Abstract
Gels containing juca seed galactomannan (JSG) were evaluated for their potential to prevent the progression of dentin erosive wear in an in vitro study with four experimental groups (n = 9). The treatments included distilled water (DW), 0.05% stannous fluoride (121 ppm F), and 0.5% or 1% JSG. The specimens underwent a cycle (3 times/day) consisting of immersion in 1% citric acid (5 minutes), treatment (5 minutes), and artificial saliva exposure (2 hours/overnight) for 5 days. Surface changes were assessed using mechanical profilometry (wear), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). The data were analyzed using ANOVA followed by Tukey's post-test (p < 0.05). The negative control group exhibited the highest wear (6.0 µm ± 3.5), significantly differing from the group treated with 0.05% stannous fluoride gel (p = 0.007), which showed less dentin loss. The groups treated with 0.5% and 1% JSG showed results similar to the negative control (p = 0.661; p = 0.212, respectively) and the stannous fluoride group (p = 0.103; p = 0.379, respectively). In the SEM images, the specimen treated with stannous fluoride showed obliterated tubules, while the JSG gels formed crystals on the dentin surface, as confirmed by the presence of oxygen and calcium in the EDS analysis. Although the JSG gels showed similar results to the stannous fluoride, did not exhibit superior efficacy at the tested concentrations.
Key Words:
erosion; dentin; gels; Caesalpinia
Resumo
Géis contendo galactomanana da semente de jucá (GSJ) foram avaliados quanto ao seu potencial na prevenção da progressão do desgaste erosivo dentinário em um estudo in vitro com quatro grupos experimentais (n = 9). Os tratamentos incluíram água destilada (AD), 0,05% de fluoreto de estanho (121 ppm F) e 0,5% ou 1% de GSJ. Os espécimes passaram por um ciclo (3 vezes ao dia) que consistia em imersão em ácido cítrico 1% (5 minutos), tratamento (5 minutos) e exposição a saliva artificial (2 horas/durante a noite) por 5 dias. As alterações de superfície foram avaliadas utilizando perfilometria mecânica (desgaste), microscopia eletrônica de varredura (MEV) e espectroscopia de raios-X por dispersão de energia (EDS). Os dados foram analisados por ANOVA, seguida do pós-teste de Tukey (p < 0,05). O grupo controle negativo apresentou o maior desgaste (6,0 µm ± 3,5), diferindo significativamente do grupo tratado com gel de fluoreto de estanho a 0,05% (p = 0,007), que apresentou menor perda de dentina. Os grupos tratados com 0,5% e 1% de GSJ apresentaram resultados semelhantes ao grupo controle negativo (p = 0,661; p = 0,212, respectivamente) e ao grupo de fluoreto de estanho (p = 0,103; p = 0,379, respectivamente). Nas imagens de MEV, o espécime tratado com fluoreto de estanho mostrou túbulos obliterados, enquanto os géis GSJ formaram cristais na superfície da dentina, como confirmado pela presença de oxigênio e cálcio na análise de EDS. Embora os géis GSJ tenham apresentado resultados semelhantes ao fluoreto de estanho, eles não demonstraram eficácia superior nas concentrações testadas.
