1012cei glass ionomer web
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Educational ObjectivesThe overall goal of this article is to provide dental profession-
als with information on tooth-colored restorations. Upon
completion of this course, the clinician will be able to do the
following:
1. Describe the early tooth-colored direct restorative
materials
2. List and compare the attributes of composite resins andglass ionomer cements
3. Describe the composition of a compomer, and compare it
to composite resins and conventional glass ionomers
4. Describe the restoratives containing nanotechnology and
the effect of nanotechnology in nano-ionomer restorations
AbstractResearchers have developed multiple tooth-colored restor-
atives in the search for a material that has optimal strength,
esthetics, handling properties and a preventive function.
Materials currently available include glass ionomer-basedmaterials, composite-based materials, compomers, giomers,
and the use of nanotechnology for composites and nano-
ionomers. Each offers benets for the individual patient case.
IntroductionThe quest for suitable tooth-colored restoratives began with
the introduction of acrylics and silicates. While weak and
offering relatively poor esthetics, as well as being difcult to
accurately mix and handle, they represented the rst efforts
at providing the clinician and patient with both esthetics and
functionality in a restoration. As researchers investigated var-ious chemistries, two main categories of direct tooth-colored
restorations evolved composite resins and glass ionomer
cements. These represented a signicant improvement over
the pre-existing options, which rapidly fell out of favor.
Figure 1. Development of early tooth-colored restoratives
1940s
Acrylics and
silicates
1950s
Composite
resins
1970s
Glass ionomer
cements
Composite ResinsComposite resins fundamentally consist of two phases: the ller
content and the monomer-based content, typically bisphenol
A glycidyl dimethacrylate (bis-GMA), tetraethyleneglycol
dimethacrylate (TEGDMA) or dimethacrylate (DMA). Set-
ting occurs strictly through polymerization of the monomers,
resulting in the llers being dispersed in the set polymer.
Early composite resins were relatively weak, with low com-
pressive strength, tensile strength and exural strength, andthey exhibited a high degree of polymerization shrinkage and
shrinkage stress. They were also poorly bonded to the clinical
site with primitive adhesive techniques, resulting in marginal
leakage and sensitivity, and subject to considerable surface
wear as a result of their relatively low surface hardness.1 Wear
resistance and strength were subsequently improved such that
posterior composites were introduced, although initially these,
too, were unsatisfactory for heavy stress-bearing situations.2
The current range of composite resin restoratives offers the
greatest strength and wear resistance of all direct tooth-colored
materials and continues to be the most esthetic option. Cur-rent adhesive techniques have resulted in improved bonding
of the tooth-adhesive and adhesive-composite interfaces,
although marginal leakage is still a consideration. Composites
typically do not contain uoride, and the uoride release from
uoride-containing composites has been found to be minimal;
at the same time, biolm adheres well and grows on rough
composite surfaces.3 Composites are now differentiated based
on ller type and load as well as unique chemistries such as
those utilized to reduce polymerization shrinkage and stress.
The physical characteristics of composites have become
well-differentiated microlled composites offer the abilityto polish and retain a high gloss and superior esthetics, while
microhybrid composites offer greater strength but result
in uneven wear due to the loss of large ller particles.4 Most
recently, nanotechnology has been introduced into composites
and is discussed later in this article.
Glass Ionomer CementsGlass ionomer cements consist of two components that
initially were available only as a powder and liquid. Funda-
mentally, these consist of uoroaluminosilicate glass particles
and an aqueous solution of polyalkenoic (or polyacrylic) acid.A major difference between glass ionomer restoratives and
composite-based restoratives is the inclusion of water in the
glass ionomer formulations and their hydrophilicity, which
results in wet contact with the tooth surface and a strong bond
over time. The setting reaction for glass ionomers is acid-
based, rather than setting through polymerization; therefore,
no polymerization shrinkage can exist. Using infrared spec-
troscopy and band-narrowing treatments to assess materials,
Arrondo et al. conrmed that glass ionomers set through an
acid-based reaction as well as cross-linking of the polycar-
boxylate with the metal ions present in the glass ionomer.5
Glass ionomer cements tolerate moist environments and are
applied to moist tooth surfaces. In addition, they adhere di-
rectly to the tooth structure and provide a solid marginal seal.
In combination, these attributes can provide for an easier and
quicker chairside experience for patient and clinician alike
compared to using composite resins. In general, however,
glass ionomer cements have lower strength than composites.
