleaching can reduce TS intensity, and the use of desensitizing gel before bleaching did not affect the bleaching efficacy. Objective 35 HP . (HP) Methods 3 selected applied 2 FN, , (FN) 5 PNSF PN SF (PN/SF blockade whitening performed days 1 minutes 4 minutessession session minutes/session (TS scale ΔE. (ΔE) p<0.05, p005 p p<0.05 0 05 (p<0.05) twoway way analysis Results experience I II treatment Conclusion inoffice office intensity efficacy (HP (FN (ΔE p00 p<0.0 (p<0.05 p0 p<0. (p<0.0 p<0 (p<0. p< (p<0 (p< (p

Abstract To analyze the surface topography and mechanical properties of a polyurethane derived from castor oil reinforced with hydroxyapatite (PU–HA) for bone fixation. The surface analysis was performed by Scanning Electron Microscopy (SEM) and the mechanical properties by Vickers microhardness and tensile tests. The SEM images showed that the PU surface presented important characteristics for materials intended for bone fixation, such as an irregular and porous surface. The analysis showed a surface with alternating areas with depressions and elevations of approximately 80±100 µm, presence of pores of 12 µm in size. The microhardness analysis showed values of 0.42±1.01 HV for PU–HA plates, lower in relation to the poly lactic-co-glycolic acid (PLGA) plate (control group). The elastic modulus and ultimate tensile strength of 317.4 MPa, and 35.57 MPa for PLGA sample, 1.187 MPa, and 0.29 MPa for PU–HA sample. The PU produced showed good surface properties, however demands better mechanical properties. PUHA HA (PU–HA fixation (SEM tests 80100 80 100 80±10 1 size 042101 0 42 01 0.42±1.0 plates lacticcoglycolic lactic co glycolic (PLGA control group. group . group) 3174 317 4 317. 3557 35 57 35.5 sample 1187 187 1.18 029 29 0.2 8010 8 10 80±1 04210 0.42±1. 31 355 3 5 35. 118 18 1.1 02 2 0. 801 80± 0421 0.42±1 11 1. 042 0.42± 04 0.42 0.4

Abstract To analyze the biocompatibility of the scaffold produced from a natural polymer derived from castor oil through hemolytic activity and antimicrobial activity, to enable the clinical application. Three in vitro tests were performed: Hemolytic activity test - Polymer partially dissolved in contact with blood agar; Hemolytic activity test in sheep's blood - Polymer extract with red blood cells solution; Antimicrobial activity test - Solid polymer in direct contact with E. Coli and S. Aureus. For hemolytic tests, none of the samples showed hemolysis. Negative hemolytic activity is a good indicator, as the maintenance of the blood clot in the area of the lesion is essential for the formation of new tissue. For the antimicrobial activity test, no significant activity was observed against the bacteria used. The polymer is not toxic to red blood cells, being viable for clinical application as a matrix for tissue regeneration.

Abstract Objective To clinically assess the effect of desensitizing gels and dentifrices on the reduction in pain sensitivity and color variation during tooth bleaching. Methodology A total of 108 volunteers were randomly separated into the following groups of n=12: GT/S-glycerine and thickener/sucralose; NF/S-potassium nitrate and sodium fluoride/sucralose; NA/S-potassium nitrate and arginine/sucralose; GT/AC-glycerine and thickener/arginine and calcium carbonate; NF/AC-potassium nitrate and sodium fluoride/arginine and calcium carbonate; NA/AC-potassium nitrate and arginine/arginine and calcium carbonate; GT/PN-glycerine and thickener/potassium nitrate; NF/PN-potassium nitrate and sodium fluoride/potassium nitrate; and NA/PN-potassium nitrate and arginine/potassium nitrate. Sensitivity was assessed with the numerical analogue scale, and color variation (ΔE) was measured with a spectrophotometer. The sensitivity values obtained were subjected to a multivariate analysis of variance (MANOVA) and color variation values were subjected to a randomized analysis of variance (p<0.05). Results The NF/AC, NA/AC, NF/PN, and NA/PN groups presented lower sensitivity values and reduced sensitivity compared to those of the other groups throughout the clinical sessions. None of the groups showed sensitivity at the 24-week assessment. Statistically, no significant difference were observed in the color values among the groups four weeks after the beginning of bleaching (p=0.074). Additionally, the color assessment of all groups was statistically similar four weeks (p=0.084) and 24 weeks (p=0.118) after the beginning. Conclusion Our results indicate that adding NF/S, NA/S, NF/AC, and NA/AC desensitizers to tooth bleaching protocols reduces pain sensitivity without affecting its effectiveness.