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base was most effective in improving the bond strength. Studies of the new alumina and glassceramic brackets indicate that high bond strengths can be attained. Most clinical failures are attributed to breakage of the wings of the ceramic brackets.
Reconditioning of metal bases by thermal treatment, chemical treatment, and grinding with a green stone have been evaluated. Reconditioning caused a 20% to 56% decrease in bond strength of several composite cements to a mesh metal base.
Fig. 20-6 Scanning electron photomicrograph of direct-bonding metal mesh base damaged by spot welds.

622

Chapter 20 CEMENTS

 

 

Bond Strength (MPa)

 

 

 

Type of Bracket

 

v p e of Cement

Base Metal

Ceramic

Plastic

Hybrid ionomer

2.9-4.2

5.8-7.4

1.4-4.5

Slightly filled composite

8.8

4.6

8.3*

Highly filled composite

13.0

5.1

8.1

Adapted from Buzzitta VAJ, Hallgren SE, Powers JM: Am J Orthod 81:87, 1982; de Pulido LG, Powers JM: Am J Orthod 83:

124, 1983;and Blalock KA, Powers JM:Am J Orthod Dentofac Orthop 107:596, 1995.

*With bracket primer.

CAVITY VARNISHES

A cavity varnish is used to provide a barrier against the passage of irritants from cements or other restorative materials and to reduce the penetration of oral fluids at the restoration-tooth interface into the underlying dentin. Varnishes help reduce postoperative sensitivity when applied to dentinal surfaces under newly placed restorations. Cavity varnishes are rapidly being replaced by bonding agents.

l.Omm COMPOSITION

I

A cavity varnish is a solution of one or more resins from natural gums, synthetic resins, or rosin. Copal and nitrated cellulose are typical examples of a natural gum and synthetic resin,

(From D~ck~nsonPT, Powers JM: Am J Orthod 78:630, 1980.) respectively. The solvents that may be used to dissolve these materials are chloroform, alcohol, acetone, benzene, toluene, ethyl acetate, and amyl acetate. Medicinal agents such as chlorobutanol, thymol, and eugenol also have been added. The volatile solvents evaporate quickly when the varnish is applied to the prepared tooth surface, thus leaving a thin resin film. The addition of fluoride to cavity varnish has not been established as effective.

MANIPULATION

Varnish solutions are usually applied by means of a small cotton pledget at the end of a wire or root

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canal reamer. Apply thin layers of the varnish with a partially saturated pledget. Use a gentle stream of air for drying, but take care to avoid forming ridges. Add a new layer only to a previously dried one. Two thin layers have been found more protective than one heavy layer. To prevent contamination of the cavity varnish, use a new cotton pledget for each application. Tightly cap varnish solutions immediately after use to minimize loss of solvent. Most varnishes are supplied with a separate bottle of pure solvent. This solvent may be used to keep the varnish from becoming too thick. Replace the loss from evaporation by adding solvent to keep the bottle at least half full by diluting the contents with the solvent. Eventually the solvent will be exhausted and a new supply should be purchased. The solvent is also useful for removing varnish from external tooth surfaces.

PROPERTIES

Cavity varnishes reduce but do not prevent the passage of constituents of the phosphoric acid cements into underlying dentin. Variations in results and the mere reduction rather than the prevention of the passage of acid appear to be a result of pinpoint holes in the varnish film formed during volatilization of the organic solvent. Greater continuity of the dried varnish film is ~ossiblebv the use of successive lavers of thin t,arnish; t h ~ stechnique is more effectitre than using just one layer of thicker varnish

~ h i ' nfilms of iesinous cavity varnishes significantly reduce leakage around the margins and walls of metallic restorations. Although the effect of the cavity varnishes is not completely known, it can be hypothesized that this reduction of fluid penetration around cavity margins would minimize postoperative sensitivity. These varnishes are applied to prepared cavity walls, including the margins. The integrity of the resin film is destroyed when composite restorative materials are placed in contact with them. The monomer contained in these resin materials dissolves the film.

Varnishes neither possess mechanical strength nor provide thermal insulation because of inad-

Chapter 20 CEMENTS

623

equate film thickness. Values of film thickness have been measured at between 1 and 40 ym for different commercial varnishes. Contact angles of varnishes on dentin range from 53 to 106 degrees. Improved integrity of a varnish film might be achieved by improvement in the spreading of the varnish on the tooth surface.

