Abstract

ORIGINAL ARTICLES

Nanoleakage phenomenon on deproteinized human dentin

Patrícia de Britto Pereira Garcia Duarte^I; Eduardo Moreira da Silva^II

^IDDS, MSc, Department of Restorative Dentistry, School of Dentistry, Federal Fluminense University, Niterói, RJ, Brazil

^IIDDS, MSC, PhD, Assistant Professor, Department of Restorative Dentistry, School of Dentistry, Federal Fluminense University, Niterói, RJ, Brazil

^{Corresponding address}Corresponding address: Dr. Eduardo Moreira da Silva Universidade Federal Fluminense Faculdade de Odontologia Rua Presidente Pedreira, nº 97 / 904 CEP 24210-470, Ingá, Niterói, RJ, Brasil Phone: 55 21 2629-9832. Fax: 55 21 2622-5739 e-mail: emsilva@vm.uff.br

ABSTRACT

OBJECTIVE: The purpose of this study was to evaluate the influence of dentin deproteinization on the nanoleakage phenomenon.

MATERIAL AND METHODS: Class V cavities were prepared in 12 human molars with cervical margins located in dentin. The cavities were assigned to 2 groups (n=6) according to dentin treatment: Group I - dentin treated in accordance with the manufacturer's instructions and Group II - dentin treated following the manufacturer's instructions + 10% NaOCl. Each group was sub-divided into three groups, according to the DBS (dentin bonding system) used: Scotchbond Multi Purpose (SBMP), Prime & Bond NT (PB) and Clearfil SE Bond (SE), which were applied according to manufacturer's instructions. The cavities were restored with composite resin, and the specimens were immersed in a tracer agent (AgNO₃ 50%) for 24 h. The teeth were sectioned buccolingually through the center of the restorations, and nanoleakage pattern was evaluated by scanning electron microscopy (SEM) using the backscattered electron image mode.

RESULTS: SEM analysis showed different nanoleakage patterns for each DBS. Irrespective of dentin treatments, all SBMP specimens showed nanoleakage. SE did not show any nanoleakage with both dentin treatments used. PB showed nanoleakage within the hybrid layer only in Group I.

CONCLUSIONS: The influence of dentin deproteinization on the nanoleakage phenomenon was dependent on dentin bonding system formulation and bonding strategies.

Uniterms: Dentin-bonding agents; Collagen; Scanning electron microscopy; Nanoleakage.

INTRODUCTION

Dentin demineralization by acid etching is a complex and superficial procedure, in which not only the smear layer is removed, but also a collagen mesh of approximately 3 to 7.5 ìm is exposed¹⁷. Underneath this demineralized layer, a partially demineralized zone appears, characterized by increased mineralization and followed by non-etched dentin²¹.

The term nanoleakage was introduced by Sano, et al.²⁶, in 1995, to describe a specific type of leakage, which exists even in the absence of marginal gaps. This leakage occurs laterally, through submicron porosities (estimated to be about 20 to 100 nm in width) at the base of the hybrid layer, which have not been filled with adhesive resin or which have been left poorly polymerized^27,37. This demineralized, but not fully hybridized dentin layer can be considered a weak point in the adhesion mechanism that could allow dentinal and oral fluid to slowly permeate the interface, and this is believed to degrade the adhesive resin²⁶.

Sodium hypochlorite (NaOCl) has been used as a deproteinizing and nonspecific agent¹⁸ capable of removing organic material exposed after dentin acid etching^10,18,24,37. Wakabayashi, et al.³⁹ (1994) findings indicate that a 60-second treatment with 10% NaOCl is sufficient for effectively eliminate the exposed collagen layer after acid etching.

Several studies have questioned the real influence of the collagen layer on the adhesion mechanism^{9,10,14,18,22,24,28,37,38}. Removal of the collagen mesh may benefit the dentin-adhesive system interaction due to the increase in dentin wettability. This adhesive protocol exposes a subsuperficial dentin layer with nearly the same characteristics as that of the etched enamel, i.e. a larger presence of hydroxyapatite crystals with high surface energy that increases adhesive strength and improves adhesion^2,4.

