Antifungal Activities and Some Surface Characteristics of Denture Soft Liners Containing Silicon Dioxide Nanoparticles

Abstract

INTRODUCTION Removable dental prostheses are the most appropriate treatment for completely and partially edentulous patients.[1] However, with aging, alveolar bone resorption becomes an endless process that negatively affects the denture’s retention,[2] can also impact a denture’s performance (e.g., chewing ability, speech, esthetics), and may induce psychological stress in elderly denture wearers, in addition to progressive changes in the denture foundation.[3] Therefore, it is necessary to correct the alignment between the ill-fitted denture base and the residual ridge via denture relining techniques.[3] There are two types of relining procedures: laboratory relining and chair-side relining. The disadvantages of laboratory relining include more visits and the patient being deprived of the denture.[45] Chair-side relining, which uses auto-polymerized acrylic resin, is faster and superior in reproducing morphological details because it captures the soft tissue directly under the denture base.[56] Soft liners can be categorized into two composition types: plasticized acrylics and silicone elastomers.[7] Long-term soft liners are used for thin, sharp residual ridges with extensive ridge resorption or severe boney undercut cases. However, short-term (temporary) soft liners are used to treat traumatized oral tissue removable denture inner surfaces, or postsurgical problems.[8] Denture-induced stomatitis (DIS) is a common inflammatory reaction of the denture-bearing mucosa.[1] DIS is a fungal infection caused by C. albicans,[9] a pathogen that is also implicated in many nondental medical problems, such as oropharyngeal infections and endocarditis.[10] The acrylic denture base is a harbor for microbes that must be removed on a daily basis by mechanical or chemical cleansing. However, in some situations, these microorganisms cannot be completely removed from the denture surfaces.[1] Therefore, an antifungal denture base material that resists C. albicans adhesion and proliferation could reduce the incidence of DIS.[9] Different approaches have been implemented to inhibit DIS, such as topical application of antifungal agents, modification of the resin denture base surface, and incorporation of antifungal agents into the denture base resin.[1112] Despite the advantages of soft liners, they are more difficult to clean than hard denture bases because they cannot be cleaned by using mechanical brushing.[47] In addition to having reduced resilience and water sorption,[47] they are easily degradable, prone to the accumulation of microorganisms, and can contribute to the progression of pathological processes that can limit the treatment options for existing infections.[13] Soft liners that lack antifungal properties allow the formation of biofilm, which is difficult to remove even using denture cleansers.[14] Recently, to overcome this problem, soft liners with antifungal properties have been formulated and proven to reduce C. albicans adhesion and prevent DIS.[10] Nanoparticles have invaded the dental field in efforts to develop dental materials with better properties. Silver, titanium dioxide, zirconium dioxide, zinc oxide, and silicon dioxide nanoparticles all possess proven antimicrobial properties when incorporated into dental materials.[10151617] A recent study explains the mechanism of the antimicrobial action of nanoparticles in terms of wrapping around the microbial cells (causing disruption of their cell membranes and leading to the inhibition of the normal budding process), producing reactive oxygen, or accumulating in the cytoplasm or on the outer cell membranes of microorganisms.[1] Moreover, the antimicrobial activity could be attributed to the disintegration of the cell membranes of C. albicans via the formation of pores that cause ion outflow followed by ultrastructural changes and programmed cell death.[18] When nanoparticles are incorporated into dental polymers, they improve the polymer characteristics because of their nano-size, great contact surface, proper bonding, and intermingling with the resin matrix of the polymer.[19] Nano-SiO2 was incorporated into polymethyl methacrylate (PMMA) in different concentrations ranging from 0.05wt% to 5wt%.[192021] Less than 1wt% showed a uniform distribution of nano-SiO2 within the resin matrix and improved its flexural strength,[19] surface properties,[20] and antifungal activity[21] whereas agglomeration occurred with more than 1%.[192021] Moreover, nano-SiO2, when used as a coat for the denture surface, reduced the adhesion of C. albicans.[22] The incorporation of nano-SiO2 as an antifungal agent into soft liners could be promising in reducing the possibility of DIS. Therefore, this investigation evaluates whether adding nano-SiO2 to a temporary auto-polymerized soft liner would impede the adhesion of C. albicans and to evaluate the roughness and contact angle of the nano-SiO2-modified soft liner. The null hypothesis was that modification of the soft liner by nano-SiO2 might not influence the antifungal or surface characteristics. MATERIALS AND METHODS SPECIMENS’ PREPARATIONS Eighty heat-polymerized acrylic disks (10 mm × 2mm) relined with a temporary resilient auto-polymerized soft liner (COE-SOFT, GC Co., Ltd, Tokyo, Japan) were prepared. As per the COE-SOFT soft-liner manufacturer’s instructions, each 2.2 g of ethyl methacrylate powder was mixed with 1.8 g of butyl phthaloylglycerol butyl ester and absolute ethanol liquid. Nano-SiO2 was silanized as explained in other investigations.