Provides a review of current safety issues and adverse effects of hydrogen peroxide tooth whitening.
Helps the reader recognise and understand any potential problems with the use of hydrogen peroxide tooth whitening agents.
Critically reviews the available literature on safety issues and adverse effects of hydrogen peroxide tooth whitening.
Outlines some simple guidelines based on the available literature for use to the reader when carrying out hydrogen peroxide tooth whitening.
Hydrogen peroxide in the form of carbamide peroxide is widely used for tooth whitening (bleaching), both in professionally- and in self-administered products. Adverse effects have become evident. Cervical root resorption is a possible consequence of internal bleaching and is more frequently observed in teeth treated with the thermo-catalytic procedure. Tooth sensitivity is experienced in 15-78% of patients undergoing external tooth bleaching. However, clinical studies addressing other adverse effects are lacking. Direct contact with hydrogen peroxide induces genotoxic effects in bacteria and cultured epithelial cells, but the effect is reduced or totally abolished in the presence of metabolising enzymes. Several carcinogenesis studies, including the hamster cheek pouch model, indicate that hydrogen peroxide (H2O2) might possibly act as a promoter. Until further clinical research is concluded to address the question of possible carcinogenicity, it is recommended that: tooth-bleaching products using concentrated H2O2 should not be used without gingival protection; that H2O2 containing products should be avoided in patients with damaged or diseased soft tissues. For nightguard vital bleaching, minimal amounts of low dose H2O2 (including in the form of carbamide peroxide) are preferred, thereby avoiding prolonged and concentrated exposures.
Contemporary tooth whitening (tooth bleaching) systems are based primarily on hydrogen peroxide (H2O2) or one of its precursors, carbamide peroxide. These bleach the chromogens within the dentine, thereby reducing the body colour of the tooth and are often used in combination with an activating agent such as heat and/or light. Such agents can be applied externally to the teeth (vital bleaching) or internally within the pulp chamber (non-vital bleaching).
Case reports and small clinical studies have confirmed that predictable tooth whitening can be achieved using a 10% carbamide peroxide gel in a bleaching tray at night, (the nightguard vital bleaching technique),1,2,3,4,5,6,7,8,9 H2O2 strips10 and 'power bleaching' using 35% H2O2 with or without light and/or heat activation.11,12 The 'walking bleach' technique introduced in 1961 for the bleaching of non-vital teeth involved sealing a mixture of sodium perborate and water into the pulp chamber between patients' visits.13 The method was later modified and water replaced by 30-35% H2O2, to improve the whitening effect.14
Concerns have been expressed over the potential adverse effects of the use of H2O2 tooth whitening agents. The adverse effects that have been reported in cellular, animal and human studies include: cervical root resorption associated with non-vital bleaching; increased tooth sensitivity associated with vital bleaching; alteration in the surface topography of enamel; reduction in bond strength of resin based materials and the possibility that H2O2 may have carcinogenic or tumour promoting capabilities.
It is the purpose of this paper to review the available information on the side effects and safety of H2O2 in tooth whitening.
Hydrogen peroxide (H2O2) is a colourless liquid with a bitter taste and is highly soluble in water to give an acidic solution. H2O2 is an oxidising agent with a wide number of industrial applications in for example, bleaching or deodorising textiles, wood pulp, hair, fur and foods, in the treatment of water and sewage, as a seed disinfectant and neutralising agent in wine distillation. Low concentrations of H2O2 have been found in rain and surface water, in human and plant tissues, in foods and beverages and in bacteria.15
Chemical reactions of hydrogen peroxide
Hydrogen peroxide is a reactive oxygen species, along with superoxide (O2-), hydroxyl (HO), peroxyl (ROO) and alkoxyl (RO).16 In human tissue, intrinsic sources of H2O2 are organelles (especially mitochondria), salivary cells, microorganisms and the lungs.17 Hydrogen peroxide production can be followed by the liberation of highly reactive oxygen species in the body via enzymatic and spontaneous redox reactions that often involve interaction with transitional metals such as iron or copper.
Enzymes such as catalase, glutathione peroxidase and superoxide dismutase catalyse the decomposition of H2O2 into water and oxygen.
Reactive oxygen radicals are a potential source of cell damage through causing DNA strand breaks, genotoxicity, and cytotoxicity, but these radicals tend neither to cross biological membranes nor travel large distances within a cell. Antioxidants provide a source of electrons that reduce hydroxyl radicals to water.