Silver nitrate solution 50% (w/v) (AgNO₃) is the most used tracer for evaluation of the nanoleakage phenomenon^{1,5,8,19,25-27,30}. This solution can penetrate the dentin due to the small silver ion size (0.059 nm in diameter)³⁵. Contrasting the size of this ion with the size of some bacteria (0.5-1.0 µm)⁷ yields considerable information about the results obtained in evaluating the nanoleakage phenomenon.

The aim of this study was to evaluate the influence of 10% NaOCl on the nanoleakage phenomenon. The research hypothesis was that dentin treatment with 10% NaOCl would prevent the occurrence of nanoleakage.

MATERIAL AND METHODS

Three commercially available adhesive systems, chosen in accordance with their different formulations (organic solvent, hydrophilic monomers and filler particle) and application protocol, were used in this study. Their compositions are described on Table 1.

Twelve extracted non-carious molars stored in a solution of 1% chloramine for 1 week and frozen in distilled water for less than two months were used in this study. Standardized saucer-shaped cervical cavities (2.0 mm high, 2.0 mm wide and 2.0 mm deep) with cervical margins located in dentin were cut on buccal and lingual surfaces of the teeth. Cylindrical diamond burs (1092; KG Sorensen, São Paulo, SP, Brazil) in a high-speed handpiece fixed in a special sample aligning device were used for cavity preparation. Hand cutting instruments (hoes – 12 5 8 26, Duflex, São Paulo, SP, Brazil) were used to provide adequate cavity finishing. The teeth were randomly assigned to 2 groups of six teeth each, according to the dentin surface treatment: Group I - Dentin surfaces were etched with 37% phosphoric acid (3M/ESPE, St. Paul, MN, USA) for 15 s, thoroughly rinsed with air-water spray for 30 s and blotted dry with tissue paper to standardize moisture; Group II - After the same procedure as applied to Group I, a 10% NaOCl gel was left on dentin surface for 1 min, water rinsed for 30 s and blotted dry with tissue paper.

After dentin treatment, the adhesive systems were applied strictly in accordance with the manufacturers' recommendations (2 sided prepared teeth, to total 4 cavities per group). For SE, a self etching primer system, the dentin surface was not etched with phosphoric acid in Group I. In Group II, the NaOCl was applied before the acidic primer. The cavities were restored with two increments of a composite resin (Z 250; 3M/ESPE, St. Paul, MN, USA) light cured for 20 s with a light-curing unit with light intensity of 500 mW/cm2 (QHL 75; Dentsply/Caulk, Milford, DE, USA). After storage in water at 37°C for 24 h, the restorations were finished using Super Snap disks (Shofu Inc., Kyoto, Japan). Root apices were sealed with a cyanoacrylate adhesive (Super Bonder^TM, 3M, São Paulo, SP, Brazil) and the teeth were coated with two layers of nail varnish up to approximately 0.5 mm from restoration margins. The specimens were immersed in a 50% (w/v) silver nitrate solution for 24 h, rinsed under running water for 5 min, immersed in a photodeveloping solution, and exposed to a fluorescent light for 8 h. After being removed from the photodeveloping solution, the specimens were rinsed under running water for 5 min, and sectioned buccolingually through the center of the restorations by using a low speed diamond saw (7016; KG Sorensen, São Paulo, SP, Brazil). The cut surfaces were embedded in epoxy resin (Resi-line, Rio de Janeiro, RJ, Brazil) and polished with increasingly fine diamond pastes (6, 3, 1? µm; Buehler Ltd., Lake Bluff, IL, USA). The specimens were ultrasonicated in distilled water for 5 minutes, air dried, mounted on aluminum stubs and sputter-coated with Au-Pd. The nanoleakage patterns were observed by scanning electron microscopy (JSM-5310, Jeol, Tokyo, Japan) using the backscattered electron image mode.

