Experimental Dental Resin Research Articles

Optimization of an ultra-bright real-time high-throughput renilla luciferase assay for antibacterial assessment of Streptococcus mutans biofilms

ObjectiveThe present work demonstrates the optimization of a renilla-based real-time, ultra-bright, non-disruptive, high-throughput bioluminescence assay (HTS) to assess the metabolism of intact Streptococcus mutans biofilms and its utility in screening the antibacterial efficacy of experimental nanofilled dental adhesive resins containing varying concentrations of nitrogen-doped titanium dioxide nanoparticles (N_TiO2). Methods. Optimization of the assay was achieved by screening real-time bioluminescence changes in intact Streptococcus mutans biofilms imposed by the various experimental biofilm growth parameters investigated (bacterial strain, growth media, sucrose concentration, dilution factor, and inoculum volume). The optimized assay was then used to characterize the antibacterial efficacy of experimental nanofilled dental adhesive resins. The assay’s ability to discriminate between bacteriostatic and bactericidal approaches was also investigated. Results. Relative Light Units (RLU) values from the HTS optimization were analyzed by multivariate ANOVA (α = 0.05) and coefficients of variation. An optimized HTS bioluminescence assay was developed displaying RLUs values (brightness) that are much more intense when comparing to other previously reported bioluminescence assays, thereby decreasing the error associated with bioluminescence assays and displaying better utility while investigating the functionalities of antimicrobial nanofilled experimental dental adhesive resins with proven long-term properties. Significance. The present study is anticipated to positively impact subsequent research on dental materials and oral microbiology because it serves as a valuable screening tool in metabolic-based assays with increased sensitivity and robustness. The assay reported is anticipated to be further optimized to be used as a co-reporter for other Luc based assays.

Antibacterial Properties of an Experimental Dental Resin Loaded with Gold Nanoshells for Photothermal Therapy Applications.

This study explored the chemical and antibacterial properties of a dental resin loaded with gold nanoshells (AuNPs) in conjunction with photothermal therapy (PTT) as a novel method against Streptococcus mutans (S. mutans) to prevent secondary caries. First, a 20-h minimum inhibitory concentration (MIC) assay was performed on solutions of AuNPs with planktonic S. mutans under an LED device and laser at 660 nm. Next, resin blends containing 0, 1 × 1010, or 2 × 1010 AuNPs/mL were fabricated, and the degree of conversion (DC) was measured using an FTIR spectroscopy. Lastly, a colony forming unit (CFU) count was performed following 24 h growth of S. mutans on 6 mm diameter resin disks with different light treatments of an LED device and a laser at 660 nm. The MIC results only showed a reduction in S. mutans at AuNP concentrations less than 3.12 µg/mL under a laser illumination level of 95.5 J/cm2 compared to the dark treatment (p < 0.010 for each). CFU and DC results showed no significant dependence on any light treatment studied. The AuNPs expressed antibacterial effects following PPT against planktonic S. mutans but not in a polymerized dental adhesive resin. Future studies should focus on different shapes, structure, and concentrations of AuNPs loaded in a resin blend.

Optimized regression model for microhardness of experimental dental composite resins with nano-hydroxyapatite filler particles

ABSTRACT Background: Bioactive materials produce a biological reaction such as stimulation of pulpal cells for dentinal repair and induction of the formation of hydroxyapatite. Aim: The study was conducted to evaluate the microhardness of experimental dental composite resins (EDCR) containing nano-hydroxyapatite, zirconia, and glass filler particles. Materials and Methods: The EDCR was prepared with varying concentrations of barium aluminum fluoride glass (5–20 nm), zirconia (4–11 nm), and hydroxyapatite (20–80 nm) filler particles added to the organic matrix. The L9 orthogonal array was used to prepare a sample size of 27 samples. Disc-shaped specimens of 10 mm diameter and 4 mm thickness were prepared using the American Society for Testing and Materials E384 standard for testing the microhardness. The Taguchi’s method of optimization was used to obtain a composite with optimum microhardness. A regression model was developed. Results: EDCR with 23.7% of zirconia, 27.5% of nano-hydroxyapatite, and 20% of glass filler particles gave the optimum microhardness of 222.67 HV. The confirmatory experimental test of EDCR gave a microhardness of 225 HV. The model developed with regression equation for the microhardness was 60–123 Z + 114 H + 17.8 G + 2.48 ZH − 0.02 HG + 0.97 Z2 − 3.40 H2. The difference between the R 2 (99.9) and adjusted R 2 values (99.4) is &lt;0.5, this shows that the model is acceptable. Conclusion: The EDCR developed after using Taguchi’s method of optimization had microhardness superior to that of the commercially available composite resins.

