Adhesive bonding of resin composite to various titanium surfaces using different metal conditioners and a surface modification system

Abstract

Objective

This study evaluated the effect of three metal conditioners on the shear bond strength (SBS) of a prosthetic composite material to cpTi grade I having three surface treatments.

Material and Methods

One hundred sixty eight rivet-shaped specimens (8.0x2.0 mm) were cast and subjected to polishing (P) or sandblasting with either 50 mm (50SB) or 250 mm (250SB) Al₂O₃. The metal conditioners Metal Photo Primer (MPP), Cesead II Opaque Primer (OP), Targis Link (TL), and one surface modification system Siloc (S), were applied to the specimen surfaces, which were covered with four 1-mm thick layers of resin composite. The resin layers were exposed to curing light for 90 s separately. Seven specimens from each experimental group were stored in water at 37ºC for 24 h while the other 7 specimens were subjected to 5,000 thermal cycles consisting of water baths at 4ºC and 60ºC (n=7). All specimens were subjected to SBS test (0.5 mm/min) until failure occurred, and further 28 specimens were analyzed using scanning electron microscope (SEM) and X-ray energy-dispersive spectroscopy (EDS). Data were analyzed by 3-way ANOVA followed by post-hoc Tukey's test (α=0.05).

Results

On 50SB surfaces, OP groups showed higher SBS means than MPP (P<0.05), while no significant difference was found among OP, S, and TL groups. On 250SB surfaces, OP and TL groups exhibited higher SBS than MPP and S (P<0.05). No significant difference in SBS was found between OP and TL groups nor between MPP and S groups. The use of conditioners on 250SB surfaces resulted in higher SBS means than the use of the same products on 50SB surfaces (P<0.05).

Conclusion

Sandblasting associated with the use of metal conditioners improves SBS of resin composites to cpTi.

INTRODUCTION

The use of titanium for dental implants and metal ceramic restorations, such as cast restorations or partial dentures, has increased over the last years because of their biocompatibility and optimum mechanical properties^6,9,23,29. However, low bond strengths between titanium and composite veneering systems have been reported^{3,11,20,21,29,32}. To overcome this limitation, several methods have been proposed to maximize the bonding of resin composite to titanium. Such methods are based on macro- and micromechanical retention, chemical bonding, or a combination of both mechanisms^6,9.

The first bonding technique was the Silicoater system, introduced in 1984 as a "system of molecular bond" between resins and metal alloy surfaces³⁴. In that system, the bonding mechanism consists of a heat fusion of a microscopic layer of silica to the metal by the so-called silica coating method, and the composite is bonded to the metal surface with a silane coupling agent in a process known as pyrolytic silanization^5,34,35.

New bonding systems that combine adhesive resins with chemically active monomers capable of bonding directly to sandblasted alloy surfaces have also been developed^15,16,17. When these new adhesive systems are used along with conditioning methods, only sandblasting of the metal surface is required for these bonding agents to provide reliable bond strength between the resin composite and metal surface¹⁴. The bonding agents lead to some mechanism of chemical bonding with different alloys, so the micromechanical retention created by sandblasting increases considerably²⁸. Phosphoric acid and carboxylic acid functional monomers used in most adhesive opaque resins and promoters are effective to bond resin composites to base metal alloys. For this reason, with the use of an appropriate adhesive metal primer, no surface preparations such as boxes, grooves, or retentive pearls are required on the metal frameworks prior to the application of light-cured veneering resins³⁸.

Now, several adhesive primers containing different functional monomers to bond resin to base metals are commercially available². However, the effects of these products on the bond strength of metals to resin have not yet been evaluated. Such an issue deserves more concern when the bonding between resin composite and titanium surface with metal primers are subjected to all the stresses created in vivo. In this regard, the combination between water storage and thermal cycling reproduces the in vivo conditions more accurately^7,8,12,22, providing evidence of the long-term effectiveness of metal primers on bond strength of resin composites to titanium surfaces.

Therefore, the purpose of this study was to evaluate whether surface pre-treatment of commercially pure titanium grade I (cpTi) with sandblasting associated with three metal conditioners or with one surface modification system would improve the bond strength of a light-activated resin composite to the base metal after thermocycling. The tested hypotheses were: (1) metal primers provide similar increase in shear bond strength (SBS); (2) and SBS values between resin and metal surfaces treated with metal primers are not impaired by thermal cycling.

