Colour stability of veneering composites after accelerated aging.

OBJECTIVES: To investigate the colour stability of four indirect composite restorative materials after accelerated aging.
METHODS: Four indirect composites (Gradia, Signum+, HFO and Adoro) were used. For each material, six specimens were prepared and subjected to accelerated aging (Suntest CPS+, Atlas, Chicago, IL, USA) according to ISO 7491. A Dr. Lange Microcolor Data Station colorimeter (Braive Instruments, Liege, Belgium) was used to measure specimen colour before and after aging. Measurements were performed according to the CIE L*a*b* system, and the mean L*, a* and b* values for each material were calculated. The equation DeltaE = [(DeltaL*)2 + (Deltaa*)2 + (Deltab*)2](1/2) was used to measure the total colour change (DeltaE), where DeltaL*, Deltaa* and Deltab* are the differences in the respective values before and after aging. One-way ANOVA were used to determine statistically significant differences in DeltaL*, Deltaa*, Deltab* and DeltaE.
RESULTS: No statistically significant differences were found in DeltaL*, Deltaa*, Deltab* and DeltaE among the materials tested (PDeltaL*=.063; PDeltaa*=.521; PDeltab*=.984 and PDeltaE=.408). After aging, Gradia specimens showed an increase in lightness (DeltaL*=0.36) and a green-yellow shift (Deltaa*=-1.18, Deltab*=0.6), while Signum+ specimens exhibited an increase in lightness (DeltaL*=0.5) and a green-blue shift (Deltaa*=-0.9, Deltab*=-0.45). HFO specimens exhibited an increase in lightness (DeltaL*=0.75) and a green-yellow shift (Deltaa*=-1.3, Deltab*=0.06), and Adoro specimens exhibited an increase in lightness (DeltaL*=2.07) and a green-yellow shift (Deltaa*=-1.3, Deltab*=0.68).
CONCLUSIONS: Colour changes were found to be within accepted values of perceptibility and clinical acceptance after accelerated aging, and no statistically significant differences were found in DeltaL*, Deltaa*, Deltab* and DeltaE among the materials tested.

INTRODUCTION

Indirect veneering composite resins are being used with increasing frequency as a viable alternative to porcelain due to their improved mechanical properties, satisfactory aesthetic performance and ease of handling. However, long-term colour stability of these resins remains a matter of concern.1 Restorations in the oral cavity are exposed to a variety of factors, such as temperature fluctuations, humidity, light, food and beverages. Composite materials change their colour as a result of external factors, such as dietary or smoking habits.2,3 Internal discoloration in the deeper layers of the materials involves a variety of factors related to their composition. More specifically, the type of photo-initiator, nature of resin matrix, filler content and particle size distribution are related to colour stability.4,5

Colour stability is also influenced by the intensity and duration of polymerisation6,7 and, consequently, by the degree of conversion.8 In addition, factors such as heat, water, and exposure to ambient and UV radiation and food colorants have been reported to affect colour stability.9–13

In an attempt to simulate long-term intraoral colour performance of composites, several in vitro methods have been developed. These methods include storage in water, dark and dry conditions6 and exposure to visible or UV radiation or several food staining solutions.14,15

The purpose of the present study was to investigate the colour stability of four indirect composite restorative materials after accelerated aging. The testing hypothesis was that the colour parameters of the tested materials remain within a clinically acceptable level after accelerated aging.

MATERIALS AND METHODS

Four indirect light-cured restorative composites of A2 dentin shade were tested (Table 1). A total of 24 specimens were fabricated, 6 specimens for each material, by filling a metal ring of 1.23 mm in height and 8.67 mm in diameter with the unset composite material, pressing it between two microscopic glass slides and covering it with transparent polystyrene matrix strips. The specimen dimensions allowed the use of a special specimen holder in the weathering device. For groups A, B, C and D, the indirect composites Gradia, Signum+, HFO and Adoro, respectively, were used. The materials were photo- and/or thermo-polymerised, according to the manufacturer’s instructions. After removing the inhibition layer from one surface of each of the disc specimens, further polishing was performed with SiC paper up to 800 grit.

Table 1.

Materials tested.

Composites	Monomers	Fillers
Gradia (GC Europe, N. V. Leuven, Belgium)	UDMA	Microfine ceramic/prepolymer filler, 75% wt
Signum+ (Heraeus Kulzer, GmbH, Hanau, Germany)	Bis-GMA,Bis-PMA,UDMA	ZrO2, SiO2, 78.5% wt
HFO (GDF mbH, Roshbach, Germany)	Bis-GMA,UDMATEGDMA	BaO2, SiO2, 75% wt
Adoro (Ivoclar-Vivadent, Schaan-Liechtenstein)	UDMA	Inorganic fillers, 65% wt

The specimens were aged immediately afterwards in a weathering device (Suntest CPS+, Atlas, Chicago, IL, USA) according to ISO 7491.16 Each aging cycle consisted of 20 min (a dry period of 17 min followed by a 3-min rinse with deionised water at 37°C). The total exposure time was 72 h under the following conditions: UV irradiation at 800–300 nm wavelength, 765 W/m2 irradiance and 66MJ/m2 daily radiant exposure.