RESULTS

Figures 1-3 are representative of dentin specimens subjected to the experimental conditions.

When the SBMP specimens were only acid-etched, the hybrid layer was approximately 5-mm-thick. Silver was deposited along the hybrid layer and inside some dentin tubules (Figure 1a). This specimen shows structures suggesting water trees, projecting from the hybrid layer up to the adhesive layer. This phenomenon represents residual water channels trapped within the adhesive layer. Figure 1b shows the resin-dentin interface of the NaOCl deproteinized specimen bonded with SBMP. The hybrid layer is not apparent. A thin and discontinuous silver deposit can be observed along the resin-dentin interface. In some parts, patches of silver deposits appeared between some resin tags and tubule walls. Silver deposits can also be seen within the adhesive layer. This finding was observed in most specimens bonded with SBMP. SBMP showed the greatest silver deposition of all tested bonding systems. For PB, in specimens only acid-etched, silver deposit occurred almost throughout the entire thickness of the hybrid layer and along the tubule walls (Figure 2a). In deproteinized specimens, PB did not show silver deposits (Figure 2b). In SE, no silver deposits were seen at the adhesive-dentin interface, irrespective of the dentin treatment (Figure 3a and 3b).

DISCUSSION

Despite their different formulations, adhesive systems should be able to provide adequate cavity wall-resin interface sealing. The adhesive systems are composed of a distinct association of hydrophilic and hydrophobic monomers dissolved in an organic solvent, such as water, ethanol or acetone. The adhesion mechanism includes dentin surface demineralization either by phosphoric acid solutions⁶ or by self-etching primers. The nanospaces created on the collagen mesh after etching are filled with resin monomers that copolymerize in situ, creating the so called hybrid layer¹⁵.

The nanoleakage phenomenon was first described by Sano, et al.²⁵ (1994) and was associated with the diffusion of ions or molecules throughout the nanometric spaces located inside the hybrid layer. It was reported that even in the absence of gaps, silver ions could penetrate the hybrid layer and that this finding could be linked to inefficient monomer diffusion through a demineralized collagen layer.

NaOCl is a well-known nonspecific proteolytic agent³⁹ and its collagen removal ability has been evaluated in previous studies^{3,9,10,18,22,24,38,39}. Furthermore, recent studies reported that collagen removal with 10% NaOCl prevented the nanoleakage phenomenon^7,20.

In the present study, a 50% (w/v) silver nitrate solution was used as a tracer to evaluate the nanoleakage phenomenon. There is a possibility, however, that the low pH of this solution may over-demineralize dentin and create artificial paths along the dentin-adhesive interface, thus masking the nanoleakage results¹⁹. Consequently, some previous studies proposed the use of less acidic silver nitrate solutions to evaluate the nanoleakage phenomenon^7,31,32. A previously published study, however, presented evidences that would support the use of 50% (w/v) silver nitrate solution in nanoleakage evaluation¹². In the aforementioned study, no differences were found between the nanoleakage patterns in specimens placed in silver nitrate solutions with high or low concentrations, and with pH ranging from 3.4 to 6. Moreover, Tay, et al.³¹ (2002) showed similar nanoleakage patterns for self-etch adhesives after immersion in both types of silver nitrate [i.e., conventional and less acidic (ammoniacal)]. Based on these studies, it may be assumed the results of the present study as useful for making inferences about the nanoleakage phenomenon.

