Abstract
Background
In this study was assessed the surface roughness and chemical composition of tooth enamel and composite resin after bleaching treatment, immersion in acidic beverages, and simulated toothbrushing.
Material and Methods
One hundred and twenty dental blocks (10 x 10 x 3 mm) were randomly assigned (n = 10) according to surface treatment [none (N), bleaching (B), toothbrushing (T), and B+T] and storage medium [saliva (S), whiskey (W), and orange juice (O)]: experimental groups - N+S, N+W, N+O, B+S, B+W, B+O, S+T, W+T, O+T, B+S+T, B+W+T, and B+O+T. Two bleaching sessions were conducted using 38% hydrogen peroxide (3 applications). Surface roughness was measured using a roughness tester and composition was determined by micro energy-dispersive X-ray fluorescence spectrometry (µ-EDXRF) before and after treatments. Calcium/phosphorus (Ca/P) ratio in enamel and silica (Si) content in composite were evaluated. Data were statistically analyzed by ANOVA and Tukey’s test (α = 0.05).
Results
Overall, increased values of surface roughness for enamel and composite were observed mainly after immersion in orange juice and bleaching/toothbrushing association. Moreover, this association and immersion in whiskey resulted in lower Ca/P ratio and after aging methods, bleached and bleached/toothbrushed groups showed decreased in Ca/P ratio compared to initial values. All groups showed Si content decrease at the end, except the group without surface treatment and immersed in saliva, and bleaching followed by immersion in orange juice and toothbrushing caused the highest Si reduction.
Conclusions
Bleaching and toothbrushing combination strengthened the effects caused by acidic drinks on roughness and chemical composition of enamel and composite.
Key words:Tooth bleaching, toothbrushing, physical properties, chemical properties.
Introduction
Smile esthetics is an important factor in individual presentation to social acceptance. Thus, dental bleaching is a conservative technique, which allows that natural or stained teeth to be changed without wearing the tooth structure, improving esthetic appearance of teeth (1). On the other hand, indiscriminate use of bleaching agents can increase the porosity and erosion on enamel surface, even using low concentration products (2,3).
Hydrogen peroxide (HP) at high concentration constitutes an alternative in cases of severe color alteration when patients have difficulty using a tray or fast treatment is needed. However, this bleaching agent causes on enamel surface increased roughness, alterations in inorganic composition and organic matrix, and decreased hardness (1,4-9).
Mineral loss and erosion of tooth hard structure can be intensified by consumption of acidic food and drinks (10,11). So, the interaction of bleaching agents with intake of acidic drinks could intensify the damage on enamel surface (10,12). Likewise, increased surface roughness of resinous materials has been reported after bleaching procedure (13,14) and intake of low pH drinks (15). In addition, abrasion caused by toothbrushing also increases the roughness (16,17).
In order to assess alterations in mineral content of enamel and inorganic component of composite, a sensitive chemical analysis can be performed using energy dispersive X-ray microanalysis (3,12). This analysis is a non-destructive method, which provides information about atomic and structural composition of substrate (12).
Thus, the purpose in this study was to evaluate the surface roughness and change in chemical composition of tooth enamel and composite resin submitted to bleaching treatment using 38% HP, immersion in low pH solutions, and/or simulated toothbrushing. The research hypothesis was that roughness and chemical composition of enamel and composite would be affected by the treatments.
Material and Methods
-Specimen preparation
The 120 bovine incisors were disinfected in 0.1% thymol solution (Byofórmula Imp Exp, São José dos Campos, SP, Brazil) for 24 h at room temperature. Then, teeth were cleaned and stored in artificial saliva (Byofórmula). Saliva was changed every two days in order to maintain a standard in mineral conditions of enamel before initial analysis of roughness and chemical composition.
The roots were separated from dental crown using a precision saw (Isomet 1000; Buehler Inc., Lake Bluff, IL, USA). So, 120 square dental blocks (10 mm x 10 mm x 3 mm) were obtained from crown, buccal surfaces were polished with -600, -800, -1000, and -1200 grit silicon carbide abrasive papers (Buehler Inc.) using polishing machine (APL-4; Arotec, Cotia, SP, Brazil) under water irrigation.
