- 1Department of Restorative Dentistry, Piracicaba School of Dentistry, State University of Campinas, Piracicaba, Brazil
- 2Division of Dental Biomaterials, The University of Oklahoma Health Sciences Center College of Dentistry, Oklahoma City, OK, United States
Introduction
Several chemical components and procedures have been used along the years to resolve dental discolorations (vital and non-vital teeth) (1, 2). However, even though promising bleaching outcomes (3–6) have been reported by numerous studies (in vitro and clinical trials), patients typically complain about the occurrence of mild-to-severe post-operatory dentin hypersensitivity (4, 7–9). These concerns have precipitated the execution of extensive studies aiming to improve the safety and efficacy of peroxide-based (hydrogen or carbamide) treatments (10). Despite the widespread clinical acceptance amongst clinicians and patients, and the perceived safety (11) associated with dental bleaching procedures, (12) studies have demonstrated the negative impacts of these so-called minimally invasive and ultraconservative techniques on enamel, (13–15) dentin, pulp and surrounding soft tissues (13, 16–18).
The fundamental mechanism of action associated with peroxide-containing products (hydrogen [HP] or carbamide [CP]) revolves around the generation of reactive oxygen species (ROS) (19). These oxidizing agents such as oxygen, hydroperoxyl, sodium hypochlorite, hydrogen peroxide, ozone and hydroxyl are associated with different redox potentials (E0, in Volts; +1.229, +1.510, +1.630, +1.780, +2.075 and +2.800, respectively) (20, 21) and according to Gentil de Moor, (21) the higher the redox potential, the higher the efficacy in breaking conjugated C=C bonds present in large organic molecules (chromophores). The breakage of conjugated bonds results in numerous small-sized molecules that efficiently scatter smaller wavelengths. This physico-chemical process alters the optical behavior of teeth (22) and the visual perception of colors from yellow-brown to bluish-white.
Even though dental bleaching agents have been reported to generate large amounts of ROS, (20) the molecular environment provided by these materials not only limit their transport, from the gel into the crystalline structure, but also hinders the efficacy of these highly reactive and short-lived species. The most common approaches to overcome these limiting factors include the utilization of high concentrations of HP (30–44%), long exposure times to CP (21 days, at-home) or the utilization of external energy sources (heat or visible light). Several light sources have been used with the purpose of improving the efficacy of bleaching procedures and to shorten the exposure of tissues (soft and mineralized) to highly caustic and oxidative agents (23, 24).
Despite the feasibility of the process, numerous reports have indicated that bleaching protocols modulated by visible light render esthetic outcomes that are only similar to those attained by at-home bleaching techniques, thereby questioning the need for the utilization of visible light (25–27). Therefore, this brief opinion article aims to contribute with information regarding the state of the art, recent developments and future perspectives in the field of dental bleaching.
Past, Present and Future of Dental Bleaching
The first attempt to improve the efficacy of hydrogen peroxide was based on the delivery of thermal energy onto the tooth structure by means of a heated spatula (28, 29). Although, the process provided with excellent esthetic results, the inability to control the diffusion of heat, and the occurrence of irreversible damage to the dentin-pulp complex restricted its widespread utilization. Subsequent developments focused on the utilization of chemical catalysts (oxalic acid) to improve the speed of the reaction and reduce the incidence of adverse effects (1). However, clinical results were associated with intense dentin hypersensitivity that could only be resolved by radical endodontic treatment.
The introduction of visible light in dental bleaching techniques started with light curing units containing quartz-tungsten halogen filament lamps. These devices emit a broad range of wavelengths (between 400 and 525 nm) (30) and tremendous amount of radiant heat (infrared) that must be filtered using band-pass optical filters. In this energy-transfer model, a colored bleaching gel is used to insulate teeth and convert photons into thermal energy. The rationale behind this approach is to raise the temperature of the gel, favor the dissociation of HP and improve the molecular mobility of ROS. Even though studies demonstrated that esthetic results were better than those attained with at-home bleaching techniques, high levels of dentin hypersensitivity were still being reported by treated patients (31).
