1http://dx.doi.org/10.20396/bjos.v20i00.8663736 Volume 20 2021 e213736 Original Article 1 Departamento of Dentistry, Federal University of Rio Grande do Norte (UFRN), Natal/RN, Brazil. 2 University of West Paulista (UNOESTE), São Paulo/SP, Brazil. Corresponding author: Ruthineia Diógenes Alves Uchôa Lins Federal University of Rio Grande do Norte – Departamento of Dentistry - Av. Sen. Salgado Filho, 1787 – Lagoa Nova, 59056-000 – Natal – Brazil. Phone: +55 84 32154100 – Mobile: +55 84 994013056 Email: aruthineia@gmail.com Editor: Dr Altair A. Del Bel Cury Received: December 24, 2020 Accepted: March 22, 2021 Effect of Spondias mombin L. extract on the wettability, roughness, color and morphology of bovine enamel Franciara Maria Gomes Alves1 , Thaís Oliveira Cordeiro1 , Ana Margarida dos Santos Melo1 , Larissa Sgarbosa de Araújo Matuda2 , Daniela Lopes da Silva Amorieli2 , Joselucia da Nóbrega Dias1 , Boniek Castillo Dutra Borges1 , Ruthineia Diógenes Alves Uchôa Lins1,* Although Spondias mombin L. extract has an excellent antimicrobial effect against oral microorganisms, it should be clarified how it affects enamel surface properties. Aim: To evaluate the color change, wettability/contact angle, surface roughness and morphology of bovine enamel submitted to the Spondias mombin L. extract. Methods: Thirty bovine teeth were distributed into the following groups: 0.12% chlorhexidine digluconate, 1:32 Spondias mombin L. extract and distilled water. Color change (CC) was evaluated after immerging specimens into the solutions for 14 days. Surface roughness (Ra) was measured using a roughness meter; wettability/contact angles (CA) were determined by the sessile drop method, and scanning electron microscopy images were obtained to characterize the morphology (SMA). The pH of the solutions was evaluated using a pHmeter. The Ra, CA, and CC data were parametric (Kolmogorov-Smirnov; p>0.05). Two-way ANOVA (for Ra and CA) and one-way ANOVA (for CC) with Tukey’s posthoc tests at a significance level of 5% were used. SMA was analyzed descriptively. Results: The Spondias mombin L. extract revealed an acidic pH, and when in contact with the bovine teeth, it increased the wettability, but it did not cause statistically significant differences in the Ra. Spondias mombin L. extract caused the highest color change. The SEM images showed differences in the specimens’ surface submitted to the extract compared to the other groups. Conclusion: Spondias mombin L. extract provided negative effects on bovine enamel’s surface, including a high color change and a more wettable substrate. Keywords: Phytotherapy. Anacardiaceae. Mouthwashes. Dental enamel. Surface properties. https://orcid.org/0000-0001-9529-4694 https://orcid.org/0000-0003-0078-715X https://orcid.org/0000-0001-7234-226X https://orcid.org/0000-0002-9033-9029 https://orcid.org/0000-0001-9755-0807 https://orcid.org/0000-0002-0435-2869 https://orcid.org/0000-0003-4313-5776 https://orcid.org/0000-0002-0047-5976 2 Alves et al. Introduction Clinical evidence shows that dental biofilm control is essential in preventive dentistry and directly reflects individuals’ oral health. The materials used for this purpose in dentistry attempt to maintain the dental surface’s natural properties, including mineral composition, hardness, smoothness, translucency and low surface free energy/wet- tability1-3. The use of mouthwashes, along with the mechanical control of the biofilm, has also shown substantial ability to prevent biofilm from growing. Although 0.12% chlorhexidine digluconate is considered the gold standard in mouthwash, it promotes adverse effects such as staining of teeth, changes in gustation, and irritation of the mucosa1,4,5. Therefore, there is a need for scientific studies that evaluate herbal med- icines’ potential as an alternative of interest for future use in the control of dental biofilm, preventing and treating oral biofilm diseases6. The species Spondias mombin has been gaining notoriety among the currently stud- ied plant extracts. In Brazil, this plant is mainly found in the North and Northeast