However, when exogenous H2O2 levels overwhelm cellular protective mechanisms, H2O2 presents a health hazard.15,18 Individuals with acatalasia lack catalase activity, leading to high endogenous H2O2 levels causing necrosis and ulceration of soft and hard tissues.19
Hydrogen peroxide toxicity
Thirty per cent H2O2 can cause severe irritation or burns on contact with skin or eyes.16 Following inadvertent irrigation of H2O2 into the periodontal ligament during root canal treatment, contact of the H2O2 with blood and tissue proteins produces effervescence, liberating oxygen and causing tissue emphysema.20
Following application of 30% H2O2 at 15 minute intervals (four applications) to the tip of rat tongue, oedema was followed by intraepithelial and some subepithelial vesiculation, changes preventable by prior administration of catalase.21
Prolonged application of a dilute 0.3 molar H2O2 solution onto the ventral tongue of dogs similarly resulted in oedema.22 Gingival tissues of dogs respond similarly to a continuous application of 1% H2O2 solution over 48 hours — oedema, followed by epithelial vacuolisation and finally destruction and sloughing of the cornified layer. A cellular response similar to that in acute inflammation occurred. Increase in vascular permeability is likely, as there is severe oedema, a large number of acute inflammatory cells, haemoconcentration in blood vessels and presence of fibrin strands. After 48 hours there was no cellular evidence of a chronic reaction replacing the acute reaction.23
Hydrogen peroxide mouth rinses can be responsible for objective and subjective adverse effects including mouth irritation and discomfort, dryness, loss of taste, elongation of filiform papillae and diffuse mucosal whitening.24 There are also changes in epithelial proliferation rate and morphological changes with epithelial thickening but fewer epithelial ridges. The PCNA (proliferating cell nuclear antigen) index, an indication of cell proliferation, increases in basal and parabasal layers of epithelium.25 At baseline, although smokers had a significantly higher PCNA index than non-smokers, this difference disappeared following bleaching indicating stimulation of cell division activity by peroxide similar to that produced by smoke. In view of this, the workers concluded that 10% carbamide peroxide could act as a tumour promoter in the presence of mutated cells.25
Weekly (for four weeks) 20 minutes applications of 10% carbamide peroxide onto the dorsal tongue of rats also increased basal layer PCNA expression, but this is only transitory, with increased PCNA expression evident only on day 0 after the last application and not on day 10 or 20. Of note were that no mucosal alterations were detected.26
At a cellular level, Schraufstatter et al. demonstrated hydrogen peroxide to induce poly-ADP-ribose polymerase activation followed by NAD depletion and a fall in ATP, resulting eventually in cell death.27
Dental pulp is reported to have a low peroxidase enzyme activity due to a sparse cell population of fibroblasts. Studies have reported the inhibition as well as inactivation of pulpal enzymes by H2O2. The quantity of peroxides penetrating the pulp chamber of extracted teeth exposed to peroxides is sufficient to produce toxic effects on cultured fibroblasts, and though there have been few reports of untoward pulpal responses, this suggests caution is warranted.28
Cervical root resorption after internal (non-vital) tooth bleaching.
Intracoronal bleaching requires healthy periodontal tissues and a root canal that is properly obturated to prevent the bleaching agent from reaching the periapical tissues.29 In vitro studies have concluded that sodium perborate in water, sodium perborate in 3% and 30% hydrogen peroxide, and 10% carbamide peroxide are all efficient at internal bleaching of non-vital teeth.30,31,32,33,34 Various heat sources may be applied to speed the reaction and improve the bleaching effect.35 The medicament is sealed in the pulp chamber for three to seven days, and is thereafter replaced regularly until acceptable lightening is achieved.
An adverse effect that has been reported following internal tooth bleaching is cervical root resorption (an inflammatory-mediated external resorption of the root).36 Table 1 summarises the available data to support a correlation between internal tooth bleaching and cervical root resorption. When interpreting the data in Table 1 it is important to note that there are a large number of cases that had suffered known trauma. In these cases it is very difficult to distinguish if the root resorption noted was due to the effect of the bleach or the trauma.
