Original Article

 

Bismuth subsalicylate as filler particle for an experimental epoxy-based root canal sealer

 

 

Eduardo Schwartzer^I; Bruna Genari^I; Fabrício Mezzomo Collares^I; Vicente Castelo Branco Leitune^I; Fabrício Aulo Ogliari^I,II; Susana Maria Werner Samuel^I

^I Dental Materials Laboratory, School of Dentistry, Federal University of Rio Grande do Sul, Porto Alegre, RS, Brazil
^II School of Engineering, Federal University of Pelotas, Pelotas, RS, Brazil

Correspondence

 

 

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ABSTRACT

AIM: To evaluate the influence of bismuth subsalicylate addition in different concentrations on theproperties ofan experimental epoxy-based root canal sealer.
METHODS: Bismuth subsalicylate in 20%, 40%, 60%, 80%, 100% and 120 wt% was added tothe sealer. Flow, film thickness, working time, setting time, dimensional change, sorption, solubility and cytotoxicity were evaluated according to ISO standard. Data were statistically analyzed by one-way ANOVA and Tukey’stest with a significance level of 5% for all tests.
RESULTS: The flow, working and setting times significantly decreased withincreasing particle concentration. The film thickness, dimensional change, water sorption and solubility values significantly increased with higher particle amount. The results for cytotoxicity showed no statistically significant differences among the particle proportions.
CONCLUSION: The results suggest that the addition up to 80% wt of bismuth subsalicylate appears to be a promising filler particle to root canal sealer development.

Keywords: root canal, cement, endodontics, bismuth subsalicylate.

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Introduction

Root canal filling is an important step in endodontic therapy after appropriate shaping and cleaning of the canals to seal off the root canal system of any irritants that remain after enlargement¹. New root canal sealers have been developed to improve properties like sealing, solubility and dimensional stability^2-4. These materials are composed, in general, by a main organic component⁵ and inorganic elements such as radiopacifiersand filler particles, such as bismuth compounds⁶.

Bismuth is a chemical element with different applications⁷. In medicine, bismuth compounds such as bismuth subsalicylate can be used for the treatment of various gastrointestinal illnesses^8-10. In Dentistry, bismuth compounds (e.g. bismuth oxide)provide an acceptable radiopacity to root canal sealers^6,11-12. Considering that resin-based endodontic sealers present good physical properties and ensure adequate biological performance^2-3, bismuth subsalicylate should be studied.

The aim of this study was to evaluate the influence of bismuth subsalicylate addition in different concentrations into an experimental epoxy-based root canal sealer regarding the flow, film thickness, working time, setting time, dimensional change, sorption and solubility and cytotoxicity of an experimental epoxy-based root canal sealer.

 

Material and methods

 

Experimental Sealer Formulation

An experimental epoxy-based root canal sealer containing bisphenol-A and epichlohydrin, (Fiberglass, Porto Alegre, RS, Brazil) at 2:1 (base: catalyst) was used in this study. To this sealer was added bismuth subsalicylate in several concentrations: 20%, 40%, 60%, 80%, 100% and 120%, in weight. The particle size distribution was assessed using a laser diffraction particle size analyzer (CILAS 1180, Orleans, France). The mean diameter particle was 9.61 μm and particle size distribution is shown in Figure 1. Colloidal silica (particle diameter of 7nm) was added at 0.05wt% to adjust the viscosity of the sealers.

 

 

 

Flow

The flow test was conducted in accordance with ISO 687613. A total of 0.05mL of each experimental sealer was placed on a glass plate (40x40x5mm) with a graduated syringe (1.5 mL). Another plate with a mass of 20±2g and a load of 100g was applied on top of the material. Ten minutes after the start of mixing, the load was removed, and the major and minor diameters of the compressed material were measured using a digital caliper (Digimess, São Paulo, Fig. 1.The particle size distribution of bismuth subsalicylate particle. SP,Brazil). For each experimental group, the test was conducted three times and the mean value was recorded.

