In-office Bleaching Activated With Violet LED: Effect on Pulpal and Tooth Temperature and Pulp Viability

Author:

Carlos NR1,Basting RT2,Kantovitz KR3,Bronze-Uhle ES4,Lisboa Filho PN5,Cavalli V6,Basting RT7

Affiliation:

1. *Natalia Russo Carlos, DDS, MSc, PhD student, Faculdade São Leopoldo Mandic, Campinis, São Paulo, Brazil

2. Rosanna Tarkany Basting, MSc, PhD, Post-doc student, Faculdade São Leopoldo Mandic, Campinis, São Paulo, Brazil

3. Kamila Rosamilia Kantovitz, DDS, MSc, PhD, professor, Faculdade São Leopoldo Mandic, Campinis, São Paulo, Brazil

4. Erika Soares Bronze-Uhle, Phys, Post-doc student, São Paulo State University (UNESP)

5. Paulo Noronha Lisboa Filho, Phys, MSc, PhD, professor, São Paulo State University (UNESP), São Paulo, Brazil

6. Vanessa Cavalli, DDS, MSc, PhD, professor, Piracicaba Dental School, University of Campinas, Piracicaba, São Paulo, Brazil

7. Roberta Tarkany Basting, DDS, MSc, PhD, professor, Faculdade São Leopoldo Mandic, Campinas, São Paulo, Brazil

Abstract

SUMMARY Objectives: This study evaluated the influence of hydrogen peroxide (HP) with or without titanium dioxide nanotubes (TiO2) associated with violet LED (VL) regarding: a) the temperature change in the pulp chamber and facial surface; b) the decomposition of HP; and c) the cytotoxicity of the gels on pulp cells. Methods and Materials: The experimental groups were: HP35 (35% HP/Whiteness HP, FGM); HP35+VL; HP35T (HP35+TiO2); HP35T+VL; HP7 (7.5% HP/White Class 7.5%, FGM); HP7+VL; HP7T (HP7+TiO2); and HP7T+VL. TiO2 was incorporated into the bleaching gels at 1%. Eighty bovine incisors were evaluated to determine temperature change in 8 experimental groups (n=10/group). A k-type thermocouple was used to evaluate the temperatures of the facial surface and in the pulp chamber, achieved by enabling endodontic access to the palatal surface, throughout the 30-minute session. HP decomposition (n=3) of gels was evaluated by using an automatic potentiometric titrator at the initial and 30-minute time points. Trans-enamel and trans-dentinal cell viability were assessed with a pulp chamber device as well as enamel and dentin discs (n=6), and the treatment extracts (culture medium + diffused components) were collected and applied to MDPC-23 odontoblast cells to evaluate cell viability according to the MTT test. Results: A temperature increase in the pulp chamber was observed in the presence of VL at 30 minutes (p<0.05) (Mann-Whitney test). Also at 30 minutes, HP35 showed greater decomposition in the presence of VL rather than in its absence (p<0.05) (mixed linear models and the Tukey-Kramer test). HP7 provided greater cell viability than the groups treated with HP35 (p<0.05) (generalized linear models test). Cell viability was significantly lower for HP7 in the presence of VL (p<0.05). Conclusion: Pulpal temperature increased with VL (maximum of 1.9°C), but did not exceed the critical limit to cause pulp damage. Less concentrated HP resulted in higher cell viability, even when associated with VL.

Publisher

Operative Dentistry

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