A high concentration of hydrogen peroxide in combination with heating seems to promote cervical root resorption.29,36 The underlying mechanism for this effect is unclear, but it has been suggested that the bleaching agent reaches the periodontal tissues through the dentinal tubules and initiates an inflammatory reaction.37 In vitro studies using extracted teeth showed that hydrogen peroxide placed in the pulp chamber penetrated the dentine,38 that heat increased the penetration39 and that the penetration is greater in teeth with cervical cemental defects.40
Increased sensitivity after external (vital) tooth bleaching
Vital tooth bleaching can be performed by 1. dentist-administered bleaching — the use of a high concentration of hydrogen peroxide (35-50%) or carbamide peroxide (35-40%), often supplemented with a heat source; 2. dentist-supervised bleaching — using a bleaching tray containing a high concentration of carbamide peroxide (35-40%) placed in the patient's mouth for 30 minutes to two hours in the dental office; 3. dentist-provided bleaching — known as 'at home' or 'nightguard' bleaching and administered by the patient applying 5-22% solution of carbamide peroxide in a custom-made tray; and 4. over-the-counter products, often based on carbamide peroxide or H2O2 of various concentrations and placed in a prefabricated tray or on strips, and adjusted by the user.
Case reports and small clinical studies have confirmed that a 10% carbamide peroxide gel used in a bleaching tray at night, (the so-called nightguard vital bleaching technique), produces predictable tooth whitening1,2,3,4,5,6,7,8,9 as do H2O2 strips10 and 'power bleaching' using 35% H2O2 with or without light and/or heat activation.11,12
Tooth sensitivity is a common adverse effect of external tooth bleaching (Table 2).53 Data from various studies of 10% carbamide peroxide indicate that from 15-65% of patients reported increased tooth sensitivity.54,55,56,57 Higher incidences of tooth sensitivity (from 67-78%) were reported after bleaching with H2O2 in combination with heat.58,59
Tooth sensitivity normally persists for up to four days after bleaching,58,60 but durations of up to 39 days have been reported.56,57 In a clinical study that compared two different brands of 10% carbamide peroxide bleaching agent, 55% of the 64 patients reported tooth sensitivity and/or gingival irritation, and 20% of those who had experienced adverse-effects terminated the treatment because of discomfort.56
The mechanisms that could account for the tooth sensitivity after external tooth bleaching have not yet been fully established, but an in vitro experiment has shown that peroxide can penetrate enamel and dentine and enter the pulp chamber.61
Effect of bleaching on the structure of enamel
Significant surface alterations in enamel topography follow vital bleaching using carbamide or H2O2.62,63 High concentrations of carbamide peroxide damage enamel surface integrity, but less so than phosphoric acid etch.63 As a result of this increased surface roughness it is possible that teeth may be more susceptible to extrinsic discolouration after bleaching.
Effects of tooth bleaching on tooth restorations
Bleaching may increase the solubility of glass-ionomer and other cements64 and reduce the bond strength between enamel and resin-based fillings in the first 24 hours,65 but not later.66 Following bleaching, H2O2 residues in the enamel may inhibit the polymerisation of resin-based materials and reduce bond strength.67 Thus tooth-bleaching agents should not be used [for 24 hours] prior to treatment with resin-based materials.
Animal, cellular and bacterial studies relating to the safety of hydrogen peroxide
An extensive review of these has been undertaken by Naik et al. (2006).68 The following provides a brief overview of this area.
In mice low doses of hydrogen peroxide (0.1% and 0.4%) administered in drinking water caused adenomas or adenocarcinomas in the duodenum.69 These findings have been questioned and it has been proposed that the most likely cause of the lesions observed were the decreased water consumption of the mice and resultant abrasion of the luminal lining on ingestion of pelleted dry rodent food.70,71 Another animal study by Weitzman et al. suggested that a known tobacco carcinogen 9, 10-dimethyl-1, 2-benzanthracene (DMBA) could be augmented in producing carcinogenesis in the buccal epithelium of hampsters by 3% H2O2.72 These results have been disputed due to the small number of animals studied. Further studies in hampsters given up to 70mg/kg of H2O2 by oral intubation for up to six months73,74 or up to 3% H2O2 in combination with DMBA applied five times daily for 16-20 weeks on the buccal epithelium75 did not show any sign of carcinogenesis. Further studies on skin have concluded that H2O2 is inactive as a tumour promoter or carcinogen.76,77
The response of mammalian cells to H2O2 is highly variable, dependent on factors such as catalase concentration and DNA repair activity. In one study, H2O2 induced a dose-dependent increase of hypoxanthine guanine phosphoribosyltransferase (HPRT) mutations in vitro in human T lymphocytes, most mutations being of the same kind as observed in T cells in vivo.78 Another study, using human lymphocytes, assessing genotoxicity showed the main event induced by extracellular application of H2O2 to be necrosis and not micronucleus formation.79
However, with these studies there is a high potential for false positive results and the studies do not take into account absorption, distribution and excretion of the H2O2. Therefore genetic effects produced in vitro cannot be immediately transposed in vivo.