Light-emitting diodes (LEDs), which are narrow-band and heat-free sources have also been used in in-office dental bleaching procedures. Despite the lower levels of dentin hypersensitivity reported, clinical outcomes were considered poor and were inferior to those from at-home bleaching techniques, which further strengthened the controversy regarding the utilization of visible light. Esteban Florez et al. (22, 28) while investigating the scientific basis of in-office power bleaching procedures, suggested that a photonic catalysis model should be used to improve bleaching outcomes when using heat-free light sources. In the model proposed, visible light irradiation is used to increase chromophores' degree of freedom and create a molecular environment that improves the reactivity of ROS and the breakage of chromophores.
A few clinical studies have investigated the effects of hybrid irradiation (infrared and visible, 780 ± 5 nm and 457 ± 15 nm, respectively) on the efficacy of in-office bleaching protocols using gels containing 6% of HP (32–34). Even though the hybrid irradiation investigated was shown to enhance the efficacy of bleaching gels with low concentrations of HP, results reported have indicated that bleaching outcomes were still inferior to those of 35% HP. According to those studies, the major benefit of the hybrid irradiation technology (LASER/LED) precipitated from the intrinsic biostimulation properties of low intensity level laser that decreased the incidence, intensity and duration of post-operatory dentin hypersensitivity, (35) thereby positively impacting patient's overall experience and comfort (36).
Photonic bleaching techniques are those that do not use any type of peroxide-containing products, (37–39) and have been suggested as an alternative to resolve dental discolorations without the occurrence of adverse side effects (40). In this pain-free approach, (40) visible radiation of adequate wavelength (405 ± 15 nm) and photon energy (3.06 μeV) (41) is used to break conjugated C=C and alter the optical behavior of teeth (42, 43). However, even though such photophysical process is feasible from the electronic standpoint, the limited penetration of near-UV wavelengths (44) associated with the desiccation of the crystalline structure, not only decreases the total amount of energy available to permanently break conjugated C=C double bonds, but also eliminates the chances for the generation of ROS. In combination, these factors are clinically translated into less-than-optimal bleaching outcomes and poor chromatic stability (days to weeks) (18, 45–47).
Other studies focused on the incorporation of calcinated metaloxide nanoparticles, such as nitrogen-doped titanium dioxide (TiO2-N), into commercially-available bleaching gels containing hydrogen peroxide (6 to 35%) (36, 48, 49). According to results reported, nanoparticles used behave as semi-conductors and efficiently convert photons into thermal energy (36). Randomized clinical trials have indicated that bleaching techniques modulated by experimental gels containing varying concentrations of HP and TiO2-N, did not result in bleaching outcomes that were better than those attained with unaltered bleaching gels under the same light irradiation conditions (36). Despite all efforts from the manufacturing and scientific communities, bleaching materials and equipment developed were not capable of vertically advancing the field.
This scenario exposes a critical need for novel materials and techniques that are capable of delivering excellent esthetic outcomes without negatively impacting the properties of teeth (surface, mechanical, chemical and biological). Recent studies (50–52) have demonstrated the synthesis of third-generation titanium dioxide nanoparticles co-doped with nitrogen and fluorine (NF_TiO2, 6–15 nm) using robust and highly reproducible solvothermal reactions. According to Huo et al. (53) the synthetic route reported renders nanoparticles that are highly crystalline, have well-defined pore-size distributions, are electron-deficient, generate substantial amounts of ROS, and display strong antibacterial properties (light and dark conditions) against non-disrupted Streptococcus mutans biofilms when functionalized in a commercially-available 5th generation dental adhesive resin (50). These findings are fundamentally important for subsequent developments in the field, because third-generation and visible-light responsive NF_TiO2 can be easily functionalized into polymers currently used in dental bleaching products (at-home and in-office). If successful, this approach may result in a novel generation of bleaching gels with low concentrations of HP and NF_TiO2 (lower than 10% HP) that are highly effective, less aggressive to the crystalline structure, and may display important teeth mineralization properties (biomimetic functionalities).
