Mechanical and Physical Properties of an Experimental Chemically and Green-Nano Improved Dental Alginate after Proven Antimicrobial Potentials

Objectives: Impression materials could be a source of cross-contamination due to the presence of microorganisms from blood and saliva inside the oral cavity. Nevertheless, routinely performed post-setting disinfection could compromise the dimensional accuracy and other mechanical properties of alginates. Thus, this study aimed to evaluate detail reproduction, dimensional accuracy, tear strength, and elastic recovery of new experimentally prepared self-disinfecting dental alginates. Methods: Two antimicrobial-modified dental alginate groups were prepared by mixing alginate powder with 0.2% silver nitrate (AgNO3 group) and a 0.2% chlorohexidine solution (CHX group) instead of pure water. Moreover, a third modified group was examined by the extraction of Boswellia sacra (BS) oleoresin using water. The extract was used to reduce silver nitrate to form silver nanoparticles (AgNPs), and the mixture was used as well in dental alginate preparation (BS + AgNP group). Dimensional accuracy and detail reproduction were examined as per the ISO 1563 standard guidelines. Specimens were prepared using a metallic mold engraved with three parallel vertical lines 20, 50, and 75 µm wide. Detail reproduction was evaluated by checking the reproducibility of the 50 µm line using a light microscope. Dimensional accuracy was assessed by measuring the change in length between defined reference points. Elastic recovery was measured according to ISO 1563:1990, in which specimens were gradually loaded and then the load was released to allow for recovery from the deformation. Tear strength was evaluated using a material testing machine until failure at a crosshead speed of 500 mm/min. Results: The recorded dimensional changes between all tested groups were insignificantly different and within the reported acceptable values (between 0.037–0.067 mm). For tear strength, there were statistically significant differences between all tested groups. Groups modified with CHX (1.17 ± 0.26 N/mm) and BS + AgNPs (1.11 ± 0.24 N/mm) showed higher tear strength values compared to the control (0.86 ± 0.23 N/mm) but were insignificant from AgNO3 (0.94 ± 0.17 N/mm). All tested groups showed elastic recovery values that met both the ISO standard and ADA specifications for elastic impression materials and tear strength values within the acceptable documented ranges. Discussion: The CHX, silver nitrate, and green-synthesized silver nanoparticles could be promising, inexpensive alternatives for the preparation of a self-disinfecting alginate impression material without affecting its performance. Green synthesis of metal nanoparticles could be a very safe, efficient, and nontoxic method, with the advantage of having a synergistic effect between metal ions and active chemical constituents of plant extracts.


Introduction
Alginates were originally developed in the 1930s, and they are among the regularly used dental materials in every dental practice for making diagnostic casts and digital models [1]. Alginates are available in the form of powder, which undergoes polymerization Gels 2023, 9,429 3 of 12 eliminating pathogens without negatively affecting the properties of the impression. The challenges associated with disinfecting irreversible hydrocolloids due to imbibition and syneresis have raised our interest in developing self-disinfecting dental alginate by mixing the powder with 0.2% CHX and 0.2% AgNO 3 (CHX group and AgNO 3 group). In addition, a Boswellia sacra plant extract was used in the green synthesis of AgNPs, and the mixture was used as well for the preparation of a third modified alginate group.
In our former study, UV-visible (UV-vis) spectroscopy, scanning electron microscopy (SEM), and energy-dispersive X-ray analysis (EDX) confirmed the biosynthesis of Ag-NPs using the Boswellia sacra extract in a simple, inexpensive, and ecologically friendly way. The chemical analysis of the Boswellia sacra (BS) extract revealed the presence of 41 different organic compounds that acted as reducing and stabilizing agents for the green synthesis of AgNPs. Moreover, the groups modified with CHX, AgNO 3 , and the BS + AgNPs showed significantly enhanced antimicrobial activity compared to the control against Candida albicans (C. albicans), Streptococcus mutans (S. mutans), Escherichia coli (E. coli), methicillin-resistant Staphylococcus aureus (MRSA), Staphylococcus aureus (S. aureus), and Micrococcus luteus (M. luteus), whereas the BS + AgNPs and CHX groups were significantly different against almost all strains, in which the CHX-modified alginate reported significantly higher results, except for with MRSA and E. coli [22,23].
Therefore, based on these findings and the fact that the green synthesis of metal nanoparticles using the Boswellia sacra extract showed promising synergistic antimicrobial effects between metal ions and the phytotherapeutic agents of the plant extract, this study aimed to assess the impact of these self-disinfection modifications of alginate on detail reproduction, dimensional changes, tear strength, and elastic recovery.

