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Brazilian Dental Journal

Print version ISSN 0103-6440On-line version ISSN 1806-4760

Braz. Dent. J. vol.16 no.3 Ribeirão Preto Sept./Dec. 2005

https://doi.org/10.1590/S0103-64402005000300003 

Apical sealing in root apex retrofilled with MTA

In vitro evaluation of apical sealing in root apex treated with demineralization agents and retrofiled with mineral trioxide aggregate through marginal dye leakage

 

 

Claudio Hideki KuboI; Ana Paula Martins GomesI; Maria Nadir Gasparoto ManciniII

IDepartment of Restorative Dentistry, Faculty of Dentistry of São José dos Campos, State University of São Paulo (UNESP), São José do Campos, SP, Brazil
IIDepartment of Bioscience and Oral Diagnosis, Faculty of Dentistry of São José dos Campos, State University of São Paulo (UNESP), São José do Campos, SP, Brazil

Correspondence

 

 


ABSTRACT

The purpose of this study was to evaluate the apical seal in root apex treated with different demineralization agents and retrofilled with mineral trioxide aggregate (MTA) using marginal dye leakage. Fifty-six, human single-rooted teeth were instrumented, filled, resected and had retrofilling cavities prepared with ultrasonic tips. Demineralizing agents were applied before the apical cavities were retrofilled with Pro Root MTA. The specimens were assigned to 4 groups (n=14), as follows: group 1 (no demineralizing agent); group 2 (35% phosphoric acid, for 15 s); group 3 (17% EDTA solution, pH 7, for 3 min); and group 4 (24% EDTA gel, pH 7, for 4 min). The extension of dye (2% rhodamine B, at 37°C, for 24 h) penetration was measured in millimeters using a stereomicroscope. Results were statistically analyzed by ANOVA and Tukey's test at 5% significance level. Among the experimental groups, the least extension of dye penetration was observed in group 1 (1.89 mm), followed by groups 2 (2.18 mm), 4 (2.54 mm) and 3 (2.64 mm). No statistically significant differences (p<0.05) were found in marginal microleakage among groups 1, 2 and 4 and groups 2, 3 and 4. Based on the results obtained in this study, it may be concluded that the application of demineralizing agents cannot be recommended when MTA is used in periradicular surgeries.

Key Words: Endodontics, demineralization agents, dye, microleakage, MTA.


RESUMO

O objetivo deste estudo foi avaliar o selamento de ápices radiculares tratados com diferentes agentes desmineralizantes e retrobturados com agregado de trióxido mineral (MTA), mediante infiltração marginal por corante. Cinqüenta e seis dentes unirradiculares humanos extraídos foram instrumentados, obturados e seccionados apicalmente. Os preparos cavitários apicais foram confeccionados com pontas ultra-sônicas e os agentes desmineralizantes foram aplicados previamente à retrobturação com Pro Root MTA. Os espécimes foram divididos aleatoriamente em 4 grupos (n=14): grupo 1 (sem agente desmineralizante); grupo 2 (ácido fosfórico 35% durante 15 s); grupo 3 (solução de EDTA 17%, pH 7, durante 3 min); grupo 4 (gel de EDTA 24%, pH 7, durante 4 min). A extensão da infiltração de corante (rodamina B 2% a 37°C, por 24 h) foi avaliada em milímetros utilizando-se um estereomicroscópio. Os resultados foram analisados estatisticamente por meio de análise de variância a um critério e do teste Tukey com nível de significância de 5%. Dentre os grupos experimentais, a menor extensão de infiltração do corante foi verificada no grupo 1 (1,89 mm), seguido pelos grupos 2 (2,18 mm), 4 (2,54 mm) e 3 (2,64 mm). Não houve diferenças estatisticamente significante (p>0.05) na infiltração marginal pelo corante entre os grupos 1, 2 e 4 e os grupos 2, 3 e 4. Com base nos resultados obtidos, pode-se concluir que a aplicação de agentes desmineralizantes não pode ser recomendada quando da utilização do MTA em cirurgias parendodônticas.