Discussion
It is clear from a simple review of the literature that significant amount of time, funds and effort have been invested by both the manufacturing and scientific communities to improve the efficacy and safety of dental bleaching procedures. Despite all efforts, in-office dental bleaching techniques modulated by visible light radiation (from heat-free sources) and HP continue to be associated with dentin hypersensitivity, (11) and negative impacts on the properties of teeth (surface, mechanical, chemical and biological) (13, 16–18, 25, 35, 54).
Since dentin hypersensitivity has a strong and positive correlation with the concentration of HP, (55) photonic bleaching approaches have been proposed as a safe, pain- and peroxide-free alternative to resolve light-to-mild dental discolorations in vital teeth. However, even though some reports have demonstrated promising immediate results, (37) the vast majority of the literature has indicated that clinical outcomes are poor and unstable. In fact, a recent study (44) has shown that 98% of the energy delivered onto the enamel (thickness of 1.0 mm) is significantly attenuated when using near-UV wavelengths (~405 nm), and results in doses of energy (at the enamel-dentin junction) that are below the threshold required to permanently break conjugated double bonds present in chromophores.
This behavior not only results in poor esthetic outcomes, but also in clinical protocols that are longer (in terms of clinical sessions). Based on the context provided, it is our opinion that light irradiation continues to be fundamentally important to improve the efficacy of peroxide-containing products (either HP or CP). It is important to underscore that bleaching protocols modulated by HP and near-UV wavelengths (~405 nm) result in bleaching outcomes that are superior than those precipitating from the combination between HP and visible light (~457 nm), (55) thereby indicating a wavelength-dependent mechanism. Two recent randomized clinical trials (56, 57) have corroborated our opinion by demonstrating that bleaching protocols modulated by near-UV radiation and CP resulted in esthetic outcomes that were comparable to those of 35% HP, were long-lasting (up to 1 year), were associated with lower levels of dentin hypersensitivity and clinical sessions that were significantly shorter (~30 min/each) (56–58).
Subsequent developments in the field should focus on improving the molecular environment of polymers to optimize the generation, transport and penetration of ROS while decreasing HP concentrations used. One possible alternative is the utilization of third-generation and visible light-responsive nitrogen and fluorine co-doped titanium dioxide nanoparticles (NF_TiO2) that are capable of generating substantial amounts of ROS and display strong antibacterial, biomimetic and biocompatibility properties (51, 52, 59). In addition, the development of improved interfacial chemistries for superior functionalization, loading and dispersion of metaloxide nanoparticles in dental polymers is expected to result in stable colloidal sols displaying superior rheological and wettability properties.
Bleaching protocols modulated by visible light radiation and nano-filled bleaching gels may not only display promising esthetic outcomes and low levels of dentin hypersensitivity, but could also display biomimetic properties. In combination, these properties are anticipated to protect the chemical make-up of treated teeth through an ion-exchange mechanism and will have the potential to render treated enamel less soluble to organic acids, thereby adding an additional therapeutic value (biomimetic properties) to dental bleaching treatments. Therefore, subsequent studies in the field should be based on mechanistic methodologies capable of elucidating the processes governing the generation and transport of ROS and the impact of polymer compositions on the efficacy of bleaching procedures.
Author Contributions
MK, PM, and RC searched the literature and wrote the initial draft. FE and VC edited the draft. VC conceptualized and supervised the article. All authors contributed to the article and approved the submitted version.