Introduction
Lifestyle changes and dietary habits play a crucial role in dental erosion 11. Gambon DL, Brand HF, Veerman ECI. Dental erosion in the 21st century: what is happening to nutritional habits and lifestyle in our society? Br Dent J2012;2013:55-7., 22. Lussi A, Megert B, Shellis P. The erosive effect of various drinks, foods, stimulants, medications and mouthwashes on human tooth enamel. Swiss Dent J 2023;133(7-8).. Over the past few decades, there has been a significant rise in the global consumption of energy drinks, carbonated beverages, fruit juices, and citrus fruits. These items contain dietary acids, which are considered external factors that contribute to erosive tooth wear (ETW) 33. Saads CT, Lussi A. Chapter 9: Acidic Beverages and Foods Associated with Dental Erosion and Erosive Tooth Wear. Monogr Oral Sci2020;28:91-8., 44. Chan AS, Tran TTK, Hsu YH, Liu SYS, Kroon JA-O. A systematic review of dietary acids and habits on dental erosion in adolescents. Int J Paediatr Dent 2020;30:713-33.. When the teeth are frequently exposed to acids, minerals are lost from the tooth surface, resulting in softening. This erosive process is often associated with mechanical factors, such as abrasion caused by oral habits, and attrition due to tooth-to-tooth contact, which further contribute to the progression of dental wear 55. Magalhães AC, Rios D, Moino AL, Wiegand A, Attin T, Buzalaf MA. Effect of different concentrations of fluoride in dentifrices on dentin erosion subjected or not to abrasion in situ/ex vivo. Caries Res 2008;42(2):112-6., 66. Johansson AK, Omar R, Carlsson GE, Johansson A. Dental erosion and its growing importance in clinical practice: from past to present. Int J Dent 2012;2012:1-17..
Clinically, repeated exposure to acidic substances results in dental enamel wear, leading to the exposure of the dentin 66. Johansson AK, Omar R, Carlsson GE, Johansson A. Dental erosion and its growing importance in clinical practice: from past to present. Int J Dent 2012;2012:1-17.. As erosive tooth wear progresses from moderate to severe levels, dentin becomes increasingly exposed. This erosive effect exposes the organic matrix, which can be degraded both mechanically and chemically 77. Ganss C, Schlueter N, Hardt M, Hinckeldey JV, Klimek J.Effects of toothbrushing on eroded dentine. Eur J Oral Sci 2007;115:390-6.. Additionally, the presence of enzymes such as matrix metalloproteinases (MMPs) can degrade this matrix, contributing to further tooth wear. Consequently, the identification and development of products that can effectively inhibit MMPs play a critical role in reducing mineral loss in dentin 88. Kato MT, Leite AL, Hannas AR, Calabria MP, Magalhães AC, Pereira JC, et al. Impact of protease inhibitors on dentin matrix degradation by collagenase. J Dent Res2012;91:1119-23..
The most common treatments for tooth erosion involve the use of fluoride-containing compounds, which can result in the formation of calcium fluoride or metal-rich precipitates 99. West NX, Seong J, Hellin N, Eynon H, Barker ML, He T. A clinical study to measure anti-erosion properties of a stabilized stannous fluoride dentifrice relative to a sodium fluoride/triclosan dentifrice. Int J Dent Hyg. 2015;15:113-9, 1010. Baig AA, Faller RV, Yan J, Ji N, Lawless M, Eversole SL. Protective effects of SnF2 - Part I. Mineral solubilisation studies on powdered apatite. Int Dent J 2014;64:4-10.. It has been reported that stannous fluoride (SnF2) is an excellent compound that significantly enhances the resistance of the dental surface to acids. 1010. Baig AA, Faller RV, Yan J, Ji N, Lawless M, Eversole SL. Protective effects of SnF2 - Part I. Mineral solubilisation studies on powdered apatite. Int Dent J 2014;64:4-10.. However, natural products are increasingly being explored as promising sources for new therapeutic agents due to their renewability and low toxicity 1111. Leal IC, Rabelo CS, Viana ÍEL, Scaramucci T, Santiago SL, Passos VF. Hesperidin reduces dentin wear after erosion and erosion/abrasion cycling in vitro. Arch Oral Biol 2021;129:1879-1506.
12. Passos VF, Melo MAS, Lima JPM, Marçal FF, Costa C, Rodrigues LKA, et al. Active compounds and derivatives of camellia sinensis responding to erosive attacks on dentin. Braz Oral Res 2018;32:40.-1313. Silveira C, Oliveira F, Dos Santos ML, De Freitas T, Imparato JC, Magalhães AC. Anacardic acid from brazilian cashew nut trees reduces dentine erosion. Caries Res 2014;48:549-56.
