Hardness and degree of conversion of dental restorative composites based on an organic-inorganic hybrid

Abstract

This paper presents a factorial design (mixture design) used to analyze the hardness and degree of monomer conversion into composites containing conventional monomers and an organic-inorganic hybrid polymer-based methacryloyloxypropyl trimethoxysilane (MEMO). For this purpose, resins (composites with SiO2) were formulated with the hybrid polymer (polycondensed, pMEMO), and two conventional monomers used in dentistry, bisphenol-A dimethacrylate (Bis-GMA) and triethyleneglycol dimethacrylate (TEGDMA). The resins were characterized through the degree of monomer conversion and Vickers hardness, and the pMEMO by means of FTIR and ¹H NMR. The results showed an increase in hardness for resins containing the hybrid material relative to the resins containing only conventional monomers. The mathematical model adjusted to the experimental data yielded an optimized formulation, which presented a higher hardness value (48.88 HV).

Hardness and degree of conversion of dental restorative composites based on an organic-inorganic hybrid

Sandro Aurélio de Souza Venter^I; Silvia Luciana Fávaro^II; Eduardo Radovanovic^II; Emerson Marcelo Girotto^II,*

^IUniversidade Tecnológica Federal do Paraná - UTFPR, Rua Marcílio Dias, 635, CEP 86812-460, Apucarana, PR, Brazil

^IIDepartamento de Química, Universidade Estadual de Maringá - UEM, Av. Colombo, 5790, CEP 87020-900, Maringá, PR, Brazil

ABSTRACT

This paper presents a factorial design (mixture design) used to analyze the hardness and degree of monomer conversion into composites containing conventional monomers and an organic-inorganic hybrid polymer-based methacryloyloxypropyl trimethoxysilane (MEMO). For this purpose, resins (composites with SiO₂) were formulated with the hybrid polymer (polycondensed, pMEMO), and two conventional monomers used in dentistry, bisphenol-A dimethacrylate (Bis-GMA) and triethyleneglycol dimethacrylate (TEGDMA). The resins were characterized through the degree of monomer conversion and Vickers hardness, and the pMEMO by means of FTIR and ¹H NMR. The results showed an increase in hardness for resins containing the hybrid material relative to the resins containing only conventional monomers. The mathematical model adjusted to the experimental data yielded an optimized formulation, which presented a higher hardness value (48.88 HV).

Keywords: organic-inorganic hybrid, sol-gel, Vickers hardness, ORMOCER^®

1. Introduction

Composites are materials prepared by mixing two or more components at macroscopic level and formed by distinct phases. Class II hybrid polymers are homogeneous materials that have an inorganic network covalently bonded to polymerizable carbon chains, which, under appropriate conditions, produce a polymer network in the hybrid system and form an Organically Modified Ceramic (ORMOCER^®)¹. These materials can be prepared through a sol-gel process by using liquid precursors, leading to systems with chemical and mechanical performances that are higher than those of mixtures of organic matrixes and inorganic inclusions².

Commercial products based on hybrid polymers, such as Definite^® (Degussa, Germany), demonstrating good mechanical properties, adhesion to teeth, elasticity and wear resistance in oral environment³ have been available for decades^4,5. However, the non-reacted diluting monomers found in Definite^® formulation may leach and cause toxic effects and tissue irritation^6,7.

The mechanical hardness property is defined as the resistance of a material to permanent penetration and is intuitively related to the wear of dental restorative resins in the oral environment⁸. In hybrid resins, an inorganic three-dimension network is formed by polycondensation of the alkoxysilanes, producing siloxane bonds (Si-O-Si) as hard as those of glass, this may explain the high hardness of these materials. Studies have demonstrated that comparatively to dental restorative resins based on conventional dimethacrylate monomers, formulations containing organic-inorganic hybrid polymers have higher hardness values⁹.

Pure organic-inorganic polymers are highly viscous, which makes their handling and consequently curing difficult¹⁰. However, some studies on resins using polycondensed (3-methacryloyloxypropyl)trimethoxysilane (pMEMO) in combination with diluting monomers have shown an increase in the hardness of the formulations with an increase in the amounts of diluents. This fact may be related to a more efficient reticulation with the use of diluting monomers due to the greater mobility of the chains of the hybrid materials in these mixtures.

The objective of this study was to evaluate the degree of conversion and Vickers hardness of dental restorative resins containing a hybrid polymer (pMEMO) as a component by a factorial design. The compositions were evaluated in the presence and in the absence of diluting monomers such as triethyleneglycoldimethacrylate (TEGDMA). The efficacy of production of pMEMO using the sol-gel process was also evaluated.

2. Material and Methods

All the reagents used in this study were acquired from Sigma-Aldrich: bisphenol A glycidyl dimethacrylate (Bis-GMA), (3-methacryloyloxypropyl)trimethoxysilane (MEMO, 98%), and triethylene glycol dimethacrylate (TEGDMA, 95%). Camphorquinone (CQ, 97%) and 2-(dimethylamino)ethylmethacrylate (DMAEMA, 99%) were used as a photoinitiation system. Microparticulated silica (V117 1075, E-3000, 7.5 mm, Esstech Inc., Essington, USA) was used as the inorganic inclusion. All the materials were used as received.