A Dr. Lange Microcolor Data Station colorimeter (Braive Instruments, Liege, Belgium) was used to measure specimen colour before and after accelerated aging.

A custom-made specimen holder, fabricated from additional type silicone (Panasil, Kettenbach, Eschenburg, Germany), was used to standardise specimen orientation against the colorimeter head to achieve consistency in repeated measurements. This procedure also ensured a standard background and elimination of the influence of external light at specimen edges. After colorimeter calibration, measurements were performed according to the CIE L*a*b* system, and the mean L*, a* and b* values for each material were calculated. The equation ΔE = [(ΔL*)2 + (Δa*)2 + (Δb*)2]1/2 was used to determine the total colour change (ΔE), where ΔL*, Δa* and Δb* are differences in the respective values before and after aging. According to the most commonly accepted values of visual perceptibility17 and clinical acceptance,14 colour changes for composites were considered to be visually perceptible when ΔE > 1 and clinically acceptable when ΔE < 3.3.

One-way ANOVA were used to determine statistically significant differences in ΔL*, Δa*, Δb* and ΔE among the materials tested. The type of the material was the independent variable. A level of statistically significant difference of α=.05 was employed in all cases.

Statistical analyses were performed using SigmaStat software (Jandel, St. Rafael, CA, US).

RESULTS

The results of the colour measurements are presented in Table 2. No statistically significant differences were found in ΔL*, Δa*, Δb* and ΔE among the materials tested. After accelerated aging, specimens of group A (Gradia) showed a low increase in lightness (ΔL*=0.36) and a predominantly green shift accompanied by a low yellow shift (Δa*=−1.18, Δb*=0.6), while specimens of group B (Signum+) exhibited a low increase in lightness (ΔL*=0.5) and a predominantly green shift accompanied by a low blue shift (Δa*=−0.9, Δb*=−0.45). Specimens of group C (HFO) exhibited a low increase in lightness (ΔL*=0.75) and a predominantly green shift (Δa*=−1.3, Δb*=0.06), while specimens of group D (Adoro) predominantly exhibited an increase in lightness (ΔL*=2.07) and a green shift (Δa*=−1.3) accompanied by a low yellow shift (Δb*=0.68).

Table 2.

Mean values and standard deviation of ΔL*, Δa*, Δb* and ΔE.

Groups	ΔL*	Δa*	Δb*	ΔE
A (Gradia)	0.36±0.19	−1.18±1.1	0.6±0.66	1.73±0.71
B (Signum+)	0.50± 0.3	−0.91±0.75	−0.45±0.56	1.35±0.57
C (HFO)	0.75± 0.83	−1.33±0.61	0.06±0.81	1.75±0.9
D (Adoro)	2.07± 1.06	−1.31±0.78	0.68±0.33	2.68±0.98

No statistically significant differences (PΔL*=.063; PΔa*=.521; PΔb*=.984 and PΔE=.408) were found among the materials tested.

DISCUSSION

The CIE L*a*b* system is a widely used system that defines colour using three parameters, L*, a* and b*.18 L* corresponds to the value of an object, ranging from white (+) to black (−). Both a* and b* are on the chromatic scale; a* measures red (+) at one end and green (−) on the other, while b* measures yellow (+) and blue (−), respectively. ΔE represents the overall colour change that could be reported by an observer.

It is widely acknowledged 9,15,19,20 that clinically acceptable ΔE values are less than 3.3. According to the results of the present study, the testing hypothesis was verified: all tested materials exhibited ΔE within clinically acceptable limits, with a deviation in measurements of Adoro (2.68±0.98). This result is in agreement with findings of other studies investigating similar materials. In a study by Stober et al,12 in which the colour stability of veneering composites was assessed, ΔE ranged between 1 and 3.3 for the majority of materials tested (Colombus, Artglass, Targis, Vita Zeta LC, BelleGlass) after 96 h of accelerated aging. Only Sinfony and Zeta HC exhibited ΔE of less than 1. After 168 h, all materials showed ΔE of more than 3.3, with the exception of Vita Zeta HC, which showed visible but acceptable discoloration (1< ΔE < 3.3). The main increase was in the colorimetric value b*, meaning that the specimens became yellowish. In a study involving 5 veneering composites (Conquest Sculpture, Thermoresin LC, Vita Zeta, Compo Plus, BelleGlass HP), Kolbeck et al10 found ΔE of 0.8 for Vita Zeta LC and 2.9 for BelleGlass HP after 72 h of UV irradiation. Most materials showed a yellow-green shift and became darker. The values of the yellow shifts were higher than those of the green shifts. Tanoue et al21 investigated the colour stability of Cesead and Newmetacolor Infinis and reported minimal colour changes (ΔE of 1.2 and 0.5, respectively) after immersion in water for 4 weeks.