Effect of Nanohydroxyapatite, Zirconia and Glass Filler Particles on the Wear and Microhardness of Experimental Dental Composite Resin.

To study the influence of nanoparticles of hydroxyapatite, zirconia, and glass on the wear and the microhardness of the organic matrix of experimental dental composite resin. The dental composite resin matrix was fabricated from bisphenol A-glycidyl methacrylate (Bis-GMA) (40 wt%), triethylene glycol dimethacrylate (TEGDMA) (36 wt%), and camphorquinone (0.4 wt%). Nanohydroxyapatite, glass, and zirconia fillers were silane treated. Nano-hydroxyapatite, glass, and zirconia were incorporated at three different concentrations. The polymerization of the dental composite resin was done using a light curing unit. Experimental dental composite resins were evaluated for wear and microhardness. The data were analyzed by one-way analysis of variance (ANOVA) test. The experimental dental composite resin composed of 32% of nanohydroxyapatite, 27% of zirconia, and 19% of glass as filler showed the minimum amount of wear. The Vickers hardness (VHN) number was observed to be minimum for the experimental dental composite resin composed of 24.1% of nanohydroxyapatite, 22% of zirconia, and 14.5% of glass. The inclusion of 32% nanohydroxyapatite, 27% of zirconia, and 19% of glass as filler into the experimental dental composite resin decreased the wear and increased the hardness. Mirajkar CK, Winnier J, Hambire U. Effect of Nanohydroxyapatite, Zirconia and Glass Filler Particles on the Wear and Microhardness of Experimental Dental Composite Resin. Int J Clin Pediatr Dent 2023;16(S-1):S81-S84.

Effect of monomer composition and filler fraction on surface microhardness and depth of cure of experimental resin composites.

This study evaluated microhardness profiles and calculated depths of cure at 80% of the surface microhardness of experimental dental resin composites having different base monomer compositions and different filler fractions. Composites were prepared using four different base monomers (bisphenol A-glycidyl methacrylate [Bis-GMA], urethane dimethacrylate [UDMA], ethoxylated bisphenol-A dimethacrylate [Bis-EMA], and Fit-852) with triethylene glycol dimethacrylate (TEGDMA) used as a co-monomer at three filler:resin matrix weight percent fractions (50:50, 60:40, and 70:30). Uncured material was placed in 3D printed molds and light cured for 40 s from the top surface only. Knoop microhardness was measured at the top of the specimen, and at every 0.5mm up to 4mm in depth. Microhardness at the surface increased in all experimental composites as the filler fraction increased. When comparing base monomers, microhardness was the highest in UDMA-based composites, while Bis-GMA-based composites showed the lowest values. When comparing depth of cure as a function of base monomer type, both Bis-GMA and Bis-EMA showed significantly lower values than UDMA or Fit-852. Composites having 50wt% filler showed a significantly higher depth of cure than those with 60 and 70wt% filler. Base monomer and filler fraction significantly influence microhardness and depth of cure in these experimental composites.

