This study aimed to assess the viability of dental cells following time-dependent carbamide peroxide teeth-whitening treatments using an in-vitro dentin perfusion assay model. 30 teeth were exposed to 5% or 16% CP gel (4 h daily) for 2 weeks. The enamel organic content was measured with thermogravimetry. The time-dependent viability of human dental pulp stem cells (HDPSCs) and gingival fibroblast cells (HGFCs) following either indirect exposure to 3 commercially available concentrations of CP gel using an in-vitro dentin perfusion assay or direct exposure to 5% H2O2 were investigated by evaluating change in cell morphology and by hemocytometry. The 5% and 16% CP produced a significantly lower (p< 0.001) enamel protein content (by weight) when compared to the control. The organic content in enamel varied accordingly to the CP treatment: for the 16% and 5% CP treatment groups, a variation of 4.0% and 5.4%, respectively, was observed with no significant difference. The cell viability of HDPSCs decreased exponentially over time for all groups. Within the limitation of this in-vitro study, we conclude that even low concentrations of H2O2 and CP result in a deleterious change in enamel protein content and compromise the viability of HGFCs and HDPSCs. These effects should be observed in-vivo.

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The quest for teeth whitening reflects patients’ demands for superior aesthetics and the considerable advancement in teeth-whitening agents and techniques. Although this procedure is routinely carried out to improve smile aesthetics, there remain two common adverse effects reported in-vivo following vital tooth-whitening therapies: gingival irritation1 and postoperative sensitivity2. Both these adverse effects are linked directly to the by-products released from the degradation of activated bleaching gels3,4. Carbamide Peroxide (CP) is one of the most commonly used treatments for vital home teeth-whitening. CP (CO(NH2) H2O2) is organic, white, and crystalline, and it will break down into hydrogen peroxide (H2O2) and urea5,6. H2O2 has a low molecular weight and a high oxidative power, favoring its rapid diffusion into enamel prisms and interprismatic spaces7. H2O2 may dissociate into water, reactive oxygen, and free radical species, such as hydroxyl radicals (OH−). In the tooth, the “whitening reaction” is thought to be carried out by H2O2-derived free radicals breaking down large dentinal chromogenic molecules (chromophores) into smaller molecules with lesser or non-absorbing optical properties, Fig. 18,9. Unfortunately, H2O2 does not remain confined to the dentin and can reach the pulp chamber mostly by diffusion through dentinal tubules. It has been suggested that upon reaching the pulp, H2O2 will lead to a decrease in cell proliferation, metabolism, and viability10, a reduction of pulp-reparative capacity11, tissue necrosis12, and finally inducing pulpal pain13. An early report suggested that at low concentrations, bleaching agents are not harmful to dental structures14. Yet, there is growing in-vitro evidence that at a low concentration (5% and 10%) of CP, the deleterious effect of H2O2-derived free radicals can be detected throughout the dentin and across the pulp chamber5,15. Although the use of teeth-whitening agents and techniques is becoming increasingly popular, there are no studies to date in the scientific literature that have investigated the possible deleterious effect of H2O2-derived free radicals directly on dental cells. Performing such experiments directly on patients would jeopardize the vitality of the tooth itself as one would require access to pulpal tissue. Considering the natural function of the dental pulp stem cells in the production of odontoblasts to create reparative dentin and for the pulp itself to support the vitality of the entire tooth, it is critical nonetheless to evaluate how these by-products impact the population of such a critical stem cell reservoir. This in-vitro study aims to evaluate the impact of exposure to a different concentration of commonly used home peroxide-based teeth-whitening on dental cells (HDPSCs and HGFCs) directly or indirectly using a dentin perfusion disc model.

Materials and methods

Following extraction, the teeth were initially stored in a 70% ethanol solution for up to 5 days at room temperature before being debrided from remaining soft tissues and finally stored in a 0.1% thymol solution at 4 °C until required for the study (storage did not exceed 2 months) (Fig. 2a-i).

