Key words:
CIE L*a*b* - color stability - esthetic restorative materials - finishing - polishing
Introduction
The quality of esthetic restorations greatly depends on the accuracy of finishing
and polishing techniques used.[1] Finishing and polishing procedures which refer to gross contouring of the restoration
to obtain the desired anatomy, to reduce the roughness and scratches, are essential
to periodontal and marginal integrity and wear reduction.[2] Polished surfaces minimize the plaque accumulation, gingival irritation, poor esthetics,
surface discoloration, and secondary caries.[3] A smooth surface is clinically important as it determines the esthetics and longevity
of the composite resin restorations.[4] Surface roughness seems to affect the initial adhesion of cells; moreover, gingival
health is subjected to surface texture of the restoration.[5]
Various techniques for polishing and finishing have been investigated: aluminum oxide
disks, fine diamond burs, carbide burs, resin points, and polishers with diamond grit.[6] Several studies suggested that certain polishing techniques may be suited to specific
materials.[7] However, it was stated that it is difficult to achieve a highly polished surface
of composite resin restorations; resin matrix and filler particles do not abrade to
the same degree due to different hardness: Craters are often formed around hard quartz
particles of conventional composites so that irregularities appear on the surface
of the restoration.[8]
Discoloration represents a significant problem for direct tooth-colored restorations,
with various studies reporting the overtime color change of composite resins due to
extrinsic or intrinsic factors.[9] Changes in color depend on several factors, such as staining agent, composite resin,
and smoothness of the polished surface.[10] Optical properties and color stability were in fact influenced by surface changes
during restorative procedures of finishing and polishing.[5] Discoloration can be assessed visually and using instrumental techniques. Instrumental
techniques eliminate the subjective interpretation inherent in a visual color comparison.
Therefore, spectrophotometers and colorimeters are widely used tools to detect the
color changes in dental restorative materials.[11] Color change (ΔE) mathematically expresses the amount of difference between the
L*a*b* coordinates of different specimens or the same specimen at different instances.[12]
The aim of this in vitro study was to evaluate and compare the color stability of various esthetic restorative
materials after surface finishing/polishing with different procedures. The null hypothesis
of the study is that the finishing treatments used had no effect on the color stability
of the esthetic restorative materials tested.
Materials and Methods
Specimens’ preparation
The experimental design of the study is shown in [Figure 1].
Figure 1:Flowchart of the experimentation
Esthetic restorative materials tested in this study are presented in [Table 1]. For each brand, the A2 Vita shade was selected.
Table 1:
Esthetic restorative materials used in this study
|
Material
|
Type
|
Composition
|
Filler content percentage (w/w)
|
Manufacturer
|
Lot #
|
|
UDMA: Urethanedimethacrylate, Bis-GMA: Bis-phenol A diglycidylmethacrylate, Bis-MPEPP:
Bisphenol A polyethoxy methacrylate, TEGDMA: Triehtylene glycol dimethacrylate, Bis-EMA:
Bisphenol A polyethylene glycol diether dimethacrylate, UV: Ultraviolet, Bis-MEPP:
2,2-bis (4-methacryloxypolyethoxyphenyl) propane
|
|
Gradia Direct
|
Microfilled composite
|
Matrix: UDMA, dymethacrylate camphoroquinone
|
73
|
GC Corporation, Tokyo, Japan
|
150527A
|
|
|
Filler: Fluoro-alumino-silicate glass silica powder
|
|
|
|
|
Filtek supreme XTE
|
Nanofilled composite
|
Matrix: Bis-GMA, TEGDMA, UDMA, Bis-EMA
|
78.5
|
3M ESPE, St Paul, MN, USA
|
N748173
|
|
|
Filler: Silica nanofillers (5-75 nm), zirconia/ silica nanoclusters (0.6-1.4 |jm)
