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Dental Health, Oral Disorders & Therapy

Research Article Volume 9 Issue 1

Evaluating the Color Change of Different Types of Composite Resins Subjected to Zoom!® in-Office Bleaching

Ameer HH AL Ameedee1

1Department of Dentistry, Beirut Arab University, Lebanon
2Department of Dentistry, Babylon University, Iraq

Correspondence: Ameer HH AL-Ameedee, Department of Dentistry, Beirut Arab University, Lebanon

Received: August 19, 2017 | Published: January 10, 2018

Citation: AL-Ameedee AHH (2018) Evaluating the Color Change of Different Types of Composite Resins Subjected to Zoom! ® in-Office Bleaching. J Dent Health Oral Disord Ther 9(1): 00321. DOI: 10.15406/jdhodt.2018.09.00321

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Abstract

This study was conducted to determine the color change of 3 types of nano-filled composite resins subjected to in-office bleaching (Zoom!® gel material 25% H2O2). 20 specimen's discs with the dimensions 5mm in diameter and 2mm in thickness were prepared from each tested material resembling 3 tested groups: Beautiful II, Ceram X mono and IPS Empress Direct composite resins. The discs were polished and stored in distilled water at 37oC for one week. Then, these were exposed to Zoom!® in-office bleaching. Colorimetric measurements were performed in the 4 different sessions, before bleaching, two weeks, 4 months and two years after bleaching (resembling 4 subgroups each of 5 discs). Data was collected and statistically analyzed using SPSS version 20.

Results: There was a significant difference between the tested materials, regarding different color parameters L*a* and b* and color change ΔΕ. A significance difference was also recorded between the different sessions of color measurements.

Conclusion: It was concluded that the tested bleaching agent affected the color of all materials, and the time was an effective factor in the color change.

Keywords: In-office bleaching; Beautiful II; Ceram X mono; IPS empress direct; Composite resins

Introduction

Beauty is a combination of qualities that delight the sight, other senses or the mind. Today, because of recent introduction and production of materials science and sophisticated dental techniques, better esthetics & improved durability of a restoration is achieved. It was found that color maintenance throughout the functional lifetime of restorations which is an indicator for the durability of a treatment. In addition color match is one of the most important characteristics of esthetic restorative materials [1,2]. Esthetic materials are now placed with minimal invasive techniques, to restore lesions or discolored teeth used to be treated previously with different approaches including crowns, direct and indirect veneers or most conservatively by bleaching [3]. The public as a conservative and economical method of improving the tooth appearance has received bleaching systems. Currently several bleaching systems are introduced in the market involving in-office bleaching, home-bleaching and over-the counter bleaching products [4-6]. Chemical methods are most recommended for tooth bleaching. Hydrogen peroxide is a common bleaching agent usually used for in-office treatment with high concentration (30-35%). Several studies have indicated a morphologic change in the tooth surface after treatment with 10% carbamide peroxide or 30% hydrogen peroxide bleaching systems [7-9]. Others indicated that these chemicals did not affect the sound tooth surface morphology [10-13]. However, the restored teeth should be considered in the investigations. A limited number of studies have reported the color change of tooth-colored restorative material due to bleaching treatments. These studies used varied concentrations of bleaching products, durations of exposure and testing materials [14,15]. The type of an esthetic restoration in terms of composition, organic and inorganic phase has been detected as a crucial factor for the degree of color and surface alternations induced by the bleaching products [16-22]. Resin materials, which are the most commonly used esthetic restorations, are especially more prone to chemical alternation compared to inert metal or ceramic [23,24]. Composite resins tend to discolor teeth due to their resin matrix, hydrophilicity and water adsorption properties. Previous studies have reported that the color changes of composites resulting from 10% carbamide peroxide were similar to those of the composites stored in water and were undetectable to the human eye [14,15]. Thus, composites with their excellent aesthetic properties may change their initial color over time because of surface and marginal staining, as well as, internal material deterioration [25]. However many reports concerning the effect of in-office bleaching on natural teeth and its effects on tooth colored composite resins are not yet fully explained [26]. Discoloration had been evaluated with various instruments as instrumental colorimetric and stereomicroscope using the CIE (Comission Internationale de l’Eclai-rage) L* a* b* color system, which is developed for characterization of colors based on human perception [27]. This system expresses ΔE as a relative color change between successive color measurements. It is generally agreed that a value of ΔE ≥ 3.3 is considered clinically perceptible. However the major parameter causing the color change was found to be L* rather than chroma (a* and b*) [28]. Thus, this study was conducted to determine the color change of three types of nano-filled composite resins subjected to in-office bleaching technique using Zoom!® bleaching material. CIE L* a* b* color system was selected for color determination. The null hypothesis was that the color change of the tested materials would respond similarly to the bleaching agent.