Bacteria lack distinct, membrane bound nuclei — their genetic material lies in the cytoplasm as a continuous loop of naked DNA and they would therefore be extremely vulnerable to H2O2. Abu-Shakra et al.82 examined effects of H2O2 on salmonella strains, and found conflicting results. Mutagenicity appeared to be more a function of the strain genotype than the amount of catalase.82 In any event, normal mammalian cells appear to have protective mechanisms able to eliminate the mutagenic response to H2O2 seen in bacteria.83
Clinical studies of hydrogen peroxide containing dental products
Hydrogen peroxide has been used as a mouthrinse for debriding oral wounds and producing a less favourable environment for anaerobic organisms.
Most often low dose H2O2 is used in mouthrinses, but in one study where 6% H2O2 was used to irrigate 122 patients with post-extraction pain, there were no reports of soft tissue irritation.16
When 1.5% H2O2 was used as a rinse for 18 months in orthodontic patients, no patients developed mucosal irritation.84
Conversely, Branemark and Ekholm studying the effects of 3% H2O2 found increased injury to damaged tissue, thus delaying wound healing.87 Rees and Orth confirmed these findings with two case reports where 3% H2O2 was used as a mouthrinse following prior tissue injury.88
Dentifrices containing low dose H2O2 were shown to produce no soft tissue changes or irritation.17 One study showed that decomposition of H2O2 in the dentifrice is enhanced six fold by the presence of baking soda. No substantial amount survived beyond brushing and after expectorating, very little material was present to interact with soft tissues in the oral cavity.17
Numerous studies have observed the clinical effects of bleaching products containing H2O2 and carbamide peroxide. In a comparison of 6.5% H2O2 strips applied in total for 56 hours over eight weeks and 10% carbamide peroxide in a tray applied for 448 hours over the same period, significant whitening was noted with both systems in the maxillary teeth. However, in the mandibular teeth, the carbamide peroxide produced significantly more whitening compared with the H2O2 system. Both products produced a similar level of sensitivity and irritation, albeit the marked difference in application times.89
With carbamide peroxide, H2O2 and urea are produced. The degradation is slower than with H2O2 and the peroxide therefore remains in contact with tooth structure and tissues for longer. In one study measuring the degradation of 10% carbamide peroxide in bleaching trays, this was highest in the first hour and closest to the teeth. The possible reasons for this may be that H2O2 penetrates the tooth, reaction with the pellicle, oral fluids/stains on the teeth or with microorganisms which degrade the material. The active agent in carbamide peroxide is available in trays for more than 10 hours (10% remained by this time).90
The method of delivery can also have an effect on the peroxide released into the mouth. Comparing a 5% H2O2 strip with 10% carbamide peroxide in a tray both applied for 30 minutes on alternate days revealed that the peroxides in saliva are higher with the strips than the tray.91
Following the application of a 19% sodium percarbonate direct bleaching gel, the peak salivary H2O2 was 0.033% and peroxide levels had returned to baseline by 30 minutes.92
Measurements of salivary pH following use of 10% carbamide peroxide (pH5.3) in a guard revealed no significant reductions, rather the pH at times increased, possibly because the carbamide peroxide degrades into H2O2 and urea (and thus ammonia). Urea is also released from salivary glands and may have contributed to the increase in pH along with the increased salivary flow and buffering systems of saliva. It can be concluded that low doses of carbamide peroxide should not demineralise tooth structure.93
Cervical root resorption is a possible consequence of internal bleaching and is more frequently observed in teeth treated with a thermo-catalytic procedure.
Tooth sensitivity is a common side effect of external tooth bleaching.