An agarose hydrogel, a natural polysaccharide, has shown benefits in dentin remineralization and dental tubule occlusion 1414. Han M, Li QL, Cao Y, Fang H, Xia R, Zhang ZH. In vivo remineralization of dentin using an agarose hydrogel biomimetic mineralization system. Sci Rep2017;7:41955.. Several plant species contain hydrophilic polysaccharides called galactomannans in their seed endosperm. Caesalpinia ferrea, commonly known as juca, is a plant commonly found in the northern and northeastern regions of Brazil. It possesses a polysaccharide with high intrinsic viscosity, forming highly viscous solutions even at low concentrations 1515. De Souza CF, Lucyszyn N, Ferraz FA, Sierakowski MR. Caesalpinia ferrea var. ferrea seeds as a new source of partially substituted galactomannan. Carbohydr Polym. 2010;82:641-7.. Additionally, C. ferrea exhibits a rich phenolic composition with antioxidant potential and enzymatic inhibitory activity 1616. Sampaio FC, Pereira MSV, Dias CS, Costa VCO, Conde NCO, Buzalaf MAR. In vitro antimicrobial activity of Caesalpinia ferrea Martius fruits against oral pathogens. J Ethnopharmacol 2009;124: 289-294., 1717. Cunha AP, Ribeiro ACB, Ricardo NMPS, Oliveira AC, Dávila LSP, Cardoso JHL, et al. Polysaccharides from Caesalpinia ferrea seeds - Chemical characterization and anti-diabetic effects in Wistar rats. Food Hydrocoll2017;65:68-76..
Therefore, considering the properties of juca, it is important to investigate its potential as a strategy for reducing dentin mineral loss during erosive challenges. However, to the best of the authors' knowledge, there have been no studies evaluating the effects of juca seed galactomannan (JSG) gels in preventing the progression of dental erosion. Therefore, this study aimed to assess the effects of JSG gels on reducing the erosive process of extrinsic origin in human root dentin. The null hypothesis stated that JSG gels would not have the ability to reduce dentin erosion in vitro.
Materials and methods
Ethical aspects
This study was submitted to and approved by the Research Ethics Committee of the Federal University of Ceará (protocol #2.611.040). Sound human third molars were used with the patient's consent. The teeth were stored in a 0.01% (w/v) thymol solution at 4°C.
Experimental design
It was a randomized, in vitro study. The experiment consisted of four experimental groups (n=9) with the following treatments: distilled water (DW), 0.5% juca seed galactomannan (JSG) gel, 1% JSG gel, and 0.05% stannous fluoride gel (121 ppm F) (Table 1). The erosive effect was assessed through quantitative measurement of tissue loss using a profilometer and qualitative analysis using SEM.
Sample size calculation
Based on the study by Silveira et al. 1313. Silveira C, Oliveira F, Dos Santos ML, De Freitas T, Imparato JC, Magalhães AC. Anacardic acid from brazilian cashew nut trees reduces dentine erosion. Caries Res 2014;48:549-56, which observed that dentin loss in a group treated with anacardic acid was significantly lower than the control group treated with sodium fluoride (1.97±1.02 vs 3.93±1.54), it was estimated that seven specimens per study group would be necessary to obtain a sample that represents the alternative hypothesis of this study with 80% statistical power and 95% confidence (Student's t-test). Considering the possibility of sample loss, an additional 20% was added to this sample, resulting in a total of nine specimens per group.
Specimen preparation
Root dentin specimens (4 × 4 × 2 mm) were obtained from human third molars using a hard tissue-cutting machine (IsoMetTM Low-Speed Saw Buehler, Lake Bluff, IL, USA). The specimens were then fixed onto acrylic resin discs. The dentin blocks were planned and polished according to the methods described in a previous study 1111. Leal IC, Rabelo CS, Viana ÍEL, Scaramucci T, Santiago SL, Passos VF. Hesperidin reduces dentin wear after erosion and erosion/abrasion cycling in vitro. Arch Oral Biol 2021;129:1879-1506.. After polishing, the specimens were sonicated in distilled water for 2 minutes. To protect the reference surface, a piece of tape was applied to each side of the specimen, leaving a center area (1 × 4 mm) exposed.