Impact of curcumin loading on the physicochemical, mechanical and antimicrobial properties of a methacrylate-based experimental dental resin

Oral biofilms are directly linked to one of the most common chronic human diseases, dental caries. Resin-based dental materials have significant potential to replace amalgam, however they lack sufficient antimicrobial power. This innovative study investigates a curcumin-loaded dental resin which can be utilized in an antimicrobial photodynamic therapy (aPDT) approach. The study evaluated the effects of curcumin loading on resin physicochemical, mechanical, and adhesive properties, as well as the antimicrobial response associated with blue light activation. Preliminary tests involving degree of conversion (DC) and sample integrity determined the optimal loading of curcumin to be restricted to 0.05 and 0.10 wt%. These optimal loadings were tested for flexural strength (FS), water sorption (WS) and solubility (SL), shear bond strength to dentin (SBS), and viability of Streptococcus mutans under 14.6 J/cm2 blue light or dark conditions, in 6 h and 24 h biofilms. The results demonstrated that 0.10 wt% curcumin had minimal impact on either FS or SBS, but detectably increased WS and SL. A 2 log10 (CFU/mL) reduction in S. mutans after light application in both 6 h and 24 h biofilms were corroborated by CLSM imaging and highlighted the significant potential of this novel aPDT approach with resin-based dental materials.

Using Copper-Doped Mesoporous Bioactive Glass Nanospheres to Impart Anti-Bacterial Properties to Dental Composites.

Experimental dental resin composites containing copper-doped mesoporous bioactive glass nanospheres (Cu-MBGN) were developed to impart anti-bacterial properties. Increasing amounts of Cu-MBGN (0, 1, 5 and 10 wt%) were added to the BisGMA/TEGDMA resin matrix containing micro- and nano-fillers of inert glass, keeping the resin/filler ratio constant. Surface micromorphology and elemental analysis were performed to evaluate the homogeneous distribution of filler particles. The study investigated the effects of Cu-MBGN on the degree of conversion, polymerization shrinkage, porosity, ion release and anti-bacterial activity on S. mutans and A. naeslundii. Experimental materials containing Cu-MBGN showed a dose-dependent Cu release with an initial burst and a further increase after 28 days. The composite containing 10% Cu-MBGN had the best anti-bacterial effect on S. mutans, as evidenced by the lowest adherence of free-floating bacteria and biofilm formation. In contrast, the 45S5-containing materials had the highest S. mutans adherence. Ca release was highest in the bioactive control containing 15% 45S5, which correlated with the highest number of open porosities on the surface. Polymerization shrinkage was similar for all tested materials, ranging from 3.8 to 4.2%, while the degree of conversion was lower for Cu-MBGN materials. Cu-MBGN composites showed better anti-bacterial properties than composites with 45S5 BG.

Development of Novel Antimicrobial Dental Composite Resin with Nano Cerium Oxide Fillers

Objectives To assess the antibacterial efficacy of experimental dental composite resin with cerium oxide nanoparticles as fillers. Methods The cerium oxide nanoparticles were prepared by the coprecipitation procedure. Synthesized 3wt% CeO2 nanoparticles were added to the composite resin as antibacterial filler. Experimental composite resin was manually prepared by adding ingredients. The resin matrix consisted of two mixed monomers, bisphenol A-glycidyl methacrylate and triethylene glycol dimethacrylate, diketone as the photo initiator, and N, N-dimethylaminoethyl methacrylate as a coinitiator. The antibacterial efficacy against Streptococcus mutans, Streptococcus mitis, Streptococcus aureus, and Lactobacillus spp. bacterial strains was tested using the microdilution method keeping commercially available 3M Filtek Z250 restorative composite as control. Results The experimental dental composite demonstrated 99.503% efficacy against Streptococcus mutans, 99.441% efficacy against Streptococcus mitis, 99.416% efficacy against Streptococcus aureus, and 99.233% efficacy against Lactobacillus spp. Conclusion Integrating cerium oxide nanoparticles as fillers into dental composite resin can be promising in terms of antibacterial activity, provided furthermore study has to be conducted to examine other properties. Clinical Significance. Previous studies attempted adding CeO2 nanoparticles into acrylic resins that showed improvement in mechanical properties, but literature is nil on the dental composite resin and cerium oxide nanoparticles. This study demonstrates the development of an experimental antibacterial dental composite resin that can resolve most of the problems related to secondary caries around dental composite restorations.