Detail Reproduction
Only the 50 and 75 µm lines were reproduced in all tested groups, while the 20 µm line did not appear in almost all specimens. As per the ISO 1563 criterion, which assesses the ability of alginate impression material to reproduce the entire length of the 50 µm line, all the specimens passed the test (100% score 1, 0% score 0).

Dimensional Accuracy
Data showed parametric distribution, and thus, the mean and standard deviation values of the dimensional changes of the tested materials are represented in Figures 1 and 2. The results indicated that the mean dimensional changes in mm were −0.038 ± 0.051 (AgNO 3 ), −0.067 ± 0.036 (BS + AgNPs), −0.042 ± 0.046 (CHX), and −0.033 ± 0.054 (control) for the vertical dimension, whereas the mean values in the horizontal dimension were −0.048 ± 0.052, −0.051 ± 0.022, −0.043 ± 0.077, and −0.037 ± 0.038 for AgNO 3 , BS + AgNPs, CHX, and control, respectively. The results showed a statistically nonsignificant difference in dimensional changes between the four tested materials in the X (p-value = 0.619) and Y (p-value = 0.958) axes.

Tear Strength
One-way ANOVA followed by Tukey's post hoc test for pairwise comparison was used to compare the three different groups. Tear strength means and standard deviation values in N/mm are illustrated in Figure 3. The results revealed that there was a statistically significant difference between the tear strength of the tested materials (p-value = 0.002). Bs + AgNPs, AgNO 3 , and CHX showed comparable and significantly highest mean tear strengths of 1.11 ± 0.24 N/mm, 0.94 ± 0.17 N/mm, and 1.17 ± 0.26 N/mm, respectively. The control (0.86 ± 0.23 N/mm) was insignificantly different from AgNO 3 but was significantly lower than CHX and BS + AgNPs.

Tear Strength
One-way ANOVA followed by Tukey's post hoc test for pairwise comparison wa used to compare the three different groups. Tear strength means and standard deviation values in N/mm are illustrated in Figure 3. The results revealed that there was a statisti cally significant difference between the tear strength of the tested materials (p-value = 0.002). Bs + AgNPs, AgNO3, and CHX showed comparable and significantly highest mean tear strengths of 1.11 ± 0.24 N/mm, 0.94 ± 0.17 N/mm, and 1.17 ± 0.26 N/mm, respectively The control (0.86 ± 0.23 N/mm) was insignificantly different from AgNO3 but was signifi  Interval plot illustrating the mean dimensional changes in millimeters in the horizonta dimension and 95% confidence interval of all tested groups.

Tear Strength
One-way ANOVA followed by Tukey's post hoc test for pairwise comparison wa used to compare the three different groups. Tear strength means and standard deviation values in N/mm are illustrated in Figure 3. The results revealed that there was a statisti cally significant difference between the tear strength of the tested materials (p-value = 0.002). Bs + AgNPs, AgNO3, and CHX showed comparable and significantly highest mean tear strengths of 1.11 ± 0.24 N/mm, 0.94 ± 0.17 N/mm, and 1.17 ± 0.26 N/mm, respectively The control (0.86 ± 0.23 N/mm) was insignificantly different from AgNO3 but was signifi

Elastic Recovery
The means and standard deviations of percentage recovery from deformation are represented in Figure 4. A one-way analysis of variance (ANOVA) indicated that there was a statistically significant difference in the elastic recovery of the four tested groups (pvalue = 0.001). The AgNO3 group had a mean elastic recovery of 98.0% ± 0.3, which was insignificantly different from the BS + AgNPs (97.8% ± 0.8) and CHX (97.7% ± 0.7). The three modified groups were significantly higher than the control (96.9% ± 0.5).