All specimens were evaluated for initial hardness through a microhardness tester (FM-ARS 9000; Future Tech Corp., Tokyo, Japan) with a Knoop diamond tip. Five indentations were performed in the center of the blocks, with a load of 10 g for 5s and a distance of 100 μm.
All specimens were assessed for their initial hardness using a microhardness tester (FM-ARS 9000; Future Tech Corp., Tokyo, Japan) equipped with a Knoop diamond tip. In the center of each block, five indentations were made with a load of 10 g for 5 seconds and a spacing of 100 μm. A total of 36 specimens with an average hardness of 58.46 ± 3.29 kg/mm² were selected and randomly assigned to the experimental groups using a computer-generated randomization list created in Microsoft Excel 365.
Isolation, purification of the JSG, and Preparation of the gels
The juca seedpods were collected at the Pici campus of the Federal University of Ceará, in Fortaleza, Ceará state, Brazil. The plant specimen was deposited in the Prisco Bezerra Herbarium at the same university, with registration number 44695.
The juca seedpods were selected, washed, and dried at 40 °C. Subsequently, the seeds were separated and soaked in distilled water at 85°C for 30 minutes. The endosperm was then extracted and subjected to a water and alcohol partition (1:4, v/v) at 60°C for 20 minutes. To extract the galactomannan, 10 grams of the depigmented endosperm were lyophilized and dissolved in 900 ml of water. The mixture was heated on a hot plate at 75°C for 4 hours, filtered, and the residue was discarded. For galactomannan purification, 97% PA ethanol (1:3, v/v) was added under stirring for 4 hours, along with NaCl (2.0 g/mol). The resulting mixture underwent three cycles of precipitation using 99% ethanol (1:1, v/v), followed by filtration and centrifugation. The gelatinous precipitate was then dried through lyophilization. 1616. Sampaio FC, Pereira MSV, Dias CS, Costa VCO, Conde NCO, Buzalaf MAR. In vitro antimicrobial activity of Caesalpinia ferrea Martius fruits against oral pathogens. J Ethnopharmacol 2009;124: 289-294.. The JSG gels were prepared by dissolving the galactomannan in distilled water at 60°C with magnetic stirring.
The copolymer PLURONIC F127® (Sigma Chemical Co., St. Louis, MO, USA) was utilized to prepare a gel containing stannous fluoride at a concentration of 20%. The distilled water was cooled in an ice bath while being agitated continuously with the addition of the copolymer PLURONIC F127® until it completely dissolved.
Erosive cycling model
The study involved a cyclic experiment that was repeated for five consecutive days, comprising three main steps: an erosive challenge, treatment with gels, and remineralization using artificial saliva. Each specimen was exposed to a 0.05 M citric acid solution (pH 1.3) for 5 minutes. Following the erosive challenge, the specimens were treated with the respective gels for 5 minutes. Subsequently, the blocks were rinsed with distilled water and immersed in artificial saliva (1.5 mM Ca; 0.9 mM PO4; 150 mM KCl; 0.1M Tris buffer) for 2 hours (11). This cycle of acid exposure, gel treatment, and remineralization was repeated three times a day for five consecutive days. To ensure optimal conditions, the specimens were stored overnight at 37°C in artificial saliva.
Surface wear evaluation
To measure tooth wear, a Hommel Tester T1000 mechanical profilometer (Hommelwerke GmbH, Germany) was used after the completion of the experimental period. The height difference between the reference surface and the treated area was assessed to quantify the extent of tooth wear. Before analysis, the tape covering the untreated area was removed, exposing the surface for evaluation. Within each sample, three measurements were taken at 100 µm intervals over a 1.5 mm distance. The average of these measurements was calculated for each sample, providing an assessment of tooth wear 1818. Passos VF, Melo MA, Vasconcellos AA, Rodrigues LKA, Santiago SL. Comparison of methods for quantifying dental wear caused by erosion and abrasion. Microsc Res Tech 2013;76:178-83..