Antimicrobial Effects of Propolis Incorporated Dental Composite Resin

Aim/Objective: The aim of this in-vitro study is to assess the antibacterial activity of a propolis-modified experimental dental composite resin in terms of reducing and preventing recurrent caries, usually caused by Streptococcus mutans. Materials and methods: Control group specimens were made using the 70/30 (filler/resin) method without the use of EPE. Group 1 specimens were made by mixing 12% EPE with 30% resin in experimental dental composite resin. The experimental dental composite was created by adding 16%EPE and 20% EPE to Group 2 and Group 3, respectively. Antibacterial testing was carried out in the inhibition zone using the minimum inhibition concentration (MIC) and minimum bactericidal concentration (MBC). Surface roughness was assessed using scanning electron microscopy. Results: The results were evaluated using one-way ANOVA and Tukey's high significant difference test (HSD). The EPE displayed antibacterial action against S.mutans, according to the findings. The inhibitory zone of 20% EPE integrated dental composite resin was 2.2mm to 2.5mm. Inhibition zones ranging from 1.2mm to 1.8mm were found in 12% and 16% of the samples, respectively. The results of the minimum inhibitory concentration showed that 20% had stronger antibacterial activity than 12 and 16 %. Scanning electron microscopy research revealed that 20% of EPE samples had decreased surface roughness. Conclusion: The experimental dental composite showed antibacterial activity against S.mutans. Antibacterial activity is increased by increasing the proportion of EPE in the experimental composite. Due to its dark color appearance it is recommended for usage as a lining material under restorative materials. Keywords: Streptococcus mutans, Secondary Caries, Antibacterial activity, Propolis, Ethanolic extract of Propolis, Dental Composite Resin

Optical characteristics of experimental dental composite resin materials

ObjectivesTo derive the K-M optical coefficients of experimental composites and compare the inherent CIE L*, a* and b* color parameters, translucency parameters and both perceptibility and acceptability thresholds. MethodsExperimental composites were prepared with 4 base-monomers: Bis-GMA, UDMA, Bis-EMA and Fit852 with TEGDMA used as a co-monomer and 3 filler:resin fractions (50:50wt%, 60:40wt% and 70:30wt%). The optical absorption (K) and scattering (S) coefficients over the visible spectra were derived. Corrected reflectivity spectra were calculated using the corrected Kubelka-Munk reflectance model and were used to calculate CIE color parameters (X, Y, Z) values. Translucency parameter (TP) was calculated using the CIEDE2000 color difference. A three-way repeated measures ANOVA was used to analyze the CIE L*a* and b* color parameters at infinite thickness. A two-way ANOVA was used to analyze the translucency parameter at 2 mm thickness. Pairwise comparisons were assessed using Bonferroni-corrected Student's t-tests. For all statistical testing α = 0.05 was used. Color parameters (ΔE00) were calculated for every experimental composite using the CIEDE2000 color differences. Perceptibility threshold (PT), acceptability threshold (AT) and translucency differences (ΔTP) were used to compare experimental composites in both filler fraction within every resin and every resin within each filler fraction. ResultsThe statistical analysis revealed a 3-way interaction (P < 0.0001) between base monomer, filler and direction factors. For the translucency parameter, when comparing filler fraction within base monomers, there were statistically significant differences between the filler fraction within all base monomers. The analysis of color differences (ΔE00) of base monomers within filler fraction revealed that the comparison between experimental composites where beyond the acceptability threshold. The comparison of the differences in translucency parameter (ΔTP) of base monomers within filler fraction were beyond the perceptibility threshold, except between base monomers UT and FT. SignificanceDifferent base monomer and filler fraction combination influences the optical characteristics of experimental composites such as: light transmission, translucency, and color appearance.

Exploring the use of a Ruthenium complex incorporated into a methacrylate-based dental material for antimicrobial photodynamic therapy.