|
|
|
|
|
Ceram.X Universal
|
Nanoceramic composite
|
Matrix: Methacrylate modified ploysiloxane, dimethacylate resin, fluorescent pigment,
UV stabilizer, stabilizer, camphoroquinone, ethyl-4 (dymethylamino) benzoate, iron
oxide pigments, aluminium sulfo silicate pigments
|
76
|
Dentsply De Trey, Konstanz, Germany
|
1507000661
|
|
|
Filler: Barium-aluminium borosilicate glass (1.1-1.5 jm), methacrylate functionalized
silicon dioxide nano filler (10 nm)
|
|
|
|
|
G-Aenial
|
Microfilled hybrid composite
|
Matrix: UDMA, dimethacrylate co-monomers
|
76
|
GC Corporation, Tokyo, Japan
|
151029A
|
|
|
Filler: Silica, strontium, lanthanoid fluoride (16-17 |jm), silica (>100 nm) fumed
silica (<100 nm)
|
|
|
|
|
Essentia
|
Microfilled hybrid composite
|
Matrix: UDMA, Bis-MEPP, Bis-EMA, Bis-GMA, TEGDMA
|
81
|
GC Corporation, Tokyo, Japan
|
151109C
|
|
|
Filler: Prepolymerised fillers, barium glass, fumed silica
|
|
|
|
|
Admira Fusion
|
Nanohybrid ormocer based composite
|
Matrix: Resine ormocer
|
84
|
Voco, Cuxhaven, Germany
|
1601121
|
|
|
Filler: Silicon oxide nanofiller, glass ceramics filler (1 μm)
|
|
|
|
|
Estelite
|
Supra-nano spherical hybrid composite
|
Matrix: Bis-GMA, Bis-MPEPP, TEGDMA, UDMA
|
82
|
Tokuyama Dental corporation, Taitou-ku, Tokyo, Japan
|
6,6E+17
|
|
|
Filler: Supra-nano spherical filler (200 nm spherical SiO2-ZrO2), composite filler (include 200 nm spherical SiO2-ZrO2)
|
|
|
|
All materials were polymerized according to the manufacturers’ instructions into silicon
rings (height 2 mm; internal diameter 6 mm; and external diameter 8 mm) to obtain
specimens identical in size. Cavities of these rings were slightly overfilled with
material, covered with transparent polyester film strip (Mylar strip, Henry Schein,
Melville, NY, USA), pressed between glass plates, and polymerized for 40 s on each
side using a curing unit (Celalux II, Voco, Cuxhaven, Germany). One light polymerization
mode was used for each material - standard: 1000 mW/cm2 for 40 s. The intensity of the light was verified with a radiometer (SDS Kerr, Orange,
CA, USA). The light was placed perpendicular to the specimen surface at a distance
of 1.5 mm to have the best intensity of light in accordance to the manufacturers’
instructions.
Finishing and polishing procedures
The specimens were randomly assigned into four groups (10 specimens of each composite
for each group). The upper surface of each specimen was finished/polished with different
finishing/polishing procedures [Table 2].
Table 2:
Finishing/polishing procedures
|
Groups
|
Manufacturers’ code
|
Type
|
Abrasive
|
Manufacturer
|
|
Group 1 (control)
|
No polishing/finishing
|
No polishing/finishing
|
No polishing/ finishing
|
None
|
|
Group 2
|
REF 4312A: 9403.204.055
|
Prepolishing
|
Diamond grit
|
Komet, Gebr. Brasseler
|
|
9404.204.055, 9405.204.055
|
Polishing
|
|
GmbH and Co., Germany
|
|
|
High shine polishing
|
|
|
|
Group 3
|
REF 4546: H135Q.314.014
|
Tungsten carbide bur
|
Tungsten carbides and diamond grit
|
Komet Gebr. Brasseler
|
|
9526UF.204.100
|
Polisher interspersed with diamonds grit
|
|
GmbH and Co., Germany
|
|
Group 4
|
REF 4652: 94025M.204.070
|
Polishing
|
Diamond grit
|
Komet, Gebr. Brasseler GmbH and Co., Germany
|
|
94025F.204.070
|
High shine polishing
|
|
|
-
Group 1: Control group (no finishing/polishing procedures)
-
Group 2: Three-polisher interspersed with diamond grit REF 4312A (9403 204 055, 9404
204 055, and 9405 204 055) (Komet, Gebr. Brasseler GmbH and Co., Germany)
-
Group 3: Two-polisher interspersed with diamond grit REF 4652 (94025M 204 070 and
94025F 204 070) (Komet, Gebr. Brasseler GmbH and Co., Germany)
-
Group 4: One tungsten carbide bur + one polisher interspersed with diamond grit REF
4546 (H135Q 314 014, 9526UF 204 100) (Komet, Gebr. Brasseler GmbH and Co.).
To reduce variability, the same investigator performed all finishing/polishing procedures.
