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University of Groningen
Predictability of clinical wear by laboratory wear methods for the evaluation of dentalrestorative materialsHeintze, Siegward Dietmar
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Publication date:2010
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155
Chapter 6
Wear of ten dental restorative materials in five wear
simulators – Results of a round robin test
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Abstract Objective: The purpose of the present study was to prove the hypothesis that different wear measurement methods generate different material rankings. Methods: Ten restorative materials, eight composites (belleGlass, Chromasit, Estenia, Heliomolar, SureFil, Targis cured at 95°C and 130°C, Tetric Ceram) an amalgam (Amalcap) and a ceramic (Empress) have been evaluated with regard to the wear with five different wear methods (IVOCLAR, ZURICH, MUNICH, OHSU, ACTA). Every centre received samples, which Ivoclar Vivadent had made using the same batch. The test centres did not know which brand they were testing. After completion of the wear test, the raw data were sent to IVOCLAR for further analysis. The statistical analysis of the data included logarithmic transformation of the data, the calculation of relative ranks of each material within each test centre, measures of agreement between methods, the discrimination power and coefficient of variation of each method as well as measures of the consistency and global performance for each material. Results: Relative ranks of the materials varied tremendously between the test centres. When all materials were taken into account and the test methods compared with each other, only ACTA agreed reasonably well with two other methods, i.e. OHSU and ZURICH. On the other hand, MUNICH did not agree with the other methods at all. The ZURICH method showed the lowest discrimination power, ACTA and IVOCLAR the highest. Material-wise, the best global performance was achieved by Empress, which was clearly ahead of belleGlass, SureFil and Estenia. In contrast, Heliomolar, Tetric Ceram and especially Chromasit demonstrated a poor global performance. The best consistency was achieved by belleGlass and SureFil, whereas the consistency of Amalcap and Heliomolar was poor. Significance: As the different wear simulator settings measure different wear mechanisms, it seems reasonable to combine at least two different wear settings to assess the wear resistance of a new material.
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Introduction
Wear is a phenomenon that occurs whenever a surface is exposed to another
surface or to chemically active substances. Material loss or wear occurs through
microploughing, microcutting, microcracking and microfatigue [1]. The various dental
materials may be grouped into five different categories: metal alloys, ceramics,
amalgams, composites and unfilled polymers. Of all these materials the composite
resins have a particular behaviour as many variables that derive from their
composition directly influence their wear resistance. Composites consist of filler
particles dispersed in a brittle polymer. Optimally, the loading force is completely
transferred from the matrix to the filler particles. The size, shape and hardness of the
fillers, the quality of the bonding between fillers and polymer matrix, the
polymerization dynamics of the polymer all have an effect on the wear characteristics
of a dental material. The various components of the composition, on the other hand,
influence physical parameters, such as flexural strength, fracture toughness, Vickers
hardness, modulus of elasticity, curing depth, etc., which may influence the wear [2].
Ceramic, on the other hand, is a brittle material. Due to its crystalline matrix, it is less
sensitive to attrition wear but more sensitive to fatigue resulting from flaws in the
material and the material composition [3].
Different approaches have been taken to relate physical properties such as fracture
toughness to wear [4-6]. Although some factors such as fracture toughness and the
modulus of elasticity seem to be predictive for wear, both universities and companies
rely more on devices that simulate wear in vitro than on physical properties alone.
Those devices are based on different approaches for both wear simulation and wear
analysis, like chewing simulators, the ACTA-machine, pin-on-disc-machine, etc.
In 2001 the International Standard Organization ISO published a technical
specification on “Guidance on testing of wear” describing eight different test methods
of two- and/or three-body contact [7]. However, no assessment of the different wear
methods has been made. Almost no efforts have been taken so far to analyze
different restorative materials of the same batch in different wear generating
environments in a blind test approach and compare the results with regard to
agreement. Although only published in the postdoctoral thesis by Kunzelmannn, an
attempt to conduct such a test was made by the ASC MD 156 Task Force on
Posterior Composites [8]. This test included four composite materials, which were
evaluated by means of four wear methods. The test revealed important variations
with regard to the ranking of the materials relative to the test method. However, the
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tests were carried out only with a limited number of materials and did not include a
comparative statistical analysis.
The aim of the present study was to compare 10 dental restorative materials in five
wear generating and wear analysing settings, including those of the latest generation.
Special attention was put to the statistical analysis focusing on the ability to
differentiate between materials, the agreement between test methods, and the
consistency of test results.
Materials and methods
The rationale for the material selection of composite materials was based on criteria
like material composition (microfiller, fine particle hybrid), market share, clinical
success record, and indication (composites for direct and indirect restorations) (Table
1). Besides these products, a ceramic and an amalgam material were chosen for
comparison.
Material Batch Composition
Amalcap Plus
C25527 Ag (70.1%), Sn (18%), Cu (11.9%). Powder:Hg = 1:0.97
Empress TC1 C35146 SiO2 (59-63%), Al2O3 (17-21%), K2O (10-14%), Na2O (3.5-65%), pigments (<5%): B2O3, BaO, CaO, CeO2,
TiO2 Matrix (weigth%) Filler (weigth%)
belleGlass enamel 911422 Bis-GMA TEGDMA
Borosilicate 0.6µm (77%)
Chromasit S4 C15082 UDMA (23.3%), Decandiol-
DMA (10%)
Copolymer (56%), SiO2 40nm (10%)
Estenia Enamel E2 202CA BisGMA, UDMA Triethylenglycol DMA
Glass ceramic 1.5µm (76%) Al2O3 20nm (16%)
Heliomolar 210 B 29157 BisGMA (14.3%), UDMA (4.4%),
Decandioldi-methyacrylate (3.3%)
Copolymer (47%), SiO2 40nm (20.2%), Ytterbium trifluoride
(10.6%)
SureFil Shade 990615 BisGMA, urethane modified
Ba-Al-F-B-silicate 0.8-10µm (82%), SiO2 (8%)
Targis Incisal S1 C05051 UDMA (9%), BisGMA (8.7%), Decandiol-
DMA (4.6%)
Ba-Al-Si-glass 1µm (72%), SiO2 40nm (5%)
Tetric Ceram 210 C16761 BisGMA (8.3%), UDMA (7.6%),
Triethylenglycol DMA (4.3%)
Barium glass 1µm (50.6%), Ba-Al-F-B-silicate 1µm (5%),
SiO2 40nm (5%), spherical mixed oxide 0.2µm (5%),
Ytterbium trifluoride (17%) Table 1: List of materials, batch-number and composition
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Furthermore, it was the special interest of Ivoclar Vivadent to find out whether
different curing procedures influence the wear rate of a specific composite material
(Targis 95°C/130°C). The same batch of each material has been used to produce flat
samples for all participating institutes. To avoid discrepancies in the production of the
samples, all samples were produced by the same employee at Ivoclar Vivadent. For
the composite materials similar colours were chosen. Table 1 enlists the materials
with their batch number and composition. The composite materials for direct
restorations were directly applied and polymerized in the material mould specific to
each test method (3 min in Spectramat, Ivoclar Vivadent). The amalgam material was
mixed for 20 sec in the Silamat 5 triturator and also directly applied and condensed in
the specific mould. The Empress and composite resins for indirect restorations
(belleGlass, Chromasit, Estenia, Targis) were fabricated according to the
manufacturer`s instructions, however curing Targis at two different temperatures,
95°C and 130°C. These specimens were luted into the mould by means of Variolink II
luting resin (Ivoclar Vivadent). The ceramic material had been additionally
conditioned with ceramic etching gel and silanized with Monobond S (Ivoclar
Vivadent). All specimens were polished with silicon carbide paper and a polishing
machine until 2500 grit.