To evaluate the effects of a blue light photosensitizer (PS), Ruthenium II complex (Ru), on the chemical, physical, mechanical, and antimicrobial properties of experimental dental resin blends. The experimental resin (BisEMA, TEEGDMA, HPMA, ethanol, and photoinitiator) was loaded with Ru at 0.00%, 0.07%, 0.14%, 0.28%, 0.56%, 1.12%, 1.2%, 1.5%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, or 10% w/w. Samples were evaluated for the degree of conversion (DC) after 30 and 60 s curing-time (n = 6). Selected formulations (0.00%, 0.28%, 0.56%, 1.12%) were further tested for shear bond strength (SBS) (n = 15); flexural strength (FS) (n = 12); and antimicrobial properties (CFUs), in dark and light conditions. These latter tests were performed on specimens stored for 24-h or 2-month in 37°C water. Water sorption (WS) and solubility (SL) tests were also performed (n = 12). Data were analyzed either by a one- or two-factor general linear model (α = 0.05). Overall, Ru concentration above 1.2% resulted in reduced DC. In SBS results, only the 1.12%Ru resin blend samples had statistically lower values compared to the 0.00%Ru resin blend at 24-h storage (p = 0.004). In addition, no differences in SBS were detected among the experimental groups after 2-month storage in water. Meanwhile, FS increased for all experimental groups under similar aging conditions (p < 0.001). Antimicrobial properties were improved upon inclusion of Ru and application of light (p < 0.001 for both) at 24-h and 2-month storage. Lastly, no detectable changes in WS or SL were observed for the Ru-added resins compared to the 0.00%Ru resin blend. However, the 0.28% Ru blend presented significantly higher WS compared to the 0.56% Ru blend (p = 0.007). Stable SBS, improved FS, and sustained antimicrobial properties after aging gives significant credence to our approach of adding the Ruthenium II complex into dental adhesive resin blends intended for an aPDT approach.

Effects of Monomer Composition of Urethane Methacrylate Based Resins on the C=C Degree of Conversion, Residual Monomer Content and Mechanical Properties.

(1) Background: This study investigated the influence of Bis-GMA, TEGDMA, UDMA, and two different polyethylene glycol (PEG)-containing, UDMO-based co-monomers on the Young’s modulus and flexural strength, degree of methacrylate C=C double bond conversion and residual monomer elution of experimental dental resins. (2) Methods: Urethane methacrylate-based monomer was synthesised via a radical chain growth polymerization mechanism using PEG in order to improve the mechanical properties. Dental resins were formulated using Bis-GMA, UDMA, or UDMO as base monomers combined with TEGDMA as a dilution monomer and DMAEM + CQ as the photo-initiator system. Degree of conversion (DC), mechanical properties, and residual monomer content of light-activated methacrylate resin formulations were evaluated and statistically analysed by ANOVA and a Tukey’s test. (3) Results: PEG-containing UDMO resins had lower Young’s modulus and elastic strength than UDMA-derived resin for all irradiation times. The highest DC (67,418%) was observed for the PEG-containing UDMO-based resin formulation when light cured for 40 s. For all samples, DC increased with the photo-polymerization time. The amount of residual monomer decreased after increasing the light-curing period from 20 to 40 s, resin with UDMO content 0.01 mol of PEG having the smallest amount of free eluted monomer. (4) Conclusions: A strong structure–property relationship exists in photo-cured dimethacrylate-based dental resins. The time and quantity of the photochemical initiation system can influence the physical–mechanical properties of the resins but also the monomers in their composition.

Evaluation of monomer elution, microhardness, and roughness of experimental dental composite resins prepared from Bis‐EFMA, a novel monomer system