Elastic Recovery
The means and standard deviations of percentage recovery from deformation are represented in Figure 4. A one-way analysis of variance (ANOVA) indicated that there was a statistically significant difference in the elastic recovery of the four tested groups (p-value = 0.001). The AgNO 3 group had a mean elastic recovery of 98.0% ± 0.3, which was insignificantly different from the BS + AgNPs (97.8% ± 0.8) and CHX (97.7% ± 0.7). The three modified groups were significantly higher than the control (96.9% ± 0.5).

Elastic Recovery
The means and standard deviations of percentage recovery from deformation are represented in Figure 4. A one-way analysis of variance (ANOVA) indicated that there was a statistically significant difference in the elastic recovery of the four tested groups (pvalue = 0.001). The AgNO3 group had a mean elastic recovery of 98.0% ± 0.3, which was insignificantly different from the BS + AgNPs (97.8% ± 0.8) and CHX (97.7% ± 0.7). The three modified groups were significantly higher than the control (96.9% ± 0.5).

Discussion
The present study was conducted on alginate hydrocolloid impression material, as it is a widely used dental material due to its attractive properties, such as acceptable detail reproduction, ease of manipulation, and low cost [1]. Disinfection of alginate impressions is a mandatory step to cease the spread of infectious diseases. Spraying and immersion techniques currently used for the disinfection of impression materials are far from ideal in alginate cases. Therefore, in the present study, some properties of alginate mixed with different disinfectant liquids instead of pure water were tested (CHX, AgNO 3 , and Boswellia sacra extract mixed with green-synthesized silver nanoparticles).
The antimicrobial activity of the modified groups was tested in our previous study using agar diffusion assays against S. aureus, methicillin-sensitive and resistant; S. mutans; M. luteus (four Gram-positive strains); one Gram-negative bacterium (E. coli); and a yeast (C. albicans). The results showed that CHX, AgNO 3 , and BS + AgNP groups were significantly more active than the control group against all tested strains. On the other hand, the antimicrobial activity of BS + AgNPs was comparable to the CHX group against C. albicans and MRSA. In addition, CHX was significantly more active compared to the other tested groups against S. mutans, S. aureus, E. coli, and M. luteus. Therefore, this study aimed to understand the impact of this new approach on the physical and mechanical properties after already exhibiting a profound antimicrobial efficacy [23].
Impression materials should have sufficient flow during impression taking to precisely replicate details of soft and hard oral tissue; consequently, it is crucial to have an optimum low viscosity [24]. The results of detail reproduction showed that all the specimens met the ISO requirement of recording the entire length of the 50 µm line. This may be attributed to the sufficient flow and the non-altered viscosity of the alginate impression before gelation even with the use of different mixing solutions other than pure water [24]. The results were in agreement with Omidkhoda et al. [25], who showed that adding silver nanoparticles to alginate for self-disinfection did not compromise the surface detail reproduction and flow properties.
The American Dental Association's specification number 18 and the International Organization for Standardization's 1563:1990, which are concerned explicitly with dental alginate, have neither specific requirements nor any limits on dimensional change values [26,27]. Dimensional accuracy measurements of alginate can be performed using several methods, including digital calipers, micrometers, dial gauges, and microscopes [28]. In this study, an optical microscope was used due to its high precision (0.0005 mm) to calculate the extent of dimensional changes after mixing alginate powder with three different antiseptic solutions (0.2% CHX, 0.2% AgNO 3 , and BS + AgNPs).
It has been reported that a range between 0.027-and 0.083-mm marginal discrepancy and/or a maximum value of 0.050 mm for a single unit is considered clinically acceptable for the fabrication of most indirect restorations [29,30]. Auspiciously, the results obtained in the vertical (between 0.038 and 0.067 mm) and horizontal dimensions (between 0.048 and 0.051 mm) for all tested groups were within the reported values and with no significant differences among all tested groups. This is in agreement with Mathew et al. [31] and Ismail et al. [32], who modified alginate material with hydrogen peroxide and povidone (PVP) iodine powder and found no changes in the dimensional accuracy of the tested groups.
The dimensional deviation between the metallic mold and alginate specimens was almost insignificantly different between all groups in the X and Y axes. The results obtained were negative for all the tested groups in the vertical and horizontal dimensions. Based on the findings, it could be hypothesized that CHX, Ag, and AgNPs consumed part of the mixing water ratio, which is crucial for the dissolution of the calcium sulfate reactor [33]. Dissolution of this reactor is important for the release of calcium ions that replace either the sodium or the potassium ions of the alginate to form an insoluble calcium alginate gel [34,35]. It was found that a reduction in the concentration of calcium ions increases the swelling capability of alginate beads and consequently causes the expansion of the material [36]. The tear strength of dental alginate is very important to be considered in areas with undercuts or insufficient thickness to resist tearing [37]. There is no defined protocol or specified values for the tear strength of impression materials in the ISO standard 1563 [27] or specification no. 18 of ANSI/ADA [26,38,39]. Tear strength evaluation in this study was performed using V-shaped specimens with a thickness of 4 mm to be similar to the clinically recommended thickness of the alginate impressions (4 to 6 mm range) [40].
The significantly higher elastic recovery and improved tear strength could be due to the presence of CHX ions, Ag ions, and silver nanoparticles that may have acted as filler particles and improved the mechanical properties. It has been hypothesized that tear strength and elastic recovery could be affected by certain factors, including the degree of cross-linking of the set alginate [43]. Moreover, a slight reduction in water amount could result in a material with a strong matrix and more tear resistance. This may be due to the role of water as a plasticizer and the presence of excess ions that can cross-link alginic chains more effectively; as a result, the final strength and elastic modulus could be improved while the setting time could be shortened [44]. This is in agreement with Fayez et al. 2016 [39] and Zarb et al. [45], who stated that any modifications of the given powder-liquid ratio, mixing technique, and filler content could result in alterations in the properties of the gel, tear energy, and elastic recovery. Several researchers also investigated the antimicrobial efficacy of metal oxide nanoparticles incorporated into alginate impression materials. They reported that these nanoparticles could be considered effective self-disinfecting agents for alginate impression materials with no adverse effect on the physical and mechanical properties [46,47].
One of the limitations of this study was that the impressions were taken with a standardized stainless-steel mold that does not fully resemble the behavior of the oral tissues, with regard to fluid absorption and the intrinsic free energy of teeth and oral soft tissues. Moreover, a future setup to examine the ability of alginate to flow and record fine details in the presence of saliva is currently being designed.