Materials & Methods

Preparation of specimens

A total of 60 discs were prepared with 5 mm in diameter and 2 mm in thickness in a Teflon cylindrical mold, twenty discs of each type of tested composite resin (Table 1). The shade was standardized for all specimens (A₁) as to eliminate this variable. The composite was applied as one increment using a custom-made Teflon mold, and covered by a mylar celluloid strip followed by a glass plate, 200 mg weight for 30 sec. The discs were cured from each side for 40 sec. using light curing was performed for 40 sec at the top and bottom surfaces using a halogen light curing unit (GNATUS, Fotopolimerizador optilight plus, Brazil) at an intensity of 450 mW/cm2 which was verified before polymerization by using a radiometer (DXI. So.V.INC. USA). The cured resin specimens were removed from the mold by pushing the Teflon condenser against the bottom. There was further polishing of the disc surface by using medium, fine, and superfine polishing discs (Sof-Lex system; 3M ESPE) with a slow-speed hand piece, rotating in one direction, although the smoothness was obtained with the celluloid strip. All specimens after cleaned followed by a 30 sec Pro’skit ultrasonic cleaner (Pro’skit, SS-802F, China). The specimens were stored in distilled water at 37 oC for one week to ensure complete polymerization, and then 5 specimens from each tested groups were blotted dry to be subjected to color evaluations were performed using correction evaluation, using Vita Easyshade compact device (VITA Zahnfabrik H. Rauter Gmbh & Co. KG, Bad Säckingen, Germany). The readings were recorded as control (before bleaching) data. The specimens were then subjected to Zoom!® in-office bleaching gel (Discus Dental Canada, 2830 Argentia Road, Unite 728 Mississauga, 0NL5N-8G4) according to the manufacturer’s instructions, the storage medium was replaced on weekly basis using an environmental water bath (BW1. PORTEX Ltd. Hythe Kent. England). The sessions for recording the color measurements preformed before bleaching, two weeks,4 months, and two years after bleaching are shown in (Table 2). This system allows the numeric definition of a color as well as the difference between two color values obtained using Hunter’s equation:

ΔE=  [ ( L 1 L 0 ) 2 +  ( a 1 a 0 ) 2 +  ( b 1 b 0 ) 2 ] ½ MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVCI8FfYJH8YrFfeuY=Hhbbf9v8qqaqFr0xc9pk0xbb a9q8WqFfeaY=biLkVcLq=JHqpepeea0=as0Fb9pgeaYRXxe9vr0=vr 0=vqpWqaaeaabiGaciaacaqabeaadaqaaqaaaOqaaKqzGeaeaaaaaa aaa8qacqqHuoarcaWHfbGaeyypa0Jaaeiia8aacaGGBbGaaiika8qa caWHmbWcdaWgaaqcfayaaKqzadGaaGymaaqcfayabaqcLbsacqGHsi slcaWHmbWcdaWgaaqaaKqzadGaaGimaaWcbeaajugib8aacaGGPaWc daahaaqcfayabeaajugWaiaaikdaaaqcLbsapeGaey4kaSIaaeiia8 aacaGGOaWdbiaahggalmaaBaaajuaGbaqcLbmacaaIXaaajuaGbeaa jugibiabgkHiTiaahggalmaaBaaabaqcLbmacaaIWaaaleqaaKqzGe WdaiaacMcalmaaCaaajuaGbeqaaKqzadGaaGOmaaaajugib8qacqGH RaWkcaqGGaWdaiaacIcapeGaaCOyaSWaaSbaaKqbagaajugWaiaaig daaKqbagqaaKqzGeGaeyOeI0IaaCOyaSWaaSbaaeaajugWaiaaicda aSqabaqcLbsapaGaaiykaSWaaWbaaKqbagqabaqcLbmacaaIYaaaaK qzGeGaaiyxaSWdbmaaCaaabeqaaKqzadGaaiyVaaaaaaa@6BA3@

The change in color from control compared to the color two weeks after bleaching was calculated as ΔE₁. The change in color 4 months after bleaching compared to two weeks after bleaching was calculated as ΔE₂ while the change in color two years after bleaching compared to 4 months after bleaching was calculated as ΔE₃. Before each assessment the instrument was calibrated according to the manufacturer’s recommendations. The discs were mounted at 90⁰ relative to the light source. For each specimen 5 readings were taken & mean of ΔE was calculated & recorded. All data was collected, tabulated according to groups & subgroups to be statistically analyzed. Data were fed to the computer & analyzed using IBM SPSS software package version 20. Quantitative data was described using mean & standard deviations. The distributions of quantitative variables were tested normally using Kolmogorov-Smirnov test, Shapiro-Wilk test & D’Agstino test. Also Histogram & Q-Q plot were used for vision test. If it revealed normal data distribution, parametric tests were applied. If the data were abnormally distributed, non-parametric tests were used. For abnormally distributed data, comparison between two independent populations was done using Mann Whitney test, while Kruskal Wallis test was used to compare different groups.