2.1. Sol-gel process

The hydrolysis and condensation process was carried out with a molar ratio of 1:3:0.01 MEMO:H₂O:HCl under magnetic stirring at room temperature for 48 h and later heated to 60 ºC for 5 h¹¹. The solvent was removed under reduced pressure and mild heating in a rotary evaporator (Fisaton, model 802, São Paulo, Brazil) till a viscous yellow liquid was obtained.

2.2.¹H NMR

¹H NMR spectra were recorded in a Varian Mercury Plus 300 model apparatus at 300.06 MHz; all samples were solubilized with a deuterated chloroform.

2.3. Resin preparation

Specific amounts of monomers were weighed in Petri dishes, to which the photoinitiaton system (0.8% camphorquinone and 3.2% DMAEMA in relation to the monomer mass) was added. Silica was weighed separately and added in small amounts to the Petri dishes. The mixtures were manually homogenized with a plastic (Teflon^®) spatula. The compositions of the resins are presented in Table 1.

2.4. FTIR: degree of conversion

The degree of conversion of double aliphatic bonds for the formation of carbon chains was evaluated after irradiation of each side of the samples formed in a Teflon^® mold of 2.10 mm thickness and 7.15 mm diameter for 180 s using a LED light curing unit (radii-cal, SDI-Ltd, Melbourne, Australia, 470 nm, 1200 mW/cm²). The irradiated samples were left in a desiccator for 24 h and pulverized before pressing into KBr pellets for measurement of infrared spectra. The infrared spectra of the non-photopolymerized resins were acquired with the samples spread on a NaCl window. The measurements were made in a FTIR Bomem MB-100 Hartmann and Bomem spectrophotometer. For the calculation of the degree of conversion, the decrease in the peak of the aliphatic C = C bond (1640 cm^-1) was compared to the peak of the C = O bond stretching (internal reference band, at 1720 cm^-1). The degree of conversion (DC) of the monomer was obtained with Equation 1, where R = intensity of the band at 1640 cm^-1 / intensity of the band at 1720 cm^-1.

2.5. Vickers hardness

For the determination of Vickers hardness, the samples were prepared in a cylindrical mold, as described in 2.4. To prevent the formation of an inhibiting surface layer due to the contact of the material with oxygen from atmosphere, a transparent PVC film was used to cover the resin during photopolymerization. Hardness measurements were performed with a Vickers tester (Digital Display Low Load Vickers Hardness Tester, model HVS-5, São Paulo, Brazil) with a load of 0.3 kg applied for 20 s. The measurements presented in this study are the means of six repetitions.

3. Results and Discussion

3.1. FTIR characterization

Figure 1 presents the infrared spectra of MEMO before and after (pMEMO) hydrolytic condensation. The band relative to the symmetric stretching of the C-H bonds of the methoxy groups at 2840 cm^-1 shown in plot (A) of MEMO before its hydrolysis is not observed in spectrum (B), indicating that the hydrolysis process effectively converted the methoxy groups bound to silica into Si-OH with the release of methanol¹². The appearance of a broad band in the 3500 cm^-1 region in (B), assigned to the stretching of O-H bonds, makes the hydrolysis of the mentioned methoxy groups evident. The condensation of the silanol groups for the formation of siloxane bonds Si-O-Si may be related to the stretching of these bonds, observed through a broader band in the 1120 cm^-1 region¹³.

3.2.1 H nuclear magnetic resonance

Figure 2 shows the chemical shifts of the hydrogens of alkoxysilane MEMO before and after hydrolysis and condensation. Two characteristics stand out for the chemical shifts before and after hydrolytic condensation. First, the signal associated with the nine hydrogens of the methoxy groups of alkoxysilane at d = 3.55 ppm is not observed in the spectrum of pMEMO (B)¹⁴, indicating the effective reaction. The broadening of the other peaks of pMEMO hydrogens indicates a polymerization and/or an oligomerization process involving the condensation of the hydroxyl groups bound to silicon atoms and the formation of siloxane bonds (Si-O-Si), which is corroborated by the band at 1120 cm^-1 in Figure 1.

3.3. Experimental design

A simplex-centroid experimental design of the mixture composition was used to evaluate the effect of components pMEMO, TEGDMA and Bis-GMA on the degree of monomer conversion and Vickers hardness. This mixture design is used to analyze the relationship involved in a process that contains several variables. Simplex-centroid design is constructed to form a triangle with data points located at each corner, three midpoints on each edge, as well as a centered point. It is highly effective at demonstrating the significance related to the three primary components. Our experimental design for the three components involved six assays and a central point in the conditions presented in Table 1. As the assays were repeated, the response variance of each assay was used to estimate the overall variance of individual responses.

The main effects of the pMEMO (x₁), TEGDMA (x₂) and Bis-GMA (x₃) contents and the combination of factors on the degree of conversion and hardness were evaluated according to the design given in Table 1 using software Design Expert^®. The quadratic models represented by Equations 2 and 3 were obtained using simplex-centroid mixture design for the degree of conversion and hardness results, respectively.