Conclusions
Within the framework of our former work and this study, CHX, AgNO 3, and BS + Ag-NPs could be considered promising additives for effective self-disinfecting alginate without compromising its physical and mechanical properties. Detail reproduction and accuracy of alginate were not negatively impacted by the different self-disinfection modifications. Elastic recovery was improved by the addition of CHX, AgNO 3, and BS + AgNPs. In addition, all groups were within the acceptable range for tear strength, with CHX and BS + AgNPs showing significantly higher tear strength values compared to the control group. Future work involving different concentrations of several metal ions and B. sacra is planned with testing their effect on the stability, setting time, hydrophilicity, and flow of alginate.

Methods
Control dental alginate and three modified antiseptic solutions were prepared to be used for mixing alginate instead of normal distilled water as follows: BS + AgNP group:Boswellia sacra (BS) resin was washed, dried, and frozen at −16 • C overnight to facilitate the grinding of the resin into a fine powder without being softened inside the blender. Afterward, the powder was soaked in distilled water for 3 days, filtered using Whatman's paper 1, and stored at 4 • C until usage. For preparation and reduction of the silver nanoparticles (AgNPs), a given amount of the above extract was added to 60 mL of 0.2% AgNO 3 solution and stirred at a speed of 800 rpm. The mixture was incubated for 3 days at room temperature in the darkness with the solution color turning from white to dark brown, signifying the formation of AgNPs. 0.2% CHX group: An amount of 2 gm of chlorohexidine powder was added to 1000 mL distilled water and vortexed for 15 min until complete dissolution of the powder in the water. 0.2% AgNO 3 group: An amount of 2 gm of 99% silver nitrate powder was added to 1000 mL of distilled water and mixed using a vortex mixer for several minutes.
Control group: Pure distilled water was used for alginate preparation without any additives.