Since NaOCl dentin treatment did not prevent the nanoleakage phenomenon with PB and SBMP dentin bonding systems, the research hypothesis was rejected. Irrespective of the dentin treatment, SBMP showed the largest silver deposition within the hybrid layer and the dentin tubules (Figures 1a and 1b). Figure 1a shows a reticular mode of nanoleakage. According to previous studies^31,32, this nanoleakage pattern represents discontinuous islands of silver deposits within the hybrid layers, and could be related to areas of incomplete water removal from dentin-resin interfaces, instead of incomplete adhesive infiltration. In addition, the authors of the present study hypothesize that the water present as solvent in SBMP primer could have contributed to this pattern of nanoleakage. Structures suggesting water tree formation with approximately 2.5 µm projecting from the hybrid layer to the adhesive layer can be seen in Figure 1a. Some previous studies have shown that fluid movement through these channels could degenerate the bonds over time^23,29. As this finding has been attributed to residual water channels trapped within the adhesive layer³¹, this phenomenon would not be expected to occur with SBMP. Reis, et al.²³ (2003), analyzing the nanoleakage patterns of water-based single step and two-step self-etching DBS have shown water tree formation within the adhesive layer. The authors claimed that the presence of water, organic solvents, and highly acidic monomers in these simplified DBS leads to poor monomer copolymerization and HEMA hydrogel formation, and might be responsible for the occurrence of this phenomenon³⁰. However, SBMP is a three-step DBS, which presents a hydrophilic primer and a hydrophobic resin in separate bottles (Table 1), and in its application protocol, the light-polymerized hydrophobic adhesive is applied over the primer. Theoretically, these features would avoid water tree formation. The only reasonable hypothesis that could be speculated to explain this water trees formation observed with SBMP is that the residual water from the primer, which is not light-activated, could not have been completely evaporated⁴¹, thus mixing with the hydrophobic resin during adhesive application. It is possible that this water might have formed hydrogen bonds with HEMA from SBMP adhesive³², delaying its evaporation, and consequently favoring water tree formation. Further research is necessary to support this possibility. Figure 1b shows isolated silver deposits within the adhesive layer and a thin and discontinuous line of silver along the resin-dentin interface. The authors speculate that this might be related to water domains formed around altered NaOCl collagen not completely removed by water-spray washing before SBMP application.

SBMP presents polyalkenoic acid copolymer in its formulation. Some authors report that this copolymer can chemically interact with calcium ions in the dentin²⁸. Van Meerbeek, et al.³⁴ (1996) also found silver ions within the hybrid layer. In a TEM study, these authors found an amorphous electron-dense phase at the top of the hybrid layer for SBMP, and recorded a high concentration of calcium and oxygen in it. They suggested that it most likely represented a phase separation of the polyalkenoic acid copolymer from the other primer components, as it reacted with calcium to form a calcium-polycarboxylate salt. This amorphous phase was not seen in specimens treated with an experimental primer that did not contain polyalkenoic acid. It can be speculated that oxygen could negatively influence monomer polymerization, allowing minute bubble formation within the hybrid layer and consequently turning it into a porous and degenerating zone. From these findings, it can be speculated that the SBMP bonding mechanism does not imply the establishment of any kind of chemical adhesion to human dentin.

No nanoleakage was observed in deproteinized PB specimens. Indeed, Goes, et al.⁷ (2004) did not find nanoleakage in specimens treated with Prime & Bond 2.1, a bond system from the same manufacturer, which only differs with respect to the presence of nanometric silica particles in its composition. The presence of acetone as organic solvent could contribute to this PB behavior. The high diffusion of acetone, together with a high water displacement capacity, could result in better PB contact with the deproteinized dentin, thus avoiding the establishment of nanoleakage. In addition, previous studies have shown that the low pH (1.5 _ 2.0) of this bonding system may be able to re-etch the mineral phase of the deproteinized dentin, creating a nanohybrid layer^22,28. From this point of view, the absence of nanoleakage seen on Figure 2b can be related to a dentin reconditioning after NaOCl treatment, increasing the substrate surface energy and enhancing the PB interaction with dentin. These findings lead the authors to presume that dentin deproteinization may benefit low pH and acetone based bonding systems.