Material

Composition

Manufacturer

Beautiful II G I

Bis phenyl glycidyl Dimethacrylate (Bis-GMA)

Shofu Dental corporation USA

7.5% triethylenglycol Dimethacrylate (TEGDMA)

5% Aluminofluoro

70% AL₂O₃ (borosilicate glass)

DL-Camphorquinone

Methacrylate modified polysiloxone.

De Tray

Di methacrylate resin.

Dentsply

Ba-Al-borosilicate glass.

Germany

Ceram. X. mono G II

70% pyrogenic Sio₂

57% camphorpuinone

ethyl-4-dimethylamino benzoate

UV stabilizer

butylated hydroxyl to luene

Paste of Dimethacrylates,

Ivochr. Vivadent

Copolymer 20-21% wt.

USA

ISP Empress Direct G III

barpum glass 77.5-79% wt.

ytterbium trifluoride (550nm)

Initiators

Stabilizers and pigments

Table 1: Materials used in the study.

Groups

Subgroups and Sessions for Recording the Color Changes Measurements

G I (n=20)

Before bleaching

Two weeks after

4 months after

6 months after

G II (n=20)

Immersion in distilled

bleaching, n=5

bleaching, n=5

bleaching, n=5

G III (n=20)

water at 37⁰ C for one week, n=5

Table 2: Grouping and sessions for recording.

Significance test results are quoted as two tailed probabilities. Significance of the obtained results was judged at the 5% level.

Results

Data were presented as mean and standard deviation (SD) values. One way ANOVA test was used to compare the color at ΔE1 data to the color after bleaching in different sessions. Effect of bleaching on color change between the three groups at different time intervals (as a factor of time) revealed a significant effect on color change of each group individually (Table 3). Effect of bleaching on color change within the group (as a factor of time), regarding GI, there was a significant effect at all-time interval. Regarding GII, there was a significant effect at all-time interval. Regarding GIII, there was a no significant effect at ΔE2. However, there was significance effect at ΔE3. Comparison between the three groups at ΔE1 revealed that GI there was significant color change. However, GII and GIII no significant difference at ΔE1. No significant differences among the three groups at ΔE2 and ΔE3 (Table 3). Regarding the color change, comparing the color change resembled in ΔE of each group using the F-test. It was found that a highly significant difference was recorded in GI and significant in each GII and GIII tested group, GI and GII revealed statistically significant changes in color differences (∆E) after bleaching at all tested time intervals. However, GIII did not show color differences (∆E) changes except at ∆E3 tested time interval (Table 3). However, concerning ΔE the significant difference among the three tested groups was recorded only ΔE1 to visual detection of the difference between three tested groups a bar graph was drawn (Figure 1). The highest mean value was seen in GI at ΔE1, and the lowest mean value was seen in GII at ΔE3 recording that the material is an effective variable in the color change (Figure 1 & Table 3). To compare the control or baseline data to the different sessions of color evaluation after bleaching Table 5 represented LSD comparison. A significant difference was recorded in both GI & GII. In Group I the significance is present between before bleaching (control) data versus all periods of color evaluation. In-group II all the significance is present between before bleaching vs. two weeks after bleaching (Table 4 & 5).

Group

ΔE1

ΔE2

ΔE3

F-Test (p)

B. Group I µ±σ

6.453a1±0.306

0.725b3±0.843

0.277b4±0.297

398.7 (p<0.01)**

C. Group II µ±σ

0.994a2±0.639

0.579b3±0.397

0.17c4±0.106

8.843 (P<0.05)*

E. Group III µ±σ

0.73b2±0.601

0.694b3±0.633

0.177c4±0.072

3.787 (P=0.04)

Table 3: Descriptive statistical study of color changes (∆E) for all the tested groups (n=5).
*The mean difference is significant at the 0.05 level. **The mean difference is highly significant at the 0.01 level.

Different letter in same row= significant differences.

Different number in same column= significant differences.