regions. However, this species is also found in several parts of the world, such as Peru, Venezuela, Bolivia, Mexico, and western India7. Its leaves present, among other characteristics, components with antimicrobial and antioxidant properties, such as flavonoids, saponins, tannins, and phenolic compounds - those last ones are also associated with antiviral and antitumor activities8. Those phytochemicals have been constantly associated with effects against oral microorganisms, including Strepto- coccus mutans. A recent study showed that the hydroethanolic extract of Spondias mombin L. has an antimicrobial activity similar to Chlorhexidine 0.12% against oral bacteria of the genus Streptococcus, also showing an anti-adherent effect on Strep- tococcus mutans9. Besides, anti-inflammatory effects and properties arising from the extract of Spondias mombin L., associated mainly with the tannin components, have also been observed6,10-16. In light of this knowledge, this in vitro study aimed to evaluate the effect of the Spon- dias mombin L. extract on the wettability, color change, surface roughness and mor- phology of bovine enamel compared with 0.12% chlorhexidine digluconate and dis- tilled water. The null hypothesis tested was that there would be no differences among the solutions concerning all properties analyzed. Methods Specimens’ preparation Specimens of bovine teeth (n=30) collected from the Nellore animal breed with a mean age of 36 months were used from the meat industry. Fractured and irregular teeth were excluded after visual inspection. Initially, the bovine teeth were cleaned with pumice and water, with the aid of a rubber cup in a slow-speed handpiece and stored in distilled water. Subsequently, a transversal section was made, dividing the root and coronal portions, 2mm below the cementoenamel junction, having as reference the labial surface. The crowns were separated from the roots using a dia- mond disc (KG Sorensen, Cotia, SP, Brazil) in a straight handpiece. It was then made 3 Alves et al. longitudinal sections in the mesial, distal, and incisal surfaces, obtaining specimens (10mm x 10mm) from the labial enamel’s flatter part. Specimens with cracks were excluded17. Finally, the specimens were stored in distilled water at room tempera- ture until the moment of the immersion protocol. Obtaining the Spondias mombin L. extract The sample of the collected raw vegetable material was deposited in the UFRN her- barium and identified by a botanist, with the number of exsiccate 12252. Spondias mombin’s collected leaves were dried at room temperature for two weeks. From 100 g of the Spondias mombin L., an extract was prepared by maceration, leaving it in con- tact with ethanol and distilled water (80:20, v/v) for seven days and subsequent lyo- philization. After this period, the hydroethanolic extract was filtered, and the organic solvent was eliminated in a rotatory evaporator (TE210, Tecnal, Piracicaba, Brazil) under a vacuum at 45° C. The hydroethanolic extract of Spondias mombin L. used in this research had a 1:32 dilution = 31.25 (mg/mL). This concentration was defined based on Lima et al.8 (2017), which found that Spondias mombin L. extract showed antimicrobial activity superior to 0.12% chlorhexidine digluconate only from that concentration. Determination of pH Ten mL of the tested solutions were analyzed in a pH meter (LUCA-210-E, LUCADEMA, São José do Rio Preto, Brazil), calibrated with phosphate and acetate buffer solutions, pH 7.0 and 4.0, respectively, at 25° C. After the extract preparation, the solutions were performed in triplicate. The pH of distilled water, 0.12% chlorhexidine digluconate, and Spondias mombin L. extract were, respectively, 7.0, 6.5, and 2.96. Immersion protocol and analyzed variables The specimens (n=30) were randomly allocated into 3 groups: CLX - 0.12% chlor- hexidine digluconate (n=10); DW - distilled water (n=10); and DE - diluted Spondias mombin L. extract (n=10). The following dependent variables were tested: wetta- bility/contact angles (CA), surface roughness (Ra), color change (CC) and surface micromorphology (SMF). For CA and Ra, solution (CLX, DW, and DE) and time (24 h and 14 days) were the independent variables. For CC and SMF, solution was the independent variable. Figure 1 presents a schematic representation of the methods. The immersion protocol used for all solutions followed the CLX manufacturer’s (Periomax©, Iodontosul, Porto Alegre, RX, Brazil). Each specimen was positioned individually inside a flask containing 10mL of the specific solution, which was disturbed for 1min twice a day, with 12 hours intervals, for 14 days. In the inter- val between immersions, the specimens were stored in 1.5mL of artificial saliva (Farmafórmula, Natal, Brazil. Composition: Single syrup [Nipagin, Nipazol, Sugar, Water] - 20%; Glycerin - 10%; Carboxymethyl Cellulose Gel [CMC] - 2.5 to 8%; Cherry Flavorant - 0.1%. pH = 7.0)17,18. The solutions and artificial saliva were renewed after each sample submission period. Then, the specimens were dried at room tempera- ture for 24 hours before the analyses4. 4 Alves et al. 10 mm 10 mm DW group (n=10) CLX group (n=10) DE group (n=10) Measurement of the PH of the solutions 14 days Drying in oven at 37° 24 hours Final analysis: Surface roughness Wettability Colour stability SEM Initial analysis: Surface roughness Wettability Colour stability Distilled water, room temperature Immersion in DW, CLX, DE 10ml, 1 min, 2x/day Storage in artificial saliva 15ml, 12 hours Figure 1. Schematic representation of the methods. Wettability/contact angles Adapting the protocol described by Costa et al.19 (2018), the wettability was evaluated using the sessile drop method. The contact angle between the dental surface and the liquid was determined. A drop of distilled water (5 μl) was released on the specimens’ surface with the aid of an automatic micropipette over a distance of 20mm, in front of a photographic camera. The surface was positioned in the central and perpendicular part of the lens. The images were captured at a distance of 30cm, 5s after the drop was dumped. Subsequently, the contact angle was measured using the Surftens 4.7 Automatic software (OEG GmbH, Frankfurt, Oder, Germany), adapting its settings for “distilled water” and “4 (four) point analysis”. Each image was analyzed in triplicate, and an average was obtained. Surface roughness assessment (Ra) For Ra analysis, the Hommel Etamic W10 roughness meter (JENOPTIK Industrial Metrology Germany GmbH, Germany) was used, equipped with a diamond needle with a radius of 2 mm. The needle was moved at a constant speed of 0.5 mm/s with a load of 0.7 mN. The cut-off value was set at 0.25 mm. The average surface roughness (Ra) of different locations (parallel, oblique and perpendicular) was obtained20,21. Color change analysis (CC) To determinate the CC, the specimens’ color was assessed at baseline (T0) and after 14 days (T14) of immersion in each solution. Four measurements were performed on enamel using a digital spectrophotometer (EasyShade, VitaZahnfabrik, Bad Säckingen, Germany), and an average value was obtained. The data recorded by the colorimeter were used to calculate the CIEDE2000 color change (ΔE00) according to the following equation: 5 Alves et al. ΔE00 = + + RT+ 1/2 ΔL’ KLSL ΔC’ KCSC ΔH’ KHSH ΔC’ KCSC ΔH’ KHSH The values of ΔL’, ΔC’, and ΔH’ are the differences in lightness, chroma, and hue between T14 and T0. SL, SC, and SH are the weighting functions for the lightness, chroma, and hue components, respectively. KL, KC, and KH are the parametric factors to be adjusted according to different viewing parameters. In this study, KL, KC, and KH were set to 1. Color change considering T14-T0 was obtained with 50:50% perceptibility (PT = 0.81 ΔE00 units) and 50:50% acceptability (AT = 1.77 ΔE00 units) thresholds22,23. Surface Microorphology Analysis (SMA) For the SMS, three specimens of each group were randomly selected (n=3) at T14. After 24h dry, the specimens were gold-sputtered, and images were recorded through a Scanning Electron Microscope (SEM-FEG, Zeiss Gemini, Germany). Images with 2000X magnification in the center of the sample were obtained and descriptively