The reliability of the models proposed was evaluated by ANOVA variance analysis. The quadratic models were found to fit the experimental data well and were significant for P values for degree of conversion and hardness of 0.1712 and 0.3928, respectively, showing that the lack of fit for the quadratic model is not significant. The residues analysis presented in Figure 3 shows that the residues are distributed in a random way in accordance to the ANOVA data. The models explain 86.32% of the degree of conversion and 92.71% of the hardness, relative to the total variation. In addition, according to ANOVA, the maximum values that could be explained (obtained by exclusion of pure error) are 88.09% and 99.59% for the degree of conversion and hardness, respectively. These results indicate that the quadratic models can be used to estimate the results within the interval of study. Thus, the quadratic models of Equations 2 and 3 are significant and fit the experimental values well, and therefore, they can be used for estimate purposes.

The analysis of the coefficients of the quadratic equation (Equation 2) for the degree of conversion shows that the main effect is that of the TEGDMA content (76.34x₂); thus, it is responsible for the high values of degree of conversion. The high degree of conversion of the resin prepared with 100% TEGDMA stands out; however, its low hardness (26.21 HV, Table 1) is an unexpected tendency for such a sample with high degree of conversion, since the literature proposes high hardness for composites with high degree of conversions. This fact can be assigned specifically to the use of diluting monomers such as TEGDMA. Although they afford greater mobility to the system components, they may also produce primary and secondary cyclizations. These cyclizations, which are TEGDMA intramolecular bonds, increase the degree of conversion; however, a three-dimension network is not formed, which explains the low hardness of the composites prepared with excess diluents¹⁵.

The coefficient of interaction of factors x₁ and x₂ is high (69.75 x₁x₂), which suggests a strong synergetic effect between components pMEMO and TEGDMA. The high viscosity of pMEMO and the known lower reactivity of methacrylate groups in hybrid systems (due to mobility restrictions) are effects that can be improved with the addition of diluting monomer TEGDMA and making the reticulation process more effective. Previous studies reported an increase in Vickers hardness of resins formed by ORMOCER^®/TEGDMA with an increase in the content of the diluting monomer, which is in agreement with the results found for the current experimental design⁹.

The quadratic model (Equation 3) showed that the pMEMO content is the most significant variable, and therefore the material that has a greater pMEMO content shows greater hardness. The formation of siloxane (Si-O-Si) bonds in the hybrid system increases the hardness of the resins due to the rigidity of these bonds when compared to the carbon bonds of resins based on a purely organic matrix (i.e., non hybrids) such as in conventional dimethacrylate monomers. Mixture x₁x₃ (xpMEMO+xBis-GMA) is negligible for the fitted model because its coefficient (4.37x₁x₃) is smaller than the associated standard deviation. The region of combination of the three variables x₁, x₂ and x₃ is observable in the level plots (response surface) given by the mathematical models, shown in Figure 4, for the degree of conversion (A) and hardness (B).

It can be noted in Figure 4a that for TEGDMA concentrations close to 100%, red regions, greater degree of conversions are obtained, which is expected, as previously discussed. For the hardness assay, Figure 4b, the best values are located close to the edge between variables x₁ (pMEMO) and x₂ (TEGDMA). However, a region that satisfies both properties simultaneously is required, that is, a region where both degree of conversion and hardness are the highest. By analyzing both response surfaces simultaneously (Figures 4a, b), we observe that the region which satisfies both properties lies near to the composition of about 50% of component x₁ (pMEMO) and 45% of component x₂ (TEGDMA).

To test the models fitted with Equations 2 and 3, an optimized composition containing 50.9% pMEMO, 46.7% TEGDMA and 2.4% Bis-GMA was prepared. The degree of conversion and Vickers hardness values obtained were 72.36% and 48.88 HV, respectively. The values predicted by the model with 95% confidence were 67.53 ± 6.76% and 46.95 ± 2.55 HV. Therefore, as the results are within this confidence interval, it can be concluded that they are very close to those of the optimal values of the proposed model, which validates the model.

4. Conclusions

An increase in hardness was observed in dental restorative resins containing hybrid polymer (ORMOCER^®), indicating a greater rigidity of these systems when they were compared to those of resins containing conventional monomers. The use of diluting monomers together with hybrid polymers improves the mechanical quality and handling of the formulations due to the decrease in the viscosity of ORMOCER^®. In addition, the mathematical model obtained was validated for prediction of the optimal resin composition to achieve higher values of DC and hardness.

Acknowledgements

The authors thank CNPQ (Process. 473279/2007-0) and Fundação Araucária (Project 385/12) for the financial support and Essthec Inc. (USA) for silica samples. Sandro A. S. Venter thanks UTFPR/Apucarana for the doctoral leave.

Received: October 29, 2012

Revised: January 14, 2013

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Publication Dates

• Publication in this collection
  11 June 2013
• Date of issue
  Aug 2013

History

• Received
  29 Oct 2012
• Accepted
  14 Jan 2013