In half of dental block, the enamel was left intact while in other half a cavity was prepared with high speed using a diamond bur wheel #3053 (KG Sorensen, Barueri, SP, Brazil). Cavity was restored with nanofilled composite resin (Filtek Z350, A3 shade, batch #BT5009; 3M ESPE, Saint Paul, MN, USA) and light cured for 20 s using a halogen unit (Soft-Start; Degussa Hüls, Postfach, Hanau, Germany) at 600 mW/cm2 of irradiance. Specimens were stored in distilled buffered water (Byofórmula) for 24 h at 37ºC. Then, restorations were polished with fine and superfine aluminum oxide abrasive discs (Sof-Lex Pop-On; 3M ESPE) for 15 s each disc.
After polishing procedure, specimens were stored in distilled buffered water for more 24 h at 37ºC. Afterwards, circular areas with 3 mm of diameter on enamel and composite were labeled with tape (Durex, 3M do Brasil Ltda, Sumaré, SP, Brazil), while the rest of surfaces were isolated with nail polish (Revlon Consumer Products Corp., Miami, FL, USA). After nail polish drying the tape was removed exposing the areas to be treated.
Specimens were randomly assigned in 12 groups (n = 10) according to surface treatment in 4 levels [none (N), bleaching (B), toothbrushing (T), and B+T] and storage medium in 3 levels [saliva (S), whiskey (W), and orange juice (O)]. Experimental design was as follows: group 1 (N+S), group 2 (N+W), group 3 (N+O), group 4 (B+S), group 5 (B+W), group 6 (B+O), group 7 (S+T), group 8 (W+T), group 9 (O+T), group 10 (B+S+T), group 11 (B+W+T), and group 12 (B+O+T). Groups were evaluated before (baseline) and after aging methods.
-Surface roughness
Arithmetical mean of roughness (Ra) was assessed using a profilometer (Surftest SJ-301; Mitutoyo Ltda., Tokyo, Japan) at constant speed of 0.5 mm/s and cut-off of 0.25 mm. Three readings in different positions were carried out with needle passing by center of specimen and rotating the same in approximately 120º after each measurement. Average of three readings was used as Ra for each specimen (14).
-Chemical composition
The chemical analysis was performed using a micro-energy dispersive X-ray fluorescence (µ-EDXRF) spectrometer (μEDX-1300; Shimadzu, Kyoto, Japan). Specimen surface was irradiated with X-ray beam of 50 µm and measurements were carried out in three points in enamel and in one point in composite. A semiconductor Si (Li) detector cooled by liquid nitrogen was used to radiation count. The tension and tube current were adjusted in 15 kV for enamel and 40 kV for composite, with reading time per point of 100 s and 25% dead time (12).
Stoichiometric synthetic hydroxyapatite (Sigma-Aldrich, St. Louis, MO, USA) was used as reference to enamel calibration with purity degree of 99.99% [Ca10(PO4)6(OH)2, batch #10818HA]. The variables to calculate the chemical formula were established for relative weights of calcium (Ca) and phosphorus (P) and the element oxygen was used as a chemical balance. The Ca/P ratio in enamel and silica (Si) content in composite were calculated by their relative weights as determined by direct reading of equipment.
-Bleaching procedure
Two bleaching sessions were performed using 38% HP (Opalescence Xtra Boost; Ultradent, South Jordan, UT, USA) with 3 applications in each session. In each application, 1 mL of bleaching agent was applied on specimen surface for 15 min. Then, gel was removed with gauze and a new application was done until completing 3 applications. Specimens were cleaned and stored in artificial saliva at 37ºC during a 7-day interval between the sessions.
-Solution immersion
Specimens were immersed in 10 mL of saliva (pH 7.1; Byofórmula), whiskey (Red Label, pH 3.7; Johnnie Walker, Kilmarnock, AD, Scotland), or orange juice (pH 3.6; Del Valle, Americana, SP, Brazil) for 10 min daily at 23ºC during 7 days. Afterwards, specimens were immersed in artificial saliva until completing a 24-h cycle. Solutions were changed daily. The pH of solutions was measured using a digital pH meter.