analyzed19. Statistical analysis Data analyses were performed through the Statistical Package for Social Sciences software (SPSS - IBM SPSS Statistics Subscription, version 25). The normality of the data was verified using the Kolmogorov-Smirnov test (p>0.05). The descrip- tive analysis presented the mean and standard deviation. The CA and RA were analyzed using two-way ANOVA/Tukey posthoc tests (solution versus time). For CC, one-way ANOVA/Tukey posthoc tests were used. The level of significance was set at 95% (p<0.05). The photomicrographs of the surface morphology were eval- uated qualitatively. Results Wettability/Contact angles (CA) There were statistically significant differences among solutions (p>0.01), times (p<0.01) and in the interaction of solutions versus times (p<0.01). Multiple compari- sons are shown in Table 1. Regardless of the time, DE showed statistically decreased contact angles than DW and CLX. Only DE provided statistically lower contact angles at T14 compared to T0. Table 1. Mean (standard deviation) of the contact angles according to the solution and time tested in this study. Solution Time Baseline (T0) 14 days (T14) Distilled water (DW) 53.81 (3.46) Aa* 48.36 (3.17) Aa 0.12% chlorhexidine digloconate (CLX) 56.86 (4.39) Aa 54.95 (4.78) Aa Spondias mombin L. extract (DE) 51.36 (3.68) Ba 39.26 (4.90) Bb *Different capital letters reveal statistically significant differences among the solutions for the same time (p<0.05). Different lowercase letters reveal statistically significant differences between times for the same solution (p<0.05). 6 Alves et al. Surface roughness (RA) There were no statistically significant differences among solutions neither between times (p>0.05). Table 2 presents detailed Ra values. Table 2. Mean (standard deviation) of surface roughness (μm) according to the solution and time tested. Solution Time Baseline (T0) 14 days (T14) Distilled water (DW) 2.12 (0.91) Aa* 1.55 (0.87) Aa 0.12% chlorhexidine digloconate (CLX) 2.04 (1.04) Aa 2.23 (0.91) Aa Spondias mombin L. extract (DE) 2.36 (0.82) Aa 1.65 (0.41) Aa *Different capital letters reveal statistically significant differences among the solutions for the same time (p<0.05). Different lowercase letters reveal statistically significant differences between times for the same solution (p<0.05). Color change (CC) There were statistically significant differences among the solutions (p<0.01). Multiple comparisons are shown in Table 3. DE showed a statistically higher CC than DW and CLX. Only DE presented ΔE00 units higher than the perceptibility (0.81) and accept- ability (1.77) thresholds. Table 4. Mean (standard deviation) of the color change (ΔE00) according to the solution tested. Solution Distilled water (DW) 0.12% chlorhexidine digluconate (CLX) Spondias mombin L. extract (DE) 0.74 (0.14) b* 0.79 (0.38) b (1.89) a *Different lowercase letters reveal statistically significant differences among the solutions (p <0.05). Surface micromorphology (SMA) The images obtained (Figure 2) point that exposition to CLX promoted mineral-like precipitation compared with DW. However, specimens exposed to the DE showed characteristics of enamel dissolution. DW CLX DE 2 µm EHT = 3.00 kV WD = 5.1 mm Mag = 2.00 K X Pixel Size = 57.29 nm Signal A = InLens Photo No. = 3307 Date: 23 Apr 2019 Time: 20:37:52 2 µm EHT = 5.00 kV WD = 7.4 mm Mag = 2.00 K X Pixel Size = 57.29 nm Signal A = InLens Photo No. = 3200 Date: 17 Apr 2019 Time: 15:06:55 2 µm EHT = 5.00 kV WD = 9.5 mm Mag = 2.00 K X Pixel Size = 57.29 nm Signal A = InLens Photo No. = 3224 Date: 17 Apr 2019 Time: 16:22:38 Figure 2. Scanning electron microscopy images of specimens exposed to distilled water (DW), 0.12% chlorhexidine digluconate (CLX), and Spondias mombin L. extract (DE). Mineral-like precipitation was observed in specimens exposed to CLX (arrows), while enamel dissolution was perceived in specimens exposed to DE (arrows). 