One of the main benets of glass ionomers is their ability to
release uoride. Based on studies of up to three years dura-
tion, uoride release is ongoing; the amount released exceedsthe initial uoride content of the uoroaluminosilicate glass
particles demonstrating the uptake of uoride from external
sources and has been found to be regulated by the phospho-
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rus at the glass ionomer surface.6 The uoride release from
glass ionomers has been shown to help prevent the formation
of secondary caries, by creating a zone of inhibition, and in
addition has been found to have a preventive effect on adja-
cent teeth.7 Since the main reason for replacement of direct
restorations is secondary caries, caries inhibition through
uoride release is highly desirable.
Bridging the GapAs a result of their respective attributes, resin-based com-
posites became the material of choice where strength and
esthetics were of greatest importance. Glass ionomers have
been favored in situations where caries control, the intraoral
environment and ease of placement were more important
considerations than strength and esthetics. Improving the
strength and esthetic properties of both composites and glass
ionomers became a strong focus, as well as improving specic
attributes (such as reducing polymerization shrinkage in res-
in-based composites). Researchers investigated and continueto investigate potential solutions that might offer all the ben-
ets of composites and glass ionomers but without any of the
drawbacks associated with either category. In the quest for a
single material that might meet all requirements for the ideal
restorative, composites and glass ionomers have both evolved.
Chemistry from each category has been incorporated into the
alternative restorative material, with differentiation of llers,
unique chemistries, delivery systems, curing mechanisms,
and single-layer versus multi-layer techniques.
Resin-modified Glass IonomersThe strength of glass ionomers was improved through the ad-
dition of methacrylate monomer in the aqueous polyalkenoic
acid solution as well as the addition of monomer containing
free radical double bonds in the uoroaluminosilicate-con-
taining component. This created a new subset within the
category that was named resin-modied glass ionomer
cement. The monomer sets through polymerization when
light-activated and cross-links, but does not interfere with the
acid-based setting reaction due to the limited amount added
to the glass ionomer.8,9 Light-curing of these glass ionomers
offers control whereby the initial self-setting is accelerated.
After exposure to polyalkenoic acid conditioner, resin-modi-
ed glass ionomer forms a hybrid layer at the dentin surface of
bur-cut dentin and a typical submicron gel phase can be ob-
served with transmission electron microscopy. Assessments
in laboratory testing found that the direct bonding to the
tooth structure was attributable to bonding of the gel phase
around the hydroxyapatite as well as to the hybrid layer (de-
pending on the product), which resulted in micro-mechanical
bonding through an interlocking mechanism.10 Interestingly,
and as a note of caution, no hybrid layer or gel phase is found
using the same protocol on Er:YAG laser-irradiated dentin,
nor any dentin demineralization or collagen melting.11 A sep-
arate study comparing the adhesion mechanism of bur-cut
and laser-irradiated dentin supports these results; althoughpartial demineralization was observed, there was still no
hybrid layer formation. It was also determined that the use
of glass ionomer conditioner was important for microtensile
bond strength in bur-cut dentin.12 The fracture resistance
of resin-modied glass ionomers has been found to be sig-
nicantly greater than that of conventional glass ionomers. In
addition, a reduction in particle size (of up to 10 microns) of
the uoroaluminosilicate-based component has been found
to increase fracture resistance as well as result in a smooth
surface.13 Resin-modied glass ionomers are still not a mate-
rial of choice for posterior stress-bearing areas, due to theirrelatively low surface hardness and fatigue resistance.14,15
Light-activated glass ionomers enable immediate nishing
and reduced incidence of subsequent microleakage.16
Metal-reinforced Glass Ionomers
Metal-reinforced glass ionomers include metal ions in the
mix typically silver-based alloys such as the silver-tin alloy
found in amalgam. These are used primarily for core buildups
and are also used to restore primary molars. A subset of this
category, the cermet, results from fusing the metal ions to
the uoroaluminosilicate glass particles; however, cermetsrelease less uoride than other glass ionomers.