In a clinical study regarding the colour stability of veneering resins, Rosentritt et al22 reported that the materials tested (Visio-Gem, Dentacolor and Vita Zeta) became darker and more yellow after 18 months of clinical performance (ΔE of 1–2.5). They attributed this change to UV stabilisers, whose action was obstructed by the accelerated aging procedure. Setz and Engel23 also reported a statistically significant yellow shift of facings made with Lucipast and Dentacolor after 2 years in the mouth. Matsumura et al24 tested the clinical performance of 110 restorations veneered with Cesead material and reported a «colour matching ability» (colour stability) of 82% after an observation period of 4 years and 5 months, 75.5% after 5 years and 3 months and 67.3% after 6 years and 3 months.

In this study, three materials (Adoro, HFO, Gradia) showed a yellow shift (positive Δb*). This phenomenon has been observed in previous studies and was attributed to the presence of residual camphorquinone, which is added to the composite materials as a photo-initiator.25,26 However, under the experimental conditions of the present study, intensive light during accelerated aging might have caused a further reaction of residual camphorquinone. Ferracane et al27 suggested that oxidation of unreacted double carbon bonds found in the polymerised resin, accelerated by UV light or heat in the presence of oxygen, leads to the formation of yellow-coloured peroxides. In addition, the by-products of tertiary aromatic amines (accelerators) may cause yellow-to-red-brown discoloration under the influence of light or heat.7,28 According to Schulze et al,29 differences in the concentration and structure of photo-initiators and amines may explain the wide spectrum of Δa* and Δb* values observed.

Matrix composition and filler type and size are thought to affect colour stability.19 During accelerated aging, specimens were rinsed with 37°C water for 3 min in every cycle, according to a specific program of the weathering device. Water can penetrate the matrix or matrix-filler interface.30,31 As matrix content has been associated with water discoloration of composites, one would expect that a higher matrix-filler ratio would lead to increased discoloration. The nature of the matrix might influence water uptake, as TEGDMA absorbs more water than UDMA,32 which in turn absorbs less than Bis-GMA.33 In the present study, the findings for Adoro (low filler content 65% wt, ΔE of 2.68 ±0.98) are in accordance with these reports. It has been reported5,9 that small ratio differences could not account for variations in water sorption, which is the case for the other three materials tested. From the composition presentation of the tested materials in Table 1 and the results of ΔE in Table 2, it may be concluded that the material presenting the lowest ΔE (Signum+, ΔE=1.35 ±0.57) had the highest filler content (78.5% wt), and its matrix is composed of Bis-GMA, Bis-PMA and UDMA.

When comparing Adoro with Gradia (similar matrix composition, different filler ratio), the above observations are verified: ΔE of Gradia is lower. When Signum+ was compared to materials with similar filler content, the lowest ΔE of Signum+ can be attributed to resin matrix composition differences. More specifically, Signum+ colour stability could be attributed to the presence of lower UDMA percentage combined with low-absorbing Bis-GMA and non-absorbing Bis-DMA34 compared to Gradia (UDMA only). The lower colour stability of HFO may be due to the presence of TEGDMA (higher water sorption).

In addition to matrix content and composition, filler size and distribution may also influence water discoloration,9,19 presumably through hydrolytic degradation of the filler-matrix interface and modification of the way light is scattered by the particles. According to Dietschi et al,5 low water sorption, high filler-resin ratio, reduced particle size, hardness and an optimal filler-matrix coupling system are related to improved resistance to discoloration.

According to Schulze,29 accelerated aging is an extrinsic post-curing factor. High temperature during accelerated aging could have increased the degree of conversion, leading to a change in the refractive index of the matrix. This in turn would make the material less translucent, a result of increased scattering.35,36 According to Kolbeck et al,10 the matrix composition combined with the quality of the polymerisation reaction is mainly responsible for the colour stability of veneering composites. According to Matsumura,24 colour stability is affected by the percentage of remaining C=C bonds (%RDB). It has also been shown that composites containing more than 35% of unconverted C=C bonds tend to be highly susceptible to discoloration.37 In a recent study, however,38 no correlation was found between unconverted C=C bonds and discoloration.

Colour difference (ΔE) evaluation using a colorimeter is a repeatable, sensitive and objective method. There are, however, some limitations concerning the use of colorimeters with different optical configurations as well as the “edge loss” phenomenon. Therefore, colour measurement may not be completely accurate.39,40

In the present study, a custom-made specimen holder was used to eliminate the “edge loss” phenomenon. In future studies, it would be useful to consider factors such as light scattering, gloss, shade and transparency when assessing overall discoloration of these materials.11,19

CONCLUSIONS

According to the results of the present study:

No statistically significant differences were found in ΔL*, Δa*, Δb* and ΔE values among the materials tested.

The predominant colour change after accelerated aging was a green-yellow shift for Gradia (Δa*=−1.18, Δb*=−0.6), a green-blue shift (Δa*=−0.9, Δb*=−0.45) for Signum+, an increase in lightness (ΔL*=0.75) and green shift (Δa*=−1.3) for HFO and an increase in lightness (ΔL*=2.06) and green-yellow shift (Δa*=−1.3, Δb*=0.6) for Adoro.

Colour changes after accelerated aging were within clinically acceptable ranges (ΔE<3.3) for all the materials tested.