T0- N=5

T1- N=5

T2- N=5

T3- N=5

F-Test (p)

B.Group I µ±σ

L*

83.151±0.51

80.071±0.05

80.71±0.70

80.491±0.88

47.07(p<0.01)**

a*

-0.371±0.17

0.871±0.05

0.621±0.36

0.551±0.314

45.25(p<0.01)**

b*

20.571±0.24

15.061±0.05

15.221±0.16

15.161±0.15

28.02(p<0.01)**

C.Group II µ±σ

L*

82.512±0.73

82.772±0.69

82.522±0.71

82.352±0.69

0.61(0.615)

a*

0.32±0.13

0.262±0.052

0.242±0.084

0.242±0.84

0.99(0.41)

b*

15.52±0.50

15.32±0.28

15.311±0.45

15.311±0.45

0.50(0.68)

E.Group III µ±σ

L*

79.083a±0.40

78.893a±0.44

79.083a±0.39

79.013a±0.40

0.83(0.49)

a*

-2.273a±0.20

-2.223a±0.24

-2.263a±0.20

-2.283a±0.27

0.13(0.94)

b*

12.853a±0.53

13.013a±0.25

12.863a±0.54

12.783a±0.53

0.75(0.75)

F-Test (p) among 3 groups

L*

151.6(p<0.01)**

179.5(p<0.01)**

37.37(p<0.01)**

59.44(p<0.01)**

a*

622.1(p<0.01)**

124.7(p<0.01)**

318.4(p<0.01)**

410.4(p<0.01)**

b*

788 (p<0.01)**

324.7(p<0.01)**

111.6(p<0.01)**

118.5(p<0.01)**

ΔE

ΔE₁

ΔE2

ΔE3

F

362.4 (p<0.01)**

0.139 (0.871)

1.017 (0.375)

Table 4: Statistical analysis between groups in different color recording sessions.

*The mean difference is significant at the 0.05 level.

**The mean difference is highly significant at the 0.01 level.

Before Bleaching Vs Two Weeks after Bleaching

Before Bleaching Vs 4 Months after Bleaching

Before Bleaching Vs Two Years after Bleaching

Group I P-value

L*

P<0.01**

P<0.01**

P<0.01**

a*

P<0.01**

P<0.01**

P<0.01**

b*

P<0.01**

P<0.01**

P<0.01**

Group IIP-value

L*

0.048*

0.34

0.71

a*

0.049*

0.44

0.85

b*

0.22

0.96

0.75

Table 5: LSD test to compare the changes in color space system within groups after the alteration by H2O2 for two years’ time follow up.

* The mean difference is significant at the 0.05 level.

** The mean difference is highly significant at the 0.01 level.

Figure 1: Bar graph representing mean color values (∆E) of the three groups in different color recording sessions.

Discussion

Discoloration of composite resins remains a major cause of the esthetic failure of materials. Such discoloration may be caused by intrinsic or extrinsic factors. The discoloration may involve the resin material itself. To ensure excellent esthetics, it is necessary for tooth colored restorations to maintain intrinsic color stability and resistance to surface staining [29]. Currently, according to the resin composite surface color it was found that evaluating the color before bleaching GI showed the statistical significant highest mean color value followed by GII, while GIII had the statistical significant lowest mean color value. After bleaching the color was evaluated in 3 different sessions. It was found that G I had the highest ΔE mean value at ΔE1, while G II showed the lowest mean ΔE value at ΔE3. These findings illustrated that bleaching agents used affected the color change of each tested group significantly. This was in accordance to Erim & Ulukapi et al. [29], who stated that the bleaching agents caused adverse effects to the tooth/restoration interface. The results collected in the present investigation showed significant differences between three tested groups in color change which might be related to differences in chemical composite size, distribution of filler particles. A larger area of interface between particle matrixes composite possibly makes it more susceptible to discoloration [31,32]. Others explained that bleaching treatment led to surface dissolution in the materials. Tiny pores on the surface, resulting from the matrix dissolution, occupied by air or saliva. The differences of optical properties among the materials, air, and water increased the reflectance on the surface [33-35]. Despite the increase in brightness that was evident for tested composites, this parameter alone was not conclusive or decisive for description of color, since color can only be described in three dimensions. Lim et al [36] concluded that the correlation between the contents of color is moderate, despite a direct relationship between content loading, scattering coefficient and reflected light and the change in ΔE mean values. This was true in the current findings showing a decrease in mean ΔE values at ΔE3 for GI and an increase in mean ΔE values for both groups II and III reaching the maximum values at ΔE3. This was also supported by other studies [37-48], who stated that micro cracks and micro voids located at the interface between the filler and the matrix are the most likely penetration pathways for stain. The roughness of the surface caused by wear and chemical degradation may also affect gloss and consequently increase the extrinsic staining [41,42]. This in this vitro study has several limitations. One is the lack of thermo-cycling that could influence the degree of total color change. The difference in thermal expansion coefficient or thermal conductivity coefficient between filler particles and resin matrix may result in a difference in thermal volumetric changes between resin matrix and filler particles. It was also reported that water absorption would be accompanied by hygroscopic expansion in the resin matrix and filler phase, thereby enhancing the weakening filler matrix interface. This should be considered in future research.

Conclusion

The Zoom!® In-office bleaching gel affects the color change of tested restorative materials in a different way.

The time affected the color changes of materials tested.

Acknowledgement

None.

Conflicts of Interest

None.

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