CompomersCompomers, also known as polyacid-modied resin com-
posites, were developed from composites. They contain ller
similar to the glass particles contained in glass ionomers, di-
methacrylate monomer and polyacid, but they do not contain
water. Setting occurs through polymerization and, as with con-
ventional composites, adhesion is achieved through the man-
datory use of bonding agents rather than direct bonding to the
tooth structure.17 Based on the absence of a COO bond, it was
determined that no acid-based reaction occurs. Finally, it was
also concluded that the release of metal ions that chelate with
the methacrylate-based polymer molecules was due to dilution
of ller particles through the presence of water.5 Compomers
have lower compressive strength and exural strength, a lower
Youngs modulus (modulus of elasticity), and reduced resis-
Glassionomers
Resin-modied
glassionomers
Metal-reinforced
glassionomers and
cermets
Giomers
Nano-ionomers
Nanolledcomposites
Compomers
Microlledand
microhybridcomposite
resins
Earlycomposite
resins
NanotechnologyFigure 2. Material categories
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tance to fracture and wear compared to composites, and should
not be used in stress-bearing areas.18,19,20 A study comparing
tooth-colored restorative materials found that the surface
nish of glass ionomers and compomers were both signi-
cantly poorer than that of conventional composites.21 Biolm
development is signicant on both compomer and composite
materials. The glass particles in compomers are responsible for
the uoride release from the set compomer which, while lowerthan with glass ionomers, is still ongoing.22,23,24,25,26 There have
been concerns about the release of HEMA from compomers,26
due to the risks of adverse pulpal responses in patients and
of allergy in patients and dental personnel. The amount of
HEMA released is inuenced by the individual material, depth
of cure and degree of curing.27,28 Although compomers do not
meet esthetic requirements where these demands are primary,
some offer greater polishability than glass ionomers and resin-
modied glass ionomers.18 Compomers may be suitable for
restorations where neither strength nor esthetics are primary
considerations, such as in pediatric restorations, and have alsobeen used as orthodontic bonding agents.
GiomersAnother approach has been the use of milled, silanized glass
ionomer llers that have already undergone the acid-base re-
action between uoroaluminosilicate glass and polyalkenoic
acid prior to milling. These llers are then used in a composite
resin base to provide uoride release from the llers together
with the strength and esthetics of composites and have been
found to be successful in these regards.29
NanotechnologyThe introduction of nanotechnology, initially in composites,
heralded improved esthetics without compromising strength
or wear resistance. Strength and wear resistance were also
improved, depending on the material.
Nanofilled Composite ResinsNanolled composite resins were designed to combine the
polishability and esthetics of microlled composites with
the strength and wear resistance of microhybrid composites.
They contain nanollers that are heavily loaded into the
composite; these improve the translucency and opalescence
of the composite, making it more natural looking and better
able to blend in with the surrounding area.4 The addition of
nanosized particles to composite resins increases their polish-
ability. Azevedo et al referred to the recent studies suggest-
ing that these particles should ideally be evenly dispersed
together with microllers.30 Nanolled composites offer
improved strength compared to microlled composites and
equal to or better than other composites.31 The addition of
pre-polymerized nanollers forming nanoclusters has beenfound to reduce polymerization shrinkage, further increase
strength and esthetics, and offer a smoother surface that is less
subject to wear and that wears more evenly.4
Nano-ionomersNano-ionomers were developed with the desire to combine
the proven benets of glass ionomers, in particular uoride re-
lease, with the proven benets of nanotechnology available in
resin-based composites discussed above notably improved
esthetics, surface smoothness, strength and wear resistance.
The nano-ionomer consists of one paste containing water,
polycarboxylic acid, nanollers and reactive resins. With theexception of the nanollers, these components are contained
in resin-modied glass ionomers and compomers. The other
paste contains a combination of nanollers (based on silica
and zirconia) and nano-clusters of these llers, together with
reactive resins and 27% uoroaluminosilicate glass particles.
The nano-ionomer is placed and light-cured after use of its
corresponding primer. It is essential that the primer be used
to optimize tensile shear bond strength. In assessing the in-
terface and the material, nano-clusters with a high ller load
and good distribution of the ller through the nano-ionomer
(KetacTM Nano, 3M ESPE) have been observed, togetherwith bonding through micromechanical locking.32 Korkmaz
et al. studied the shear bond strength of nano-ionomer to
enamel and dentin after use of primer with or without the ad-
dition of 37% phosphoric acid etching, with some specimens
receiving laser etching rst. It was found that the use of only
primer resulted in the greatest shear bond strength in den-
tin; in enamel, use of phosphoric acid provided the greatest
bond strength. Interestingly, as with the resin-modied glass
ionomers discussed earlier, laser treating the tooth structure
prior to use of the primer and nano-ionomer results in poor
shear bond strengths.33 The setting reaction of the nano-ionomer involves the rapid free radical polymerization of the
monomers when exposed to light-curing, followed for a much
longer time by a slower acid-base reaction involving the uo-
roaluminosilicate glass ller and aqueous acid solution. The
nano-ionomer has been found to have compressive strength at
least equal to conventional glass ionomers and resin-modied
glass ionomers, to have good exural strength and diametral
tensile strength, and to be less brittle than resin-modied
Figure 3. SEM of nano-ionomer
Courtesy of Dr. William Douglas and Dr. Daranee Tantibirojn
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glass ionomers. Equivalent uoride release and recharge oc-
cur, and the inclusion of nanollers in the material results in
a smooth surface, with wear resulting in loss of the ne par-
ticles (as with nanolled composites). The end result of use
of the nanotechnology is a nano-ionomer that offers greater
strength, the esthetics of nanotechnology and the release of
uoride on an ongoing basis.