The materials were coded and sent to the test centres, whereas the time interval until
testing occurred was taken into account. This interval was different for each test
method.
Ivoclar Vivadent method (IVOCLAR)
After processing and before testing, the samples (n=8) were kept dry at a
temperature of 37°C for 24 hours. The samples were mounted in a chewing
simulator, which is commercially available from Willytec (Germany). Antagonists were
made of pressed IPS Empress ceramic (Ivoclar Vivadent) and were glazed two times
at a temperature of 870°C. The diameter of the antagonist was 2.36 mm at a height
of 0.6 mm from the cuspal tip to the base. This value has been validated by analyzing
the curvatures of the palatal cusp of upper first molars of young adults (unpublished
data). The load was set at 50 N, the sliding movement at 0.7 mm. A total of 120,000
cycles of unidirectional antagonist movements with a frequency of 1.6 Hz were
carried out. Furthermore, the specimens underwent 320 cycles of thermocycling
(5°C/55°C). After completing the wear generating procedure, impressions of the
material were taken by using a low viscosity silicone material (President light,
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Coltène, Switzerland). After the impression material was allowed to set for four hours,
replicas were made with white super hard plaster (Fuji Superhard rock, GC, Japan)
by means of a vacuum, vibrator and pressure device. The plaster replicas were
analysed by means of a commercially available laser device (Laserscan 3D, Willytec,
Germany) and the appropriate match-3-D-software using the procedures “fit plane”
and “subtract plane”; the method is described elsewhere [9]. The software calculated
the volumetric (IVVOL) as well as the maximal vertical loss (IVVERT) (1% percentile).
The reason for using the 1% percentile was to eliminate extreme values produced by
fine dust particles as well as other discrepancies.
Zurich method (ZURICH)
This method has been described in detail elsewhere [10]. After processing and
before testing, the specimens (n=8) were kept in water at a temperature of 36.5°C for
2 weeks. For generating wear palatal cusps, which were cut out of similar upper
molars, were pushed against the surface of the specimens (n=6) with a load of 49 N
and a frequency of 1.7 Hz. The specimens were mounted on a rubber socket at a 45°
angle, allowing the antagonist to glide over the surface of the test specimen. The test
specimens were kept in water with changing temperatures according to a
thermocycling protocol (3,000x 5°C/55°C). After 120,000, 240,000, 640,000, and
1,200,000 loading cycles, the samples were subjected to toothbrushing with a slurry
of toothpaste for 30 min, 30 min, 100 min, and 140 min respectively [11]. Additionally,
at the end of the first phase (120,000 cycles) the samples were put into a solution of
75% ethanol for 20 hours to simulate chemical degradation. After each thermo-
mechanical sequence, the maximal vertical loss of both the specimens (OCA
occlusal contact area) and the antagonists as well as the vertical loss in the contact
free area (CFA) were calculated by using a computerized 3D-scanner [12]. The
scanner is driven by step motors which scan the object in 1µm steps in the z-
direction and in 100 µm steps in the xy-direction [2]. In each test sequence six
different materials, which were randomly allocated to the six test chambers, were
subjected to wear.
OHSU method (OHSU)
This method has been described in detail elsewhere [13]. In principle, enamel cusps
were forced into contact with the specimens through a layer of food like slurry
(mixture of poppy seeds and PMMA beads). The enamel cusps were drilled out of
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human upper molars of similar shape, giving them a spherical shape of a diameter of
10mm. The enamel stylus was first ground with 600 grit and 1000 grit silicon carbide
slurry, polished with 5µm aluminium oxide paste and then ultrasonically cleaned for 1
min. The specimens (n=10 ) were stored in water for 24 hours at 37°C before being
mounted in the chewing simulator. The cusp was first forced onto the specimen
surface with a load of 50N, sliding across a linear path of 8mm to produce abrasive
wear. At the end of each path, a static load of 80N was applied to produce localized
attrition wear. For an entire test sequence, 100,000 cycles at 1Hz with unidirectional
movements were run. The mean vertical loss of the abrasion and attrition wear facets
were measured with a profilometry device at 10 defined tracks. The values of tracks 4
to 6 correspond to the abrasion wear (OHSUABR) and the tracks 8 to 9 to the
attrition wear (OHSUATT).
Munich Method (MUNICH)
For this method, a prototype of the wear simulator used for the Ivoclar Vivadent
method was utilized, though with a different machine configuration. After processing
and before testing, the samples (n=8) were kept in physiological sodium chloride
solution at room temperature for 7 days. During wear testing the test specimens
(n=8) were kept under permanent contact to the spherical antagonist (Degusit
aluminium oxide, 5 mm diameter) with a linear sliding distance of 8 mm (back-and-
forth-movement) and a vertical load of 50N. During chewing simulation the samples
were rinsed with distilled water at 37°C. At 10,000, 30,000, and 50,000 double cycles
(bidirectional forth-and-back-movement), replicas were taken with a polyvinylsiloxane
impression material (Permadyne Garant, 3MESPE) and poured out with white plaster
(Fuji Superhard rock, GC, Japan). The volumetric loss of the wear facet was
determined on the plaster models with the 3D laser device (Laserscan 3D, Willytec,
Germany), as briefly described above. In the course of each test sequence, eight
different materials, which were randomly allocated to the eight test chambers, were
subjected to wear.
ACTA method (ACTA)
Two metal wheels rotate in different directions with about 15% difference in the
circumferential speed while having close contact [14]. The test specimens (between
24 and 28) were placed on the circumference of one wheel while the other wheel
serves as antagonist. The force with which the two wheels are put together was
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adjusted to 15 N. The wheels were placed in a slurry of white millet seeds in a buffer
solution. After 50,000, 100,000 and 200,000 cycles the maximal vertical loss of the
test specimens was measured with a profilometry device.