 

 

INTRODUCTION

The use of manual, rotary and/or ultrasonic cutting instruments on root dentin surface during periradicular surgery produces smear layer, which is composed of organic and inorganic material and can contain microorganisms and its endotoxins (1). It has been reported (1,2) that the application of demineralizing agents, either acids or chelating, can improve the action of root canal dressings, adhesion and penetration of retrofilling materials, and make root surface more biocompatible, optimizing periodontal healing and not interfering with apical retrofilling seal. On the other hand, smear layer removal can increase dentin permeability, facilitating bacterial penetration and reinfection of dentinal tubules if the sealing fails (1).

Different materials have been used to seal the pathways of communication between the root canal system and the oral cavity or periradicular tissues. These materials must be biocompatible and should favor regeneration of the involved tissues to their prediseased status (3). Mineral trioxide aggregate (MTA) has been developed at Loma Linda University as a promising option to seal communications between the tooth and the external surfaces (4). This material is currently marketed under the brand name Pro Root MTA (Dentsply, Tulsa, Oklahoma, USA). Several studies have shown the clinical applicability of MTA, especially in periradicular surgeries (5-10).

This in vitro study evaluated the effects of different demineralizing agents on marginal leakage on root-end fillings with Pro Root MTA.

 

MATERIAL AND METHODS

Fifty-six human single-rooted teeth were used in this experiment. All teeth were extracted for periodontal reasons and the study protocol was approved by the local Ethics in Research Committee (Protocol number 051/2000 - PH/CEP). After extraction, the teeth were kept in 10% buffered formalin for 1 week and then stored in saline prior to instrumentation. The teeth were decoronated using a #57 carbide bur (Sybron Canada, Ontario, Canada) at high-speed with water spray coolant. Average root length was 18 mm.

After enlarging the apical foramen up to a size 20 K-file (Maillefer, Ballaigues, Switzerland), root canals were instrumented at 1 mm from the apex up to a size 50 K-file (Maillefer), cleaned and shaped using standard step-back technique. Five milliliter of 1% sodium hypochlorite (Byofórmula Tecnopharma, São José dos Campos, São Paulo, Brazil) was used as irrigant at each change of file. After final irrigation, canals were dried with paper points (Diadent, Chongju City, Korea) and obturated with laterally condensed gutta-percha (Diadent) and AH Plus sealer (Dentsply De Trey GmbH, Konstanz, Germany). After removing 3 mm of excess filling material, the access cavities were closed with Cavit cement (ESPE, Premier Sales Corp., Norristown, PA, USA). The roots were stored in a closed glass recipient containing sterile saline and maintained in an incubator at 37 ± 1°C for one week.

Apical root resections were made by removing 3 mm of the apex at a 90-degree angle to the long axis of the root with a water-cooled #57 carbide bur (Sybron) at high-speed. The resected root-ends were smoothed with a double-sided carborundum disk (23.8 mm x 0.6 mm; Dentorium Export Ltd, New York, NY, USA).

A supporting matrix was developed for apical cavity preparation. This device was composed of two nylon plates with an inner channel (in each plate), which locked the roots at 45° inclination and allowed standardizing the position of cavity preparation. This matrix protected the specimens from the pressure of the vice (#3; Fort Line, São Paulo, SP, Brazil) and kept them gripped during ultrasonic preparation.

The root-end cavities were prepared using an ultrasonic unit (Jet Sonic Plus; Gnatus Equipamentos Médico-Odontológicos, Ribeirão Preto, SP, Brazil) with ultrasonic tips (S12D-90 model; Satelec, Merignac Cedex, France). A 3-mm deep class I root-end cavity was made in the resected root-end at the highest frequency setting. Cutting with the ultrasonic tips was performed using a feather-like back and forth motion with the tip enveloped in water spray.