MATERIAL AND METHODS

The materials used in this study are given in Figure 1. A total of 196 rivet-shaped specimens (8.0 x 2.0 mm) were cast with cpTi (Tritan^®, Dentaurum J. P. Winkelstroeter KG, Pforzheim, Germany) using electric plasma arc in an inert gas-conditioned casting machine (EDG Equipments, São Carlos, SP, Brazil)¹ according to the manufacturer's instructions. After casting, the disk surfaces were gradually polished with up to 600-grit silicon-carbide papers under constant cooling water. The metal specimens were then washed with isopropyl alcohol for 10 min with ultrasonic agitation.

Figure 1.

Materials used in this study

Material	Identification	Abbreviation	Manufacturer	Component
Metal	Tritan	cp Ti grade I	Dentaurum, Germany	Ti 3 99.5%, others 0.5%
Metal conditioners	Metal Photo Primer	MPP	Shofu, Kyoto, Japan	4-acryloyloxyethyl trimellitate
	Targis link	TL	Ivoclar, Liechtenstein	10-methacryloyloxydecyl dihydrogen phosphate
	Cesead II Opaque Primer	OP	Kuraray, Osaka, Japan	10-methacryloyloxydecyl dihydrogen phosphate
Metal surface modification system	Siloc Bonding System	S	Heraeus Kulzer, Wehrheim, Germany	Methacryloxypropl trimethoxysilane
Opaque resin	C & B Opaque	O	Heraeus Kulzer, Wehrheim, Germany	Opaque OA3
Composite veneering material	Artglass	A	Heraeus Kulzer, Wehrheim, Germany	Dentin A3

Experimental design

The study design is illustrated in Figure 2. The specimens were assigned to 3 groups, and were submitted to 3 surface treatments: (1) polishing control with 600-grit silicon-carbide paper (P), (2) Sandblasting with either 50 µm Al₂O₃ (50SB) or (3) 250 µm Al₂O₃ (250SB). Sandblasting was performed perpendicularly to the metal surface at a distance of 5 mm and at 0.5 MPa for 15 s (Basic Classic; Renfert GmbH, Hilzingen, Germany)^37,39.

Figure 2.

Flowchart of the experimental design

After surface preparation was completed, each group (56 specimens) was divided into four subgroups, according to the metal conditioners and metal surface modification system applied to the disk surfaces. In addition, 14 specimens from the 50SB group and 14 specimens from the 250SB group were left untreated to receive only opaque and dentin resins (control groups - OD).

The following metal conditioners were applied to the metal surfaces: MPP (Metal Photo Primer, Shofu Inc., Kyoto, Japan), OP (Cesead II Opaque Primer, Kuraray Co. Ltd., Osaka, Japan), S (Siloc Bonding System, Heraeus-Kulzer GmbH, Wehrheim, Germany) - a metal surface modification system, and TL (Targis link, Ivoclar Vivadent, Schaan, Liechtenstein) (Figure 3). When the metal conditioner was presented as a single bottle product, the product was brushed directly on the alloy surface, according to the manufacturers' instructions. For the Siloc Bonding System, one coat of primer (Siloc Pre, Heraeus-Kulzer GmbH, Wehrheim, Germany) was applied to the specimen surfaces with a single brush application. The primed specimens were allowed to dry for 2 min and were placed in an activation chamber (Silicoater MD, Heraeus-Kulzer, Wehrheim, Germany), as recommended by the manufacturer. At the end of the cycle, the specimens were removed from the oven and were left at room temperature for 4 min.

Figure 3.

Failure patterns of all experimental groups at T0 (A) and T1 (B)

Afterward, one coat of the bonding agent (Siloc Bond, Heraeus-Kulzer, Wehrheim, Germany) was applied with a single brush and was allowed to dry for 5 min. Two 1-mm thick layers of an opaque resin (O) were applied to the metal surfaces and each layer was exposed to light for 90 s in a laboratory light-curing unit (Dentacolor XS, Heraeus-Kulzer, Wehrheim, Germany), according to the manufacturers' recommendation. A cylindrical stainless steel split mold having an internal hole having 8 mm of diameter and being 2-mm thick was positioned on the specimen and two 1-mm-thick layers of dentin composite (A) were inserted into the mold. The mold was removed and each layer was then exposed to light for 90 s using the same light-curing unit, resulting in a total light exposure of 180 s.