-Simulated toothbrushing
Specimens were submitted to 30,000 cycles of toothbrushing (Equilabor, Piracicaba, SP, Brazil), in line course of 20 mm extension, at a frequency of 4.5 cycles/s and constant load of 200 g. Oral B Indicator (Procter & Gamble, Manaus, AM, Brazil) medium-sized toothbrushes with soft-rounded bristles and a slurry (1:3) of whitening dentifrice (Colgate Ultra Branco; Colgate Palmolive, Osasco, SP, Brazil) and distilled water were used (12). At end, specimens were rinsed with running water and cleaned using an ultrasonic cleaner (USC-700; Unique, Indaiatuba, SP, Brazil) for 10 min.
-Statistical analysis
After exploratory data analysis, roughness, Ca/P ratio, and Si content data were statistically analyzed by three-way proc-mixed analysis of variance (ANOVA) for repeated measures followed by Tukey’s test at a pre-set of 5% significance level (version 9.1; SAS Institute Inc., Cary, NC, USA).
Results
-Surface roughness
ANOVA showed interaction between the factors “surface treatment”, “storage medium”, and “time” for enamel and composite (p = 0.0001 and p = 0.0003, respectively).
In Table 1, enamel bleached and toothbrushed presented the highest roughness values, followed by groups only bleached, which showed higher roughness compared to groups only toothbrushed. Bleached group immersed in whiskey showed the lowest roughness compared to group immersed in orange juice. In other surface treatments the results were statistically similar in both acidic drinks.
Table 1. Surface roughness mean (standard deviation) of tooth enamel according to surface treatment and storage medium.
In Table 2, bleaching and toothbrushing association also promoted higher surface roughness on composite, while the groups only bleached or toothbrushed showed similar roughness values. Group immersed in orange juice presented the highest roughness values compared to group immersed in whiskey, except for bleached group and immersed in whiskey.
Table 2. Surface roughness mean (standard deviation) of composite resin according to surface treatment and storage medium.
All groups showed an increase in values of surface roughness for enamel and composite, except for the group without surface treatment and immersed in artificial saliva (control). The lowest roughness was observed for group immersed in saliva, regardless of aging method.
-Chemical composition
ANOVA showed interaction between the factors “surface treatment”, “storage medium”, and “time” for enamel and composite (p = 0.0056 and p = 0.00001, respectively).
In Table 3, bleached and toothbrushed groups showed similar Ca/P ratio, regardless of storage medium. Furthermore, bleaching/toothbrushing association and immersion in whiskey promoted lower Ca/P ratio compared to group immersed in saliva, while the group immersed in orange juice promoted intermediate values. After aging methods, bleached and bleached/toothbrushed groups showed decrease in Ca/P ratio, which was statistically significant when compared to baseline.
Table 3. Calcium/phosphorus ratio mean (standard deviation) of tooth enamel according to surface treatment and storage medium.
In Table 4, surface treatments and low pH solutions promoted higher change in Si proportion, but bleaching followed by immersion in orange juice and toothbrushing caused the highest reduction in Si content. Toothbrushed groups showed intermediate values without significant difference between acidic drinks. All groups showed Si decrease at the end, except the control group.
Table 4. Silica content mean (standard deviation) of composite resin according to surface treatment and storage medium.
Discussion
In the present study, bleaching treatment effects on enamel and composite surfaces was evaluated by roughness assessment and by µ-EDXRF to analyze of calcium and phosphate content in enamel and silica content in composite. Surface roughness and chemical composition of tooth enamel and composite resin were affected by treatments; thus, research hypothesis was accepted.
Tooth bleaching using 38% HP increased the surface roughness of bovine enamel, corroborating with other studies that also showed morphological changes on enamel surface after bleaching treatment (1-4,8,18). On the other hand, previous investigations reported no change on enamel surface (19,20). Probably, chemical composition of bleaching agents and method used to assess the roughness could influence the different results obtained.