Funding
This study was supported in part by Coordenação de Aperfeiçoamento de Pessoal do Nível Superior (CAPES) – 001. This study was also supported by São Paulo State Research Foundation (FAPESP) - #2019/02393-6 and #2020/06782-4.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1. Alqahtani MQ. Tooth-bleaching procedures and their controversial effects: a literature review. Saudi Dent J. (2014) 26:33–46. doi: 10.1016/j.sdentj.2014.02.002
2. Carey CM. Tooth whitening: what we now know. J Evid Based Dent Pract. (2014) 14:70–6. doi: 10.1016/j.jebdp.2014.02.006
3. de Freitas MR, de Carvalho MM, Liporoni PC, Fort AC, Zanatta RF. Effectiveness and adverse effects of over-the-counter whitening products on dental tissues. Front Dental Med. (2021) 2:507. doi: 10.3389/fdmed.2021.687507
4. Basting RT, Amaral FL, França FM, Flório FM. Clinical comparative study of the effectiveness of and tooth sensitivity to 10 and 20% carbamide peroxide home-use and 35 and 38% hydrogen peroxide in-office bleaching materials containing desensitizing agents. Oper Dent. (2012) 37:464–73. doi: 10.2341/11-337-C
5. Pinto AV, Bridi EC, Amaral FL, França FM, Turssi CP, Pérez CA, et al. Enamel mineral content changes after bleaching with high and low hydrogen peroxide concentrations: colorimetric spectrophotometry and total reflection X-ray fluorescence analyses. Oper Dent. (2017) 42:308–18. doi: 10.2341/16-032-L
6. Cavalli V, Silva BG, Berger SB, Marson FC, Tabchoury CP, Giannini M. Decomposition rate, pH, and enamel color alteration of at-home and in-office bleaching agents. Braz Dent J. (2019) 30:385–96. doi: 10.1590/0103-6440201902484
7. Liu XX, Tenenbaum HC, Wilder RS, Quock R, Hewlett ER, Ren YF. Pathogenesis, diagnosis and management of dentin hypersensitivity: an evidence-based overview for dental practitioners. BMC Oral Health. (2020) 20:220. doi: 10.1186/s12903-020-01199-z
8. Ortega-Moncayo MG, Aliaga-Sancho P, Pulido C, Gutierrez MF, Rodriguez-Salazar E, Burey A, et al. Is the use of a potassium nitrate dentifrice effective in reducing tooth sensitivity related to in-office bleaching? A randomized triple-blind clinical trial. J Esthet Restor Dent. (2021). doi: 10.1111/jerd.12826
9. Piknjač A, Soldo M, Illeš D, Knezović Zlatarić D. Patients' Assessments of tooth sensitivity increase 1 day following different whitening treatments. Acta Stomatol Croat. (2021) 55:280–90. doi: 10.15644/asc55/3/5
10. Tredwin CJ, Naik S, Lewis NJ, Scully CB. Hydrogen peroxide tooth-whitening (bleaching) products: review of adverse effects and safety issues. Br Dent J. (2006) 200:371–6. doi: 10.1038/sj.bdj.4813423
11. Oldoini G, Bruno A, Genovesi AM, Parisi L. Effects of amorphous calcium phosphate administration on dental sensitivity during in-office and at-home interventions. Dent J. (2018) 6:52. doi: 10.3390/dj6040052
12. Li Y, Greenwall L. Safety issues of tooth whitening using peroxide-based materials. Br Dent J. (2013) 215:29–34. doi: 10.1038/sj.bdj.2013.629
13. Sun L, Liang S, Sa Y, Wang Z, Ma X, Jiang T. Surface alteration of human tooth enamel subjected to acidic and neutral 30% hydrogen peroxide. J Dent. (2011) 39:686–92. doi: 10.1016/j.jdent.2011.07.011
14. Grazioli G, Valente LL, Isolan CP, Pinheiro HA, Duarte CG, Münchow EA. Bleaching and enamel surface interactions resulting from the use of highly-concentrated bleaching gels. Arch Oral Biol. (2018) 87:157–62. doi: 10.1016/j.archoralbio.2017.12.026
15. Silva AP, Oliveira R, Cavalli V, Arrais CA, Giannini M, Carvalho RM. Effect of peroxide-based bleaching agents on enamel ultimate tensile strength. Oper Dent. (2005) 30:318–24.