Tooth-bleaching agents should not be used [for at least 24 hours] prior to restorative treatment with resin-based materials.
Urgent clinical studies are required on the genotoxic and tumour-promoting effects of hydrogen peroxide bleaching agents. Until such studies are available it is recommended that tooth-bleaching products using concentrated H2O2 should not be used without gingival protection to prevent exposure of the gingival tissues or mucosae. The use of H2O2 containing products should be avoided in patients with damaged or diseased tissues. For nightguard vital bleaching, minimal amounts of low dose H2O2 (10% carbamide peroxide) is preferred, avoiding prolonged and long-term use. Patients undergoing nightguard vital beaching should be regularly reviewed and monitored.
Haywood VB, Heymann HO . Nightguard vital bleaching. Quint Int 1989; 20: 173– 176.
Howard J . Patient-applied tooth whiteners. J Am Dent Assoc 1992; 132: 57– 60.
Kowitz GM, Nathoo SA, Rustogi KN et al. Clinical comparison of Colgate Platinum Tooth Whitening system and Rembrant Gel Plus. Comp Contin Educ Dent 1994; 17: S46– 51.
Matis BA, Cochran MA, Eckert G, Carlson TJ . The efficacy and safety of a 10% carbamide peroxide bleaching gel. Quint Int 1998; 29: 555– 563.
Reinhardt JW, Eivins SC, Swift EJ . Clinical study of nightguard vital bleaching. Quint Int 1993; 24: 379– 384.
Russell CM, Dickinson GL, Johnson MH . Dentist-supervised home bleaching with ten per cent carbamide peroxide gel: a six month study. J Esthet Dent 1996; 8: 177– 182.
McCaslin AJ, Haywood VB, Potter BJ et al. Assessing dentin colour changes from nightguard vital bleaching. J Am Dent Assoc 1999; 130: 1485– 1490.
Heymann HO, Swift EJ, Bayne SC et al. Clinical evaluation of two carbamide peroxide tooth whitening agents. Compend Contin Educ Dent 1998; 19: 359– 362.
Papathanasiou A, Bardwell DS, Kugel GA . A clinical study evaluating a new chairside and take-home whitening system. Compend Contin Educ Dent 2001; 22: 289– 294.
Gerlach RW, Zhou X . Vital bleaching with whitening strips: summary of clinical research on effectiveness and tolerability. J Contemp Dent Prac 2001; 2: 1– 15.
Haywood VB . History, safety and effectiveness of current bleaching techniques and application of the nightguard vital bleaching technique. Quint Int 1992; 27: 471– 488.
Sulieman M, Addy M, Rees JS . Development and evaluation of a new method in vitro to study the effectiveness of tooth bleaching. J Dent 2003; 31: 415– 422.
Spasser HF . A simple bleaching technique using sodium perborate. NY State Dent J 1961; 27: 332– 334.
Nutting EB, Poe GS . A new combination for bleaching teeth. J So CA Dent Assoc 1963; 31: 289– 291.
IARC. Hydrogen peroxide. 1999; 671– 689.
Walsh LJ . Safety issues relating to the use of hydrogen peroxide in dentistry. Aust Dent J 2000; 45: 257– 269.
Marshall MV, Gragg PP, Packman EW et al. Hydrogen peroxide decomposition in the oral cavity. Am J Dent 2001; 14: 39– 45.
Desesso JM, Lavin AL, Hsia SM, Mavis RD . Assessment of the carcinogenicity associated with oral exposures to hydrogen peroxide. Food and Chemical Toxicology 2000; 38: 1021– 1041.
Delgado WA, Calderon R . Acatalasia in two Peruvian siblings. J Oral Pathol 1979; 8: 358– 368.
Bhat KS . Tissue emphysema caused by hydrogen peroxide. Oral Surg Oral Med Oral Pathol 1974; 38: 304– 307.
Seltzer S . Catalase protection against hydrogen peroxide-induced injury in rat oral mucosa. Oral Surg Oral Med Oral Pathol 1993; 75: 744– 750.
Dorman HL, Bishop JG . Production of experimental edema in dog tongue with dilute hydrogen peroxide. Oral Surg Oral Med Oral Pathol 1970; 29: 38– 43.
Martin JH, Bishop JG, Guentherman RH, Dorman HL . Cellular response of gingiva to prolonged application of dilute hydrogen peroxide. J Periodontol 1968; 39: 208– 210.