AbstractThis study aimed to compare the monomer elution, microhardness, and roughness of experimental resin‐based composites (RBCs) prepared from a novel monomer system derived from 9,9‐Bis[4‐(2‐hydroxyethoxy)phenyl]fluorene) (Bis‐EFMA), bisphenol A‐glycidyl methacrylate (Bis‐GMA), and urethane dimethacrylate (UDMA) with each other, also with a commercial RBC, 3 M ESPE FiltekTM Z250 (FZ). Experimental Bis‐EFMA (ET), Bis‐GMA (BT), and UDMA (UT) based composites were prepared (20% Bis‐EFMA or 20% Bis‐GMA or 20% UDMA, and 20% triethylene glycol dimethacrylate [TEGDMA], and 60% glass filler). 60 specimens were produced (n = 5) and exposed to ethanol solution for 7 days. Then specimens were tested at baseline (T0), first (T1), third (T2), and seventh (T3) days. ET and FZ released significantly lower TEGDMA than other RBCs did (p &lt; 0.05). BT released significantly higher TEGDMA than other RBCs did at T1 (p &lt; 0.05). However, no significant difference was found between FZ and ET at T1 (p &gt; 0.05). FZ exhibited the highest microhardness at all‐time points; besides, the microhardness of BT was lowest at T0, while the microhardness of BT and UT was lower than that of FZ and ET at T1, T2, and T3 (p &lt; 0.05). BT exhibited higher roughness at T2 than the UT did at T0 and T1, significantly (p &lt; 0.05). However, no significant difference was found between the other RBCs (p &gt; 0.05). Bis‐EFMA, a novel bisphenol A‐free monomer system, has the potential to be used in commercial RBCs as a substitute for Bis‐GMA in terms of lower monomer elution and higher microhardness.

Polymerization kinetics of experimental resin composites functionalized with conventional (45S5) and a customized low-sodium fluoride-containing bioactive glass

This study aimed to investigate polymerization kinetics and curing light transmittance of two series of experimental dental resin composites filled with 0–40 wt% of either 45S5 bioactive glass (BG) or a customized low-Na F-containing BG. Polymerization kinetics in 0.1-mm and 2-mm thick layers were investigated through real-time degree of conversion measurements using a Fourier transform infrared (FTIR) spectrometer. FTIR spectra were continuously collected at a rate of 2 s−1 during light-curing (1340 mW/cm2). Light transmittance through 2-mm thick composite specimens was measured using a UV–Vis spectrometer at a rate of 20 s−1. Unlike BG 45S5, which led to a dose-dependent reduction in the rate and extent of polymerization, the customized low-Na F-containing BG showed a negligible influence on polymerization. The reduction in light transmittance of experimental composites due to the addition of the low-Na F-containing BG did not translate into impaired polymerization kinetics. Additionally, the comparison of polymerization kinetics between 0.1-mm and 2-mm thick layers revealed that polymerization inhibition identified for BG 45S5 was not mediated by an impaired light transmittance, indicating a direct effect of BG 45S5 on polymerization reaction. A customized low-Na F-containing BG showed favourable behaviour for being used as a functional filler in light-curing dental resin composites.

Comparative Evaluation of Mechanical Properties of Titanium Dioxide Nanoparticle Incorporated in Composite Resin as a Core Restorative Material

To compare and evaluate the mechanical properties of 2.5% titanium dioxide nanoparticle (TiO2 NP) incorporated as filler in an experimental composite resin with everX Flow and MultiCore Flow. TiO2 was prepared and incorporated into experimental dental composite resin. The experimental and traditional composite resin was grouped as follows: Group I: The experimental composite resin with 2.5% of TiO2 fillers, Group II: everX Flow (GC EUROPE), and Group III: MultiCore Flow (Ivoclar Vivadent). Based on International Standards Organization (ISO) 4049, the samples were prepared for the compressive, diametral tensile, and flexural test. Statistical analysis was done, and the results were tabulated. Compared to the other tested materials, the experimental composite resin had relatively high compressive strength, diametral tensile strength, and flexural strength. Compared to MultiCore Flow, the everX Flow showed strong mechanical properties. Based on the result of the study, it can be concluded that the 2.5% TiO2 NP incorporated as filler in an experimental composite resin demonstrated higher mechanical properties compared to the conventional material. The unique photoactivities of TiO2 NP and their superior mechanical properties make them one of the ideal additives to enhance the performance of polymeric materials.

Incorporation of Copper-Doped Mesoporous Bioactive Glass Nanospheres in Experimental Dental Composites: Chemical and Mechanical Characterization.