Experimental ApproachesExperimental llers such as trimethyletoxysilane and the use
of N-vinylpyrrolidone have been investigated as additives
to composites and glass ionomer cements, and the inclusion
of a methacryloyl derivative of l-proline in glass ionomers
was found to result in greater diametral tensile strength,
higher compressive strength and higher biaxial exural
strength.30,34,35 Nanosized particles of nanohydroxyapatite
and uorapatite were created and incorporated into glass
ionomer cement in another study, resulting in increased bond
strength, compressive strength, diametral tensile strengthand exural strength.36 One investigation involved creat-
ing novel llers for a resin-based composite by combining
ground cured glass ionomer with ceramic whiskers composed
of silica fused onto silicon nitride that were then silanized.
The resulting material was found to have superior exural
strength and moderate uoride release, the degree of release
inuenced by the proportions of ground glass ionomer and
ceramic whiskers.37 Experimental light-cured HEMA-free
glass ionomer cements have been studied and found to offer
promise.38 Self-etch adhesives to further strengthen adhesion
to tooth structure have also been researched for both com-posites and resin-modied glass ionomers.39
Handling and Placement
As with restorative materials themselves, substantial devel-
opments have occurred with the mixing and application of
tooth-colored restoratives. Initially, glass ionomers consisted
of powder and a water and polyacrylic acid-based liquid,
and were always hand-mixed. Similarly, early composites
consisted of two pastes and they, too, were hand-mixed.
There was no possibility of a one-component delivery sys-
tem, nor did mixing tips/double-barrel applicators exist.
Currently, a number of options are available for the handling
and application of composites and glass ionomers as well as
their derivative products. For composites, one option is a
multi-dose syringe from which the material is extruded onto
a mixing pad before being applied to the tooth; another is
direct application from a unit-dose capsule or, for owable
composites, directly into the preparation from a disposable
single-use applicator tip on a multi-dose syringe. Focus has
also been placed on the shapes of the syringes, the amount of
pressure required for extrusion of the material, the hand gripand thumb comfort during extrusion, methods for measuring
the amount extruded (such as clicks or lines representing an
average extruded dose), and the overall ease of use. Although
still available, hand-mixed dual-paste composites are difcult
to mix accurately and without the inclusion of voids. For glass
ionomers and resin-modied glass ionomers, several options
exist. These include the use of a powder and liquid, or paste-
paste (using the same hand-mixing method used for early
glass ionomers) and the use of a unit dose that is activated by
pressing on, or twisting, the unit dose and then triturated for
10 to 15 seconds (product dependent) before being applieddirectly to the preparation with or without the use of an ap-
plicator. A third option is the use of a Paste Pak that is placed
in an applicator, after which a disposable mixing tip is added
to mix premeasured amounts of each component and to dis-
pense the material onto a pad or directly to the site of use.
Figure 4. Unit doses, powder liquid, syringes
The use of predosed, as well as premixed, materials auto-
matically regulates the quality of the mix as well as the ap-propriate proportion of components. This is important, since
measuring and mixing errors can result in incorrect ratios of
two-component materials that will lead to reduced strength
and surface hardness of the nal restoration. One study found
resin-modied glass ionomers less affected than traditional
glass ionomers and other materials, but not immune to these
effects.40 Nonetheless, depending on whether a dispropor-
tionate amount of powder or liquid is used in a hand-mixing
system without premeasuring, it has been found that surface
hardness, exural strength and fracture resistance can be
affected.41,42 This led to the researchers in one investigation
advocating the use of precapsulated unit doses.42 A nano-
ionomer (Ketac Nano) utilizes a novel unit dose that does
not require activation or trituration and can be applied to the
preparation after taking it out of its foil pouch and placing it in
the matching applier (AplicapTM,3M ESPE). This approach
provides premeasured unit dosing with mixing occurring as
the material is extruded through the mixing tip built into the
unit dose itself. This system can save time and provides ease
of use. Alternatively, if preferred, the same nano-ionomer
can be dispensed as two separate premeasured pastes froma dual-paste double-barrel syringe system clicker dispenser
and hand-mixed prior to direct application to the preparation
using hand instruments.