Tombes MB, Galluci B . The effects of hydrogen peroxide rinses on the normal oral mucosa. Nurs Res 1993; 42: 332– 337.
da Costa Filho L C, Da Costa C C, Soria M L, Taga R . Effect of home bleaching and smoking on marginal gingival epithelium proliferation:a histologic study in women. J Oral Pathol Med 2002; 31: 473– 480.
Albuquerque Rde C, Gomez R S, Dutra R A et al. Effects of a 10% carbamide peroxide bleaching agent on rat oral epithelium proliferation. Braz Dent J 2002; 13: 162– 165.
Schraufstatter IU, Hyslop PA, Jackson J, Cochrane CC . Oxidant injury of cells. Int J Tissue React 1987; 9: 317– 324.
Bowles WH, Burnes H Jr . Catalase/Peroxidase activity in dental pulp. J Endod 1992; 18: 527– 534.
Baratieri LN, Ritter AV, Monteiro S et al. Nonvital tooth bleaching: guidelines for the clinician. Quint Int 1995; 26: 597– 608.
Rotstein I, Zalkind M, Mor C et al. In vitro efficacy of sodium perborate preparations used for intracoronal bleaching of discoloured non-vital teeth. Endod Dent Traumatol 1991; 7: 177– 180.
Rotstein I, Mor C, Friedman S . Prognosis of intracoronal bleaching with sodium perborate preparations in vivo: 1 year study. J Endod 1993; 19: 10– 12.
Ari H, Ungor M . In vitro comparison of different types of sodium perborate used for intracoronal bleaching of discoloured teeth. Int Endo J 2002; 35: 433– 436.
Freccia WF, Peters DD, Lorton L, Bernier WE . An in vitro comparison of nonvital bleaching techniques in discoloured teeth. J Endod 1982; 8: 70– 77.
Vachon C, Vanek P, Friedman S . Internal bleaching with 10% carbamide peroxide in vitro. Pract Periodon Aesthet Dent 1998; 10: 1145– 1148, 1150, 1152.
Howell RA . Bleaching discoloured root-filled teeth. Br Dent J 1980; 148: 159– 162.
Friedman S, Rotstein I, Libfelt H et al. Incidence of external root resorption and esthetic results in 58 bleached pulpless teeth. Endod Dent Traumatol 1988; 4: 23– 26.
Cvek M, Lindvall AM . External root resorption following bleaching of pulpless teeth with oxygen peroxide. Endo Dent Traumatol 1985; 1: 56– 60.
Rotstein I . In vitro determination and quantification of 30% hydrogen peroxide penetration through dentin and cementum during bleaching. Oral Surg Oral Med Oral Pathol 1991; 72: 602– 606.
Rotstein I, Torek Y, Lewinstein . Effect of bleaching time and temperature on the radicular penetration of hydrogen peroxide. Endod Dent Traumatol 1991; 7: 196– 198.
Rotstein I, Torek Y, Lewinstein I . Effect of cementum defects on radicular penetration of 30% H2O2 during intracoronal bleaching. J Endod 1991; 17: 230– 233.
Lewinstein I, Hirschfeld Z, Stabholz A, Rotstein I . Effect of hydrogen peroxide and sodium perborate on the microhardness of human enamel and dentin. J Endod 1994; 20: 61– 63.
Chng HK, Palamara JEA, Messer HH . Effect of hrdrogen peroxide and sodium perborate on mechanical properties of human dentin. J Endod 2002; 28: 62– 67.
Latcham NL . Postbleaching cervical resorption. J Endod 1986; 12: 262– 264.
Latcham NL . Management of a patient with severe postbleaching cervical resorption. A clinical report. J Prosthet Dent 1991; 65: 603– 605.
Goon EY, Cohen S, Borer RF . External cervical tooth resorption following bleaching. J Endod 1986; 12: 414– 418.
Harrington CV, Natkin E . External resorption associated with bleaching of pulpless teeth. J Endod 1979; 5: 344– 348.
Lado EA, Stanley HR, Weisman MI . Cervical resorption in bleached teeth. Oral Surg Oral Med Oral Pathol 1983; 55: 78– 80.
Gimlin DR, Schindler WG . The management of postbleaching cervical resorption. J Endod 1990; 16: 292– 297.