The 56 roots were randomly assigned to 4 groups (n=14): in group 1, no demineralizing agent was applied to the roots; in group 2, the root-end cavities and resected apical surface were etched with 35% phosphoric acid gel (Scotchbond Etching Gel; 3M/ESPE, St. Paul, MN, USA) for 15 s; in groups 3 and 4 the demineralizing agents were 17% ethylenediaminetetraacetic acid (EDTA) aqueous solution, pH 7.0, for 3 min (Byofórmula Tecnopharma) and 24% EDTA gel, pH 7.0, for 4 min (Farmavida, Guaratinguetá, SP, Brazil), respectively. The agents were applied passively with 1.0 mL syringes (SR Hospital Products, São Paulo, SP, Brazil), in a way that the root-end cavities and resected root surfaces were evenly coated. After application, the agents were aspirated and the canals were irrigated with 10 mL saline and dried with absorbent paper points.

The root-end cavities were retrofilled with Pro Root MTA (Dentsply), mixed according to the manufacturer's instructions. The material was condensed into the cavities using small pluggers (#10670, SSWhite, Rio de Janeiro, RJ, Brazil). Excess material was removed with wet cotton pellets and the roots were kept in a 100% humidity environment at 37° C for 24 h. Each pouch of Pro Root MTA contained 1 g and was used to retrofill one group (14 specimens).

Twenty-four hours after retrofilling, the roots were mounted on a utility wax plate and were surface-coated with three layers of red nail varnish (Colorama, São Paulo, SP, Brazil). The varnish was applied onto the entire root surface, except for the area corresponding to the resected apical surface, and was left drying. Afterwards, the area protected with the varnish was coated with a layer of sticky wax (Horus, Dentsply Ind. e Com. Ltda, Rio de Janeiro, RJ, Brazil) to complete sealing. Eight roots were used as positive and negative controls (two roots per group). For the specimens used as positive controls, the canals were obturated only with gutta-percha, and the demineralization agent was applied in the same way as for the corresponding experimental group, keeping root surface without any coating. For the specimens used as negative controls, the canals were obturated with gutta-percha and sealer, the demineralization agent was applied in the same way as for the corresponding experimental group and root surface was coated varnish and wax, as previously described.

The roots were then immersed in 2% rhodamine B (mol wt 479; Synth, Labsynth Ltda, Diadema, SP, Brazil) aqueous solution (pH 7.03) in 0.2 M phosphate buffer. The specimens were first submitted to low-pressure conditions (25 polHg for 90 min; Dia-Pump, Model CAL - BF1725, FANEM Ltd, São Paulo, SP, Brazil) and then kept in an environment at 37 ± 1°C and 100% relative humidity for 24 h. This methodology took in consideration the findings of a previous study (11), which reported that leakage is higher when air is removed by a vacuum pump and teeth are immersed in dye for 24 h. In this study, the air was removed with a vacuum pump in a way that trapped air could not affect apical microleakage results.

After dye testing, the teeth were washed in running water for 5 min and left drying at room temperature for 24 h. The varnish and sticky wax coatings were removed with a scalpel blade and a guide groove was prepared with a diamond disc (#7020, KG Sorensen, Barueri, SP, Brazil) in a crown-apex direction on both buccal and lingual surfaces to nearly the depth of the canal. Roots were longitudinally split using a large spoon excavator and each half was fixed on a glass slide with epoxy resin (Ciba-Geigy, São Paulo, SP, Brazil). Linear dye penetration was measured using a stereomicroscope (Stemi 2000-C model, Carl Zeiss, Germany) with a 0.1-mm ocular grid at X10 magnification. The extension of dye penetration between the retrofilling material and tooth structure along both coronal and apical interfaces was assessed by two experienced examiners calibrated for the technique and blinded to the groups. Eight leakage measurements were obtained for each specimen.

The highest leakage values per specimen attributed by the examiners were selected and microleakage means recorded for the experimental groups were analyzed statistically by one-way ANOVA and Tukey's test. Statistically significant differences among the groups were set at p<0.05.