SEM and EDS evaluations of the dentin surfaces
Two dentin samples from each group were subjected to scanning electron microscopy (SEM). They were immersed in a 2.5% glutaraldehyde fixative solution in a 0.1 mol/L sodium cacodylate buffer for 24 hours and then washed with the same buffer. Subsequently, the samples were dehydrated using ethanol solutions with increasing concentrations and dried at room temperature for 24 hours in a desiccator 1919. Toledano M, Yamauti M, Ruiz-Requena ME, Osorio R. A ZnO-doped adhesive reduced collagen degradation favouring dentine remineralization. J Dent. 2012;40:756-65.. The dried specimens were fixed onto metal stubs and coated with a layer of gold using a metallizer (Hammer VI - Sputtering System, Anatech Ltda, Alexandria, USA).
The samples were analyzed using the SEM Quanta FEG 450 (FEI Company, Oregon, USA). Subsequently, an EDS analysis was conducted to examine the chemical composition of the dentin surface. The acceleration voltage was set at 20 kV, and a magnification of 5000x was used.
Statistical analysis
The mean and standard deviation data were analyzed using the SPSS 22.0 software for Windows (SPSS Inc., Chicago, IL, USA). Preliminary Kolmogorov-Smirnov tests for normality were conducted. Based on the normal distribution observed in the evaluated data, parametric analysis of variance (ANOVA) tests, one-factor, were performed. Post-hoc comparisons were conducted using the Tukey test for the wear data, with a significance level set at 5%.
Results
The wear values (µm) of the root dentin (Table 2) revealed a statistically significant difference between the groups (p = 0.011). The negative control group (distilled water) exhibited the highest wear pattern (6.0 µm ± 3.5), which was significantly different from the group treated with 0.5% stannous fluoride gel (p = 0.007), as it showed the lowest dentin loss. The groups treated with 0.5% and 1% JSG gel showed similar results to the negative control (p = 0.661; p = 0.212, respectively) and stannous fluoride (p = 0.103; p = 0.379, respectively). However, there was no significant difference in comparison to the galactomannan gel concentration (p = 0.850).
The SEM images reveal that the negative control group (Figure 1a) exhibits wider dentinal tubules. In contrast, the specimen treated with stannous fluoride (Figure 1b) shows more obliterated tubules. The specimen treated with JSG at a concentration of 0.5% (Figure 1c) displays the formation of poorly defined crystals, whereas the one treated with JSG at 1% exhibits a higher quantity of crystals with a more distinct shape (Figure 1d). Energy dispersive X-ray spectroscopy (EDS) analysis enables the detection of calcium and oxygen on the surface of the dentin specimen treated with JSG 1% (Figure 2).
Representative SEM micrograph (x5000) of erosion-treated area. Distilled water (A), stannous fluoride (B), JSG 0.5% (C), and JSG 1% (D).
EDS images of the treated area with JSG 1%. The yellow color indicates the presence of oxygen (A) and the blue color indicates the presence of calcium (B) in the dentin surface.
Discussion
According to our results, the null hypothesis stating that JSG gels do not significantly prevent the progression of dental erosion was accepted. In terms of wear analysis, the group treated with stannous fluoride gel showed a significant difference compared to the negative control group, exhibiting less dentin loss. Both concentrations of JSG did not demonstrate statistical differences compared to the negative control. However, they were also similar to the positive control (stannous fluoride).
In this in vitro study, surface profilometry was employed to detect surface loss in dentin specimens. This technique quantifies surface loss by comparing it to an untreated reference area. It has been utilized in numerous studies and is considered a reliable method for evaluating surface loss in specimens subjected to significant erosion. 1111. Leal IC, Rabelo CS, Viana ÍEL, Scaramucci T, Santiago SL, Passos VF. Hesperidin reduces dentin wear after erosion and erosion/abrasion cycling in vitro. Arch Oral Biol 2021;129:1879-1506., 1313. Silveira C, Oliveira F, Dos Santos ML, De Freitas T, Imparato JC, Magalhães AC. Anacardic acid from brazilian cashew nut trees reduces dentine erosion. Caries Res 2014;48:549-56, 1818. Passos VF, Melo MA, Vasconcellos AA, Rodrigues LKA, Santiago SL. Comparison of methods for quantifying dental wear caused by erosion and abrasion. Microsc Res Tech 2013;76:178-83..