Seven specimens from each experimental group (n=7) were stored in distilled water at 37ºC for 24 h (T0), while the other 7 specimens were stored in distilled water at 37ºC for 24 h followed by 5,000 thermal cycles (T1), which consisted of water baths at 4ºC and 60ºC with a dwell time of 15 s in each bath (MSCT-3 Plus; Marcelo Nucci - ME; São Carlos, SP, Brazil). All specimens were then subjected to an SBS test using a machine of mechanical test MTS 810 (Material Test System Corporation, Minneapolis, MN, USA) at a crosshead speed of 0.5 mm/min until failure occurred^21,30. The SBS values were obtained in Kgf and converted into megapascals (MPa).

Fractured surfaces were evaluated with an optical stereomicroscope (Carl Zeiss Jena GmbH, Jena, Germany) at 40x magnification to determine the failure pattern, which was classified as follows: cohesive, when the fracture was located within the resin composite; adhesive, when the fracture was located between the resin composite and metal surface; or mixed, when the fracture was located within the resin composite and between the resin composite and metal surface. In addition, a representative specimen surface of each experimental group was evaluated with a scanning electron microscope (SEM) operating at 20 kV (JSM-T33AO, JEOL Ltd., Tokyo, Japan), before and after particle abrasion. All representative specimen surfaces were also examined by X-ray energy-dispersive spectroscopy - EDS (JSM-T33AO, JEOL Ltd., Tokyo, Japan) at 20 kV and live time of 100 s.

Levene and Shapiro-Wilk tests (Statistica 6.0, Statsoft Inc., Tulsa, OK, USA) were applied to evaluate the homogeneity and normality among SBS means (P>0.05) respectively. The SBS means were submitted to 3-way ANOVA (surface treatment, conditioner, and thermocycling) at a 95% confidence level. One-way ANOVA (Statistica 6.0, Statsoft Inc., Tulsa, OK, USA) was performed to compare the differences in SBS means of groups having different conditioners only within the group with polished surfaces (P). Differences among means were determined by post-hoc Tukey's test at a pre-set alpha of 5%. The OD group was not included in the statistical tests because this group was only added to the study to provide the SBS values when no conditioners are used.

RESULTS

Forty-two thermocycled specimens without any treatment agent showed premature adhesive failures prior to the mechanical testing and were excluded from the study. The 3-way ANOVA detected a significant interaction between "treatment" and "conditioner" factors as well as between "thermocycling" and "conditioner" (P<0.05). Within the 50SB group, the SBS values of OP (9.3 MPa) were only higher than those of MPP (6.7 MPa) (P<0.05), while no significant difference was noted between OP, S, and TL (Table 1). Within the 250SB group, OP (13.2 MPa) and TL (12.4 MPa) showed significantly higher SBS means than MPP (9.8 MPa) and S (10.2 MPa) (P<0.05), while no significant difference was noted neither between OP and TL nor between MPP and S (Table 1). Overall, the SBS means of most 250SB groups with surface conditioners were higher than those of 50SB (P<0.05). The only exception was observed when S was used, as no significant difference in SBS was noted between 50SB and 250SB groups (from 6.6 MPa to 9.7 MPa, P>0.05).

Table 1.

Shear bond strength (MPa) mean values (±standard deviations) of resin composite to sandblasted cpTi surfaces with metal primers. Means followed by the same capital letters in a column and lower case on the lines do not differ significantly by the Tukey test (α=0.05)

Metal primers	Sandblasting
	50SB	250SB
MPP	6.7(0.9)Bb	9.8(1.4)Ba
OP	9.3(2.1)Ab	13.2(2.0)Aa
S	8.5(1.2)ABa	10.2(0.9)Ba
TL	8.4(1.2)ABb	12.4(2.0)Aa

No significant difference in SBS means was observed between T0 and T1 (P>0.05). At T0, no significant difference in the SBS values was observed between TL (10.6 MPa) and OP (10.4 MPa), or between MPP (8.4 MPa) and S (9.6 MPa) (P>0.05) (Table 2). The SBS means of OP and TL were higher than those of MPP (P<0.05). At T1, OP (12.1 MPa) showed higher SBS values than MPP (8.1 MPa), S (9.1 MPa), and TL (10.2 MPa) (P<0.05) (Table 2). One-way ANOVA (Table 2) indicated no significant differences in SBS among groups with conditioners (P>0.05).

