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The decomposition rate and bleaching efficacy of in-office bleaching gels with different pHs: a randomized controlled
Fernanda Novak Gumy1, Karine Letícia da Silva1, Marcela Novak Gumy2
1Department of Restorative Dentistry, State University of Ponta Grossa, Av. General Carlos Cavalcanti, 4748, Ponta Grossa, Brazil.
Background:
To evaluate the decomposition rate of active hydrogen peroxide (HP) and bleaching efficacy during in-office bleaching using high-concentration HP gels with different pHs.
Method:
A randomized, parallel, double-blind controlled trial was conducted with 40 volunteers randomized into four groups (pH 5.4; pH 7.0; pH 7.7, and pH 8.0). During the first session in-office bleaching, approximately 0.01 g of the gel was collected and titrated with potassium permanganate to obtain the concentration of active HP and pH values were measured using an electrode. Bleaching efficacy was assessed using a spectrophotometer [∆Eab, ∆E00, and WID], Vita Classical and Vita Bleachedguide scales [∆SGU]. The decomposition rate of HP concentration and pH values change were calculated using ANOVA one-way. The bleaching efficacy was assessed using two-way repeated measures ANOVA. Tukey's test was applied as a post-hoc test (p < 0.05).
Results:
All gels experienced decreasing HP concentration over time. pH 5.4 gel showed greatest reduction after 50 min (p < 0.001). pH 8.0 and 7.7 gels remained stable; pH 5.4 remained acidic, while pH 7.0 turned acidic (p < 0.001). No significant difference in bleaching degree was observed among gels. They all showed a similar and clinically important color change after two clinical sessions, remained stable 1-month post-treatment (p > 0.05).
Conclusions:
All bleaching gels kept at least 70% of their HP content after 50 min, suggesting that there is a surplus of HP. They provided similar whitening efficacy 1-month after bleaching.
Practical Implications:
It is possible that lower HP concentrations may be equally effective in achieving desired results while reducing the potential for side effects.
Clinical Trial Registry Name:
RBR-35q7s3v.
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