Statistical methods
For the sake of clarity, only the wear data after completing all cycles are presented.
As the wear analysis of the antagonist is not part of all wear methods, only the wear
of the material specimens are shown. For the ZURICH method, only the material loss
results of the occlusal contact area (OCA) are presented. Thus, we will compare
seven variables related to five methods. The seven variables will be denoted by
IVVOL, IVVERT, ZURICH, OHSUABR, OHSUATT, MUNICH and ACTA. As each
variable has a different scale it is impossible to compare the variables with each
other. In order to apply an analysis of variance for a given variable, the “within-
material" variance should be similar for each material. This was obviously not the
case for the raw data (data not shown). Thus, a transformation of the data was
needed to fulfil this requirement.
Several transformations were tried, including a square-root, a cubic-root and a
logarithm transformation. It turns out that the logarithm transformation was adequate
to stabilize the variance for each variable (see Figure 1).
ANOVA and power of discrimination
ANOVA was applied for each of the seven variables using the log-transformed data.
The power of discrimination for each variable could then be measured by the R2-
value provided by ANOVA. This value represents the percentage of the total variance
in the data, caused by the variation between materials.
Agreement between methods
The sample means of the log-transformed data were used for ranking the 10
materials with respect to each variable. Instead of "absolute ranks", we have defined
"relative ranks", which should take into account the fact that some materials
performed nearly equally well for some variables, whereas other materials were
clearly better or worse. For each variable, the relative rank was assigned 1 to the
best material (the material with the lowest mean log-value, denoted by m) and the
relative rank 10 to the worst material (the material with the highest mean log-value,
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denoted by M). Then, relative ranks were defined in order to respect the relative
differences between materials. Thus, the relative rank of a material with mean log-
value x was set to 1+9(x-m)/(M-m).
While these rankings are useful to compare the materials (see below), they can also
be used to measure the agreement between two variables. A possible measure of
agreement between two variables V1 and V2 is provided by
MADR (V1,V2) = ∑
= 1
10
i | Rank (i:V1) – Rank (i:V2) | / 10
Rank (i:V) denoting the rank of the i th material with respect to the variable V. Thus
MADR is the Mean of the Absolute Deviations of the Ranks obtained from two
variables. The smaller MADR(V1,V2) the stronger V1 and V2 agree.
Comparison of materials
Ranks can also be used to compare the materials with each other with respect to
“global performance" and “consistency of performance" (across the methods). In
order to give the same weight to each method, only the variable IVVERT for the
method IVOCLAR and the variable OHSUABR for the method OHSU were
considered for this procedure. The global performance Gi of a material can be
measured by the median of its relative ranks with respect to the five methods. The
consistency of performance Ci was calculated by the mean of absolute deviations
with respect to global performance.
Reliability of methods
The reliability of the different wear measurement methods is related to its variabilities
with respect to the measurement of the same material. In order to assess this
parameter the standard deviation could not be used, since the scale differed from
variable to variable. Instead, the coefficient of variation, which is the standard
deviation divided by the mean, was employed. Thus, lower coefficients of variation
indicate a lower relative variability, which in turn may indicate a better reliability. For
this procedure the original data have been used since logarithms may happen to be
negative and the coefficient of variation is not defined for variables with negative
values.
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Results
As the focus of this study lays on the comparison between the methods the
presentation of single results for each test method has been dispensed. Figure 1
illustrates a plot of the logarithms of the raw data and the “within-material" variance,
which was stabilized by the data transformation. Some clear outliers were identified
in the data (one for the ZURICH method and four for the ACTA method) and were
discarded for the rest of the analysis. In the MUNICH method, problems with the
wear simulation affecting different materials method led to the exclusion of several
specimens (n=7), affecting different materials. Only in the IVOCLAR and OHSU wear
tests all specimens of each material could be analysed for wear. Fig. 1 shows a plot
of the logarithms of the raw data and the “within-material” variance which was
stabilized by the data transformation.
For Figure 1 and Tables 3 and 5 the materials were arranged according to their
global performance given in Table 3.
Figure 1. Logarithmic transformation of raw data for each test method The 10 materials are represented on the horizontal axis and coded as: 1: Empress, 2: belleGlass, 3: SureFil, 4: Estenia, 5: Targis 130°C, 6: Amalcap, 7: Targis 95°C, 8: Heliomolar, 9: Tetric Ceram, 10: Chromasit. Specimens are represented by their identification numbers within each material.
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ANOVA and power of discrimination
ANOVA led to clear-cut significant results (p<0.0001) for each variable, meaning that
at least some of the materials differed from the others.
Each method achieved a good discrimination power (about 90% or more), except for
the ZURICH method (R2 only about 50%) (Table 2). This could already be seen in
Figure 1, where the materials do not differ much from each other for this method.
ACTA 97.2% IVVOL 95.8% IVVERT 94.3% MUNICH 90.8% OHSUABR 89.7% OHSUATT 89.4% ZURICH 52.2% Table 2: Discrimination power of the different variables
Agreement between methods
The relative ranks of the materials in relation to each variable are given in Table 3.
One can see at first glance that the MUNICH method was very different from all the
other methods. This was confirmed by the MADR values provided in Table 4. By
contrast, the values IVVERT and IVVOL, as well as the variables OHSUABR and
OHSUATT, strongly agreed with each other (MADR=0.7 in both cases). It is also
noteworthy that ACTA was the method which agreed the most with the other
variables, in particular with ZURICH, OHSUABR and OHSUATT.