The etched-only PB specimens showed extensive silver deposit in the hybrid zone and inside the dentinal tubules (Figure 2a). This finding is in agreement with Li, et al.¹¹ (2000). Two aspects could explain this behavior. Firstly, PB does not contain HEMA in its composition. The -OH groups in these hydrophilic monomers increase the surface free energy of dentin, enhancing the adhesive system wettability². Consequently, it is reasonable to speculate that the absence of HEMA could reduce the ability of PB to diffuse through collagen fibers exposed after etching¹⁶. Secondly, UDMA and PENTA are high molecular weight monomers that also possibly reduce the PB ability to diffuse through demineralized dentin²⁸. Further studies should be done in order to establish whether PENTA is less efficient than HEMA with regard to the dentin adhesion mechanism¹¹.

SE is a water-based self-etching system, which has an acidic primer that dissolves the smear layer and demineralizes superficial dentin. As this system does not require previous acid-etching, some of the drawbacks, such as dentin over-etching, over-moistening and over-drying can be avoided, thus making this bonding system less sensitive to clinical variations. Moreover, according to Toba, et al.³³ (2003) an important feature related to successful bonding is averting the collapse of the collagen mesh exposed after acid-etching

In the present study, SE primer was applied after dentin treatment with NaOCl in Group II, and at first sight, this may seem illogical. However, Inai, et al.¹⁰ (1998), showed a significant increase in the bond strength of a self-etching experimental adhesive when applied after dentin NaOCl treatment. According to these authors, some kind of interaction between the phosphate groups of the phosphoric acidic ester present in the adhesive formulation and the calcium ions left on dentin surface after NaOCl treatment could have been responsible for this increase in bond strength. The 10-MDP present in the SE formulation also has phosphate groups in its molecules, and a previous study³⁵ showed that this acidic monomer has the ability to chemically adhere to the calcium in dentin. From this point of view, the authors thought reasonable to investigate the effect of NaOCl dentin treatment before SE primer application on the nanoleakage phenomenon.

Figures 3a and 3b show that irrespective of dentin treatment, no nanoleakage was observed in SE specimens. In NaOCl treated specimens no hybrid layer could be observed, as shown in Figure 3b. It is reasonable to assume that these findings are associated with the presence of 10-methacryloyloxydecyl dihydrogen phosphate (10-MDP) in SE formulation. As a phosphoric acid ester, 10-MDP has a mild decalcification power (pH – 2.0) causing less dentin mineral removal and less collagen exposure. As a self-etching system, the monomers demineralize and penetrate the dentin simultaneously, theoretically allowing complete adhesive diffusion, thus producing a hybrid layer with fewer defects⁷. This behavior reflects the results shown in a previous study⁸, which concluded that simultaneous monomer infiltrations allow adequate adhesion and restoration sealing.

While no differences in nanoleakage were found between the groups, the authors speculated that dentin treatment with NaOCl before SE primer application in Group II could have removed the organic content of the smear layer, acting as a cleaning agent, thus enhancing the contact between the 10-MDP acidic monomer and the intact superficial dentin. Another aspect that could explain the SE performance is the presence of camphoroquinone as a photoinitiator in its primer. Miyazaki, et al.¹³ (1995), showed an increase in bond strength for DBS that have camphoroquinone as a photoinitiator in their primers and claimed that this increase in bond strength would suggest an improvement in the polymerization of the DBS impregnated into the dentin substrate. Since SBMP and PB also have camphoroquinone as a photoinitiator, the same behavior claimed here for SE could be expected. Two aspects, however, must be taken into account: firstly, in SBMP, the camphoroquinone is present only in the hydrophobic resin; secondly, PB is a DBS in which organic solvent, hydrophilic and hydrophobic monomers are mixed in a single bottle. Thus, it is possible that the absence of HEMA and the presence of high molecular weight monomers, i.e. UDMA and PENTA, as aforementioned, could have masked this effect of camphoroquinone in PB.

CONCLUSIONS

The influence of NaOCl dentin treatment on the nanoleakage phenomenon was dependent on bond system formulation and on its interaction with the substrate. The tested acetone-based system was the only DBS that showed beneficial results when used in association with the deproteinizing pre-treatment agent.

Received: August 16, 2006

Modification: December 14, 2006

Accepted: April 04, 2007

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