Experimental dental resin composites incorporating copper-doped mesoporous bioactive glass nanospheres (Cu-MBGN) were designed to impart antibacterial and remineralizing properties. The study evaluated the influence of Cu-MBGN on the mechanical properties and photopolymerization of resin composites. Cu-MBGN were synthesized using a microemulsion-assisted sol–gel method. Increasing amounts of Cu-MBGN (0, 1, 5, and 10 wt %) were added to the organic polymer matrix with inert glass micro- and nanofillers while maintaining a constant resin/filler ratio. Six tests were performed: X-ray diffraction, scanning electron microscopy, flexural strength (FS), flexural modulus (FM), Vickers microhardness (MH), and degree of conversion (DC). FS and MH of Cu-MBGN composites with silica fillers showed no deterioration with aging, with statistically similar results at 1 and 28 days. FM was not influenced by the addition of Cu-MBGN but was reduced for all tested materials after 28 days. The specimens with 1 and 5% Cu-MBGN had the highest FS, FM, MH, and DC values at 28 days, while controls with 45S5 bioactive glass had the lowest FM, FS, and MH. DC was high for all materials (83.7–93.0%). Cu-MBGN composites with silica have a potential for clinical implementation due to high DC and good mechanical properties with adequate resistance to aging.

Development of Chlorhexidine Loaded Halloysite Nanotube Based Experimental Resin Composite with Enhanced Physico-Mechanical and Biological Properties for Dental Applications

Objective: The objective of this study was to explore the effect of Chlorhexidine-loaded Halloysite nanotubes (HNT/CHX) fillers (diverse mass fractions from 1 to 10 wt.%) on physicochemical, morphological and biological properties of newly developed experimental dental resin composite, in order to compare with the properties of composites composed of conventional glass fillers. Methods: The dental resin composites were prepared by incorporating various proportions of HNT/CHX. Six different groups of specimens: control group and five groups composed of varied mass fractions of HNT/CHX (e.g., 1.0, 2.5, 5.0, 7.5 and 10 wt.%) as fillers in each group were fabricated. Mechanical properties of the composites were monitored, using UTM. The degree of conversion of dental resin composites and their depth of cure were also evaluated. Antimicrobial properties of dental composites were studied in vitro by applying agar diffusion test on strain Streptococcus mutans and cytotoxicity were studied using NIH-3T3 cell line. Results: The incorporation of varied mass fractions (1.0 to 5.0 wt.%) of HNT/CHX in dental resins composites enhanced mechanical properties considerably with significant antibacterial activity. The slight decrease in curing depth and degree of conversion values of composites indicates its durability. No cytotoxicity was noticed on NIH-3T3 cell lines. Significance: Consistent distribution of HNT/CHX as a filler into dental composites could substantially improve not only mechanical properties but also biological properties of dental composites.

Physicochemical and biological assessment of silver nanoparticles immobilized Halloysite nanotubes-based resin composite for dental applications

ObjectiveThe purpose of this study was to investigate the effect of Silver nanoparticle immobilized Halloysite Nanotubes (HNT/Ag) fillers on physicochemical, mechanical, and biological properties of novel experimental dental resin composite in order to compare with the properties of corresponding composites containing conventional glass fillers. MethodsDental resin (Bis-GMA/TEGDMA with ratio 70/30) composites were prepared by incorporation of varied mass fraction of HNT/Ag. Experimental composites were divided into six groups, one control group and five experimental groups containing mass fraction 1 to 10.0 wt. % of HNT/Ag. Mechanical properties of the dental composites were recorded. Degree of conversion and depth of cure of the dental resin composites were assessed. Antimicrobial properties were assessed using agar diffusion test and evaluation of cytotoxicity were performed on NIH-3T3 cell line. ResultsThe inclusion of mass fractions (1–5 wt. %) of the HNT/Ag in dental resins composites, significantly improved mechanical properties. While, addition of larger mass fractions (7.5 and 10 wt. %) of the HNT/Ag did not show further improvement in the mechanical properties of dental resins composites. Theses composites also demonstrated satisfactory depth of cure and degree of conversion. A significant antibacterial activity was observed on S. mutans. No significant cytotoxicity was found on NIH-3T3 cell lines. ConclusionThe incorporation of HNT/Ag in Bis-GMA/TEGDMA dental resins composites resulted in enhancement in mechanical as well as biological properties for dental applications. Clinical significanceHNT/Ag containing dental composite is proposed to be highly valuable in the development of restorative dental material for patients with high risk of dental caries.