Bleaching occurs by HP dissociation in free radicals that penetrate into tooth structure and eventually can reach in the pulp. These free radicals are highly unstable and have capacity to oxidize the chromophores, which are pigmented organic molecules (3,9). After bleaching treatment, as on enamel surface, was also observed increase on roughness of the nanofilled composite, corroborating with findings of other authors (13,14). Organic matrix oxidation of composite by the bleaching agent provides water absorption and loss of the inorganic filler particles, compromising the surface integrity of resinous material (13).
Surface changes on tooth structure and restorative material can appear after toothbrushing, especially when using dentifrices of high abrasiveness (17,21-23), as the whitening dentifrice used in this study. Association of toothbrush bristles with abrasive particles of dentifrice increases the surface roughness of composite by degradation of organic matrix, exposition and loss of inorganic filler during the simulated toothbrushing procedure (21). In this study, increased roughness was observed after simulated toothbrushing for composite resin, as reported by previous studies (16,21), and for tooth enamel (24). On the other hand, the use of singly dentifrice not changes surface roughness of enamel (25). However, toothbrushing procedure associated to bleaching treatment increased the enamel roughness (4,17,22).
In the present investigation, immersion in different low pH beverages increased the bleaching agent and toothbrushing effects on surface roughness of enamel and composite. Acidic drinks consumption can cause deterioration of resinous materials, causing alteration in organic matrix and loss of inorganic filler particles (15). At enamel, acidic beverages promote dissolution of its surface by an erosive process (11). In both cases, these alterations increased the roughness on enamel and composite surfaces, being dependent of exposure time, pH, and chemical composition of solutions (26,27).
In addition, composite resin exposure to ethanol causes decrease on its physical properties (28). Alcohol is a solvent that penetrates the polymer matrix causing surface deterioration and decreases the physical properties of resin-based material (27,29). However, alcohol not causes apparent effects on enamel surface, but the low pH of an alcoholic drink can cause erosive process on this surface (26). Overall, orange juice storage caused higher roughness values for composite and enamel compared to whiskey. Even with close pH values of these two solutions, the citric acid present in orange juice has been considered an aggressive medium be storage tooth hard tissues and resinous materials (30).
Bleached enamel, immersed in acidic drinks, and toothbrushed showed the highest mineral loss. As observed in present investigation, use of different bleaching agents caused calcium and phosphorus loss, assessed by µ-EDXRF and FT-Raman analysis (12). However, no mineral loss after dental bleaching was reported by others studies (5,18). Severity of changes on enamel during bleaching treatment depends of exposure time, concentration, and pH of bleaching agent (1,2,5,8,9), which could explain the controversial results.
The µ-EDXRF analysis of composite resin showed that all treatments promoted silica loss. As for enamel, association of bleaching treatment, immersion in low pH, and simulated toothbrushing caused the highest reduction of silica content. So, oxidation of organic matrix caused by bleaching increases water absorption (13), which combined to abrasion after toothbrushing compromises the composite surface even more, causing loss of filler particles (21). In addition, acidic solutions used also promoted surface erosion as well as the softening of resinous matrix (15).
Conclusions
Toothbrushing and bleaching association strengthened the effects of superficial changes and chemical composition of tooth enamel as well as composite. Bleaching combined to low pH beverages and brushing caused higher alteration on chemical composition and roughness of enamel and composite.
Acknowledgments
The authors acknowledge by use of the Laboratory of Biomedical Vibrational Spectroscopy from Research and Development Institute at University of Paraíba Valley and Laboratory of Dental Materials from the Piracicaba Dental School. We would like to thank the São Paulo Research Foundation (FAPESP), for the X-ray microfluorescence equipment (Grant no. 05/50811-9).