Detail Reproduction and Dimensional Accuracy
Surface detail reproduction of alginate impression materials was determined according to ISO specification 1563 but with a slight modification of the specified metallic mold to allow measurements of the dimensional accuracy in the X and Y axes [27]. A stainless-steel mold was used, which was engraved with three vertical orientation lines (20, 50, and 75 µm depth and 25 mm length, Figure 5) and two horizontal lines. For detail reproduction assessment, the different alginate groups were prepared and placed inside the mold, and then covered with a metal plate with 1 kg weight on top to simulate the impression-taking process and allow for the outflow of excess material. After gelation, the surface of each specimen (n = 6 for each group) was examined using a stereomicroscope (Wild Lecia M8, Heerbrugg, Switzerland) at 10× magnification. Detail reproduction was examined according to the ISO specification number 1563, in which the alginate impression materials had to reproduce the full length of the 50 µm line over the full 25 mm length. A score of one was set to a line that was fully and continuously reproduced, and otherwise, a zero score was given.

Methods
Control dental alginate and three modified antiseptic solutions were prepared to be used for mixing alginate instead of normal distilled water as follows: BS + AgNP group: Boswellia sacra (BS) resin was washed, dried, and frozen at −16 °C overnight to facilitate the grinding of the resin into a fine powder without being softened inside the blender. Afterward, the powder was soaked in distilled water for 3 days, filtered using Whatman's paper 1, and stored at 4 °C until usage. For preparation and reduction of the silver nanoparticles (AgNPs), a given amount of the above extract was added to 60 mL of 0.2% AgNO3 solution and stirred at a speed of 800 rpm. The mixture was incubated for 3 days at room temperature in the darkness with the solution color turning from white to dark brown, signifying the formation of AgNPs.
0.2% CHX group: An amount of 2 gm of chlorohexidine powder was added to 1000 mL distilled water and vortexed for 15 min until complete dissolution of the powder in the water. 0.2% AgNO3 group: An amount of 2 gm of 99% silver nitrate powder was added to 1000 mL of distilled water and mixed using a vortex mixer for several minutes.
Control group: Pure distilled water was used for alginate preparation without any additives.

Detail Reproduction and Dimensional Accuracy
Surface detail reproduction of alginate impression materials was determined according to ISO specification 1563 but with a slight modification of the specified metallic mold to allow measurements of the dimensional accuracy in the X and Y axes [27]. A stainlesssteel mold was used, which was engraved with three vertical orientation lines (20, 50, and 75 µm depth and 25 mm length, Figure 5) and two horizontal lines. For detail reproduction assessment, the different alginate groups were prepared and placed inside the mold, and then covered with a metal plate with 1 kg weight on top to simulate the impressiontaking process and allow for the outflow of excess material. After gelation, the surface of each specimen (n = 6 for each group) was examined using a stereomicroscope (Wild Lecia M8, Heerbrugg, Switzerland) at 10× magnification. Detail reproduction was examined according to the ISO specification number 1563, in which the alginate impression materials had to reproduce the full length of the 50 µm line over the full 25 mm length. A score of one was set to a line that was fully and continuously reproduced, and otherwise, a zero score was given.  For dimensional change examination, the samples of the detail reproduction test were photographed using the stereomicroscope (Wild Lecia M8, Heerbrugg, Switzerland) combined with a digital camera (Leica DFC 420 C, Leica Mikrosysteme, Wetzlar, Germany) at 18× magnification. The vertical dimension between reference points (X, X ) and horizontal dimensions between X and Y in each specimen were measured using Leica LAS AF LITE Gels 2023, 9, 429 9 of 12 4.10.0 software ( Figure 6). Dimensional changes were assessed by calculating the difference between reference points of the master model and its replica, shortly after impression making [48]. The value for dimensional change was calculated as an average of three measurements and was recorded to the nearest 0.1 mm.
For dimensional change examination, the samples of the detail reproduction test were photographed using the stereomicroscope (Wild Lecia M8, Heerbrugg, Switzerland) combined with a digital camera (Leica DFC 420 C, Leica Mikrosysteme, Wetzlar, Germany) at 18× magnification. The vertical dimension between reference points (X, X′) and horizontal dimensions between X′ and Y in each specimen were measured using Leica LAS AF LITE 4.10.0 software ( Figure 6). Dimensional changes were assessed by calculating the difference between reference points of the master model and its replica, shortly after impression making [48]. The value for dimensional change was calculated as an average of three measurements and was recorded to the nearest 0.1 mm. Figure 6. Schematic drawing of the stainless-steel analog indicating the lines measured between reference points X-X' (Vertical dimension) and X'-Y (horizontal dimension).