Previous studies have demonstrated positive outcomes in terms of reducing the progression of dental erosion using stannous fluoride. 99. West NX, Seong J, Hellin N, Eynon H, Barker ML, He T. A clinical study to measure anti-erosion properties of a stabilized stannous fluoride dentifrice relative to a sodium fluoride/triclosan dentifrice. Int J Dent Hyg. 2015;15:113-9, 1010. Baig AA, Faller RV, Yan J, Ji N, Lawless M, Eversole SL. Protective effects of SnF2 - Part I. Mineral solubilisation studies on powdered apatite. Int Dent J 2014;64:4-10.. Stannous fluoride functions by creating a protective barrier on the tooth surface, facilitated by the strong affinity between stannous ions and hydroxyapatite 1010. Baig AA, Faller RV, Yan J, Ji N, Lawless M, Eversole SL. Protective effects of SnF2 - Part I. Mineral solubilisation studies on powdered apatite. Int Dent J 2014;64:4-10.. The findings of the current study further support the beneficial effects of SnF2 gel in preventing erosion caused by citric acid, as it was observed to decrease wear compared to the negative control.
The present study examined a gel formulation based on a natural product intended for in-office application. Previous studies have also investigated gels containing natural products 2020. Sales-Peres Ade C, Marsicano JA, Garcia RP, Forim MR, Silva MF, Sales-Peres SH. Effect of natural gel product on bovine dentin erosion in vitro. J Appl Oral Sci. 2013;21:597-600., 2121. Boteon AP, Kato MT, Buzalaf MAR, Prakki A, Wang L, Rios D, et al. Effect of Proanthocyanidin-enriched extracts on the inhibition of wear and degradation of dentin demineralized organic matrix. Arch Oral Biol2017;84:118-24.. In a study simulating extrinsic erosion using bovine dentin blocks, a Neem gel (10% Neem extract) did not show a significant difference compared to the negative control in reducing dentin loss. Only when combined with sodium fluoride gel was there a reduction in dentin loss 2020. Sales-Peres Ade C, Marsicano JA, Garcia RP, Forim MR, Silva MF, Sales-Peres SH. Effect of natural gel product on bovine dentin erosion in vitro. J Appl Oral Sci. 2013;21:597-600.. Similarly, in the present study, JSG also did not demonstrate a significant difference. However, the gels in this study were prepared using isolated galactomannan. It is possible that incorporating another active ingredient could provide additional benefits. In another study utilizing bovine dentin blocks, a 10% cranberry extract gel was effective in reducing dentin loss 2121. Boteon AP, Kato MT, Buzalaf MAR, Prakki A, Wang L, Rios D, et al. Effect of Proanthocyanidin-enriched extracts on the inhibition of wear and degradation of dentin demineralized organic matrix. Arch Oral Biol2017;84:118-24.. The concentrations of JSG used in this study were 0.5% and 1%, which are much lower compared to the concentrations employed in the previously mentioned studies. Therefore, it is believed that using a higher concentration of JSG may yield better results in reducing dentin loss.
SEM analysis is commonly utilized to assess changes in dentin morphology 1313. Silveira C, Oliveira F, Dos Santos ML, De Freitas T, Imparato JC, Magalhães AC. Anacardic acid from brazilian cashew nut trees reduces dentine erosion. Caries Res 2014;48:549-56. In an in vitro study, the closure of dentinal tubules was observed using various concentrations of SnF22222. Takamizawa T, Tsujimoto A, Ishii R, Ujiie M, Kawazu M, Hidari T, et al. Laboratory evaluation of dentin tubule occlusion after use of dentifrices containing stannous fluoride. J Oral Sci2019;61:276-83.. In the current study, SEM analysis of specimens treated with stannous fluoride revealed a reduction in tubule diameter compared to the control group, along with the occlusion of certain dentinal tubules. In the SEM images of blocks treated with JSG, crystal deposition was observed on the dentin surface in both concentrations tested, with the gel containing the higher concentration of galactomannan displaying more clearly defined crystals. To determine the composition of these crystals, an EDS analysis was performed.