APPLICATIONS

Cavity varnishes are indicated for use (1) on dentinal surfaces to minimize the penetration of acid from zinc phosphate cements, and (2) on enamel and dentinal walls to reduce the penetration of oral fluids around metallic restorations. Cavity varnishes appear also to retard the penetration of discolored corrosion products from dental amalgam into dentin. Varnishes are not used under composite restorations, because bonding agents effectively seal the dentin tubules. A cavity varnish is applied to the dentinal walls of those tubules in direct contact with the pulp when a base of zinc phosphate cement is used. When therapeutic action is expected from a low-strength base or liner or when the cement base material itself is bland in its action on the pulp, a cavity varnish is not used on the underlying dentin. The varnish may be applied over the cement base in these situations.

CAVITY LINERS

A cavity liner is used like a cavity varnish to provide a barrier against the passage of irritants from cements or other restorative materials and to reduce the sensitivity of freshly cut dentin. Unlike a varnish, a liner may provide some therapeutic benefits to the tooth. Liners, however, do not set as the calcium hydroxide pulp-capping agents do.

COMPOSITION

Cavity liners are suspensions of calcium hydroxide in an organic liquid such as methyl ethyl ketone or ethyl alcohol or in an aqueous solution

624

Chapter 20 CEMENTS

of methyl cellulose. The methyl cellulose functions as a thickening agent. Liners also may contain acrylic polymer beads or barium sulfate. Fluoride compounds such as calcium monofluorophosphate have been added to some liners. On evaporation of the volatile solvent, the liner forms a thin film on the prepared tooth surface.

MANIPULATION

Cavity liners are fluid in consistency and are easily flowed or painted over dentinal surfaces. The solvents evaporate to leave a thin film residue that protects the underlying pulp. Certain products are claimed to have better integrity and pulpal protection when used with composite restorative materials.

PROPERTIES

Like varnishes, cavity liners neither possess mechanical strength nor provide any significant thermal insulation. The calcium hydroxide liners are soluble and should not be applied at the margins of restorations.

Fluoride compounds have been added to some cavity liners to reduce the possibility of secondary caries around permanent restorations or to reduce sensitivity. Effectiveness of the fluoride for either purpose would depend on its availability to enamel and dentin through its solubility. Although in vitro studies with one material have shown reduced solubility of tooth tissue, clinical studies have not yet demonstrated its efficacy. However, such an investigation has shown an absence of bacteria at the resin composite-tooth tissue interface when a cavity liner containing calcium monofluorophosphate is used.

LOW-STRENGTH BASES

 

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Low-strength (low-rigidity) bases are two-paste calcium hydroxide or ZOE cements that set to a hard mass when mixed. These cements are commonly referred to as liners, intermediay bases, or pulp-capping agents (calcium hydroxide prod-

ucts only). Glass ionorner, hylxid ionorner, and compoiner bases are discussed in the section on high-strength bases.

COMPOSITION AND CHEMISTRY

OF SETTING

Calcium Hydroxide Bases The base paste of a typical product contains calcium tungstate, tribasic calcium phosphate, and zinc oxide in glycol salicylate. The catalyst paste contains calcium hydroxide, zinc oxide, and zinc stearate in ethylene toluene sulfonamide. The ingredients responsible for setting are calcium hydroxide and a salicylate, which react to form an amorphous calcium disalicylate. Fillers such as calcium tungstate or barium sulfate provide radiopacity.

A light-cured calcium hydroxide base consists of calcium hydroxide and barium sulfate dispersed in a urethane dimethacrylate resin.

Zinc Oxide-Eugenol Bases These bases are non-modified (Type IV) ZOE cements as described in ANSI/ADA Specification No. 30 (IS0 3107). They are typically two-paste systems in which the zinc oxide and eugenol are formulated with inert oils and fillers. The cement sets to a hard mass when mixed. The setting reaction is accelerated by moisture and an increase in temperature.

MANIPULATION

Calcium hydroxide bases and ZOE low-strength bases are supplied as two-paste systems. Equal lengths of the different-colored pastes are dispensed on a paper pad and then mixed to a uniform color.

PROPERTIES

Calcium hydroxide cements are used for lining deep cavities or for direct pulp capping. The antibacterial action of calcium hydroxide makes these cements useful in indirect pulp-capping procedures involving carious dentin. ZOE cements are used in deep cavities to retard pene-

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tration of acids and reduce possible discomfort to the pulp. Both calcium hydroxide and ZOE lowstrength bases are often used with a highstrength base in restoring a tooth. Root canal sealers containing calcium hydroxide have been developed.