 

RESULTS

Total dye penetration was observed between gutta-percha and dentinal walls in the positive control samples. No dye penetration was observed in the negative control specimens. The lowest dye penetration means was observed in group 1 (1.89 ± 0.79 mm), followed by groups 2 (2.18 ± 0.37 mm), 4 (2.54 ± 0.88 mm) and 3 (2.64 ± 0.33 mm). Statistical analysis by one-way analysis of variance and Tukey's test did not show significant differences (p>0.05) in marginal microleakage among groups 1, 2 and 4 and groups 2, 3 and 4. Group 3 (17% EDTA solution, pH 7.0) had significantly higher microleakage than group 1 (no demineralizing agent) (p<0.05).

 

DISCUSSION

In this study, the smear layer of root-end cavities was removed because it can be disintegrated or dissolved by soluble products from bacterial metabolism, such as acids and enzymes (1) or saliva, thus causing gap formation between the filling material and the root canal walls (12). These gaps can allow leakage of bacteria or their components and byproducts into the dentinal tubules and periapical tissues (1,12). Furthermore, it has been observed that plastic filling materials and sealers penetrate better into dentinal tubules after smear layer removal (13). It may be assumed that such penetration can increase the interface between the filling and the dentin, which may improve the material's ability to prevent further leakage (1). Peters and Harrison (2), using a dye leakage model, reported that citric acid demineralization of resected root surfaces had no significant effect on the sealing ability of amalgam, IRM or gutta-percha retrofils in comparison to similar undermineralized groups.

In the present study, the root-end cavities and resected apical surface were either not treated (group 1) or treated (groups 2, 3 and 4) with demineralizing agents for smear layer removal prior to Pro Root MTA retrofilling. Wu et al. (8), in a previous study using fluid transport model, did not remove the smear layer from the root sections before obturation with MTA.

Dye penetration is often used for leakage studies because dyes are relatively easy to be stored, applied and to have their penetration assessed quantitatively (1,14). Moreover, if a filling material does not allow penetration of small molecules such as dyes, it is likely that it has potential to prevent leakage of larger molecules, such as bacteria and their byproducts (5). Several types of dyes, i.e., methylene blue (6,10,14), fuchsine (15), India ink (12,14) and rhodamine (5,10) have been used.

In a pilot study, 2% rhodamine B solution was prepared by dissolving rhodamine B crystals in distilled water and the resulting dye was found to be acidic (pH 1.8). Starkey et al. (16), while evaluating the effect of 2% methylene blue dye at different pHs (1, 1.96, 2.66, 2.73, 4.84 and 6.78) on apical leakage, observed dissolution of the exposed root apices in the groups at pH 5.0 or lower. Therefore, in the present study, 2% rhodamine B aqueous solution at pH 7.03 in a phosphate buffer was prepared by mixing 2 g of rhodamine B powder with 100 mL of 0.2 M phosphate buffer solution at pH 7.0.

The mean extension of dye penetration at tooth/material interface in group 1 was 1.89 mm. This result is not in agreement with the findings of previous studies (5,6,9). On the other hand, it is consistent with the results of Zanetti et al. (17), who also used rhodamine B and observed mean leakage of 1.10 mm.

Gilheany et al. (18) reported that the permeability of the resected apical dentin and microleakage around the retrograde filling material had a significant influence on apical leakage. Torabinejad et al. (5) reduced the amount of rhodamine B dye penetration through the exposed dentinal tubules by sealing the resected surface with a layer of adhesive. Moreover, it has been shown that, in the fluid-conductive device, the fluid movement could take place in the MTA retrofil because it is a hydrophilic aggregate material that requires moisture for its setting reaction (19). In this study, the exposed dentinal tubules of apical root resections were not sealed with an adhesive layer and dye were prepared in aqueous solution. This may partly explain why the dye could penetrate at least 6-fold deeper over the full length of the root-end cavities in eight of the tested specimens.