Material IVVOL IVVERT ZURICH OHSUABR OHSUATT MUNICH ACTA Global Perfor-mance Gi
Consist-ency Ci
Empress 5.1 4.0 1.0 1.6 1.9 6.8 1.0 1.6 1.8 belleGlass 4.4 4.2 2.6 6.2 4.6 3.1 7.2 4.2 1.5 SureFil 5.6 4.9 6.3 5.0 6.4 2.6 7.2 5.0 1.2 Estenia 7.4 6.3 5.1 3.1 1.1 10.0 4.6 5.1 1.7 Targis 130 7.1 6.0 5.2 8.8 9.3 2.4 8.3 6.0 1.9 Amalcap 1.4 2.5 8.0 1.0 1.0 7.7 6.2 6.2 2.5 Targis 95 6.6 5.7 7.4 8.5 8.8 2.5 8.5 7.4 1.8 Heliomolar 1.0 1.0 9.7 8.2 8.1 1.0 8.8 8.2 3.3 Tetric Ceram
7.7 7.2 9.2 10.0 10.0 3.7 8.6 8.6 1.7
Chromasit 10.0 10.0 10.0 10.0 9.2 1.5 10.0 10.0 1.7 Table 3: Relative ranks of materials with respect to each variable (rounded up or down to one decimal place) as well as global performance and consistency for each material
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IVVOL IVVERT ZURICH OHSUABR OHSUATT MUNICH ACTA IVVOL 0 0.7 2.8 2.3 2.6 3.6 2.8 IVVERT 0.7 0 2.6 2.5 2.8 3.4 2.8 ZURICH 2.8 2.6 0 2.2 2.3 4.6 1.3 OHSUABR 2.3 2.5 2.2 0 0.7 5.9 1.3 OHSUATT 2.6 2.8 2.3 0.7 0 6.0 1.7 MUNICH 3.6 3.4 4.6 5.9 6.0 0 5.4 ACTA 2.8 2.8 1.3 1.3 1.7 5.4 0 Table 4: Agreement between methods measured by MADR (rounded up or down to one decimal place). Comparison of materials
The best global performance was achieved by Empress (G=1.6) which was clearly
ahead of belleGlass (G=4.2), SureFil (G=5.0) and Estenia (G=5.1) (Table 3). In
contrast to these materials, Heliomolar (G=8.2), Tetric Ceram (G=8.6) and especially
Chromasit showed a poor global performance (G=10.0). The best consistency was
achieved by belleGlass (C=1.5) and SureFil (C=1.2), whereas Amalcap and
Heliomolar demonstrated a poor consistency (C=2.5 and C=3.3). The consistency of
all the other materials was between 1.7 and 1.9.
Reliability of method
When the coefficients of variation are compared with each other (Table 5), it can be
noted that the variables IVVERT and ACTA were those which vary the least, followed
by IVVOL. In this respect the variables OHSUABR, OHSUATT, MUNICH and above
all ZURICH did not perform that well (Table 5).
Material IVVOL IVVERT ZURICH OHSUABR OHSUATT MUNICH ACTA
Empress 42.4 19.5 34.8 15.5 26.3 25.8 51.1 belleGlass 12.3 12.5 53.6 16.7 27.7 10.9 13.0 SureFil 17.9 11.4 47.2 21.1 18.6 24.2 10.7 Estenia 26.9 14.3 50.3 19.2 45.4 46.0 14.6 Targis 130 15.4 16.0 29.1 26.7 25.2 13.4 14.0 Amalcap 10.6 9.0 28.9 46.1 45.5 30.7 13.5 Targis 95 20.6 15.8 55.0 36.6 27.6 45.7 12.6 Heliomolar 17.8 9.2 29.9 16.8 17.7 18.8 8.0 Tetric Ceram
21.1 8.8 27.1 32.8 27.7 37.7 7.3
Chromasit 17.5 8.7 44.3 18.2 21.9 34.4 8.3 Mean 20.2 12.5 40.0 25.0 28.4 28.8 15.3
Median 17.8 12.0 39.6 20.2 27.0 28.2 12.8
Table 5: Coefficient of variation (multiplied by 100) for each material and each variable, as well as mean and median of 10 coefficients of variation for each variable.
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Discussion
In the present study 10 restorative materials, eight composites, one amalgam and
one ceramic have been evaluated with regard to wear with five wear methods, every
centre receiving specimens made at Ivoclar Vivadent by the same employee with the
same batch. The test centres did not know which brands they were testing. A similar
attempt of round robin testing was carried out by the ASC MD 156 Task Force on
Posterior Composites, including 4 composite materials (Ful-fil, Heliomolar, Silux and
Herculite XR) evaluated by four wear simulators (ACTA, Alabama, Minnesota, Zurich)
and two “pin-on-disc” sliding wear machines (NIST, University of Indiana). There has
been no official publication, but the results were discussed in the postdoctoral thesis
of Kunzelmann [8]. Although the statistical analysis was not as comprehensive as in
the present study, considerable variations could be seen between the test centres
with regard to the ranking of the materials. A similar conclusion can be drawn from
the present study. When the relative ranks of the materials were calculated, the
results varied tremendously between the test centres. When taking all materials into
account and comparing the test methods, only ACTA agreed reasonably well with
two other methods, ZURICH and OHSU, achieving mean values of absolute
deviations of the ranks below 2 (Table 4). On the other hand, MUNICH did not agree
with all the other methods at all.
Two test methods produced two result values for the same material. IVOCLAR
calculated both the volumetric and the maximal vertical loss and OHSU calculated
the mean vertical loss at two different sites within the wear facet related to different
forces. However, both variables within the same test method were strongly
associated (mean values of absolute deviations of the ranks equal to 0.7, Table 4).
Considering the single materials and relative ranks, a difference of more than 1.5
units between the variables OHSUABR and OHSUATT was only found for the
materials Estenia and belleGlass, whereas for IVOCLAR the differences between
IVVOL and IVVERT were 1.1 ranks or lower. Although different forces and number of
cycles were used, similar findings were observed in other studies which employed
the OHSU method [13,15]. For this method no clear tendency between abrasion and
attrition could be seen (Table 5). For IVOCLAR the volumetric loss had higher
coefficients of variation than the vertical loss, whereas both OHSU variables were
similar in this respect. However, the abrasion variables varied less than the attrition
variable. For IVOCLAR, vertical loss varied less than volumetric loss. This may
indicate a better reliability of the vertical wear. This may be explained by the fact that
168
with IVOCLAR a transversal movement is included in the test set, which generates
material loss related to both attrition and microfatigue. Volumetric loss may thus vary
more than vertical loss as material breakdown at the margins of the wear facet
contributes to a higher scatter of the values.
ACTA achieved the highest discrimination power among the various methods,
followed by IVOCLAR (Table 2).
The test centres used different wear simulators, different forces, different antagonist
materials, different number of cycles, with or without thermocycling, etc. Some used
abrasive mediums and different methods to evaluate the material loss. ZURICH
additionally included five hours of simulated toothbrushing between the phases as
well as storage of the samples in ethanol. Wear produced by toothbrushing devices
on restorative materials in vitro is in the range of 2-5 µm when using a toothpaste of
medium abrasivity [16] and seems to be negligible when compared to the wear of the
contact area which is in the range of 50 and 180 µm for the ZURICH device.
A force of 50 N is used with ZURICH, MUNICH, IVOCLAR and OHSU (for tests on
abrasion). This value is regarded to be a mean value of the physiological biting
forces of non-bruxist patients [17]. Higher forces during in vitro simulation lead to
higher wear rates [18]. Although the simulators use the same loading force, the
actual force created on the material depends on the contact area, which not only
varied from simulator to simulator due to differences in the configuration of the
antagonist but also changes during the simulation due to flattening of the antagonist.