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Figures 5a and 5b. Unit dose and Aplicap
Clinical ApplicationThe two cases below illustrate the use of nano-ionomer for
anterior restorations.
Case 1.The patient presented with a large distal and buccal carious
cavity on tooth #27 which served as the support for a partial
denture clasp. An esthetic, wear-resistant restoration was
required, and it was decided to create a closed-sandwich
restoration using nano-ionomer and composite. After
applying primer (Ketac Nano), a stand-alone air syringe
was used (rather than a three-in-one air-water syringe)
to maximally air-dry the primer and avoid any possible
contamination of the site with water prior to light-curing.
Nano-ionomer (Ketac Nano) was then placed in the site forthe internal sandwich layer and light-cured, with the light-
curing tip held close to the material to ensure maximum
cure. Once cured, a soft composite nishing bur was used
to prepare the surface of the nano-ionomer, after which a
total-etch technique was used for bonding (XP Bond,
Dentsply Caulk) of the composite to the enamel. The com-
posite (FiltekTM Supreme A3, 3M ESPE) was then placed
and the composite light-cured and nished. The end result
was a durable, esthetic restoration.
Figure 6. Disto-buccal cervical lesion
Figure 7. Application of primer
Figure 8. Air-drying of primer
Figure 9. Light-curing of primer
Figures 10a and 10b. Application of nano-ionomer
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Figure 11. Light-curing of nano-ionomer
Figure 12. Nano-ionomer prepared prior to composite placement
Figure 13. Finished closed-sandwich restoration
Case 2.The patient in this case was an 89-year-old woman with xero-
stomia. She presented with extensive carious cervical lesions
under a xed anterior prosthesis, indicative of high caries
activity, and the selected clinical solution was use of nano-
ionomer. Primer (Ketac Nano) was applied, dried using an airsyringe and light-cured. For the restorations, nano-ionomer
(Ketac Nano) was applied and shaped using a plastic instru-
ment prior to light-curing. The nal restorations were n-
ished using a nishing bur. To help prevent recurring caries
and to recharge the nano-ionomer with uoride, the patient
was then placed on a preventive protocol that involved the use
of ClinproTM 5000 with TCP (3M ESPE) in the morning and
Crest PRO-HEALTHTM (Procter and Gamble) toothpaste
in the evening, followed by MI PasteTM (GC America) in a
custom-made soft tray overnight.
Figure 14. Carious cervical lesions under fixed prosthesis
Figure 15. Excavation of caries
Figure 16. Application of primer
Figure 17. Application of nano-ionomer
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Figures 18a and b. Final cervical restorations
SummaryTooth-colored restorations have changed greatly since
their initial introduction. Over time, these have developed
to include several types of packable composites, owable
composites, glass ionomers and compomers and the use of
nanotechnology. When selecting a material, the require-
ments for the patient and individual restorations are factors
of paramount importance.
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32 CoutinhoE,CardosoMV,DeMunckJ,NevesAA,VanLanduytKL,PoitevinA,PeumansM,LambrechtsP,VanMeerbeekB.Bondingeffectivenessandinterfacialcharacterizationofanano-lledresin-modiedglass-ionomer.DentMater.2009;25(11):1347-57.
33 KorkmazY,OzelE,AttarN,OzgeBicerC. Inuenceofdifferentconditioningmethodson theshearbondstrength ofnovel light-curingnano-ionomerrestorativetoenamelanddentin.LasersMedSci.2010;25(6):861-6.
34 Moshaverinia A, Roohpour N, Rehman IU. Synthesis andcharacterization of a novel fast-set proline-derivative-containingglassionomercementwithenhancedmechanicalproperties.ActaBiomater.2009;5(1):498-507.
35 CulbertsonBM.Newpolymericmaterialsforuseinglass-ionomer
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cements.JDent.2006;34(8):556-65.36 MoshaveriniaA,Ansari S,MoshaveriniaM,Roohpour N,DarrJA, Rehman I. Effects of incorporation of hydroxyapatite anduoroapatite nanobioceramics into conventional glass ionomercements(GIC).ActaBiomater.2008;4(2):432-40.