[192021] Nano-SiO2 was measured digitally (Motorized Analytical Balance Scale, Denver Instrument, Bohemia, NY, USA), and it was added at 0.25%, 0.5%, and 1% concentrations to the soft-liner powder, whereas pure specimens constituted the control group. The concentration selection was based on a pilot study using 0.25% to 5%, in which concentrations higher than 1% caused a huge increase in C. albicans count. An electric home mixer with a blunt blade was used for powder mixing to ensure the homogenous distribution of nanoparticles within the soft-liner powder. Two customized split stainless-steel molds were used for specimens’ fabrication. The first mold (10 mm × 2mm) was used for heat-polymerized acrylic specimens, whereas the second one (10 mm × 3.3 mm) was used for soft-liner application. According to the technique used for denture base fabrication, the first mold was used to construct the wax specimens (Vertex Dental B. V., Soesterberg, Netherlands), which were invested by using dental stone (Fujirock EP; GC Corporation, Tokyo, Japan) in a dental flask (61B Two Flask Compress; Handler Manufacturing). All the wax was melted to obtain mold spaces. Heat-polymerized acrylic resin (Major base 20; Prodotti Dentari SPA, Italy) was mixed as per the manufacturer’s instructions after the application of a separating medium (Isolmajor, Major Prodotti Dentari SPA, Moncalieri, Italy). The acrylic dough was packed and polymerized by using a short polymerization cycle using a thermal curing unit (KaVo Elektrotechnisches Werk, Leutkirch, Germany). Finishing of completely polymerized specimens was done by using a tungsten carbide bur (HM 79GX-040 HP; Meisinger, Centennial, Colorado) followed by a polishing machine (Metaserve 250 grinder-polisher; Buehler, Lake Bluff, Illinois) to polish one side of the specimen’s surface, as described in previous studies,[2021] whereas the other side remained unpolished.[23] The dimensions of all specimens were measured via a digital caliber, with 0.01-mm accuracy (Neiko 01407A Electronic Digital Caliper; Neiko Tools US, LaPorte, Indiana), and they were also checked for smooth surfaces free of any porosity by the naked eye of two evaluators. Distilled water was used to keep the approved specimens at 37ºC for 48 h. RELINING PROCEDURES All relining procedures were performed by the same operator for standardization. The specimens’ surfaces were polished by using #240 silicon carbide abrasive paper (Silicon grinding paper, Buehler-MIT II, Buehler, Lake Bluff, IL, USA) fixed to a mechanical polisher (Metaserve 250 grinder-polisher, Buehler) in a wet condition.[2021] A detergent was used to clean the abraded surface, and then it was washed under running water and dried.[24] Before relining, the prepared specimens were randomly selected and placed in the second mold with the abraded surface facing up. The primer was painted by using a brush in two layers in one direction, and then the soft liner was mixed and applied in the mold containing the heat-polymerized denture base specimens. A glass slab was placed over the mold and pressed until glass-to-metal contact was obtained, and it was kept under pressure till complete polymerization.[6] After the polymerization process was completed, the flashes and edges of the specimens were removed, and the dimensional accuracy was verified as described earlier. Distilled water was used to store the specimens at 37oC for 48 h, and then they were subjected to testing. FUNGAL ADHERENCE ASSAY C. albicans (ATCC 10231) were spread on Sabouraud dextrose plates and cultured at 37°C for 48 h. A single isolated fresh colony was inoculated overnight in 4 mL Sabouraud dextrose broth (SDB Acumedica Co., Manufacturers, Lansing, Michigan) at 37°C with shaking for additional 24h followed by centrifugation to collect cells. Phosphate-buffered saline (PBS) was used to wash collected cells twice and then resuspended for concentration standardization by a spectrophotometer to 1.7×107 colony-forming unit (CFU/mL).[2122] The acrylic disks were ultrasonically cleaned and then subjected to ultraviolet (UV) light for 30 min.[10] For biofilm formation on an acrylic disk, each disk was submerged in the broth (200 µL) and incubated at 37°C for 48 h. PBS was used to wash the acrylic disks twice to eliminate nonadherent cells, followed by placement of the specimens with adherent cells in sterile tubes containing 1 mL of PBS with sonication for 15 min. To remove adherent cells for counting, a vortex was used for 10 min to vibrate the tubes, and then centrifugation was conducted for 5 min at 4,500 rpm. Then, 10 mL of the centrifuged solution was diluted serially and spread on a petri dish containing Sabouraud dextrose Agar and incubated for 24 h at 37ºC.[25]C. albicans colonies in each quadrant were counted by using a marker pen counter (colony counter “Scienceware- bel-art products,” Wayne, New Jersey), and the total colonies number was multiplied by the dilution factor displayed Candida count (CFU/mL).