References
- 1.Favaro JC, Geha O, Guiraldo RD, Lopes MB, Aranha AMF, Berger SB. Evaluation of the effects of whitening mouth rinses combined with conventional tooth bleaching treatments. Restor Dent Endod. 2019;44:e6. doi: 10.5395/rde.2019.44.e6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Pimenta-Dutra AC, Albuquerque RC, Morgan LS, Pereira GM, Nunes E, Horta MC. Effect of bleaching agents on enamel surface of bovine teeth: A SEM study. J Clin Exp Dent. 2017;9:e46–50. doi: 10.4317/jced.53011. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Sabel N, Karlsson A, Sjölin L. XRMA analysis and X-ray diffraction analysis of dental enamel from human permanent teeth exposed to hydrogen peroxide of varying pH. J Clin Exp Dent. 2019;11:e512–20. doi: 10.4317/jced.55618. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Melo CF, Manfroi FB, Spohr AM. Microhardness and roughness of enamel bleached with 10% carbamide peroxide and brushed with different toothpastes: an in situ study. J Int Oral Health. 2014:18–24. [PMC free article] [PubMed] [Google Scholar]
- 5.Lima DA, Aguiar FH, Pini NI, Soares LE, Martin AA, Liporoni PC. In vitro effects of hydrogen peroxide combined with different activators for the in-office bleaching technique on enamel. Acta Odontol Scand. 2015;73:516–21. doi: 10.3109/00016357.2014.997793. [DOI] [PubMed] [Google Scholar]
- 6.Lago AD, de Freitas PM, Araújo EM, Matos AB, Garone-Netto N. Is it necessary to prepare the enamel before dental bleaching? Int J Dent. 2017;2017:5063521. doi: 10.1155/2017/5063521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Pinto A, Bridi EC, Amaral F, França F, Turssi CP, Pérez CA. 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. [DOI] [PubMed] [Google Scholar]
- 8.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. [DOI] [PubMed] [Google Scholar]
- 9.Mushashe AM, Coelho BS, Garcia PP, Rechia BN, da Cunha LF, Correr GM. Effect of different bleaching protocols on whitening efficiency and enamel superficial microhardness. J Clin Exp Dent. 2018;10:e772–5. doi: 10.4317/jced.54967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.de Araújo LS, dos Santos PH, Anchieta RB, Catelan A, Briso AL, Zaze AC. Mineral loss and color change of enamel after bleaching and staining solutions combination. J Biomed Opt. 2013;18:108004. doi: 10.1117/1.JBO.18.10.108004. [DOI] [PubMed] [Google Scholar]
- 11.Aykut-Yetkiner A, Wiegand A, Ronay V, Attin R, Becker K, Attin T. In vitro evaluation of the erosive potential of viscosity-modified soft acidic drinks on enamel. Clin Oral Investig. 2014;18:769–73. doi: 10.1007/s00784-013-1037-9. [DOI] [PubMed] [Google Scholar]
- 12.Paula SS, Soares LE, do Espirito Santo AM, Martin AA, Cavalli V, Liporoni PC. FT-Raman and energy dispersive X-ray fluorescence spectrometric analyses of enamel submitted to 38% hydrogen peroxide bleaching, an acidic beverage, and simulated brushing. Photomed Laser Surg. 2010;28:391–6. doi: 10.1089/pho.2008.2426. [DOI] [PubMed] [Google Scholar]
- 13.Wang L, Francisconi LF, Atta MT, Dos Santos JR, Del Padre NC, Gonini Jr A. Effect of bleaching gels on surface roughness of nanofilled composite resins. Eur J Dent. 2011;5:173–9. [PMC free article] [PubMed] [Google Scholar]
- 14.de Oliveira Lima M, Catelan A, Hernandes NM, Giorgi MC, Ambrosano GM, Lima DA. In vitro evaluation of the effect of different polishing techniques on the surface roughness of composite resins submitted to at-home and in-office bleaching procedures. J Conserv Dent. 2015;18:483–7. doi: 10.4103/0972-0707.168820. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Rajavardhan K, Sankar A, Kumar M, Kumar K, Pranitha K, Kishore K. Erosive potential of cola and orange fruit juice on tooth colored restorative materials. Ann Med Health Sci Res. 2014;4:S208–12. doi: 10.4103/2141-9248.141960. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Takahashi R, Jin J, Nikaido T, Tagami J, Hickel R, Kunzelmann KH. Surface characterization of current composites after toothbrush abrasion. Dent Mater J. 2013;32:75–82. doi: 10.4012/dmj.2012-160. [DOI] [PubMed] [Google Scholar]