In their studies, Torabinejad et al. (6) and Aqrabawi (9) used 72-h immersion in 1% methylene blue dye to penetrate MTA root-end fillings. These authors observed mean dye penetration of only 0.28 - 0.31 mm and no leakage, respectively. Wu et al. (20) reported that 1% methylene blue dye solution may be discolored by some dental filling materials (amalgam, calcium hydroxide, zinc oxide eugenol cement, Cavit and MTA), which may result in unreliable results for these materials in dye leakage studies. This was one of the reasons why 2% rhodamine B aqueous solution was the dye of choice in of pH 7.03 in a phosphate buffer for 24 h.

Wu et al. (8) reported that the seal produced by MTA leaked after 24 h. However, MTA sealing was greatly improved during the first 3 months and was maintained until the end of the experiment (8). This may probably be attributed to further hydration of MTA powder by moisture, which can result in an increase in compressive strength and decrease in leakage. In the present study, MTA sealing was assessed 24 h after retrofilling. This may possibly explain why dye penetration means ranged from 1.89 to 2.64 mm after 24-h immersion in dye solution.

In a previous study (2), a demineralizing agent (1% citric acid, pH 1) was applied only on apical section surface, after insertion of the retrofilling material. It was observed that the use of demineralizing agents did not affect retrofil sealing. Accordingly, in this study, groups 1, 2 and 4 had statistically similar results (p>0.05).

Group 3 (17% EDTA solution, pH 7.0, for 3 min) had dye leakage means statistically similar (p>0.05) to those of groups 2 (35% phosphoric acid, for 15 s) and 4 (24% EDTA gel, pH 7.0, for 4 min). These findings confirm the hypothesis that the demineralizing agents possibly produce changes in dentin surface permeability (1).

Gagliani et al. (15) reported that the extension of leakage on marginal interface of apical retrofils (Super Seal), assessed with 0.5% fuchsin after application of 17% EDTA buffered solution pH 7.5 on the sectioned surface, was never greater than 2.4 mm. However, in the present study, the application of 17% EDTA solution at pH 7.0 for 3 min (group 3) and 24% EDTA gel at pH 7.0 for 4 min (group 4) on root-end cavities and resected apical surface yielded greater leakage of 2% rhodamine B (2.64 mm and 2.54 mm, respectively).

Dye marginal leakage in group 3 produced significantly higher leakage means than the group in which no demineralizing agent was used (group 1). In group 4, however, four specimens showed leakage >3 mm and other two specimens had 2.95 mm, while in group 3 only two specimens showed leakage >3 mm. A possible explanation could be the small sample size, composed by fourteen specimens in each group.

Several studies using different methodologies have been carried out to assess the marginal sealing of the MTA and have shown its effectiveness in preventing or reducing leakage, as well as its good adaptation and less amount of marginal cracks (5-9,17). However, in this investigation, MTA retrofils showed dye leakage means from 1.89 to 2.64 mm.

Based on the data presented herein, it is not possible to state which demineralizing agent should be used in periradicular surgeries with Pro Root MTA retrofils because other factors (i.e., biocompatibility and effect of the agent on the biological properties of MTA) may influence its clinical performance. No significant differences in retrofilling leakage with Pro Root MTA were observed when 35% phosphoric acid and 24% EDTA gel were used.

 

ACKNOWLEDGEMENTS

The authors would like to thank Gnatus Equipamentos Médico-Odontológicos for supplying the Ultasonic tips (S12D-90 model); Dr. Clóvis Pagani for helpful technical assistance; Dr. Marco A.

Leonel Caetano and Ivan Balducci (Department of biostatistics, Faculty of Dentistry of São José Campos) for assistance in statistical analysis; and Dr. Cristiane Y. Koga Ito (Department of Bioscience and Oral Diagnosis, Faculty of Dentistry of São José Campos) for assistance in manuscritpt preparation.

 

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Correspondence:
Dr. Claudio Hideki Kubo
Rua Guaripé, 95, c.1, Bairro Saúde
04147-070 São Paulo, SP, Brasil
Tel: +55-11-5584-0872. Fax: +55-12-3921-2036
e-mail: chkubo1@ig.com.br

Accepted August 28, 2003

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