16. Kemaloglu H, Tezel H, Ergücü Z. Does post-bleaching fluoridation affect the further demineralization of bleached enamel? An in vitro study. BMC Oral Health. (2014) 14:113. doi: 10.1186/1472-6831-14-113
17. Cavalli V, Rosa DA, Silva DP, Kury M, Liporoni P, Soares LE, et al. Effects of experimental bleaching agents on the mineral content of sound and demineralized enamels. J Appl Oral Sci. (2018) 26:e20170589. doi: 10.1590/1678-7757-2017-0589
18. Kury M, Antonialli FM, Soares LE, Tabchoury CP, Giannini M, Florez FL, et al. Effects of violet radiation and non-thermal atmospheric plasma on the mineral contents of enamel during in-office dental bleaching. Photodiag Photodyn Ther. (2020) 31:101848. doi: 10.1016/j.pdpdt.2020.101848
19. Kwon SR, Wertz PW. Review of the mechanism of tooth whitening. J Esthet Restor Dent. (2015) 27:240–57. doi: 10.1111/jerd.12152
20. De Moor RJ, Verheyen J, Diachuk A, Verheyen P, Meire MA, De Coster PJ, et al. Insight in the chemistry of laser-activated dental bleaching. Sci W J. (2015) 2015:650492. doi: 10.1155/2015/650492
21. Pretel H, Costa JL, Florez FL, Nogueira BR, de Oliveira OB. Assessment of the temporal variation of electrical potential and pH of different bleaching agents. Heliyon. (2021) 7:e08452. doi: 10.1016/j.heliyon.2021.e08452
22. Esteban Florez, F.L., E. Lins, P.P. Portero, R.d.F.Z. Lizarelli, O.B.d. Oliveira, and V.S. Bagnato. Investigation of photo-bleaching through transmittance method in pigmented solution: understanding possible mechanisms and advantages for photo dental whitening. SPIE BiOS. (2007). doi: 10.1117/12.700517
23. Florez FL, Lins EC, Portero PP, Lizarelli RF, Oliveira Jr OB, Bagnato VS. Evaluation of temperature increase during in-office bleaching. J Appl Oral Sci. (2016) 24:136–41. doi: 10.1590/1678-775720150154
24. Nam SH, Choi BB, Kim GC. The whitening effect and histological safety of non-thermal atmospheric plasma inducing tooth bleaching. Int J Environ Res Public Health. (2021) 18:4714. doi: 10.3390/ijerph18094714
25. Hahn P, Schondelmaier N, Wolkewitz M, Altenburger MJ, Polydorou O. Efficacy of tooth bleaching with and without light activation and its effect on the pulp temperature: an in vitro study. Odontology. (2013) 101:67–74. doi: 10.1007/s10266-012-0063-4
26. Maran BM, Burey A, de Paris Matos T, Loguercio AD, Reis A. In-office dental bleaching with light vs. without light: a systematic review and meta-analysis. J Dent. (2018) 70:1–13. doi: 10.1016/j.jdent.2017.11.007
27. SoutoMaior JR, De Moraes SL, Lemos CA, Vasconcelos BD, Montes MA, Pellizzer EP. Effectiveness of light sources on in-office dental bleaching: a systematic review and meta-analyses. Operat Dent. (2019) 44:E105–17. doi: 10.2341/17-280-L
28. Florez FL, Figueiredo AC, Moriyama LT, Junior OO, Bagnato VS. In vitro study of the influence of the pigments of three colored gels over the light distribution of visible light by digital images. BiOS. (2009). doi: 10.1117/12.809359
29. Florez FL, Vollet-Filho JD, Oliveira-Junior OB, Bagnato VS. Time-course diffusion of hydrogen peroxide using modern technologies. Proceed SPIE. (2017) 7162:716209-1- 716209-8. doi: 10.1117/12.809285
30. Elvidge CD, Keith DM, Tuttle BT, Baugh KE. Spectral identification of lightning type and character. Sensors. (2010) 10:3691. doi: 10.3390/s100403961
31. Martin J, Fernandez E, Bahamondes V, Werner A, Elphick K, Oliveira Jr OB, et al. Dentin hypersensitivity after teeth bleaching with in-office systems. Randomized clinical trial. Am J Dent. (2013) 26:10–4.