Enamel as antagonist material is used with ZURICH and OHSU. However, the
configuration is totally different. While in the ZURICH method, palatal cusps are cut
out of first upper molars, in the OHSU test, a spherical stylus with a diameter of 10
mm is fabricated out of extracted molars. The sharper the antagonist, the higher will
the wear rate be [8,19]. In a study on 20 extracted first upper molars, a ball with a
radius of 0.6 mm was assumed to be the most suitable for the anatomical variations
in human molar cusps [20]. No other measurements of this kind were found in the
literature. However, analyses of plaster models of ten 20-25-year old patients carried
out with 3D laser device revealed that the mean radius was 1.04 mm in the frontal
segment of the cusp and 1.79 mm in the sagital segment (unpublished data by
IVOCLAR). The latter finding was the basis for choosing a radius of 1.18 mm for the
IVOCLAR method. One explanation for the scattering of the results of the ZURICH
method, which was also expressed by its low discrimination power and high
coefficient of variation, is the use of enamel as antagonist material. This, however,
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could not be seen with the OHSU method, which also uses enamel as stylus. While
in the OHSU method, the enamel of the antagonist is prepared to a standardized
shape and polished, in the ZURICH method the enamel cusps are only standardized
by subjective molar selection and cleaned with a rotating nylon brush. Thus, the
cusps may differ widely with regard to anatomical form, fluoride content in the outer
surface and the amount of aprismatic enamel; the latter two parameters have an
effect on the hardness of the enamel stylus. Another factor that may contribute to the
scatter of the results is the rubber socket on which the samples are mounted. The
rubber socket should simulate the periodontal ligament and should produce a sliding
movement of the sample, thus leading to a dampening effect during wear simulation.
Using finite element analysis Kunzelmann reported in his postdoctoral thesis that the
sliding movement was very much dependent on where the sample was mounted in
the chamber [8]; a deviation of 1 mm from the centre resulted in a tilting movement
rather than a sliding movement. Together with changes in the elastic modulus of the
rubber over time, this uncontrollable movement, which is accelerated by
thermocycling, may be the cause for the high coefficient of variation. High standard
deviation of material loss was also reported in other publications using the same
simulator setting [18,19,21]. A substitute for enamel as antagonist may reduce both
the variability and the time required to fabricate the antagonists. Steatite, a synthetic
material mainly composed of magnesium silicate, has been regarded as a suitable
substitute by some authors [8,22,23] while denied by others [20,24]. The MUNICH
method uses Degusit material as stylus – a material that consists mainly of highly
condensed aluminium oxide. Degusit was chosen because tests revealed a similar
material wear rate for spherical Degusit antagonists as that of palatal cusps of upper
molars. The coefficient of variation after 50,000 cycles of mastication of the Degusit
spheres was lower than that of steatite and enamel. The IVOCLAR method uses IPS
Empress (Ivoclar Vivadent) ceramic material for wear testing. Recently, it was
reported that Empress ceramic material as antagonist produced a similar wear rate
on different composites as enamel antagonists [25,26].
Concerns about the reproducibility of the test results arise as the present wear data
do not necessarily match the wear data on the same material using the same wear
method. While in the case of Heliomolar, for instance, the Zurich method provided a
similar result as that published in other studies elsewhere [21], the result for Tetric
Ceram was 25% lower in the present study than that of the study by Kersten et al.
One confounder in this particular case may be the fact that the ZURICH simulation
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normally uses mod-fillings in extracted teeth for wear testing, while, by contrast, the
present study utilized flat samples. As far as reproducibility is concerned, a similar
finding was noted for the ACTA method, as in the present study Heliomolar produced
a lower vertical loss after 200,000 cycles than the loss after 100,000 cycles published
in another study (mean vertical loss 68 µm versus 84 µm) [27]. Furthermore, the
reported standard deviations were much higher than in the present study. For the
MUNICH method, SureFil and Tetric Ceram were in the same statistical subgroup,
while another study, which employed the same approach, revealed a significant
difference between both materials [6]. For the ACTA method, these differences may
be explained by the quality of the abrasive medium used (millet seeds) [28]. For the
other methods, however, which do not use abrasive media, these differences are not
readily explainable. For the OHSU method it is difficult to compare data of the
present study with those in the literature, as different forces and number of cycles
were applied [13]. However, a critical issue for the OHSU wear simulator is the need
for calibration before running tests as some mechanical features of the machine may
alter decisive wear parameters of the machine.
A striking fact was that the MUNICH method did not correspond at all with either of
the other methods. The specific test parameters may account for this result. A sliding
movement of 8 mm was chosen as an early publication indicated that the sliding
distance should be at least twice the diameter of the stylus to ensure that the
abraded material particles are easily washed away and the creep effects are reduced
[29]. In the other two-body wear approaches, IVOCLAR and ZURICH, the sliding
movements simulate the sliding of teeth that come into contact with each other [30].
In those cases, the antagonist are not in permanent contact with the specimen’s
surface, Therefore, the worn particles can be easily washed away by the water flow
during the simulation. It can be argued whether the MUNICH approach does reflect
wear mechanisms that occur clinically. As for the OHSU method a spherical stylus
with a diameter well above the diameter of molar cusps was chosen as pre-tests
showed less scattering of results and lower wear [8]. It can be argued whether both
effects may result in an additional lower degree of differentiation between the
materials. Another influence that has not been systematically evaluated may be the
material of the antagonist. The rationale to use 50,000 cycles for the MUNICH
method was that experiments with different composite resins showed that during the
first 50,000 cycles (bidirectional movement = 100,000 cycles back and forth
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movements) the increase in wear resulted in a non-linear curve, whereas after
50,000 cycles the wear increased on a linear basis.
From the comparison of the results provided by five test centres and the seven wear
parameters respectively, it is clear that at least three different types of wear can be
distinguished [3,31]:
Type 1, produced by IVVERT and IVVOL. The wear is a consequence of a direct
contact between material and antagonist and can be described as a mixed wear
(adhesion, attrition and fatigue). For composite materials the discriminating
characteristics which control the wear rate are above all the friction coefficient and
the surface roughness, which are influenced by the composite structure, the elastic
modulus, and the shear strength. The dimension and the volume of filler particles
influence the wear resistance as well. A low elastic modulus, for example, leads to a
higher contact area, thus to lower pressure. Large filler particles can cause a high
friction coefficient, leading to high internal shear stresses in the polymer matrix. A
high filler volume content can be beneficial by decreasing the tendency of the
material to creep.
Type 2, produced by ACTA, which agreed quite well with OHSUABR. This three-
body-wear test is mainly an abrasive process with low pressure loads. The wear rate
of this test is principally influenced by the hardness and fracture toughness of the
material. The OHSU simulator is very different from the ACTA machine.