The force used in the polishing procedure was controlled with a dynamometer (Taylor
Dynamometer Inc., Milwaukee, WI, USA). The instruments were used parallel on the surface
and each polisher was used for 10 s.
Staining process
The staining solution used was coffee (Nescafe Classic, Nestle, Vevey, Switzerland).
The coffee was prepared using a proportion of two spoons of powder for 250 ml of water
at room temperature. The specimens were immersed in staining solution at room temperature
over a 28-day test period. The control samples have not been subjected to the staining
process and were stored in distilled water during the whole experimentation period.
Staining solution was changed daily and put in vials with cover that prevent evaporation.
Spectrophotometric analysis was made before staining, after staining, and after 7,
14, 21, and 28 days after the beginning of the experimentation. We indicate each time
interval as D0, D1, D2, D3, and D4. Before each measurement, the specimens were rinsed
with distilled water and air-dried.
Color testing
A blind trained operator performed the colorimetric evaluation according to the CIE
L*a*b* system at six experimental periods: Immediately after light polymerization,
after finishing/polishing procedures, and at 7, 14, 21, and 28 days of the staining
process. To simulate the absence of light in the mouth, the color of the specimens
was measured against a black background with a spectrophotometer (SP820λ; Techkon
GmbH, Konig-Stein, Germany). All specimens were chromatically measured four times
and the average values were calculated; then, each color parameter for each specimens
of the same shade was averaged. The total color differences (ΔEab*) were calculated
as follows:
Where L* is lightness, a* is green-red component (-a* = green; +a* = red), and b*
is blue-yellow component (-b* = blue; +b* = yellow). A value of ΔEab* <3.3 was considered
clinically acceptable in the present study. Color measurements of the experimental
groups were compared with those of the control group.
Statistical analysis
Statistical analysis was performed using computer software (Stata 12.0, Stata Corp.,
Station College, TX, USA). Descriptive statistics including the mean, standard deviation,
median, and minimum and maximum values were calculated for each color coordinate for
all the groups. The distributions were assessed and found to be nonnormal (Shapiro–Wilk
Test). Nonparametric Kruskal–Wallis one-way analysis of variance (ANOVA) by the factor
of material was performed with the differences in color (ΔE*ab) and three-color coordinates
(CIE L*, CIE a*, and CIE b*) between different immersion protocols in the specimen
conditions such as before staining and after staining at the significance level of
0.05. Changes in color coordinates were calculated as “color coordinate of stained
surfaces.” Means of the different polishing/finishing groups were compared with Scheffe’s
multiple comparison test at the 0.05 level of significance.
Results
The mean values and standard deviations of the color changes (ΔE) for each material
are reported in [Table 3]. Every subsequent weekly measurement was collected to assess the color change in
relation to the time of immersion. Thus, for each experimental group, every material
has five mean values (D0, D1, D2, D3, and D4). Before immersion in staining solutions,
the materials presented similar values (P > 0.05). According to ANOVA, the restorative material, time of exposure to the staining
agent, and polishing/finishing technique were found statistically significance (P < 0.05) in color change. The absence of any polishing/finishing technique as control
caused a significant lower staining for Essentia, Admira Fusion, and Estelite if compared
to the other restorative materials that significantly changed their colorimetric parameters
in 4 weeks (P > 0.05) [Figure 2]. The polishing/finishing technique used in Group 2 (three polishers interspersed
with diamond grit) caused a significantly different color change for all the materials
tested if compared to control group. Filtek Supreme XTE, G-aenial, and Ceram.X Universal
showed a significantly lower degree of staining than in Group 1 (P < 0.05). The other
restorative materials showed significantly higher values than in Group 1 with the
main increase between the 1st and the 3rd week [Figure 3]. Data deriving from samples in Groups 3 and 4 showed similar staining degree of
the restorative materials [Figures 4] and [5], except for Essentia which registered the highest discoloration in time (P < 0.05).
The polishing/finishing technique used for Group 3 tended to maintain lower staining
when compared with Group 4, except for Essentia.