Tear Strength
A tear strength test was performed according to ISO standard 1563:1990 [27] for irreversible hydrocolloid impression materials. A polymeric mold was printed using a 3D printer (Renkforce RF100, Conrad, Hirschau, Germany) with dimensions of 10 cm length, 2 cm width, and 4 mm thickness at the tearing point (Figure 7). The mold was placed over a glass plate and filled with the freshly mixed alginate prepared for each group. The filled mold was then covered with a second glass plate and a weight of 500 gm was added over the top to ensure uniform alginate thickness. After setting, the specimens were inspected for defects, excess material was trimmed, and the thickness of each sample was recorded using a digital caliper (Mitutoyo GmbH, Neuss, Germany). Each specimen was fixed to the grips of a Zwick materials testing machine (Zwick Zmart Pro, ZwickRoell GmbH & Co. KG, Ulm, Germany) and subjected to tensile load at a crosshead speed of 500 mm/minute until rupture. Tear strength was calculated according to the following equation:

Tear strength
Force required for tearing Thickness of sample

Tear Strength
A tear strength test was performed according to ISO standard 1563:1990 [27] for irreversible hydrocolloid impression materials. A polymeric mold was printed using a 3D printer (Renkforce RF100, Conrad, Hirschau, Germany) with dimensions of 10 cm length, 2 cm width, and 4 mm thickness at the tearing point (Figure 7). The mold was placed over a glass plate and filled with the freshly mixed alginate prepared for each group. The filled mold was then covered with a second glass plate and a weight of 500 gm was added over the top to ensure uniform alginate thickness. After setting, the specimens were inspected for defects, excess material was trimmed, and the thickness of each sample was recorded using a digital caliper (Mitutoyo GmbH, Neuss, Germany). Each specimen was fixed to the grips of a Zwick materials testing machine (Zwick Zmart Pro, ZwickRoell GmbH & Co. KG, Ulm, Germany) and subjected to tensile load at a crosshead speed of 500 mm/minute until rupture. Tear strength was calculated according to the following equation: Tear strength = Force required for tearing Thickness of sample For dimensional change examination, the samples of the detail reproduction test were photographed using the stereomicroscope (Wild Lecia M8, Heerbrugg, Switzerland) combined with a digital camera (Leica DFC 420 C, Leica Mikrosysteme, Wetzlar, Germany) at 18× magnification. The vertical dimension between reference points (X, X′) and horizontal dimensions between X′ and Y in each specimen were measured using Leica LAS AF LITE 4.10.0 software ( Figure 6). Dimensional changes were assessed by calculating the difference between reference points of the master model and its replica, shortly after impression making [48]. The value for dimensional change was calculated as an average of three measurements and was recorded to the nearest 0.1 mm. Figure 6. Schematic drawing of the stainless-steel analog indicating the lines measured between reference points X-X' (Vertical dimension) and X'-Y (horizontal dimension).