Nevertheless, it seems that the wear processes are similar and only Amalcap and
Tetric Ceram represent exceptions in the correlation. Although claimed as “attrition
wear”, the parameter OHSUATTR is affected by the foregoing abrasion process, and
differs only in the load amplitude (80 N instead of 50 N). It should actually approach
the Type 1 of wear, yet as previously seen, its results agree more with OHSUABR
and ACTA than with the IVOCLAR method.
Type 3, produced by MUNICH. The simulator is the same as the one employed at
IVOCLAR, yet the different configuration parameters yield different results. Mainly
because of the much harder antagonist and the permanent back-and-forth 8 mm long
sliding, the wear mechanism is mostly due to fatigue. Important material parameters
are the elastic modulus, the strain-to-break and the type of filler. A low elastic
modulus leads to a large contact area and low contact stresses, material with high
strain-to-break are usually more resistant to fatigue, and once abraded, the filler
particles can cause a three-body abrasion, enhancing the wear rate: since the
contact is permanent, debris are entrapped between antagonist and material surface.
172
Thus, the larger and the harder the composite filler particles, the higher could this
“self-abrading” effect be.
The ZURICH method is difficult to interpret because of the large scattering of the
results. If the type of configuration parameters is taken into account, the wear
mechanism should theoretically lie between the wear types 1 and 2.
If these differences and the specific mechanical and structural characteristics are
taken into consideration, it is now possible to explain the reasons why the same
material behaved differently in different wear simulators.
Heliomolar showed low wear at IVOCLAR and MUNICH but high wear at the other
test centres. Heliomolar is a composite with microfillers (40 nm) and can be polished
to very low roughness values. In two-body attrition wear simulations like IVOCLAR
and MUNICH the friction generated during the simulation is very low, resulting in low
shear forces and low incidence of microfatigue, which ultimately causes wear [32]. By
means of a pin-on-disc wear simulator with on-line wear measurement, Kunzelmann
was able to determine the friction force generated by the stylus on different materials
[8]. Heliomolar showed a slow increase of friction force with a maximum of 7 N
compared to Tetric, which had a rapid increase with a maximum friction force of 16 N.
Additionally, abraded Heliomolar particles are transferred to the antagonist, filling the
voids of the abraded antagonist and thereby reducing the friction and wear [32]. This
effect was confirmed in the present study when the Empress antagonists were
examined for ytterbium trifluoride, the typical ingredient of Heliomolar, using EDX. In
chewing simulators like ACTA and OHSU, which use an abrasive medium, wear of
Heliomolar was higher, indicating that the abrasives together with the shear forces of
the moving stylus weaken the matrix-filler bond. Materials with a low modulus of
elasticity and low filler content are more prone to wear in the ACTA machine
compared to materials with high modulus of elasticity and high filler content [33].
However, it cannot be explained with certainty why Heliomolar showed high wear
rates in the ZURICH two-body wear simulator. Possible explanations are the above-
mentioned uncontrollable tilting movements of the rubber socket. The hydrolysis of
the matrix described in the literature [34] may have played only a negligible role,
even when the long storage time of two weeks and the long simulation procedure are
taken into account. The effect of thermocycling on wear (IVOCLAR, ZURICH) has not
been systematically evaluated, in spite of the fact that some studies revealed a wear-
increasing effect with some materials [35-37]. As the ZURICH method includes 3,000
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cycles, as compared to IVOCLAR, which uses only 320 cycles, the thermocycling
effect may be more pronounced in the ZURICH simulator.
The microfilled composite Chromasit showed the highest wear of all materials in all
wear simulators except for the MUNICH method. This material has a low filler content
of only about 30% weight, resulting in a low modulus of elasticity, flexural strength,
fracture toughness and hardness. These properties lead to early wear due to
microploughing or plastic flow. The very low elastic modulus (low contact stresses),
the low filler percentage (low friction) and the nano-size of the particles (minor self-
abrading effect) could explain the low wear in the MUNICH simulator. One study
using another approach of wear simulation showed equally high wear rates for
Chromasit [38].
belleGlass, a highly filled hybrid composite, produced low to medium wear rates in all
wear simulators. This material possesses general good mechanical properties, partly
due to the post-heat-curing procedure and the special glass fillers, which are well
bonded to the matrix. Consequently, the material is characterized by a general
favourable resistance to adhesion, abrasion and fatigue wear. This finding
corresponds with the findings of other in vitro studies using the ZURICH simulator
[39], the Alabama wear simulator [40] and a pin-on-disc apparatus [41]. The
performance of belleGlass was superior to that of Targis in the IVOCLAR, OHSU and
ZURICH simulator and equal to Targis in the ACTA and MUNICH simulator. Like
belleGlass Targis is a fine-particle hybrid composite with a high filler content and it is
also post-cured at a high temperature. The mechanical properties are also similar,
with the type of filler (the glass particles of Targis contain barium oxide) and size
(Targis incorporates slightly larger particles, about 1 µm vs. 0.6 µm of belleGlass)
being the main differences between the two materials. The susceptibility of Ba-
containing glasses to leaching as reported in the literature [42] or a weak bond
between filler and matrix could be the reason for the differences between the wear
rates. This result is in line with other publications on wear [40,41] but differs from a
publication which used the ZURICH simulator [39]. Again, the MUNICH simulator
provided different results for that material. The different curing procedures
(130°C/95°C) had no influence on the wear of Targis, although studies have shown
an improvement of physical properties of heat-treated materials compared to light-
cured ones in vitro [43] and in situ [44].
Estenia contains a hard glass-ceramic filler and nano-size aluminium oxide particles,
which render the material very hard, stiff and highly fracture resistant [45].
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Consequently, Estenia exhibited low wear in the OHSU and ACTA simulators,
medium wear in the IVOCLAR and ZURICH simulator (high contact stresses due to
the high elastic modulus and high friction due to the large hard particles) but
excessive wear in the MUNICH simulator. This may be explained by the fact that in
the MUNICH simulator aluminium oxide antagonists are used. These antagonists
come into contact with the glass-ceramic fillers of the composite, resulting in a high
roughness of the antagonist, which further damages the composite material. The
“self-abrading” effect through worn debris is particularly significant for this composite
as well. In the literature a low wear rate was found in conjunction with the Alabama
wear simulator [40].
SureFil, a packable composite whose physical properties are similar to other hybrid
composites [46] showed wear rates similar to belleGlass in all simulators except for
ZURICH. Although only light-cured, SureFil possesses stiffness, hardness, fracture
toughness and particle size which are similar to belleGlass. For the OHSU this result
is in line with another study [47].
Tetric Ceram is a direct composite. Its structure is similar to that of Targis, with a
similar type and size of Ba-containing glass fillers. The mechanical properties are in
general lower than those of Targis; consequently it showed higher wear rates. Like
Targis it can suffer from the possible leaching of barium, resulting in an additional
drawback.