Al-Nazhan S . External root resorption after bleaching: a case report. Oral Surg Oral Med Oral Pathol 1991; 72: 607– 609.
Abou-Rass M . Long-term prognosis of intentional endodontics and internal bleaching of tetracycline stained teeth. Compend Contin Educ Dent 1998; 19: 1034– 1044.
Anitua E, Zabalegui B, Gil J, Gascon F . Internal bleaching of severe tetracycline discolourations: four-year clinical evaluation. Quint Int 1990; 21: 783– 788.
Holmstrup G, Palm AM, Lambjerg-Hansen H . Bleaching of discoloured root-filled teeth. Endod Dent Traumatol 1988; 4: 197– 201.
Tam L . The safety of home bleaching techniques. J Can Dent Assoc 1999; 65: 453– 455.
Haywood VB, Leonard RH, Nelson CF, Brunson WD . Effectiveness, side effects and long term status of nightguard vital bleaching. J Am Dent Assoc 1994; 125: 1219– 1226.
Schulte JR, Morrissette DB, Gasior EJ, Czajewski MV . The effects of bleaching application time on the dental pulp. J Am Dent Assoc 1994; 125: 1330– 1335.
Leonard RH, Haywood VB, Phillips C . Risk factors for developing tooth sensitivity and gingival irritation associated with nightguard vital bleaching. Quint Int 1997; 28: 527– 534.
Tam L . Clinical trial of three 10% carbamide peroxide bleaching products. J Can Dent Assoc 1999; 65: 201– 205.
Cohen SC, Chase C . Human pulpal responses to bleaching procedures on vital teeth. J Endod 1979; 5: 134– 138.
Nathanson D, Parra C . Bleaching vital teeth — a review and clinical study. Compend Contin Educ Dent 1987; 8: 490– 498.
Schulte JR, Morrissette DB, Gasior EJ, Czajewski MV . The effects of bleaching application time on the dental pulp. J Am Dent Assoc 1994; 125: 1330– 1335.
Thitinanthapan W, Satamanont P, Vongsavan N . In vitro penetration of the pulp chamber by three brands of carbamide peroxide. J Esthet Dent 1999; 11: 259– 264.
Shannon H, Spencer P, Gross K, Tira D . Characterization of enamel exposed to 10% carbamide peroxide bleaching agents. Quint Int 1993; 24: 39– 44.
Ernst CP, Marroquin BB, Willershausen-Zonnchen B . Effects of hydrogen peroxide-containing bleaching agents on the morphology of human enamel. Quint Int 1996; 27: 53– 56.
Swift E J Jr, May K N Jr, Wilder A D Jr et al. Two-year clinical evaluation of tooth whitening using an at-home bleaching system. J Esthet Dent 1999; 11: 36– 42.
Dishmann MV, Covey DA, Baughan LW . The effects of peroxide bleaching on composite to enamel bond strength. Dent Mater 1994; 9: 33– 36.
Homewood C, Tyas M, Woods M . Bonding to previously bleached teeth. Austr Orthodont J 2001; 17: 27– 34.
Lai SC, Tay FR, Cheung GS et al. Reversal of compromised bonding in bleached enamel. J Dent Res 2002; 81: 477– 481.
Naik S, Tredwin CJ, Scully C . Hydrogen peroxide tooth-whitening (bleaching): Review of safety in relation to possible carcinogenesis. Oral Oncol 2006; Epub ahead of print.
Ito A, Naito M, Watanabe H . Implication of chemical carcinogenesis in the experimental animal-tumorigenic effect of hydrogen peroxide in mice. Hiroshima Daigaku Genbaku Hoshanou Igaku Kankyusho Nenpo 1981; 22: 147– 158.
Ito A, Naito M, Naito Y, Watanabe H . Induction and characterization of gastro-duodenal lesions in mice given continuous oral administration of hydrogen peroxide. Gann 1982; 73: 315– 322.
Ito A, Watanabe H, Naito M et al. Correlation between induction of duodenal tumor by hydrogen peroxide and catalase activity in mice. Gann 1984; 75: 17– 21.
Weitzman SA, Weitberg AB, Stossel TP et al. Effects of hydrogen peroxide on oral carcinogenesis in hamsters. J Periodontol 1986; 57: 685– 688.