7 Alves et al. Discussion The null hypothesis tested in this experiment - that there would be no differences among the solutions concerning all properties analyzed - was rejected since expo- sition to the Spondias mombin L. extract promoted enamel color and micromor- phology changes. Although the SEM images demonstrated possible changes in the specimens’ surface from the Spondias mombin L. extract group, the surface roughness before and after immersion protocol did not indicate statistically significant changes in any of the groups. According to Field et al.24 (2013), the assessment of surface roughness may not provide details on the surface texture, wear resistance and the ability to retain liquids, limiting this type of analysis. However, the analysis of surface roughness can indicate possible changes in the dental structure, especially when associated with other variables’ analysis25. It is likely that an acidic pH presented by the Spondias mombin L. extract caused enamel dissolution and changes on enamel topography (Figure 2DE), which were not detected employing the roughness test. Dantas et al.26 (2015) defined wettability as the liquid’s ability to wet a solid, exempli- fying it as a drop of liquid resting on a solid surface which the liquid may or may not spread. Water is a polar liquid that tends to spread over a surface with high surface energy and form a drop in areas with low energy. Regarding surface wettability, the contact angle data indicate that the dental enamel has undergone significant changes when exposed to the extract of Spondias mombin L. A decrease in the contact angle was observed, which suggests an increase in the free surface energy and, conse- quently, in wettability. According to Luz et al.27 (2008), the two main factors that can affect the wetting behav- ior of a solid by a liquid are: topographic inhomogeneity, caused by surface roughness or porosity and chemical inhomogeneity, caused by the presence of contaminants on the solid surface. Likely, the acidic pH of the Spondias mombin L. extract promoted enamel dissolution, increasing porosity (Figure 2) and wettability. Regarding color change, the specimens submitted to the Spondias mombin L. extract presented the highest color change compared to distilled water and 0.12% chlorhex- idine digluconate. Since this extract has a brown color, an acidic pH, and contains alcohol, it presents greater potential to cause specimens darkness23,28. Comparatively, the CLX group showed no clinically noticeable color changes. How- ever, chromatic changes on the dental surface exposed to CLX are related to its ability to precipitate pigments on the dental surface, whether from drinks or food1,29,30. The fact that the present study did not establish a contact of specimens with any drink or food may explain this result. Therefore, before clinical use of the Spondias mombin leaf extract, their dark color and acidic pH should be modified to avoid enamel dam- age and darkening. As this work involved bovine enamel as the first substitute from human enamel, fur- ther investigations should perform similar evaluations using human enamel. Finally, it is worth mentioning that one of the limitations of in vitro studies is the reproduc- tion of real conditions. Even when it is conducted as close as possible to a clinical 8 Alves et al. situation, laboratory conditions do not reproduce exact oral conditions, known for their extreme complexity. Thus, further clinical trials should be designed to investigate the interaction between Spondias mombin L. extract and oral tissues. Conclusion The Spondias mombin L. extract altered the micromorphology, promoted color change and a more wettable bovine enamel surface. Acknowledgements We are grateful to the Departments of Materials Engineering and Pharmacy at the Universidade Federal do Rio Grande do Norte to support the production of extract and SEM analysis, respectively. References 1. Zanatta FB, Antoniazzi RP, Rösing CK. Staining and calculus formation after 0.12% chlorhexidine rinses in plaque-free and plaque covered surfaces: a randomized trial. J Appl Oral Sci. 2010 Sep- Oct;18(5):515-21. doi: 10.1590/s1678-77572010000500015. 2. Rodrigues JA, Lussi A, Seemann R, Neuhaus KW. 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