Myristyltrimethylammonium Bromide (MYTAB) as a Cationic Surface Agent to Inhibit Streptococcus mutans Grown over Dental Resins: An In Vitro Study.

This in vitro study evaluated the effect of myristyltrimethylammonium bromide (MYTAB) on the physical, chemical, and biological properties of an experimental dental resin. The resin was formulated with dental dimetacrylate monomers and a photoinitiator/co-initiator system. MYTAB was added at 0.5 (G0.5%), 1 (G1%), and 2 (G2%) wt %, and one group remained without MYTAB and was used as the control (GCtrl). The resins were analyzed for the polymerization kinetics, degree of conversion, ultimate tensile strength (UTS), antibacterial activity against Streptococcus mutans, and cytotoxicity against human keratinocytes. Changes in the polymerization kinetics profiling were observed, and the degree of conversion ranged from 57.36% (±2.50%) for G2% to 61.88% (±1.91%) for G0.5%, without a statistically significant difference among groups (p > 0.05). The UTS values ranged from 32.85 (±6.08) MPa for G0.5% to 35.12 (±5.74) MPa for GCtrl (p > 0.05). MYTAB groups showed antibacterial activity against biofilm formation from 0.5 wt % (p < 0.05) and against planktonic bacteria from 1 wt % (p < 0.05). The higher the MYTAB concentration, the higher the cytotoxic effect, without differences between GCtrl e G0.5% (p > 0.05). In conclusion, the addition of 0.5 wt % of MYTAB did not alter the physical and chemical properties of the dental resin and provided antibacterial activity without cytotoxic effect.

Preparation of low shrinkage stress dental composite with synthesized dimethacrylate oligomers

Two dimethacrylate oligomers named polypropylenglycol bis(2-hydroxy-3-methoxypropyl) dimethacrylates (380PPMA and 640PPMA) with different molecular weight were synthesized through ring opening addition reaction between epoxy terminated oligomers PPDE and methacrylic acid, and their structures were confirmed by FT-IR and 1H-NMR spectra. The PPMAs were used to replace TEGDMA partially in Bis-GMA/TEGDMA (50/50, wt./wt.) with the aim to reducing volumetric shrinkage and shrinkage stress of dental resin composites. Dental resin composite without PPMAs was used as control. Double bond conversion (DC), volumetric shrinkage (VS), shrinkage stress, water sorption (WS) and solubility (SL), flexural strength (FS) and modulus (FM) of experimental dental resin composites were investigated. Dynamic mechanical analysis (DMA) was used to evaluate the glass transition temperature (Tg), heterogeneity, and crosslink density (υ). The results showed that dental resin composites contained 640PPMA had slower polymerization rate. Only dental resin composites with 20 wt% of 640PPMA in resin matrix had lower VS than control group (p < 0.05). All of PPMAs containing composites had lower shrinkage stress than control group (p < 0.05). Before water immersion, all of experimental dental resin composites had the same FS and FM (p > 0.05), while after water immersion, FM of dental resin composites with PPMAs became lower than control (p < 0.05). Higher WS and SL were observed in composites with 640PPMA (p < 0.05). Incorporation of PPMAs into dental resin composites could decrease Tg and crosslink density (p < 0.05), but more homogeneous materials could be obtained (p < 0.05). Therefore, PPMAs could be used to reduce volumetric shrinkage and shrinkage stress of dental resin composites, but further studies concerned biocompatibility and service life should be taken because of the higher WS and SL.