[1025] SURFACE ROUGHNESS (RA, μm) A noncontact profilometer (Contour GT; Bruker Nano gmbH, Schwarzschildstrasse, Berlin, Germany) was used to measure Ra. With a standard camera (20×), three areas were scanned and then the average Ra (μm) was calculated for each specimen.[2021] CONTACT ANGLE The sessile drop method was used to measure the contact angle by a goniometer (DM-501; Kyowa Interface Science Co., Japan). After specimens’ surface dryness, a (2-μL) droplet of distilled water was dispensed on the dried surface by using an autopipette. The angle of the tangent to the water droplet surface was measured thrice per specimen, and then the average contact angle was calculated for each specimen.[2122] The interpretation of images was done by using software (Kyowa Interface Science Co., Japan). STATISTICAL ANALYSIS The Statistical Package for the Social Sciences (SPSS) software program, version 23.0 was used for data entry and analysis. The normality of the data was checked first by using the Shapiro–Wilk test, and insignificant results revealed that the data were normally distributed; thus, parametric tests were used for the analysis. For the descriptive statistics, mean and standard deviations were computed. For the inferential statistics, one-way analysis of variance (ANOVA) was used to test the significance of the relationships between the tested properties and nano-SiO2 concentration levels, followed by Tukey’s post hoc test. P-values less than 0.05 were considered statistically significant. RESULTS The one-way ANOVA results are summarized in Table 1, which showed the significant variation in means due to nano-SiO2 concentration levels. Tukey’s post hoc test is used to test the pairwise comparison of the means [Table 2].Table 1: One-way ANOVA results of tested propertiesTable 2: Mean (standard deviation) and significance between groups for tested propertiesThe Candida count was lower in nano-SiO2 groups than in the control group (P < 0.001). In addition, there were significant differences between the nano-SiO2 groups. The Candida count was found to be highest in the control group, whereas the lowest Candida count was observed in a 0.5% nano-SiO2 concentration [Figure 1].Figure 1: Direct culture count of tested groups according to nano-SiO2%: (A) 0.25% nano-SiO2, (B) 0.50% nano-SiO2, (C) 1% nano-SiO2, and (D) unmodified group (0% nano-SiO2)In comparison with the control group, Ra significantly decreased with nano-SiO2 addition (P < 0.001), except for the 1% nano-SiO2 group (P = 0.816). However, there was no significant difference in Ra between the 0.25% and the 0.5% groups (P = 0.084). The lowest Ra value was found in the 0.25% concentration group, whereas the control and 1% groups showed the highest Ra values [Table 2]. The contact angles of the nano-SiO2 groups were significantly lower than the control group (P < 0.001). Comparison of the contact angles among nano-SiO2 groups revealed that the 0.25% concentration group differed from the 0.5% and 1% concentration groups to a statistically insignificant degree (P = 0.28 and P = 0.184 respectively). Moreover, there was a significant difference between 0.5% and 1% concentration levels of nano-SiO2 (P < 0.001). Among the nano-SiO2 groups, the lowest contact angle was found at the 0.5% concentration level, and the highest contact angles were recorded at the 1% and 0.5% concentration levels [Table 2]. Figure 2 confirms the contact angle finding, as the addition of nano-SiO2 decreased the contact angle [Figure 2A–C] in comparison to the control group [Figure 2D].Figure 2: Contact angle of tested groups according to nano-SiO2%: (A) 0.25% nano-SiO2, (B) 0.50% nano-SiO2, (C) 1% nano-SiO2, and (D) unmodified group (0% nano-SiO2)DISCUSSION A combination of soft liner and antifungal agent can facilitate the treatment of DIS by minimizing the tissue trauma induced due to friction with the inner surface of the rigid removable dentures and preventing interaction between oral tissues and contaminated denture surfaces. Thus, the antifungal agents within the soft liner can interrupt the re-infection cycle.[11] According to the manufacturer’s claims, the soft liner used in the present study polymerizes intra- or extraorally within 15 min and lasts for about three months of clinical use. This study investigated the antifungal activity, surface roughness, and contact angles of soft liners while incorporating different concentrations of nano-SiO2. The results reveal that the use of all these nano-SiO2 concentrations with an auto-polymerized soft denture liner decreased C. albicans adherence, surface roughness, and contact angle, with the greatest effects obtained with a 0.5% concentration. Therefore, the null hypothesis was rejected, because all tested properties were influenced by incorporating nano-SiO2. The displayed antifungal activity of the tested nano-SiO2-modified soft liner can be attributed to the large total surface area of the nanoparticles in contact with C. albicans cell membranes. This interaction is consistent with the nanoparticle–Candida contact theory, which states that nano-SiO2 may penetrate or disrupt C. albicans cell membranes, leading to a change in the membrane permeability and abnormal diffusion of ions.