37 XuHH,EichmillerFC,AntonucciJM,SchumacherGE,IvesLK.Dentalresincompositescontainingceramicwhiskersandprecuredglassionomerparticles.DentMater.2000;16(5):356-63.
38 Xie D, Chung ID,WuW,Mays J. Synthesis and evaluation ofHEMA-freeglass-ionomer cements fordentalapplications.Dent
Mater.2004;20(5):470-8.39 CoutinhoE,Van Landuyt K,DeMunck J, Poitevin A,YoshidaY,InoueS, PeumansM,SuzukiK,LambrechtsP,VanMeerbeekB. Development of a self-etch adhesive for resin-modied glassionomers.JDentRes.2006;85(4):349-53.
40 Behr M, Rosentritt M, Loher H, Kolbeck C, Trempler C,StemplingerB,KopzonV,HandelG.Changesofcementpropertiescausedbymixingerrors:thetherapeuticrangeofdifferentcementtypes.DentMater.2008;24(9):1187-93.
41 BehrM,RosentrittM,LoherH,HandelG.Effectofvariationsfromtherecommendedpowder/liquidratioonsomepropertiesofresin-modiedcements.ActaOdontolScand.2006;64(4):214-20.
42 DowlingAH,FlemingGJ.Areencapsulatedanteriorglass-ionomerrestoratives better than their hand-mixed equivalents? J Dent.
2009;37(2):133-40.
Author ProfileLou Graham, DDS
Dr. Lou Graham is a graduate of Emory
Dental School. He is the past Dental
Director at the University of Chicago
and currently holds a part-time faculty
position there. Dr. Graham is an inter-
nationally recognized lecturer involved incontinuing education that focuses on incorporating current
clinical advancements through conservative dentistry. Dr.
Graham practices full time in Chicago, IL.
DisclaimerThe author(s) of this course has/have no commercial ties with the sponsors or
the providers of the unrestricted educational grant for this course.
Reader FeedbackWe encourage your comments on this or any PennWell course. For your conve-
nience, an online feedback form is available at www.ineedce.com.
Questions
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answers. An immediate grade report will be provided and upon receiving a passing grade your Verication Form will be provided immediately for viewing and/or printing. Verication Forms can be viewed
and/or printed anytime in the future by returning to the site, sign in and return to your Archives Page.
1.Asresearchersinvestigatedvariousmaterials,twomaincategoriesofdirecttooth-colored restorationsevolved;thesewere_______.
a. composite resins and silicatesb. silicates and glass ionomer cementsc. composite resins and glass ionomer cementsd. acrylics and silicates
2.Themonomer-basedcontentincompos-iteresinsistypically_______.a. bis-GMAb. TEGDMAc. DMAd. any of the above
3.Settingofcompositeresins_______.a. occurs through polymerization of the monomersb. results in the llers being dispersed in the set
polymer
c. occurs through an acid-based reactiond. a and b
4.Earlycompositeresinsexhibited_______.a. low strengthb. a high degree of polymerization shrinkagec. a high level of shrinkage stressd. all of the above
5.Thecurrentrangeofcompositeresinrestorativesoffersthe_______ofalldirecttooth-coloredmaterials.a. greatest strength and wear resistanceb. lowest strength and wear resistancec. greatest strength and poorest estheticsd. none of the above
6.Compositestypically_______.a. contain iodideb. contain uoridec. do not contain uorided. a and b
7.Microlledcompositesoffer_______.a. the ability to polish the composite to a high glossb. the ability to retain a high gloss
c. superior estheticsd. all of the above
8._______isafundamentalcomponentofglassionomercements.a. Fluoroaluminosilicate glassb. Polyalkenoic (or polyacrylic) acidc. Resind. a and b
9.Theinclusionofwateringlassionomersandtheirhydrophilicityresultsin_______.a. wet contact with the tooth surfaceb. a weak bond over timec. a strong bond over time
d. a and c10.Thesettingreactionforglassionomers
is_______.a. acid-basedb. alkali-basedc. ploymerization-basedd. none of the above
11.Glassionomercements_______.a. tolerate moist environmentsb. adhere directly to the tooth structurec. are applied to moist tooth surfacesd. all of the above
12.Inthequestforasinglematerialthatmightmeetallrequirementsfortheideal
restorative,_______haveevolved.a. compositesb. acrylicsc. glass ionomer cementsd. a and c
13.Thestrengthofglassionomerswasimprovedthroughtheadditionof_______.a. methacrylate monomerb. polymer containing free radical double bonds
c. compomer particles
d. none of the above
14.Themonomerinresin-modiedglassionomers_______.a. cross-links
b. sets through polymerization when light-activated
c. does not interfere with the acid-based setting
reaction