Calcium Hydroxide Bases The important properties of these bases are mechanical and thermal properties, solubility, and pH. Calcium hydroxide (self-curedl bases have low values of tensile strength and compressive strength, or elastic modulus, compared with high-strength bases (Table 20-15). Although setting times vary between 2.5 and 5.5 minutes, compressive strengths of these cements continue to increase over a 24-hour period. For a group of five commercial products, compressive strengths ranged from 6.5 to 14.3MPa at 10 minutes to from 9.8 to 26.8 MPa at 24 hours. The low elastic modulus of calcium hydroxide bases restricts their usage to areas not critical to the support of restorations. Mechanical support should be provided by sound dentin or by a high-strength base. Calcium hydroxide bases are, however, considered strong enough to support the forces of condensation of amalgam.

Chapter 20 CEMENTS

625

Calcium hydroxide bases may provide some thermal insulation to the pulp if used in sufficiently thick layers. A thickness greater than 0.5 mm is not suggested. Practically, thermal protection should be provided by the overlying high-strength base.

The solubility of calcium hydroxide bases has been measured in several solvents for various periods of immersion. For a group of five commercial products, values ranged from 0.4% to 7.8%in distilled water at 37' C for 24 hours, from 0.1% to 6.2% in 35% phosphoric acid for 60 seconds, and from 0.3% to 1% in ether for 10 seconds. One product that was resistant to dissolution in water and in acid disintegrated when exposed to ether. Some solubility of the calcium hydroxide is necessary to achieve its therapeutic properties, although an optimum value is not known. Clearly the use of acid-etching procedures and varnish in the presence of calcium hydroxide bases must be done with care. Over a long term, some calcium hydroxide products seem to "disappear" from the cavity. The cause of this dissolution is unclear, but some products have been reformulated in an attempt to minimize the problem.

The pH of commercial products has been

Compressive Strength

Tensile Strength

Elastic Modulus

(MPa)

(MPa)

(GPa)

LOW-STRENGTH (LOW-RIGIDITY) BASES

Calcium hydroxide (light-cured) Calcium hydroxide (self-cured) Glass ionomer (light-cured) Glass ionomer (self-cured)

Zinc oxide-eugenol (Type 111)

HIGH-STRENGTH (HIGH-RIGIDITY) BASES

Glass ionomer Hybrid ionomer

Polymer-reinforced zinc oxide-eugenol (Type IV)

Zinc phosphate Zinc polyacrylate

626

Chapter 20 CEMENTS

measured at between 9.2 and 11.7.Free calcium hydroxide in excess of that necessary to form the calcium disalicylate stimulates secondary dentin in proximity to the pulp and shows antibacterial activity.

One light-cured calcium hydroxide base is reported to have a surface pH of 11.9, low dissolution in acid (<O.5%),low 24-hour solubility in water (<1.0%), and high compressive strength (80 MPa). Whereas two-paste calcium hydroxide bases show antibacterial activity, a light-cured type did not.

ZINC OXIDE-EUGENOL BASES

ANSI/ADA Specification No. 30 (IS0 3107) requirements for zinc oxide-eugenol liners are listed in Table 20-8. The mechanical properties of these cements are compared with those of calcium hydroxide bases and high-strength bases (see Table 20-15). ZOE products tend to be weaker and less rigid than calcium hydroxide pastes that set. Because the base is used in thin layers, it provides little thermal insulation. The eugenol has a sedative (obtundent) effect on the pulp. The base should not be used when a composite is to be placed, because eugenol can inhibit polymerization of the bonding agent and composite.

HIGH-STRENGTH BASES i ',

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,'

High-strength bases are used to provide thermal protection for the pulp and mechanical support for a restoration. Bases are usually prepared from a base or secondary consistency (higher powder/ liquid ratio) of zinc phosphate, zinc polyacrylate, glass ionomer, hybrid ionomer, or compomer cements. A polymer-reinforced ZOE base is also available.

Recently, self-cured and light-cured glass ionomer and hybrid ionomer cements have become available as lowand high-strength bases. The low-strength bases (liners) typically flow more readily than the high-strength bases and are less rigid, as shown in Table 20-15. Light-cured

glass ionomers are water-based cements but have a unique chemistry of setting that involves both an acid-base reaction between carboxylate ions and the glass particles and a lightaccelerated polymerization of dimethacrylate oligomers. Most of the light-cured liners are premixed pastes or powder-liquid systems mixed by hand, but one recent light-cured liner is encapsulated. The composition and setting reaction of the hybrid ionomers used as bases are identical to those of the luting cements discussed earlier in this chapter.