[26] This could cause cell structural changes, deterioration of cell metabolism, inhibition of normal budding, and ultimately cell death.[118] Although adding 1% nano-SiO2 to the soft liner reduced C. albicans adherence, this antifungal activity was inferior to that exhibited in the lower nano-SiO2 concentration groups. These results were in agreement to other studies that demonstrated that a homogenous spread of nanoparticles in the resin matrix is required to obtain an improved polymer with efficient, continuous antimicrobial activity.[27] Karci et al.[28] reported that the low density of nano-SiO2 increased particle amount per unit area when compared with the same concentration of metal oxides, which means that higher concentrations of nano-SiO2 will lead to their agglomeration in the matrix. Thus, our results can be explained as follows: When nano-SiO2 concentration was low enough to allow a homogenous, individual distribution in the polymer matrix without clustering, the nanoparticles displayed higher antifungal activity than when the concentration increased until they agglomerated into clusters and thus exhibited reduced total active surface area.[10] These results align with those of de Castro et al.,[29] who found that increasing the concentration of silver vanadate nanoparticles from 2.5% to 5% and 10% resulted in reduced antifungal activity. As previously mentioned, this can be explained by the clustering of the nanoparticles, leading to a reduction in the total surface area exposed to C. properties by the contact angle, such as surface roughness and can C. albicans accumulation and adhesion to the soft-liner The the surface roughness, the higher the of biofilm formation due to the increased surface the the of microorganisms, and the increased surface present to microorganisms the applied The results reveal a between surface roughness and nano-SiO2 in which the addition of low concentrations to 0.5% resulted in reduced surface roughness and thus soft-liner surfaces. These results are consistent with the reduction of C. albicans count that occurred when nano-SiO2 was added to the soft liner at concentrations of 0.25% and This could be explained by the of low concentrations of nano-SiO2 to be within the resin matrix as as their proper via which resulted in its chemical to the methacrylate resin of the soft liner in the of from the surface and the to The 1% concentration of nano-SiO2 increased the surface roughness when it was added to the soft which can be explained by the agglomeration and clustering of these These results align with those of et who that adding nano-SiO2 to at higher concentrations increased its surface The results of study also that surface roughness increased after the addition of lower concentration resulted in higher surface was reported that a surface roughness of can increase the microbial Ra values lower than can be considered For this nano-SiO2 added to the soft liner resulted in the highest reported Ra it was to the as previously The contact angle the surface of dental methacrylate which is the of soft denture liners, is to in its The interaction between and the C. albicans been proven to be an factor in C. albicans albicans less to surfaces than to The acrylic denture base surface properties of and roughness have been to C. albicans adherence, which the of In addition, microorganisms are more difficult to remove from surfaces than from easily surfaces. been proven that increasing the of the acrylic resin surface C. albicans thus, the of et that nano-SiO2 on the surface of dentures the contact angle, and the adhesion of C. In addition, et found that the incorporation of nano-SiO2 into C. albicans adhesion due to increased surface by a reduced contact angle in comparison to that of the In this adding nano-SiO2 at 0.25% and 0.5%, reduced the contact angle, increased surface of the soft liner. This can be attributed to a reduction in surface by the nano-SiO2 These results align with those of et who found that nano-SiO2 In addition, our results align with those of et who that nano-SiO2 increased surface by the contact angle as compared with the the lowest contact angles were with the highest added nano-SiO2 which was not the for our For our the highest added concentration of nano-SiO2 increased the contact angle, it was the contact angle of the control group. This increase in the contact angle a reduction in surface which could be caused by a reduction in the total surface area of the nano-SiO2 due to their agglomeration into surface roughness and contact angle to the decreased C. albicans adhesion the antifungal of soft liners containing nano-SiO2 at low concentrations and that such liners could be used to prevent DIS and is after procedures to the possibility of The of this investigation include using a single of soft and of the of the oral such as thermal changes, and of that could the properties of soft liner with antifungal Therefore, of properties and of different of soft liner with low nano-SiO2 concentrations in oral are and nano-SiO2 into temporary auto-polymerized soft liners to a significant in C. albicans surface roughness, and contact In higher nano-SiO2 concentrations reduced antifungal and increased the surface roughness and contact AND AND In addition to the data in the additional data can be on