Sample preparation for enamel‑protein (weight) ratio analysis. Tirty teeth were assigned randomly to the control and two treatment groups (N=10/group). This study’s power was set at 80% with a p-value of 0.05 by estimating the required sufficient sample size in a pilot study. A high (16%) and a low (5%) concentration of CP was selected to follow dentist-directed home teeth-whitening as recommended by the Council of European Dentists (CED-DOC-2012-061-E August 2012 Guidelines). The teeth were exposed to 5% or 16% CP gel for 4 h daily for 2 weeks and were kept in artificial saliva between treatments. The control group was kept in artificial saliva over the same period. The peroxide gel was homogeneously dispensed into an individual thermoplastic vacuum-formed (non-spaced) tray for each tooth and the excess was removed as recommended by the manufacturer. Although teeth vary in size, we ensure that the crown of each tooth was completely immersed in the CP gel for the duration of the treatment. The artificial saliva was prepared using the ingredients outlined by McKnight-Hanes and Whitford16 (Table 1) and kept at 4 °C following preparation. Following treatment, each tooth was longitudinally sectioned into buccal and lingual halves (Fig. 2a-ii) that underwent complete dentin, pulp, and EDJ removal using diamond and stainless-steel burs in a fast turbine handpiece. The remaining enamel shell (0.3–0.5 mm thick) was cleaned in ultrasonic deionized water for 30 s (Fig. 2a-iii). The enamel shells were then pulverized to a fine powder for thermogravimetry testing using a “Spartan, Vibratory Sieve Shaker” (FRITSCH GMBH, GERMANY) (Fig. 2a-iv).

Enamel‑protein (weight) ratio analysis pre and post‑whitening. Thermogravimetric analysis (TGA) was carried out using the TGA 50 analyzer (SHIMADZU CORPORATION, JAPAN). Each sample consisted of (4.00±0.25) mg of powdered enamel placed in a platinum crucible. The TGA cycle was run between room temperature and 800 °C, at a rate of 10 °C/min with a 1-min hold at 30 °C. The measurements were carried out under oxygen (50 ml/min). The TGA curves are presented as a percentage of weight loss on the Y-axis (TGA%) and temperature (°C) in Fig. 2b.

Cell culture. Impact of CP on human dental pulp stem cells (HDPSCs) survivability. Dentin discs were obtained from a total of 34 human teeth. The teeth were sectioned transversely at the mid-coronal level to obtain a standardized dentin thickness of 3 mm-thick disc samples using a diamond microtome (STRUERS, ACCUTOM-50, STRUERS LTD., SOLIHULL, WEST MIDLANDS, UK). The discs were immersed in 37% phosphoric acid in a sonic bath for up to 15 s to remove the smear layer, followed by 2 min of rinsing in distilled water17. The dentin tubules’ vertical orientation and their opening were checked by Scanning Electron Microscopy (FLEXSEM 1000. HITACHI HIGH TECHNOLOGIES; TORONTO, CANADA) on selected discs. Cell culture well plates were modified with a transwell insert (THERMO FISHER SCIENTIFIC, WHITBY, CANADA) to support the 3 mm-thick dentin discs with a diameter<4 mm (Fig. 3). Gaps between the transwell insert walls, and the edges of the dentin discs were sealed using a flowable composite resin material (FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE, 3M ESPE) (Fig. 3a) to ensure that any CP gel deposited on top of the dentin disc could only perfuse through the dentin tubules (Fig. 3b) Additionally, we ensured that the cell growth medium was in direct contact with the dentin disc’s underside to mimic the partial pressure in the dentinal tubules. HDPSCs (LONZA WALKERSVILLE, INC. MD 21793-0127 USA) were cultured in the dental pulp stem cell (DPSC) basal medium supplemented with dental pulp stem cell growth supplement (DPSCGS), 50 ml; l-glutamine, 10.0 ml; Ascorbic Acid, 5.0 ml; Gentamicin/Amphotericin-B (GA) (LONZA WALKERSVILLE, INC. MD 21793-0127 USA). Cells from the 4th passage were used with a minimum of 50,000 cells present in each well of the 12 well-plate the day before the treatment. Te HDPSCs sub-cultures and dentin discs were randomly assigned to three treatment groups: exposure to 5%, 10%, 35% CP gel, and control. For the treatment groups, a drop of activated CP gel (using a drop of artificial saliva) at relevant concentrations was directly applied on top of the dentin disc mounted in the transwell insert (Fig. 3a) to simulate the exposure of the HPSCs to the whitening treatment. Artificial saliva was used for the control group. A time assay of HDPSCs survivability was performed for up to 4 h by evaluating the change in cell shape and morphology optically, as presented in Fig. 4a. In Addition, the ratio of live/dead cells at each time point was obtained by hemocytometry after trypan blue staining.

Impact of H2O2 on human gingival fibroblast cells (HGFCs) survivability. HGFCs (SCINCELL RESEARCH LABORATORIES, CARLSBAD, CA 92008, UNITED STATES) were cultured in Dulbecco’s Modified Eagle Medium (DMEM) (SIGMA CHEMICAL CO., ST. LOUIS, MO) supplemented with 10% fetal calf serum (GIBCO, GRAND ISLAND, NY) and 10% antibiotics at 37 °C (ISOTEMP FISHER SCIENTIFIC, PITTSBURGH, PA). Cells from the 4th passage were used with a minimum of 50,000 cells present in each well of the plate (12 wells) the day before treatment. Cultured HGFCs were exposed directly to a 5% H2O2 solution, as depicted in Fig. 5a-i. A time assay of HGFCs survivability was performed for up to 4 h by evaluating the change in cell shape and morphology optically as presented in Fig. 5a-ii, iii, iv, v & vi. Additionally, the ratio of live/dead cells at each time point (30 min, 1 h, 2 h, and 4 h) was obtained by hemocytometry after trypan blue staining.