32. Zanin F, Brugnera Jr A, Marchesan MA, Pecora JD. Laser and LED external teeth-bleaching. Biomedical Optics. (2004) 2004:5313 doi: 10.1117/12.537428
33. Torres CR, Barcellos DC, Batista GR, Borges AB, Cassiano KV, Pucci CR. Assessment of the effectiveness of light-emitting diode and diode laser hybrid light sources to intensify dental bleaching treatment. Acta Odontol Scand. (2011) 69:176–81. doi: 10.3109/00016357.2010.549503
34. Kossatz S, Dalanhol AP, Cunha T, Loguercio A, Reis A. Effect of light activation on tooth sensitivity after in-office bleaching. Oper Dent. (2011) 36:251–7. doi: 10.2341/10-289-C
35. Benetti F, Lemos CA, de Oliveira Gallinari M, Terayama AM, Briso AL, de Castilho Jacinto R, et al. Influence of different types of light on the response of the pulp tissue in dental bleaching: a systematic review. Clin Oral Investig. (2018) 22:1825–37. doi: 10.1007/s00784-017-2278-9
36. Trevisan TC, Bortolatto JF, Rizzi G, Meloto BT, Dantas AA, de Oliveira Junior OB. Clinical performance of 6% hydrogen peroxide containing TiO(2)N nanoparticles activated by LED in varying wavelengths-a randomized clinical trial. Lasers Med Sci. (2022). 37:2017–24. doi: 10.1007/s10103-021-03464-1
37. Panhoca VH, Oliveira B, Rastelli AS, Bagnato VS. Dental bleaching using violet light alone: clinical case report. Dentistry. (2017) 7:459. doi: 10.4172/2161-1122.1000459
38. Santos AE, Bussadori SK, Pinto MM, Zanin FA, Silva T, Martinbianco AL, et al. Clinical evaluation of in-office tooth whitening with violet LED (405 nm): a double-blind randomized controlled clinical trial. Photodiag Photodyna Therapy. (2021) 35:102385. doi: 10.1016/j.pdpdt.2021.102385
39. Kury M, Resende BA, Silva DP, Wada EE, Antonialli FM, Giannini Met al. Clinical application of violet LED In-office bleaching with or without traditional systems: case series. Oral Health Dent Stud. (2018) 2. doi: 10.31532/OralHealthDentStud.2.1.001
40. Brugnera AP, Nammour S, Rodrigues JA, Mayer-Santos E, De Freitas PM, Brugnera A, et al. Clinical evaluation of in-office dental bleaching using a violet light-emitted diode. Photobiomodul Photomed Laser Surg. (2020) 38:98–104. doi: 10.1089/photob.2018.4567
41. Nakonieczna-Rudnicka M, Bachanek T, Madejczyki M, Grajewskai I, Kobyłecka E. Teeth Whitening vs. the Influence of Extrinsic Factors on Teeth Stains. Przeglad lekarski. (2015) 72:126–30.
42. Zanin F. Recent advances in dental bleaching with laser and LEDs. Photomed Laser Surg. (2016) 34:135–6. doi: 10.1089/pho.2016.4111
43. Zanin F, Brugnera Jr A, Windlin MC. Dental bleaching with LEDs and lasers. Lasers Dent. (2015):92–103. doi: 10.1002/9781118987742.ch14
44. Kury M, Rueggeberg FA, Soto-Montero JR, André CB, Resende BA, Giannini M, et al. Characterization and effectiveness of a violet LED light for in-office whitening. Clin Oral Investig. (2022) 3:1–12 doi: 10.1007/s00784-021-04357-x
45. Kury M, Perches C, da Silva DP, Andre CB, Tabchoury CP, Giannini M, et al. Color change, diffusion of hydrogen peroxide, and enamel morphology after in-office bleaching with violet light or non-thermal atmospheric plasma: an in vitro study. J Esthetic Restorative Dent. (2020) 32:102–12. doi: 10.1111/jerd.12556
46. de Oliveira Gallinari M, Cintra LT, Barboza AC, da Silva LM, de Alcantara S, Dos Santos PH, et al. Evaluation of the color change and tooth sensitivity in treatments that associate violet LED with carbamide peroxide 10 %: a randomized clinical trial of a split-mouth design. Photodiag Photody Therapy. (2020) 30:101679. doi: 10.1016/j.pdpdt.2020.101679