Table 2.

Shear bond strength (MPa) mean values (±standard deviations) of resin composite to sandblasted cpTi surfaces with metal primers after 24 h of water storage (T0) or after thermocycling (T1). Means followed by the same capital letters in a column and lower case on the lines do not differ significantly by the Tukey test (α=0.05)

Metal primers	Storage condition
	T0	T1
MPP	8.4(1.3)Ba	8.1(1.0)Ba
OP	10.4(2.2)Aa	12.1(1.9)Aa
S	9.6(1.2)Ba	9.1(0.9)Ba
TL	10.6(1.9)Aa	10.2(1.4)Ba

At T0 and T1 (Figure 3), debonded surfaces from most groups showed 100% adhesive failures located between the metal surface and opaque resin. At T0, only the OP/S250 group exhibited 100% of mixed failures, while OP/50SB (14%), S/250SB (28%), and TL/250SB (28%) showed small amounts of mixed failures. A similar pattern was observed at T1, but a small increase in mixed failures (14%) was observed in MPP/250SB and TL/50SB groups in comparison to the failure patterns at T0. In contrast to the failure pattern of the S/250SB group at T0, the S/250SB group at T1 showed a 100% adhesive failure pattern. The effect of sandblasting on the surface morphology and composition of specimens from groups P, 50SB, and 250SB can be seen on SEM micrographs and EDS spectra (Figures 4, 5, and 6). It is possible to note the effects of varying sizes of aluminum oxide on surface morphology (Figures 5A and 6A), since pressure, time of sandblasting, and distance from the metal surface were the same in all groups. EDS analysis detected the presence of aluminum and oxide on the sandblasted cpTi surfaces (Figures 5B and 6B).

Figure 4.

Scanning electron microscopy analysis for cpTi before sandblasting

Figure 5.

Scanning electron microscopy analysis for cpTi after sandblasting with 50 μm Al₂O₃

Figure 6.

Scanning electron microscopy analysis for cpTi after sandblasting with 250 μm Al₂O₃

DISCUSSION

The present study evaluated the SBS of a resin composite to cpTi after sandblasting with varying sizes of Al₂O₃ particles associated with three metal conditioners or with one surface modification. Overall, the association of metal conditioners and sandblasting increased the SBS in comparison to the values obtained on polished surfaces. The effectiveness of the conditioners on SBS to cpTi airborne-particle-abraded surfaces (50SB and 250SB) and either under the influence of 24 h water storage or thermal stress (T0 and T1) was more evident when monomers having phosphoric acid (OP and TL) in their composition were used in comparison with those having the carboxylic derivative (MPP). These results are in agreement with those from previous studies^36,37 that attributed this greater effectiveness to the presence of a hydrophobic group in their compositions. According to Taira, et al.^30,31 (1995,1998) the pure Ti surface is covered with a layer of titanium oxides that guarantees the resin/metal bond by its reaction with the monomers derived from carboxylic and phosphoric acids. Ban³ (2003) reported that carboxylic acid (4-AET and 4-META) and phosphoric (MDP) derivatives interact with the oxide film on the surface of basic metals, including titanium, via hydrogen bridges, and with the hydroxyl ions (OH^- present on the metal surface. Therefore, the first hypothesis, stating that the metal primers provide similar increase in SBS, was not validated in the current study. We observed a 1.5 times increase in the resin/Ti bond strength values in comparison with the values observed on a noble alloy. Such increase could be related to the great ability for titanium to oxidate. The micromechanical retention appears to contribute much more than chemical bonding does.

The bond between polymers and metal is not completely justified by these two bonding mechanisms. This conclusion is in agreement with our results, when we compared the polishing group with the 50SB/OD and 250SB/OD groups. The effectiveness of OP and TL may be also attributed to chemical affinity of the phosphoric acid group for the aluminum oxide particles trapped on the metal surface due to sandblasting^14,25.