Author disclaimer. The authors have purposely decided not to disclose the brand or manufacturer of the commercially available products used in this study was done in our previous submission15.

Results

Enamel permeability. Figure 2b shows a typical thermogravimetry (TGA) curve of weight change with temperature for the selected enamel sample. This change is shown more clearly in the DrTGA curve (1st derivative of the TGA curve), presenting the largest rate of mass change at T=464 °C. The 16% CP treatment group showed an organic variation of 4.0%, whereas the 5% CP treatment group showed a variation of 5.4% (Fig. 2c) with no significant difference. Both treatment groups exhibited significantly lower (p<0.001) enamel protein content by weight following CP treatment when compared to the control group (~50% on average).

HDPSCs. After 240 min, HDPSCs, exposed to all CP treatments, presented non-native cellular morphological appearances (round) when compared to the control (no exposure to CP). Cell death was confirmed by hemocytometry counting using trypan blue stain (Fig. 4a). Figure 4b presents the fitted plots of the percentage of live/dead cells over time for the control group (no CP exposure) (Fig. 4b-i) and the three CP gel concentrations (Fig. 4b-ii, iii & iv). There was an exponential decrease in the number of live cells remaining over time for the three treatment groups. By plotting the percentage of live/dead cells over time (Fig. 4b), it is possible to fit an exponential decay over the population of live cells remaining. Upon calculating the decay constant (1/e or of 70% drop in the original population) for each of the groups, it appears that both the T10%CP and T35%CP are close to one another (27.9±12.5) min and (28.3.6±4.3) min (Fig. 4b-iii & iv), respectively. In contrast, T5%CP=(203.4±246.0) min (Fig. 4b-ii).

HGFCs. HGFCs start to lose their morphological appearances after 30 min and cell death was confirmed by hemocytometry counting using trypan blue stain. Over 95% cell death can be recorded after 120 min exposure to H2O2. Te 1/e time constant occurs at TH2O2=(24.6±4.6) min (Fig. 5b).

Discussion

Enamel permeability. Enamel encounters whitening agents first. However, enamel consists of > 98% of a hydroxyapatite mineral phase, and < 2% of the enamel consists of protein (90% amelogenin, 10% enamelin, and ameloblastin). These proteins form an enamel sheath around the enamel rods in mature teeth18. Any loss in these proteins would increase the enamel permeability and promote extrinsic reagents’ penetration19. Our results suggest that enamel protein is susceptible to oxidative degradation from the CP breakdown reaction by-products. The main mass change (430–500  °C) reflects the oxidative degradation of the enamel’s organic content leaving only enamel mineral content in the crucible20. A low CP (5%) concentration is sufficient to alter the protein content in the enamel. Peroxide-based whitening agents have been shown to induce alterations in the surface texture and morphology of enamel8,21. Ferreira et al. demonstrated that 35% hydrogen peroxide (HP) affected enamel morphology, producing porosities, depressions, and superficial irregularities to various degrees 22. CP specifically induced uniform etching-like erosion of surface and subsurface enamel due to mineral dissolution and decalcifcation23. It can also cause a decrease in enamel hardness and higher enamel roughness 24. An electron microscopy study observed that whitening treatment with either CP or HP induced various surface alterations, including reducing the prismatic layer, demineralization of the enamel prisms, and greater porosity within and between the enamel prisms25. Our approach extended this funding as we confirmed that enamel’s protein content is also significantly reduced, asserting the opening of the inter-prismatic spaces that would act as conduits for the penetration of CP breakdown reactions by-products to the inner part of the tooth, including the pulp. However, as changes in enamel composition can be reversible in-vivo, this alteration in the enamel composition is not final.

The effect of teeth‑whitening on HDPSCs and HGFCs. Dental hypersensitivity occurs in about two-thirds of patients during vital bleaching26. It is principally attributable to peroxide diffusion into the enamel and dentin, resulting in dehydration and subsequent fluid movement in the dentinal tubules, which stimulates the nerve endings, leading to sensitivity14. The over-exposure of the by-products released from the whitening gel to most cells causes oxidative stress27. An increase in ROS (Reactive Oxygen Species) levels causes deleterious effects on several cell components, including lipid peroxidation, oxidative alterations of protein, and DNA cell damage28. Decay constants can be used to indicate when the culture is no longer viable. Interestingly, both 10% and 35% CP exposure impacted the cell culture similarly, whereas 5% CP exposure affects the culture to a much lesser extent, as proven by the wider error on the constant value. Translating these findings in-vivo may result in the partial mitigation of this rapid cell death due to positive pulp pressure, dental fluid, and the cell’s inherent defense against oxidative stress. One of the limitations of our study was not to investigate cellular recovery and host immune response following exposure to H2O2-derived free radicals.