d. all of the above
15.Thedirectbondingtothetoothstructureobservedwithglassionomerswasfound
inonestudytobeattributableto_______.a. bonding of the gel phase around the hydroxyapatite
b. the hybrid layer
c. monomer
d. a and b
16.FollowingEr:YAGlaser-irradiationofdentin,_______hasbeenobservedwiththeuseofglassionomers.a. a deeper hybrid layer
b. no hybrid layer
c. no setting reaction
d. a and c
17.Theuseofglassionomerconditioneris
importantfor_______inbur-cutdentin.a. microtensile bond strengthb. shrinkage
c. stress reduction
d. all of the above
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Questions
18.Metal-reinforcedglassionomers_______.a. typically include silver-based alloys in the mixb. are used primarily for core buildupsc. can be used to restore primary molars
d. all of the above
19.Thecermet_______.a. results from fusing metal ions to uoroaluminosili-
cate glass particlesb. is a subset of metal-reinforced glass ionomersc. releases less uoride than other glass ionomersd. all of the above
20.Compomersarealsoknownas_______.a. polyacid-modied glass ionomersb. polyacid-modied acrylicsc. polyacid-modied compositesd. none of the above
21.Compomerscontain_______.a. ller similar to the glass particles contained in glassionomers
b. dimethacrylate monomer and polyacidc. no waterd. all of the above
22.Settingofcompomersoccursthrough_______.a. polymerization onlyb. an acid-based reaction onlyc. both polymerization and an acid-based reactiond. none of the above
23.Ithasbeenfoundthat_______withthemethacrylate-basedpolymermolecules
isduetodilutionofllerparticlesthroughthepresenceofwater.a. the release of metal ions that hydrateb. the release of metal ions that chelatec. the release of carboxyl bonds that chelated. all of the above
24.Compomershave_______comparedtocomposites.a. lower compressive and exural strengthb. a lower modulus of elasticityc. less resistance to fracture and weard. all of the above
25.Therehavebeenconcernsaboutthereleaseof_______fromcompomers.
a. uorideb. EDTAc. HEMAd. b and c
26.Biolmformationissignicanton_______.a. compomersb. amalgamc. compositesd. a and c
27.Agiomercontains_______.a. milled, silanized glass ionomer llersb. a composite resin basec. a silicate base
d. a and b
28.Giomershave_______.a. the strength of compositesb. the esthetics of compositesc. been shown to release uorided. all of the above
29.Theintroductionofnanotechnology_______.a. occurred initially in compositesb. heralded improved estheticsc. did not compromise strength
d. all of the above
30.Nanolledcompositeresinsweredesignedtocombinethe_______.a. polishability and esthetics of microlled compositesb. strength and wear resistance of microhybrid
compositesc. strength and wear resistance of compomersd. a and b
31.Nanollersincomposites_______.a. improve the translucency of compositesb. improve the opalescence of compositesc. make composites more natural lookingd. all of the above
32.Nanolledcompositesoffer_______microlledcomposites.a. improved strength compared tob. reduced strength compared toc. the same strength asd. none of the above
33.Theadditionofpre-polymerizednanollersformingnanoclustershasbeenfoundto_______incomposites.a. reduce polymerization shrinkageb. increase shrinkage stressc. increase strengthd. a and c
34._______arecontainedinnano-ionomers.a. Water and polycarboxylic acid
b. Nanollersc. Reactive resinsd. all of the above
35.Thenanollersinnano-ionomerarebasedon_______.a. silica and phosphateb. zirconia and phosphatec. uoride and zirconiad. zirconia and silica
36.Nano-ionomercontains_______uoroaluminosilicateglassparticles.a. 17%b. 27%c. 37%
d. none of the above
37.Primermustbeusedpriortoplacementofnano-ionomerstooptimize_______.a. compressive strengthb. tensile shear bond strengthc. exural strengthd. all of the above
38._______studiedtheshearbondstrengthofnano-ionomertoenamelanddentin.a. Korovsky et alb. Korkmaz et alc. Korbovskia et ald. none of the above
39.Theuseofonlyprimerhasbeenfoundtoresultinthegreatestshearbondstrengthto_______.a. enamelb. dentinc. cementumd. a and b
40.Theuseofphosphoricacidhasbeenfoundtoprovidethegreatestbondstrengthto_______.a. enamelb. dentin
c. cementumd. a and c
41.Nano-ionomerhasbeenfoundto______.a. have compressive strength at least equal to glass
ionomersb. have good exural and diametral tensile strengthc. be less brittle than resin-modied glass ionomersd. all of the above