EDS analysis conducts a mapping of the dentin surface, allowing for the identification of chemical elements present 2323. Basting RT, Leme AA, Bridi EC, Amaral FL, França FM, Turssi CP, et al. Nanomechanical properties, SEM, and EDS microanalysis of dentin treated with 2.5% titanium tetrafluoride, before and after an erosive challenge. J Biomed Mater Res B Appl Biomater. 2015;103:783-9.. A significant presence of oxygen and calcium was observed in the region where the crystals were located. Furthermore, the morphology of the crystals formed by JSG gels resembled that of calcium oxalate crystals reported in previous studies 2424. Pereira JC, Segala AD, Gillam DG. Effect of desensitizing agents on the hydraulic conductance of human dentin subjected to different surface pre-treatments--an in vitro study. Dent Mater 2005;21:129-38., 2525. Sauro S, Gandolfi MG, Prati C, Mongiorgi R. Oxalate-containing phytocomplexes as dentine desensitisers: an in vitro study. Arch Oral Biol 2006;51:655-64.. In one study, phytocomplexes containing oxalates were found to reduce dentin permeability through crystal deposition within the dentinal tubules 2525. Sauro S, Gandolfi MG, Prati C, Mongiorgi R. Oxalate-containing phytocomplexes as dentine desensitisers: an in vitro study. Arch Oral Biol 2006;51:655-64.. These findings suggest that JSG may play an important role in decreasing dentin permeability.
Some species of the Caesalpinia genus are well-known and extensively studied, but only a few of the polysaccharides extracted from their pods and seeds are utilized for therapeutic and commercial purposes 1717. Cunha AP, Ribeiro ACB, Ricardo NMPS, Oliveira AC, Dávila LSP, Cardoso JHL, et al. Polysaccharides from Caesalpinia ferrea seeds - Chemical characterization and anti-diabetic effects in Wistar rats. Food Hydrocoll2017;65:68-76.. Although there was no significant difference observed between the concentrations of JSG gels, SEM images of the JSG 1% group showed a notable formation of well-defined crystals, indicating that this concentration warrants further investigation. Considering the morphological changes in dentin observed in the SEM images, it is plausible to consider the potential use of JSG in the treatment of dentin hypersensitivity, which is one of the complications associated with erosion-induced wear.
As this study was conducted in vitro, it is important to note that the results cannot be directly extrapolated to in vivo situations, as the oral cavity's natural protective factors are absent. One limitation of the study is the use of artificial saliva, which lacks the proteins necessary to simulate the formation of acquired pellicle, thus preventing the assessment of its protective effect against erosive wear. Additionally, the study did not evaluate erosion associated with abrasion, which means the impact of mechanical brushing on dentin wear could not be examined. Therefore, further studies employing different methodologies are needed to investigate the preventive effects of JSG gels on the progression of dentin erosion.
The JSG gels, while showing similar results to the positive control, did not exhibit superior efficacy at the tested concentrations. Consequently, stannous fluoride remains a viable option for the treatment of erosive tooth wear.
Acknowledgments
The authors express their gratitude to the Central Analítica-UFC for conducting the microscopy measurements, which were supported by Finep-CT-INFRA, CAPES-Pró-Equipamentos, and MCTI-CNPq-SisNano2.0. This research also received support from PROAP/PRINT/CAPES and Portal de Periodicos CAPES - Finance Code 001.
References
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1Gambon DL, Brand HF, Veerman ECI. Dental erosion in the 21st century: what is happening to nutritional habits and lifestyle in our society? Br Dent J2012;2013:55-7.
-
2Lussi A, Megert B, Shellis P. The erosive effect of various drinks, foods, stimulants, medications and mouthwashes on human tooth enamel. Swiss Dent J 2023;133(7-8).