Tear Strength
A tear strength test was performed according to ISO standard 1563:1990 [27] for irreversible hydrocolloid impression materials. A polymeric mold was printed using a 3D printer (Renkforce RF100, Conrad, Hirschau, Germany) with dimensions of 10 cm length, 2 cm width, and 4 mm thickness at the tearing point (Figure 7). The mold was placed over a glass plate and filled with the freshly mixed alginate prepared for each group. The filled mold was then covered with a second glass plate and a weight of 500 gm was added over the top to ensure uniform alginate thickness. After setting, the specimens were inspected for defects, excess material was trimmed, and the thickness of each sample was recorded using a digital caliper (Mitutoyo GmbH, Neuss, Germany). Each specimen was fixed to the grips of a Zwick materials testing machine (Zwick Zmart Pro, ZwickRoell GmbH & Co. KG, Ulm, Germany) and subjected to tensile load at a crosshead speed of 500 mm/minute until rupture. Tear strength was calculated according to the following equation:

Tear strength
Force required for tearing Thickness of sample

Elastic Recovery
Elastic recovery was evaluated using a split cylindrical mold (20 mm in length and a 12.5 mm interior diameter), surrounded by a fixation ring as recommended by ISO 1563:1990 ( Figure 8) [26]. Alginate powder was mixed with the designated liquid for each group and allowed to set inside the mold (n = 10). After the setting time recommended by the manufacturer, the samples were inspected and measured using a digital caliper by the same practitioner for standardization. A Zwick material testing machine (Zwick Zmart Pro, Zwick Roell GmbH & Co. KG, Ulm, Germany) was used to gradually deform each sample by 20% of the original length (L) for 5 s, and then the samples were gradually unloaded to allow for recovery from the deformation. After 40 s as a recovery time, samples were measured again and the recovery from deformation was calculated as percentages by using the following formula: where L is the original length and ∆L is the length after deformation. Elastic recovery was evaluated using a split cylindrical mold (20 mm in length and a 12.5 mm interior diameter), surrounded by a fixation ring as recommended by ISO 1563:1990 ( Figure 8) [26]. Alginate powder was mixed with the designated liquid for each group and allowed to set inside the mold (n = 10). After the setting time recommended by the manufacturer, the samples were inspected and measured using a digital caliper by the same practitioner for standardization. A Zwick material testing machine (Zwick Zmart Pro, Zwick Roell GmbH & Co. KG, Ulm, Germany) was used to gradually deform each sample by 20% of the original length (L) for 5 s, and then the samples were gradually unloaded to allow for recovery from the deformation. After 40 s as a recovery time, samples were measured again and the recovery from deformation was calculated as percentages by using the following formula: Elastic recovery ΔL L 1 100 where L is the original length and ΔL is the length after deformation.

Statistical Analysis
The Shapiro-Wilk test was used to check normality, and results were presented as mean and standard deviation (SD). All quantitative variables showed parametric distribution; therefore, one-way analysis of variance (ANOVA) was used for comparison between the groups. Tukey's post hoc test was used for pairwise comparison between the groups when the ANOVA test was significant. The significance level was set at p ≤ 0.05. Statistical analysis was performed using Minitab 17.1.0 for Microsoft Windows.
Author Contributions: L.S. and C.B. designed the concept and methodology, and L.S. investigated, collected, and analyzed the data. C.B. provided the resources, and visualization was conducted by L.S. and C.B. Writing and original draft preparation were performed by L.S. C.B. substantially revised the manuscript and performed the final editing. All authors have read and agreed to the published version of the manuscript.
Funding: This research received no external funding.

Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable, as this article does not contain any studies with human participants or human data, or animals performed by any of the authors.

Data Availability Statement:
The datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request.

Conflicts of Interest:
The authors declare no conflict of interest.

Statistical Analysis
The Shapiro-Wilk test was used to check normality, and results were presented as mean and standard deviation (SD). All quantitative variables showed parametric distribution; therefore, one-way analysis of variance (ANOVA) was used for comparison between the groups. Tukey's post hoc test was used for pairwise comparison between the groups when the ANOVA test was significant. The significance level was set at p ≤ 0.05. Statistical analysis was performed using Minitab 17.1.0 for Microsoft Windows.
Author Contributions: L.S. and C.B. designed the concept and methodology, and L.S. investigated, collected, and analyzed the data. C.B. provided the resources, and visualization was conducted by L.S. and C.B. Writing and original draft preparation were performed by L.S. C.B. substantially revised the manuscript and performed the final editing. All authors have read and agreed to the published version of the manuscript.