Based on the EDS analysis, oxygen and aluminum were only detected on the sandblasted metal surfaces, demonstrating the presence of remaining Al₂O₃ particles, as also observed by Ohkubo, et al.²³ (2000). However, the influence of aluminum on the bonding mechanism is not well known¹⁹. Cobb, et al.⁶ (2000) described changes in the surface morphology of gold alloys due to the differences in particle sizes and the range in pressure during sandblasting. They also found an increase in the amount of aluminum on the metal surface and the possible chemical affinity of aluminum for functional monomers and phosphoric derivatives. In addition to the micromechanical retention, Kern and Thompson¹⁴ (1994) reported that the remaining aluminum particles on the metal surface play an important role in the bonding mechanism created by bonding systems with functional monomers.

According to the EDS analysis, it was not possible to observe the presence of remaining compounds from conditioners on the metal surfaces, or even the silicon layer of the S group. According to Kern and Thompson¹³ (1994) the pyrolytically deposited silicon results in a layer that is invisible to SEM, while Ekstrand, Ruyter and Øysaed¹⁰ (1988) observed that the presence of polymer molecules on the surfaces of metals can only be detected by infrared spectroscopy. The effects of remaining aluminum particles also hels explain the higher amount of mixed failures in the 250SB group in comparison to those observed in 50SB groups, confirming the greater retention demonstrated by that group.

Thermocycling in a water bath has been used frequently to simulate the intraoral aging effect on resin composite adhesion. However, these simulations vary considerably and any evidence of the number of cycles corresponding to those experienced in vivo was not yet found^7,18. In the present study, thermocycling had no significant effect on conditioners. Therefore, the metal primers demonstrated reliable bonding without a reduction in bond strength after thermocycling. Thus, the second research hypothesis - establishing that SBS values between resin and metal surface treated with metal primers is not impaired by thermocycling - was validated.

The results of the present study are in agreement with those observed by Özcan and Valandro^26,27 (2012, 2011) that observed higher bond strength of resin composite to titanium with phosphoric acid derivatives. According to the authors²⁷, the effectiveness of the bond strength can also be influenced by the opaque resin layer applied after the surface treatment and previously the application of aesthetic covering material. The effect of opaquers can be attributed to differences in their chemical composition and form of presentation (powder/liquid or paste) that lead to various consistencies²⁴. Özcan and Kumbuloglu²⁴ (2009) concluded that although thickness did not affect the bond strength between resin composite to titanium, type of opaquers had a significant effect in the results with higher bond strength for power-liquid form than paste form in both thin and thick application. Moreover, the authors suggested that the degree of water uptake of the opaquers, specifically due the hydrophilic character of the dimethacrylates could influence in bond strength²⁴. Since only one opaque resin was tested in the present investigation, further studies are needed in order to evaluate more carefully the influence of this material on the bonding process.

The shear bond strength test was used in this study because shearing forces are the most predominant during chewing⁴. For this reason, this test reproduces more closely what happens to materials in the mouth. On the other hand, it is important to point out that some methods, such as finite analysis and mathematical analysis of stress, demonstrated that nominal bond strength obtained after specimen fracture divided by the cross-sectional area may not represent the true stress generated at the interface³³. Such a difference between the stress generated during the test and that created during chewing may be attributed to other influencing factors, such as specimen geometry, load type, moment of load application and cynzel position³³.

The results of this in vitro study suggest that the use of chemical bonding systems combined with a mechanical retention improved the bonding between a resin composite and commercially pure titanium (cpTi). This evidence implies that clinicians may consider the use of techniques that combine chemical bond and mechanical retention when reliable bonding is required between a metal surface and resin composite. Thus, clinicians can be more confident when using composite veneering systems coupled to metals.

CONCLUSIONS

According to the results of the current study, it was concluded that an increase in SBS of resin to cpTi may be achieved by associating the mechanical retention provided by sandblasting with 250 µm aluminum oxide particles with the chemical bonding created by metal conditioners, mainly by those containing functional monomers derived from phosphoric acid (Cesead II Opaque Primer and Targis link).