42.Experimentally,theinclusionofamethacryloylderivativeofl-prolineinglassionomerswasfoundtoresultin_______.a. greater strengthb. greater polishabilityc. lower reectanced. all of the above
43.Self-etchadhesivestofurtherstrengthenadhesiontotoothstructurehavebeenresearchedfor_______.a. compositesb. gold inlaysc. resin-modied glass ionomersd. a and c
44.Earlycomposites______.a. were weakb. consisted of two pastesc. were hand-mixedd. all of the above
45._______isanoptionforthehandlingandapplicationofcomposite.a. A multi-dose syringe with a mixing pad
b. Direct application from a unit-dose capsulec. Use of a disposable tip and multi-dose syringe for
owablesd. all of the above
46.Theuseof_______isanoptionformixingglassionomers.a. a powder and liquidb. a capsulec. a Paste Pakd. all of the above
47.Measuringandmixingerrorscanresultinincorrectratiosoftwo-componentmaterialsandcanleadto_______.a. reduced strengthb. reduced surface hardness
c. reduced fracture resistanced. all of the above
48.Usingpremeasuredunitdosingwithmixingoccurringasthematerialisextrudedcan_______.a. save timeb. provide ease of usec. increase wasted. a and b
49.Researchersinoneinvestigationonthemixingofglassionomersadvocatedtheuseof_______.a. powder and liquidb. precapsulated unit dosesc. a dual paste system
d. none of the above50.The_______isafactorwhenselectinga
tooth-coloredrestorative.a. requirements for the patientb. gender of the patientc. individual restorationd. a and c
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P.O.Box116,Chesterland,OH44026orfaxto:(440)845-3447
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Educational Objectives
1. Describetheearlytooth-coloreddirectrestorativematerials
2. Listandcomparetheattributesocompositeresinsandglassionomercements
3. Describethecompositionoacompomer,andcompareittocompositeresinsandconventionalglassionomers
4. Describetherestorativescontainingnanotechnologyandtheefectonano technologyinnano-ionomerrestorations
Course Evaluation
Pleaseevaluatethiscoursebyrespondingtotheollowingstatements,usingascaleoExcellent=5toPoor=0.
1.Weretheindividualcourseobjectivesmet? Objective#1:YesNo Objective#3:YesNoObjective#2:YesNo Objective#4:YesNo
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8.Doyoueelthatthereerenceswereadequate? Yes No
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___________________________________________________________________
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___________________________________________________________________
ANSWER SHEET
Advances in Tooth-Colored Restorations
Name: Title: Specialty:
Address: E-mail:
City: State: ZIP: Country:
Telephone:Home(
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Requirementsforsuccessfulcompletionofthecourseandtoobtaindentalcontinuingeducationcredits:1)Readtheentirecourse.2)Completeall
informationabove.3)Completeanswersheetsineitherpenorpencil.4)Markonlyoneanswerforeachquestion.5)Ascoreof70%onthistestwillearn
you3CEcredits.6)CompletetheCourseEvaluationbelow.7)MakecheckpayabletoPennWellCorp.For Questions Call 216.398.7822
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This course was made possible through an unrestricted educational grant from 3MESPE. No manufacturer or third party has had any input into the development of coursecontent. All content has been derived from references listed, and or the opinions ofclinicians. Please direct all questions pertaining to PennWell or the administration ofthis course to Machele Galloway, 1421 S. Sheridan Rd., Tulsa, OK 74112 or [email protected].
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Completing a single continuing education course does not provide enough informationto give the participant the feeling that s/he is an expert in the eld related to the coursetopic. It is a combination of many educational courses and clinical experience thatallows the participant to develop skills and expertise.
COURSE CREDITS/COSTAll participants scoring at least 70% on the examination will receive a verication
form verifying 3 CE credits. The formal continuing education program of this sponsoris accepted by the AGD for Fellowship/Mastership credit. Please contact PennWell forcurrent term of acceptance. Participants are urged to contact their state dental boardsfor continuing education requirements. PennWell is a California Provider. The CaliforniaProvider number is 4527. The cost for courses ranges from $49.00 to $110.00.
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