-
3Saads CT, Lussi A. Chapter 9: Acidic Beverages and Foods Associated with Dental Erosion and Erosive Tooth Wear. Monogr Oral Sci2020;28:91-8.
-
4Chan AS, Tran TTK, Hsu YH, Liu SYS, Kroon JA-O. A systematic review of dietary acids and habits on dental erosion in adolescents. Int J Paediatr Dent 2020;30:713-33.
-
5Magalhães AC, Rios D, Moino AL, Wiegand A, Attin T, Buzalaf MA. Effect of different concentrations of fluoride in dentifrices on dentin erosion subjected or not to abrasion in situ/ex vivo. Caries Res 2008;42(2):112-6.
-
6Johansson AK, Omar R, Carlsson GE, Johansson A. Dental erosion and its growing importance in clinical practice: from past to present. Int J Dent 2012;2012:1-17.
-
7Ganss C, Schlueter N, Hardt M, Hinckeldey JV, Klimek J.Effects of toothbrushing on eroded dentine. Eur J Oral Sci 2007;115:390-6.
-
8Kato MT, Leite AL, Hannas AR, Calabria MP, Magalhães AC, Pereira JC, et al. Impact of protease inhibitors on dentin matrix degradation by collagenase. J Dent Res2012;91:1119-23.
-
9West NX, Seong J, Hellin N, Eynon H, Barker ML, He T. A clinical study to measure anti-erosion properties of a stabilized stannous fluoride dentifrice relative to a sodium fluoride/triclosan dentifrice. Int J Dent Hyg. 2015;15:113-9
-
10Baig AA, Faller RV, Yan J, Ji N, Lawless M, Eversole SL. Protective effects of SnF2 - Part I. Mineral solubilisation studies on powdered apatite. Int Dent J 2014;64:4-10.
-
11Leal IC, Rabelo CS, Viana ÍEL, Scaramucci T, Santiago SL, Passos VF. Hesperidin reduces dentin wear after erosion and erosion/abrasion cycling in vitro. Arch Oral Biol 2021;129:1879-1506.
-
12Passos VF, Melo MAS, Lima JPM, Marçal FF, Costa C, Rodrigues LKA, et al. Active compounds and derivatives of camellia sinensis responding to erosive attacks on dentin. Braz Oral Res 2018;32:40.
-
13Silveira C, Oliveira F, Dos Santos ML, De Freitas T, Imparato JC, Magalhães AC. Anacardic acid from brazilian cashew nut trees reduces dentine erosion. Caries Res 2014;48:549-56
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14Han M, Li QL, Cao Y, Fang H, Xia R, Zhang ZH. In vivo remineralization of dentin using an agarose hydrogel biomimetic mineralization system. Sci Rep2017;7:41955.
-
15De Souza CF, Lucyszyn N, Ferraz FA, Sierakowski MR. Caesalpinia ferrea var. ferrea seeds as a new source of partially substituted galactomannan. Carbohydr Polym. 2010;82:641-7.
-
16Sampaio FC, Pereira MSV, Dias CS, Costa VCO, Conde NCO, Buzalaf MAR. In vitro antimicrobial activity of Caesalpinia ferrea Martius fruits against oral pathogens. J Ethnopharmacol 2009;124: 289-294.
-
17Cunha AP, Ribeiro ACB, Ricardo NMPS, Oliveira AC, Dávila LSP, Cardoso JHL, et al. Polysaccharides from Caesalpinia ferrea seeds - Chemical characterization and anti-diabetic effects in Wistar rats. Food Hydrocoll2017;65:68-76.
-
18Passos VF, Melo MA, Vasconcellos AA, Rodrigues LKA, Santiago SL. Comparison of methods for quantifying dental wear caused by erosion and abrasion. Microsc Res Tech 2013;76:178-83.
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Publication Dates
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Publication in this collection
22 Dec 2023 -
Date of issue
Sep-Oct 2023
History
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Received
02 Apr 2023 -
Accepted
29 Aug 2023