HDPSCs. It is known that HDPSCs represent a heterogeneous culture from pulp tissue, including a population of mesenchymal stem cells29,30. We decided to use this heterogeneous culture for this investigation as mesenchymal stem cells are recruited as precursors to new odontoblast-like cells, responsible for dentin-pulp complex regeneration following lethal odontoblast damage as expected following exposure to ROS31. Odontoblasts are also involved in the initiation, development, and maintenance of the pulp inflammatory/immune response, representing the host’s first defense line 32. It is thus essential to evaluate the survivability of HDPSCs in a highly damaging environment. Our results suggest that both the 10% and 35% CP gel exposure to the dentin disc affect HDPSCs in the same manner (based on the time constant) as if the cells were exposed directly to the 5% H2O2 as done for HGFCs. The dentin disc (3 mm thick) cannot withhold the penetration of the CP breakdown reactions by-products to reach the cell culture when the CP’s concentration exceeds 5% CP, as demonstrated by cell viability measurements. This is consistent with our previous in-vitro study15, which had proven that even with a low concentration (5% CP) whitening agent, the peroxide and free radicals could diffuse through the dentin into pulp tissue, causing collagen degradation and reduction in organic dentinal components (Amide I and Amide III). All teeth-whitening protocols evaluated in the present study resulted in trans-enamel and trans-dentinal peroxide diffusion, directly related to the teeth-whitening gel’s concentration and the time of application to dentin. However, the pulp cells from human tissue were still highly sensitive to all bleaching protocols tested in this investigation, albeit the response to 5% differed from 10% and 35%. Previous studies demonstrated pulp cell oxidative stress induced by H2O2 in a time-/concentration-dependent manner10,33. In vital teeth, oxidative stress causes inflammatory pulp response directly related to the enamel and dentin thickness of bleached teeth31,34. A study by Sato et al. demonstrated that in-vivo oxidative stress generated by a 35%-H2O2 gel in the pulp tissue of young human premolars increased the activity of metalloproteinases and cysteine cathepsin B, which both play an essential role in protein matrix degradation. According to data from the present study, these negative side effects may be minimized by shortening the contact time with the enamel or dentin or reducing the concentration of H2O2 in teeth-whitening agents. Several clinical trials have shown that teeth-whitening gels with H2O2 concentration (15–20%) applied to enamel for 45–60 min can promote a significant color change caused by a high 35% H2O2 gel concentration. In these studies, tooth sensitivity incidence ranged from 24 to 78%, considered mild in severity from 35–37. Moreover, a more recent clinical study revealed that the whitening efficiency of low 5% CP gels was as effective as those containing 10% CP38. Thus, by reducing the concentration of peroxide and exposure time, it is possible to execute an effective and less aggressive home tooth-whitening protocol. However, in-vivo studies in vital human teeth are needed to assess tooth-whitening effectiveness and pulp responses after applying the teeth-whitening protocols evaluated in the present study. Although our study did not intend to replicate an ‘in-vivo” like tooth model, we produced a simple perfusion model that facilitates testing the impact of whitening approaches on dental cells to evaluate their short-term viability.

HGFCs. Human gingival fibroblasts play an essential role in the structure of tissues, function, and immune defense of the host39. Some reports indicate that H2O2 caused irritation, ulceration, burning, and certain adverse effects on the gums40,41. It was reported that hydrogen peroxide promoted PKC and ERK 1/2 activation and decreased cell viability42. An in-vitro study reported that hydrogen used at concentrations of 10 to 200 mM promoted apoptosis. The characteristic apoptotic events such as morphological changes, including chromatin condensation, and nuclear and DNA fragmentation, considered a hallmark of cells undergoing apoptosis, were detected in hydrogen peroxide HGFCs43. In the present study, we found that 5% H2O2 reduced the viability of HGFCs. The immediate impact of H2O2 in gingival fibroblast viability does not directly reproduce events in the pulp chamber but indicates why gingival irritation can occur and supports limiting direct contact with the gingiva44. Reversal of this gingival effect has been reported after 2 weeks with 10 and 16% CP45.

Conclusions

References

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For more info: david.deng@wecistanche.com  WhatApp:86 13632399501