Figure 2:Color change values for the esthetic restorative materials tested reported at D0,
D1, D2, D3, and D4 for Group 1
Figure 3:Color change values for the esthetic restorative materials tested reported at D0,
D1, D2, D3, and D4 for Group 2
Figure 4:Color change values for the esthetic restorative materials tested reported at D0,
D1, D2, D3, and D4 for Group 3
Figure 5:Color change values for the esthetic restorative materials tested reported at D0,
D1, D2, D3, and D4 for Group 4
Table 3:
ΔE mean values for the esthetic restorative materials tested
|
Gradia Direct
|
Filtek Supreme XTE
|
Ceram.X Universal
|
G-Aenial
|
Essentia
|
Admira Fusion
|
Estelite
|
|
Same superscript letters indicate no significant differences in row (P>0.05). DO,
D1, D2, D3, and D4 indicate time intervals between each spectrophotometric measurement.
In row, if significance indicator is missing, there are significant differences among
restorative materials
|
|
Group 1
|
|
DO
|
1.9A
|
2.1A
|
2.3A
|
2.2A
|
2.6A
|
2.1A
|
1.6A
|
|
D1
|
4.2B
|
5.2B
|
3.3C
|
4.2B
|
5.8
|
2.6C
|
3.1C
|
|
D2
|
10.1D
|
12.1D
|
5.2E
|
6.7E
|
8.3
|
4.4F
|
4.7F
|
|
D3
|
13.5
|
20.2
|
10.1G
|
10G
|
10.1G
|
6.9H
|
6.3H
|
|
D4
|
17.4
|
24.4
|
14.81
|
15.11
|
11.4
|
9.9
|
7.7
|
|
Group 2
|
|
DO
|
0.4A
|
0.6A
|
0.8A
|
0.7A
|
1.1A
|
0.6A
|
0.1A
|
|
D1
|
0.9B
|
2.4C
|
2.5C
|
3.7D
|
3.8D
|
4D
|
1.3B
|
|
D2
|
4.4E
|
3F
|
4E
|
4.9E
|
9.8G
|
11G
|
2.3F
|
|
D3
|
11.5H
|
61
|
5.51
|
61
|
11.8H
|
12.6H
|
6.81
|
|
D4
|
19.6
|
7L
|
7L
|
7.5L
|
13.2
|
16
|
10.8
|
|
Group 3
|
|
DO
|
0.6A
|
0.8A
|
1A
|
0.9A
|
1.3A
|
0.8A
|
0.3A
|
|
D1
|
3.5B
|
6.3
|
3.7B
|
4.9
|
8.3
|
2.3C
|
2.3C
|
|
D2
|
6.4D
|
8E
|
5.7D
|
8.4E
|
13.5
|
5.8D
|
3.7
|
|
D3
|
9.9F
|
10F
|
6.9G
|
12.4
|
20.5
|
7G
|
6.7G
|
|
D4
|
12.9H
|
13.6H
|
9.7
|
14.8
|
27.5
|
13.5H
|
7.6
|
|
Group 4
|
|
DO
|
0.3A
|
0.5A
|
0.7A
|
0.6A
|
1A
|
0.5A
|
0.1A
|
|
D1
|
2.8B
|
5.7
|
2.9B
|
2.2B
|
8
|
3.2B
|
1.6B
|
|
D2
|
5C
|
7.2D
|
7.9D
|
5.5C
|
11.1
|
6.9D
|
5C
|
|
D3
|
9.7E
|
10.3E
|
10.4E
|
7.2
|
17.2
|
14
|
11E
|
|
D4
|
14.2
|
16.9F
|
12.6G
|
10.2
|
21.4
|
16.5F
|
12.5G
|
Discussion
The null hypothesis of the study that the finishing treatments used had no effect
on the color stability of the esthetic restorative materials tested was rejected.
In fact, not only the time of exposure to the staining agent but also the polishing/finishing
technique played a significant role in color change. Visually and/or specific instruments
can be used to assess color change of dental materials.[11] Various studies reported the advantages of using the CIE L*a*b* coordinate system,
such as its repeatability, sensitivity, and objectivity. This technique was chosen
to evaluate the color variation (ΔE) because it is well suited for the determination
of small color variations.[13] Several authors have reported that ΔE values ranging from 1 to 3 are perceptible
to the naked eye and ΔE values >3.3 are clinically unacceptable.[13],[14] In this study, almost all the materials tested presented an unacceptable color variation
(ΔE ≥ 3.3) after 1 week of the staining process regardless of the finishing treatment
performed.