47. Gallinari MO, Fagundes TC, da Silva LM, de Almeida Souza MB, Barboza AC, Briso AL. A new approach for dental bleaching using violet light with or without the use of whitening gel: study of bleaching effectiveness. Operat Dent. (2019) 44:521–9. doi: 10.2341/17-257-L
48. Thacker M, Chen YN, Lin CP, Lin FH. Nitrogen-doped titanium dioxide mixed with calcium peroxide and methylcellulose for dental bleaching under visible light activation. Int J Mol Sci. (2021) 22:3759. doi: 10.3390/ijms22073759
49. Zhang F, Wu C, Zhou Z, Wang J, Bao W, Dong L, et al. Blue-light -activated nano-TiO2@PDA for highly effective and non-destructive tooth whitening. ACS Biomat Scie Enginee. (2018) 4:3072–7. doi: 10.1021/acsbiomaterials.8b00548
50. Florez FL, Hiers RD, Larson P, Johnson M, O'Rear E, Rondinone AJ, et al. Antibacterial dental adhesive resins containing nitrogen-doped titanium dioxide nanoparticles. Mater Sci Eng C Mater Biol Appl. (2018) 93:931–43. doi: 10.1016/j.msec.2018.08.060
51. Florez FL, Hiers RD, Zhao Y, Merritt J, Rondinone AJ, Khajotia SS. Optimization of a real-time high-throughput assay for assessment of Streptococcus mutans metabolism and screening of antibacterial dental adhesives. Dent Mater. (2020) 36:353–65. doi: 10.1016/j.dental.2019.12.007
52. Esteban Florez FL, Trofimov AA, Ievlev A, Qian S, Rondinone AJ, Khajotia SS. Advanced characterization of surface-modified nanoparticles and nanofilled antibacterial dental adhesive resins. Sci Rep. (2020) 10:9811. doi: 10.1038/s41598-020-66819-8
53. Huo Y, Bian Z, Zhang X, Jin Y, Zhu J, Li H. Highly active TiO2-xNx visible photocatalyst prepared by N-doping in Et3N/etoh fluid under supercritical conditions. J Phy Chemistry C. (2008) 112:6546–50. doi: 10.1021/jp711966c
54. Barcellos DC, Borges AB, Torres CR, Batista GR. Analysis of the pulp chamber temperature of teeth submitted to light activation with and without bleaching gel. W J Dent. (2011) 2:23–7. doi: 10.5005/jp-journals-10015-1048
55. Camargo SE, Valera MC, Camargo CH, Mancini MN, Menezes MM. Penetration of 38% hydrogen peroxide into the pulp chamber in bovine and human teeth submitted to office bleach technique. J Endod. (2007) 33:1074–7. doi: 10.1016/j.joen.2007.04.014
56. Kury M, Wada EE, da Silva Palandi S, Picolo MZ, Giannini M, Cavalli V. Colorimetric evaluation after in-office tooth bleaching with violet LED: 6- and 12-month follow-ups of a randomized clinical trial. Clin Oral Investig. (2022) 26:837–47. doi: 10.1007/s00784-021-04062-9
57. Kury M, Wada EE, Silva DP, Tabchoury CP, Giannini M, Cavalli V. Effect of violet LED light on in-office bleaching protocols: a randomized controlled clinical trial. J Appl Oral Sci. (2020) 28:e20190720. doi: 10.1590/1678-7757-2019-0720
58. Youssef SA, Cunha SR, Mayer-Santos E, Brito SA, de Freitas PM, Ramalho J, et al. Influence of 35% hydrogen peroxide gel renewal on color change during in-office dental photobleaching with violet LED: a split-mouth randomized controlled clinical trial. Photodiagnosis Photodyn Ther. (2021) 36:102509. doi: 10.1016/j.pdpdt.2021.102509
Keywords: tooth bleaching, hydrogen peroxide, light, nanoparticles, in-office
Citation: Cavalli V, Kury M, Melo PBG, Carneiro RVTSM and Esteban Florez FL (2022) Current Status and Future Perspectives of In-office Tooth Bleaching. Front. Dent. Med. 3:912857. doi: 10.3389/fdmed.2022.912857
Received: 04 April 2022; Accepted: 03 May 2022;
Published: 31 May 2022.
Edited by:
Mutlu Özcan, University of Zurich, SwitzerlandReviewed by:
Sandrine Bittencourt Berger, Universidade Norte do Paraná, BrazilCopyright © 2022 Cavalli, Kury, Melo, Carneiro and Esteban Florez. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Vanessa Cavalli, cavalli@unicamp.br