- 17.Soares AF, Bombonatti JF, Alencar MS, Consolmagno EC, Honório HM, Mondelli RF. Influence of pH, bleaching agents, and acid etching on surface wear of bovine enamel. J Appl Oral Sci. 2016;24:24–30. doi: 10.1590/1678-775720150281. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Llena C, Esteve I, Forner L. Effects of in-office bleaching on human enamel and dentin. Morphological and mineral changes. Ann Anat. 2018;217:97–102. doi: 10.1016/j.aanat.2018.01.003. [DOI] [PubMed] [Google Scholar]
- 19.Cadenaro M, Navarra CO, Mazzoni A, Nucci C, Matis BA, Di Lenarda R. An in vivo study of the effect of a 38 percent hydrogen peroxide in-office whitening agent on enamel. J Am Dent Assoc. 2010;141:449–54. doi: 10.14219/jada.archive.2010.0198. [DOI] [PubMed] [Google Scholar]
- 20.Machado LS, Anchieta RB, dos Santos PH, Briso AL, Tovar N, Janal MN. Clinical comparison of at-home and in-office dental bleaching procedures: a randomized trial of a split-mouth design, Int. J. Periodontics Restorative Dent. 2016;36:251–260. doi: 10.11607/prd.2383. [DOI] [PubMed] [Google Scholar]
- 21.da Cas NV, Ruat GR, Bueno RP, Pachaly R, Pozzobon RT. Effect of whitening toothpaste on superficial roughness of composite resin. Gen Dent. 2013;61:e8–11. [PubMed] [Google Scholar]
- 22.Pinto SC, Hilgenberg SP, Wambier DS, Farago PV, Bandeca MC, Santos FA. Characterization of dentifrices containing desensitizing agents, triclosan or whitening agents: EDX and SEM analysis. Braz Dent J. 2014;25:153–9. doi: 10.1590/0103-6440201302209. [DOI] [PubMed] [Google Scholar]
- 23.Borges AB, Santos LF, Augusto MG, Bonfiette D, Hara AT, Torres CR. Toothbrushing abrasion susceptibility of enamel and dentin bleached with calcium-supplemented hydrogen peroxide gel. J Dent. 2016;49:54–9. doi: 10.1016/j.jdent.2016.03.009. [DOI] [PubMed] [Google Scholar]
- 24.Wiegand A, Burkhard JP, Eggmann F, Attin T. Brushing force of manual and sonic toothbrushes affects dental hard tissue abrasion. Clin Oral Investig. 2013;17:815–22. doi: 10.1007/s00784-012-0788-z. [DOI] [PubMed] [Google Scholar]
- 25.Turssi CP, de Magalhaes CS, Serra MC, Rodrigues Junior AL. Surface roughness assessment of resin-based materials during brushing preceded by pH-cycling simulations. Oper Dent. 2001;26:576–84. [PubMed] [Google Scholar]
- 26.Ablal MA, Kaur JS, Cooper L, Jarad FD, Milosevic A, Higham SM. The erosive potential of some alcopops using bovine enamel: an in vitro study. J Dent. 2009;37:835–9. doi: 10.1016/j.jdent.2009.06.016. [DOI] [PubMed] [Google Scholar]
- 27.Bansal K, Acharya SR, Saraswathi V. Effect of alcoholic and non-alcoholic beverages on color stability and surface roughness of resin composites: an in vitro study. J Conserv Dent. 2012;15:283–8. doi: 10.4103/0972-0707.97961. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.de Moraes Porto IC, das Neves LE, de Souza CK, Parolia A, Barbosa dos Santos N. A comparative effect of mouthwashes with different alcohol concentrations on surface hardness, sorption and solubility of composite resins. Oral Health Dent Manag. 2014;13:502–6. [PubMed] [Google Scholar]
- 29.Soares LE, Nahorny S, Martin AA. FT-Raman spectroscopy study of organic matrix degradation in nanofilled resin composite. Microsc Microanal. 2013;19:327–34. doi: 10.1017/S1431927612014225. [DOI] [PubMed] [Google Scholar]
- 30.Erdemir U, Yildiz E, Eren MM, Ozel S. Surface hardness of different restorative materials after long-term immersion in sports and energy drinks. Dent Mater J. 2012;31:729–36. doi: 10.4012/dmj.2012-054. [DOI] [PubMed] [Google Scholar]