According to Ertaş et al.,[15] in this study, a long-term staining protocol of 28 days was performed. This time
of exposure should simulate around 2 years of clinical exposure to the staining agents
(24 h in vitro corresponds to about 1 month in vivo), which is considered sufficient for long-term staining susceptibility evaluation.
Coffee was selected as the staining agents, in accordance with the studies which demonstrated
that certain substances (e.g., coffee) may cause more severe staining than other.[16]
The effectiveness of finishing/polishing procedures on composite surface is an important
goal to be achieved in the restorative process; resin composite restoration can be
imperceptible only if its surface closely resembles the enamel surface. It is well
known that the smoothest obtainable surface is achieved by curing the material in
direct contact with a Mylar strip.[17] For recontouring restorations or removing excess material, some abrasive instruments
such as flexible discs and finishing burs are used. Numerous studies indicate that
rubber polishers with diamond grit produce smoother surfaces than diamond finishing
burs, tungsten carbide burs, or mounted stones.[3],[18] Similarly, in this study (except for Essentia), the finishing technique used for
Groups 2 and 3 (polishers alone) tended to maintain lower staining when compared with
Group 4 (tungsten carbide bur + polisher). Hence, we can say that rubber polishers
created smoother surfaces and therefore lower staining susceptibility if compared
to the use of carbide burs.
According to Paravina et al.,[5] a decrease in the particle size of the abrasive produces a superior surface. The
grit in the polishing material should be smaller than the particle size of the restorative
material that is being polished to produce better results. A recent study showed that
polishers’ capability of producing smooth surfaces was related to their ability to
cut the filler particle and matrix equally.[19] In the present study, carbide burs produced higher color variations than the other
groups. These instruments are necessary for contouring anatomically structured and
concave surfaces such as the lingual surface of anterior teeth or the occlusal surfaces
of posterior teeth.[3] Furthermore, while diamond burs were best suited for gross removal and contouring
because of their high cutting efficiency, carbide burs would be best suited for smoothing
and finishing because of their low cutting efficiency. However, various studies are
in accordance with the findings of this study, underlying that finishing carbide produce
rough surfaces and therefore higher discoloration compared with those produced by
rubber polishers or aluminum discs.[20]
As regards the type of composite resin, in this study, in the absence of any finishing
treatment (control group), the lower staining was recorded for the hybrid composites
(Essentia, Admira Fusion, and Estelite) if compared to the other restorative materials.
Without finishing procedure, these three different hybrid composites demonstrated
lower staining susceptibility if compared to the other microfilled and nanofilled
materials tested. Similar results were reported in our previous study, in which Estelite
and Admira Fusion showed similar results, thus demonstrating the lowest ΔE.[21] Our results are also in accordance with recent studies which reported higher discoloration
for nanofilled composites compared to nanohybrid ones.[22],[23] Ayad showed for Ormocer composites significantly lower color susceptibility if compared
to nanofilled resins.[24]
However, in this study, after the polishing/finishing protocols, the behavior of the
materials tested changed. Finishing caused a significantly different color change
for all the materials tested if compared to control group and the nanofilled composites
Filtek Supreme XTE and Ceram.X Universal showed a significantly lower degree of staining.
After finishing, the other restorative materials showed significantly higher values
and particularly the microhybrid composite Essentia reported the highest values of
discoloration after all the three different finishing protocols. This finding can
be explained by the polishability of the resin composite, which is directly affected
by the filler particle size. Generally, the smaller the average particle size, the
easier it will be to polish the resin.[25] The filler content of the composite affects its roughness; consequently, nanofilled
composites showed smoother surfaces than microfilled composites.[26] In addition to this, in the present study, polished nanofilled composites showed
lower discoloration (and probably lower surface roughness) if compared to polished
hybrid resins. As it was stated before, nanofilled composite resins contain fillers
with size ranging from around 5 to 100 nm, and the particle size is similar.[10] However, hybrid composite resins contain fillers with different particle sizes.
The finishing burs or the polisher cut better particles with similar size while the
presence of inhomogeneous fillers (as for hybrid composites) reduce the effect of
polishing of the instrument used. For this reason, after the finishing procedures,
the nanofilled composite resin tested in this study showed lower discoloration than
hybrid composite resin materials.
Conclusions
Within the limitations of this study, the finishing treatments used had a significant
effect on the color stability of the esthetic restorative materials tested. The time
of exposure to the staining agent and the polishing/finishing technique influenced
the color change.
Financial support and sponsorship
Nil.