Contrary to composite resins, the wear mechanisms of amalgam and ceramic
materials are different. Amalgam materials exhibit good wear resistance in many
wear simulators, which can be explained by the fact that surface tension is partly
compensated by plastic deformation. During the simulation process an oxide layer is
continuously formed and removed. Furthermore, in the two-body wear simulators,
amalgam is transferred to the antagonist, thus reducing its roughness. It was
surprising that the amalgam showed high wear in the ZURICH, MUNICH and ACTA
wear simulators. The reasons for that are not easily explainable, especially since
studies using the ACTA machine reported low wear rates for amalgam [48].
The Empress ceramic material showed low wear in the OHSU, ZURICH and ACTA
simulators but high wear in the MUNICH method and medium wear at IVOCLAR.
This may be explained by the type and hardness of antagonist material. In the two
latter simulator settings, a ceramic material is used as antagonist, accelerating the
wear processes on the ceramic specimen; this is more pronounced with aluminium
oxide than with leucite-containing ceramic (correspondingly the Degusit material is
175
also harder than the antagonist used in the IVOCLAR method). It may be argued
whether ceramic is a suitable stylus material to test ceramic samples for wear or
whether enamel should rather be used in this case. Other studies in vitro, however,
confirm the low wear rate of Empress [49].
All of the wear simulators lack the scientific evidence that the in vitro simulation
corresponds to the in vivo situation, in spite of the fact that publications related to
three of the simulators tried to establish clinical correlations. The ZURICH method
even claims that 1,200,000 cycles in the simulator corresponds to 5 years in vivo.
However, this assumption has not been systematically verified in longitudinal clinical
studies with different materials and is only based on the extrapolation of 4-year-
clinical wear data on 14 mod Dispersalloy amalgam fillings and 6-month data on
inlays made of an experimental composite [50,51]. With ACTA and OHSU, which
also published reasonable correlation coefficients between in vitro and in vivo data
[13,14], these correlations, however, were made using semi-quantitative methods for
assessing wear in vivo on pooled data from clinical trials. Methods which use scale
models, like the Vivadent Scale or ML Scale, with defined steps at the restoration
margin assume wear at the margin to be predictive for general wear and occlusal
contact wear [52]. However, they systematically underestimate wear [53], as marginal
breakdown, and under-/overfilling are possible confounders. Furthermore, wear at
the margins is not correlated with wear of the occlusal contact area. More
sophisticated methods employ special microscopic devices [54], mechanical
computer-aided scanners [2,12,55], or, more recently, laser equipment [9]. The
problems with all these methods are related to the quality of the impression for the
replica production and the need to determine reference points that are assumed to
be unchanged. However, randomized prospective clinical trials with an adequate
number of subjects, standardized clinical protocols and reliable, valid wear
assessment methods are necessary to evaluate the significance of wear methods in
vitro.
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Conclusions
• IVOCLAR (vertical loss) and ACTA were the best methods with respect to the
coefficient of variation. The discrimination power of the ZURICH method was
clearly inferior to that of the other methods.
• The variables related to the same method largely agreed with each other
(volumetric and vertical wear for IVOCLAR method; abrasion and attrition for
OHSU method).
• The MUNICH method strongly disagreed with the other methods.
• As the different wear simulator settings measure different wear mechanisms, it
seems reasonable to combine at least two different wear settings to assess
the wear resistance of a new material.
• Well-designed clinical studies, which use an adequate sample size and
quantitative methods to measure the wear, are needed to better assess the
clinical significance of the different wear simulator settings.
Acknowledgements
The authors would like to thank Till Göhring (University of Zurich), Karl-Heinz
Kunzelmann (University of Munich), Martin Rosentritt (University of Regensburg), and
John Sorensen (University of Portland) for conducting the wear tests in the
respective wear simulator settings and sending the raw data to IVOCLAR for further
analysis. Furthermore, we would like to thank W. Längle for the preparation of the
specimens and Mrs. G. Zellweger for conducting the wear analysis for the Ivoclar
method.
References [1] Suh NP. Tribophysics. New Jersey: Prentice-Hall, 1986. [2] Roulet J-F. Degradation of dental polymers. Basel: Karger, 1987. [3] Baran G, Boberick K, McCool J. Fatigue of restorative materials. Crit Rev Oral Biol Med 2001;12:350-60. [4] Lewis G. Predictors of clinical wear of restorative dental composite materials. Biomed Mater Eng 1993;3:167-74. [5] Tyas MJ. Correlation between fracture properties and clinical performance of composite resins in Class IV cavities. Aust Dent J 1990;35:46-9.
177
[6] Manhart J, Kunzelmann KH, Chen HY, Hickel R. Mechanical properties and wear behavior of light-cured packable composite resins. Dent Mater 2000;16:33-40. [7] ISO. Dental materials - Guidance on testing of wear. Part 2: Wear by two-and/or three body contact. Technical Specification 2001;No. 14569-2. [8] Kunzelmann K-H. Verschleissanalyse und -quantifizierung von Füllungsmaterialien in vivo und in vitro. Aachen: Shaker Verlag, 1998. [9] Mehl A, Gloger W, Kunzelmann KH, Hickel R. A new optical 3-D device for the detection of wear. J Dent Res 1997;76:1799-807. [10] Krejci I, Reich T, Lutz F, Albertoni M. In-vitro-Testverfahren zur Evaluation dentaler Restaurationssysteme. 1. Computergesteuerter Kausimulator. Schweiz Monatsschr Zahnmed 1990;100:953-960. [11] Krejci I, Albertoni M, Lutz F. In-vitro-Testverfahren zur Evaluation dentaler Restaurationssysteme. 2. Zahnbürsten-/Zahnpastaabrasion und chemische Degradation. Schweiz Monatsschr Zahnmed 1990;100:1164-1168. [12] Krejci I, Reich T, Bucher W, Lutz F. Eine neue Methode für die dreidimensionale Verschleissmessung. Schweiz Monatsschr Zahnmed 1994;104:160-9. [13] Condon JR, Ferracane JL. Evaluation of composite wear with a new multi-mode oral wear simulator. Dent Mater 1996;12:218-26. [14] de Gee AJ, Pallav P. Occlusal wear simulation with the ACTA wear machine. J Dent 1994;22:S21-7. [15] Condon JR, Ferracane JL. In vitro wear of composite with varied cure, filler level, and filler treatment. J Dent Res 1997;76:1405-11. [16] McCabe JF, Molyvda S, Rolland SL, Rusby S, Carrick TE. Two- and three-body wear of dental restorative materials. Int Dent J 2002;406-416. [17] Gibbs CH, Mahan PE, Lundeen HC, Brehnan K, Walsh EK, Holbrook WB. Occlusal forces during chewing and swallowing as measured by sound transmission. J Prosthet Dent 1981;46:443-9. [18] Lutz F, Krejci I, Barbakow F. Chewing pressure vs. wear of composites and opposing enamel cusps. J Dent Res 1992;71:1525-9. [19] Krejci I, Lutz F, Zedler C. Effect of contact area size on enamel and composite wear. J Dent Res 1992;71:1413-6. [20] Krejci I, Albert P, Lutz F. The influence of antagonist standardization on wear. J Dent Res 1999;78:713-9. [21] Kersten S, Lutz F, Besek M. Zahnfarbene adhäsive Füllungen im Seitenzahnbereich. Zürich: Eigenverlag PPK, 2001. [22] Wassell RW, McCabe JF, Walls AW. A two-body frictional wear test. J Dent Res 1994;73:1546-53. [23] Wassell RW, McCabe JF, Walls AW. Wear characteristics in a two-body wear test. Dent Mater 1994;10:269-74.