Takahashi M, Hasegawa R, Furukawa F et al. Effects of ethanol, potassium and metabisulfite, formaldehyde and hydrogen peroxide on gastric carcinogenesis in rats after initiation with N-methyl N Nitro N Nitrosoguanidine. Jpn J Cancer Res 1986; 77: 118– 124.
Li Y, Noblitt T, Zhang A et al. Effect of long-term exposure to a tooth whitener. J Dent Res 1993; 72: 1162– 1248.
Marshall MV, Kuhn JO, Torrey CF et al. Hamster cheek pouch bioassay of dentifrices containing hydrogen peroxide and baking soda. J Amer College Toxicol 1996; 15: 45– 61.
Klein-Szanto AJ, Slaga TJ . Effects of peroxides on rodent skin:epidermal hyperplasia and tumor promotion. J Invest Dermatol 1982; 79: 30– 34.
Kurokawa Y, Takamura N, Matsushima Y et al. Studies on the promoting and complete carcinogenic activities of some oxidizing chemicals in skin carcinogenesis. Cancer 1984; 24: 299– 304.
Diaz-Llera S, Podlutsky A, Osterholm AM et al. Hydrogen peroxide induced mutations at the HPRT locus in primary human T-lymphocytes. Mutat Res 2000; 469: 51– 61.
Fenech M, Crott J, Turner J, Brown S . Necrosis, apoptosis, cytostasis and DNA damage in human lymphocytes measured simultaneously within the cytokinesis-block micronucleus assay: description of the method and results for hydrogen peroxide. Mutagenesis 1999; 14: 605– 612.
Estervig D, Wang RJ . Sister chromatid exchanges and chromosome aberrations in human cells induced by H2O2 and other photoproducts generated in fluorescent light-exposed medium. Photochem Photobiol 1984; 40: 333– 336.
Bradley MO, Hsu IC, Harris CC . Relationships between sister chromatid exchange and mutagenicity, toxicity and DNA damage. Nature 1979; 282: 318– 320.
Abu-Shakra A, Zeiger E . Effects of Salmonella genotypes and testing protocols on H202-Induced mutation. Genetics 1982; 7: 7445– 7449.
De Flora S, Camoirano A, Zanacchi P, Bennicelli C . Mutagenicity testing with TA97 and TA102 of 30 DNA-damaging compounds, negative with other Salmonella strains. Mutat Res 1984; 134: 159– 165.
Boyd RL . Effects on gingivitis of daily rinsing with 1.5% H2O2. J Clin Periodontol 1989; 16: 557– 562.
Clark WB, Magnusson I, Walker CB, Marks RG . Efficacy of Perimed antibacterial system on established gingivitis. (I). Clinical results. J Clin Periodontol 1989; 16: 630– 635.
Rosling BG, Slots J, Webber RL et al. Microbiological and clinical effects of topical subgingival antimicrobial treatment on human periodontal disease. J Clin Periodontol 1983; 10: 487– 514.
Branemark PI, Ekholm R . Tissue injury caused by wound disinfectants. J Bone Joint Surg Am 1967; 49: 48– 62.
Rees TD, Orth CF . Oral ulcerations with use of hydrogen peroxide. J Periodontol 1986; 57: 689– 692.
Donly KJ, Donly AS, Baharloo L et al. Tooth whitening in children. Compend Contin Educ Dent 2002; 23: 22– 28.
Matis BA, Gaiao U, Blackman D et al. In vivo degradation of bleaching gel used in whitening teeth. JADA 1999; 130: 227– 235.
Hanning C, Zech R, Henze E et al. Determination of peroxides in saliva-kinetics of peroxide release into saliva during home-bleaching with Whitestrips and Vivastyle. Arch Oral Biol 2003; 48: 559– 566.
Mahony C, Barker ML, Engel TM, Walden GL . Peroxide degradation kinetics of a direct application percarbonate bleaching film. Am J Dent 2003; 16 Spec No: 9B– 11B.
Leonard RH Jr, Bentley CD, Haywood VB . Salivary pH changes during 10% carbamide peroxide bleaching. Quint Int 1994; 25: 547– 550.
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Tredwin, C., Naik, S., Lewis, N. et al. Hydrogen peroxide tooth-whitening (bleaching) products: Review of adverse effects and safety issues. Br Dent J 200, 371–376 (2006). https://doi.org/10.1038/sj.bdj.4813423
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