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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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    23 GroblerSR, RossouwRJ,VanWykK.Acomparison ofuoridereleasefromvariousdentalmaterials.JDent.1998;26:259-65.

    24 Shaw AJ, Carrick T, McCabe JF. Fluoride release from glass-ionomerandcompomerrestorativematerials:6-monthdata.JDent.

    1998;26:355-9.25 Asmussen E, Peutzfeldt A. Long-term uoride release from aglassionomercement,a compomer,and fromexperimentalresincomposites.ActaOdontolScand.2002;60(2):93-7.

    26 KawaiK,TakaokaT.Fluoride,hydrogenionandHEMAreleasefromlight-curedGICrestoratives.AmJDent.2002;15(3):149-52.

    27 PalmerG,AnsticeHM,PearsonGJ.Theeffectofcuringregimeonthe releaseofhydroxyethylmethacrylate(HEMA)fromresin-modiedglass-ionomercements.JDent.1999;27(4):303-11.

    28 Beriat NC, NalbantD.Water absorption and HEMA release ofresin-modiedglass-ionomers.EurJDent.2009;3(4):267-72.

    29 IkemuraK,TayFR,EndoT,PashleyDH.Areviewof chemical-approachandultramorphological studieson thedevelopmentofuoride-releasing dental adhesives comprising new pre-reactedglassionomer(PRG)llers.DentMatJ.2008;27(3):315-39.

    30 AzevedoC,TavernierB,VignesJL,CenedeseP,DubotP.Structureandsurfacereactivityofnovelnanoporousaluminallers.JBiomedMaterResBApplBiomater.2009;88(1):174-81.

    31 BeunS,GlorieuxT,DevauxJ,VrevenJ,LeloupG.Characterizationof nanolled compared to universal andmicrolled composites.DentMater.2007;23(1):51-9.

    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

    Online CompletionUse this page to review the questions and answers. Return towww.ineedce.comand sign in. If you have not previously purchased the program select it from the Online Courses listing and complete the

    online purchase. Once purchased the exam will be added to your Archives page where a Take Exam link will be provided. Click on the Take Exam link, complete all the program questions and submit your

    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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    PLEASE PHOTOCOPY ANSWER SHEET FOR ADDITIONAL PARTICIPANTS.

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    Educational Objectives

    1. Describetheearlytooth-coloreddirectrestorativematerials

    2. Listandcomparetheattributesocompositeresinsandglassionomercements

    3. Describethecompositionoacompomer,andcompareittocompositeresinsandconventionalglassionomers

    4. Describetherestorativescontainingnanotechnologyandtheefectonano technologyinnano-ionomerrestorations

    Course Evaluation

    Pleaseevaluatethiscoursebyrespondingtotheollowingstatements,usingascaleoExcellent=5toPoor=0.

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    ANSWER SHEET

    Advances in Tooth-Colored Restorations

    Name: Title: Specialty:

    Address: E-mail:

    City: State: ZIP: Country:

    Telephone:Home(

    ) Ofce(

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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.

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    M2011.All

    rightsreserved.3M,ESPEandKetacaretrademarksof3Mor3MESPEAG.UsedunderlicenseinCanada.

    *Source:Externalstudyfor3MESPE,n=120

    Call 800-634-2249 or visit www.3MESPE.com/KetacNano

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