178
[24] Condon JR, Ferracane JL. Factors effecting dental composite wear in vitro. J Biomed Mater Res 1997;38:303-13. [25] Shortall AC, Hu XQ, Marquis PM. Potential countersample materials for in vitro simulation wear testing. Dent Mater 2002;18:246-54. [26] Ferracane JL, Egge A, Heintze SD. Comparison of antagonists for producing wear of dental composites in the OHSU oral wear simulator; 2003: Annual meeting of the the Academy of Dental Materials, Charleston, USA. [27] Pelka M, Ebert J, Schneider H, Kramer N, Petschelt A. Comparison of two- and three-body wear of glass-ionomers and composites. Eur J Oral Sci 1996;104:132-7. [28] Schnabel C, Kunzelmann K-H, Hickel R. The influence of different abrasion media o three-body-wear of composites. J Dent Res 1995;74.90, Abstr. no 625. [29] Powell JM, Phillips RW, Norman RD. In vitro wear response of composite resin, amalgam, and enamel. J Dent Res 1975;54:1183-95. [30] Gibbs CH, Lundeen HC, Mahan PE, Fujimoto J. Chewing movements in relation to border movements at the first molar. J Prosthet Dent 1981;46:308-22. [31] Mair LH, Stolarski TA, Vowles RW, Lloyd CH. Wear: mechanisms, manifestations and measurement. Report of a workshop. J Dent 1996;24:141-8. [32] Friedrich K. Friction and wear of polymer composites. Amsterdam: Elsevier, 1986. [33] Braem M, Finger W, Van Doren VE, Lambrechts P, Vanherle G. Mechanical properties and filler fraction of dental composites. Dent Mater 1989;5:346-8. [34] Söderholm KJ, Zigan M, Ragan M, Fischlschweiger W, Bergman M. Hydrolytic degradation of dental composites. J Dent Res 1984;63:1248-54. [35] Shinkai K, Suzuki S, Leinfelder KF, Katoh Y. How heat treatment and thermal cycling affect wear of composite resin inlays. J Am Dent Assoc 1994;125:1467-72. [36] Chadwick RG. Thermocycling--the effects upon the compressive strength and abrasion resistance of three composite resins. J Oral Rehabil 1994;21:533-43. [37] Yap AU, Wee KE, Teoh SH, Chew CL. Influence of thermal cycling on OCA wear of composite restoratives. Oper Dent 2001;26:349-56. [38] Koczorowski R, Wloch S. Evaluation of wear of selected prosthetic materials in contact with enamel and dentin. J Prosthet Dent 1999;81:453-9. [39] Göhring TN, Besek MJ, Schmidlin PR. Attritional wear and abrasive surface alterations of composite resin materials in vitro. J Dent 2002;30:119-27. [40] Suzuki S, Nagai E, Taira Y, Minesaki Y. In vitro wear of indirect composite restoratives. J Prosthet Dent 2002;88:431-6. [41] Knobloch LA, Kerby RE, Seghi R, van Putten M. Two-body wear resistance and degree of conversion of laboratory-processed composite materials. Int J Prosthodont 1999;12:432-8. [42] Söderholm KJ, Yang MC, Garcea I. Filler particle leachability of experimental dental composites. Eur J Oral Sci 2000;108:555-60.
179
[43] Peutzfeldt A, Asmussen E. The effect of postcuring on quantity of remaining double bonds, mechanical properties, and in vitro wear of two resin composites. J Dent 2000;28:447-52. [44] Ferracane JL, Mitchem JC, Condon JR, Todd R. Wear and marginal breakdown of composites with various degrees of cure. J Dent Res 1997;76:1508-16. [45] Yamaga T, Sato Y, Akagawa Y, Taira M, Wakasa K, Yamaki M. Hardness and fracture toughness of four commercial visible light-cured composite resin veneering materials. J Oral Rehabil 1995;22:857-63. [46] Cobb DS, MacGregor KM, Vargas MA, Denehy GE. The physical properties of packable and conventional posterior resin-based composites: a comparison. J Am Dent Assoc 2000;131:1610-5. [47] Ferracane JL, Choi KK, Condon JR. In vitro wear of packable dental composites. Compend Contin Educ Dent Suppl 1999;S60-6(Supplement No. 25). [48] Pallav P, Davidson CL, de Gee AJ. Wear rates of composites, an amalgam, and enamel under stress-bearing conditions. J Prosthet Dent 1988;59:426-9. [49] Ramp MH, Suzuki S, Cox CF, Lacefield WR, Koth DL. Evaluation of wear: enamel opposing three ceramic materials and a gold alloy. J Prosthet Dent 1997;77:523-30. [50] Lutz F, Krejci I. Mesio-occlusodistal amalgam restorations: quantitative in vivo data up to 4 years. A data base for the development of amalgam substitutes. Quintessence Int 1994;25:185-90. [51] Krejci I, Lutz F. In-vitro-Testverfahren zur Evaluation dentaler Restaurationssysteme. 3. Korrelation mit In-vivo-Resultaten. Schweiz Monatsschr Zahnmed 1990;100:1445-1449. [52] Bryant RW. Comparison of three standards for quantifying occlusal loss of composite restorations. Dent Mater 1990;6:60-2. [53] Perry R, Kugel G, Kunzelmann KH, Flessa HP, Estafan D. Composite restoration wear analysis: conventional methods vs. three-dimensional laser digitizer. J Am Dent Assoc 2000;131:1472-7. [54] Christensen R, Bangerter V. Apparatus for automated, non-contact measurements of surface changes. J Dent Res 1990;69:126 Abstr. no. 140. [55] DeLong R, Pintado M, Douglas WH. Measurement of change in surface contour by computer graphics. Dent Mater 1985;1:27-30.
180