Film thickness

This evaluation was made according to ISO 687613. Two glass plates (5x10mm) were placed together and their combined thickness was measured. An amount of 0.5mL of experimental sealer was placed at the center of one of the plates, and a second plate was placed on top of the material. At 180±5s after the start of mixing, a load of 150±3N was applied vertically onto the top glass plate. Ten minutes after the start of mixing, the thickness of the two glass plates and the interposed sealer film was measured using a digital caliper. The film thickness was recorded by the difference between the thickness of the two glass plates with and without sealer. The mean value of three measurements was recorded as the film thickness of the material.

Working time

The test to measure the time to mix the components to obtain the cement with appropriate properties was based in ISO 687613. This test had the same sequence of the flow test, but it was repeated at longer time intervals between manipulation and setting time. The working time was recorded when the diameter of the specimen were 10% lowerthan the diameter of the immediate manipulated cement. The test was repeated three times and the mean values were recorded.

Setting time

The setting time was recorded according to ISO 687613. Rings measuring 10mm in diameter and 1mm in height were filled with the material. These specimens were maintained under controlled temperature and humidity conditions, 37±1oC and 95% respectively. Measurements were conducted using Gilmore needles, weighing 100±0.5g and a flat end of 2.0±0.1mm diameter. The needle was lowered vertically onto the horizontal surface of each sample in such a way that it touched the surface every 5 min. The setting time was recorded when the needle did not produce any visible indentation on the sealer surface.

Dimensional change following setting

The dimensional change was measured based in ISO 687613. The cylindrical matrixes were filled with the sealer. These specimens were positioned between two glass plates (25x70x1mm). Five minutes after the start of mixing, the specimens were placed in desiccators at 37oC and 95% relative humidity and held for a period three times the setting time. The specimens were removed from the matrixes and the thickness was measured. Then, they were immersed in distilled water at 37oC during 30 days and a new measurement was made. A micrometer (Aus-JENA, Jena, Germany) with 0.001mm accuracy was used for measuring purposes. The difference between before and after storage was calculated. Measurements were made three times and the mean value of these measurements was recorded as the dimensional change of the material.

Water sorption and solubility

Water sorption and solubility were determined based on the ISO 404914. Root canal sealer disks were produced in a silicone matrix (10.0mm diameter, 1.0mm thick). Specimens were placed in a desiccator at 37°C for 22 hand in a desiccator at 23°C for 2 h. The disks were repeatedly weighed in an analytical balance (Shimadzu Corp., Tokyo, Japan) until a constant mass (m1) was obtained (i.e., until the mass variance of each specimen was no more than 0.1mg in any 24 h period). Diameter and thickness of each specimen were measured with a digital caliper to calculate the volume (V) of each disk (in mm3). Thereafter, the specimens were stored in sealed glass vials with 10 mL of distilled water at 37°C for seven days. After 7 days, the disks were weighed after being washed under running tap water and gently wiped with an absorbent paper to obtain themass (m2) and then returned to the desiccator. Next, the specimens were weighed until a constant mass (m3) was obtained (as described for m1). Water sorption (WS) and solubility (SL), in micrograms per cubic millimeter, were calculated using the following formulae:

WS = m₂– m₃/ V (1)

SL = m₁– m₃/ V (2)

Cytotoxicity

According to ISO 10993-515, the cell viability was analyzed using mononuclear cells obtained from human peripheral blood. These cells were routinely maintained in Dulbecco’s modified Eagle’s medium (DMEM) with HEPES - HDMEM, with 10% fetal calf serum. The cells were maintained with endodontic sealers incubated for 72 h at 37oC and 5% CO2. The controls consisted of cells incubated without endodontic cement. The rate of viable cells was quantified by testing(3-4,5- dimethylthiazol-2-yl)-2,5-diphenol tetrazoliumbromide) MTT assay after 24hin contact with the endodontic cement.

Statistical analysis

Data normality distribution was analyzed by Kolmogorov- Smirnov and the tests used in this study were one-way ANOVA and Tukey’s multiple-comparison test with a significance level of 5% for all tests.

 

Results

Flow

The flow significantly decreased with increasing filler particles concentration comparing 20% and 40% with the other percentages(p<0.05), ranging from 15.13 to 21.72mm. The results of flow measurements are set out in Table 1.

 

 

 

Film thickness

The film thickness values significantly increased with increasing filler particle concentration (p<0.05), ranging from 113 to 483 μm. The film thickness measurements are shown in Table 1.

Working time

The means and standard deviations of working time are shown in Table 1. The working time significantly decreased with increasing filler particle concentration (p<0.05), ranging from 53.3 to25.67 min.

Setting time

The setting time significantly decreased with increasing filler particle concentration (p<0.05). These values varied from 03:51 to 06:35h. The setting time measurements are shown in Table 1.

Dimensional change following setting

The means and standard deviations of the dimensional change are shown in Table 2. The significantly highest dimensional change occurred with 80% filler particle concentration and the lowest was with 20%. The values ranged from -0.14 to -0.75%. The specimens of the groups with 100 and 120 wt% of filler particles were solubilized and the dimensional change measurement could not be performed.

 

 

 

Water sorption and solubility

Water sorption and solubility means and standard deviations are shown in Table 2. Water sorption significantly increased with higher addition of filler particle concentration (p<0.05), ranging from 33.85 to 177.9 μg/mm3. Solubility of the specimens with 120wt% filler particle concentration was statistically higher than groups with other filler particle concentration (p<0.05). The values of solubility ranged from 13.19 to 39.45μg/mm3.

Cytotoxicity

There were no statistically significant differences (p>0.05) amongthe filler particle concentrations regarding cytotoxicity. The results are shown in Figure 2.

 

 

 

Discussion

In the present study, the addition of bismuth sub salicylate influenced the tested properties. The groups higher than 60% did not achieve the standards¹³. Previous study that evaluated flow presented values of 8.9 mm for Gutta flow, 10.9 mm for AH Plus and 12.2 mm for Epiphany¹⁶. A high flow value could lead to an increased risk of sealer extrusion, but low flow values could difficult the penetration of materials in dentin root canal walls^17-18.The sealers with bismuth subsalicylate showed higher values than the standard (50 μm)¹³. Increased concentration of particles led to an increased volume of sealer particles, decreasing the flow and film thickness of sealer. However, flow and film thickness values of the experimental sealer of the present study are consistent to the values presented by commercial resin-based sealers¹⁹.The working and setting times must be long enough to manipulate the material to fill adequately the root canal²⁰. ISO 687613 requires that a sealer should present working timeless than 30 min and setting time ranged from 30 min to 72 h. In the present study, the working time of group with 120 wt% fulfilled the requirement. For the setting time, all groups fulfilled the requirements.

Water sorption could cause hydrolysis and plasticizing of the resin-based materials. These processes could result in the separation of the polymer chains, changing the dimension of the material, and consequently leading to gap formation and fluid infiltration²¹. According to ISO687613, the endodontic sealer should not shrink more than 1% and swell more than 0.1% to avoid gaps between sealer and dentin. In the present study, the experimental endodontic sealers presented swelling higher than 0.1%13 accordingly to commercial available sealers^22,24.Any uptake of water isdetermined by the intrinsic hydrophilicity of the copolymer, the type and amount of filler particles²⁵ and it could result in lower mechanical properties of root canal sealers^21,26.The water sorption could also lead to degradation of the sealer, due to the unreacted monomers leach through porosities²¹.According to ISO 404914, the water sorption of the resin-based material cannot be more than 40 μg/mm3 and the water solubility must be up to 7.5 μg/mm3. In the present study, the water sorption of the sealers with 20 wt% of bismuth subsalicylate presented water sorption in accordance to the requirement. The other concentrations did not fulfill the standard. Solubility also presented higher values than required. However, this standard is for restorative materials; there is no specific standard for resin-based root canal sealers. The values of water sorption and solubility are consistent with commercial resin-based root canal sealers²⁷. Solubility of unreacted components could lead to cytotoxicity of periapical region tissues^21,28. Low cytotoxicity is a desirable characteristic for new root canal sealers. In the present study, addition of bismuth subsalicylate did not increase the cytotoxicity of the experimental sealer.

It was concluded that addition up to 80% wt of bismuth subsalicylate appears to be a promising filler particle for root canal sealer development.

 

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Correspondence:
Fabrício MezzomoCollares
Rua Ramiro Barcelos, 2492, CEP: 90035-003
Rio Branco, Porto Alegre, RS, Brasil
E-mail: fabricio.collares@ufrgs.br

Received for publication: May 28, 2013
Accepted: September 13, 2013