PROPERTIES

The tensile strength, compressive strength, and elastic modulus of five types of high-strength bases are compared in Table 20-15. The secondary consistencies of these cements result in higher values of strength and elastic modulus than values obtained from mixes of a primary (luting) consistency (see Table 20-3). Zinc phosphate cements are the most rigid of the five types, whereas the polymer-modified ZOE cements (Type 111) have the lowest properties. ANSI/ ADA Specification No. 96 specifies the net setting time, minimum compressive strength, and maximum values of acid erosion and acid-soluble arsenic and lead content for zinc phosphate, zinc polyacrylate and glass ionomer bases, as listed in Table 20-2.

The ability of a cement base to support a restoration during function has been studied by stress analysis techniques, as described in Chapter 4. The thickness and elastic modulus of the base affect the deflection of the base and restoration. Mismatches in the moduli of the base and restorative material can cause tensile stresses at the cement-restoration interface that can lead to failure of either material. Studies have recommended that a zinc phosphate base be used to support an amalgam restoration, whereas zinc phosphate, glass ionomer, or zinc polyacrylate may be used to support a Class 1resin composite restoration.

The glass ionomer lining cements and bases are unique in their ability to bond to dentin. Bond

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strengths measured in tension vary from 2.0 to 4.9 MPa. These cements also can be etched to provide additional retention to a composite restoration (so-called sandwich technique). Glass ionomer lining cements and bases release fluoride ions and are radiopaque.

Chapter 20 CEMENTS

627

The thermal conductivity and diffusivity of dental cements (see Tables 3-4 and 3-6) are similar to those of enamel and dentin. Thus cement bases provide thermal protection to the pulp if used in a sufficiently thick layer

(>0.5 mm).

I SELECTED PROBLEMS

Problem 1

A provisional acrylic crown was difficult to remove, and upon removal was found to be soft. What caused these problems, and how can they be resolved?

Solution

The use of reinforced ZOE cement makes the removal of a provisional acrylic crown difficult, and the eugenol softens the acrylic. Therefore a low-strength, non-eugenol-zinc oxide or provisional resin cement is recommended for use with acrylic crowns.

Problem 2

A low-gold alloy bridge with normal retention is to be temporarily cemented. Which cement is recommended for this application?

Solution

Low-strength ZOE cement is suggested to allow for easy removal and cleanup of the bridge for final cementation.

Problem 3

A low-gold content MOD inlay with normal retention is to be cemented permanently. Which cements are recommended for this application? Which are not?

Solution a

Glass ionomer, hybrid ionomer, zinc phosphate, and zinc polyacrylate cements are suf-

ficiently strong and insoluble in oral fluids for this application.

Solution b

EBA ZOE cements are weaker and more soluble in oral fluids than are other cements and are generally not recommended for final cementation.

Problem 4

A gold alloy casting seated properly before cementation but failed to seat when cemented with zinc phosphate cement. What factors might have caused this difficulty, and how can it be corrected?

Solution

An excessive film thickness of zinc phosphate cement may result from (1) too high a mixing temperature, (2) too high a powder/liquid ratio, (3) water contamination during mixing,

(4) a glass slab temperature below the dew point, (5) too long a time between completion of mixing and cementation, or (6) cement being placed on the tooth before being placed on the casting.

Problem 5

A clinician experienced difficulties in reproducing the consistency of mixes of a zinc polyacrylate cement. The mixes were too thick. What were the probable causes of this problem, and how can they be corrected?

628

Chapter 20 CEMENTS

Solution a

The liquid of a zinc polyacrylate cement (excluding the anhydrous type) is very viscous and difficult to dispense accurately. The dropper bottle should be held perpendicular to the mixing pad when the liquid is dispensed. Try to dispense drops of uniform size.

Solution b

The loss of water by evaporation will increase the powder/liquid ratio. The liquid should be dispensed just before mixing, and a waterresistant mixing pad should be used.

Solution c

A mixing temperature higher than 23" C or overmixing will result in a mix that is too thick. Use a cool slab for mixing, and carefully follow the recommended mixing time for more consistent mixes.

Problem 6

During the insertion of a zinc phosphate cement base into an extensive cavity preparation, the mix became dry and friable and did not adhere well to the cavity walls. What factors might be related to such a change in consistency, and how can the consistency be improved?

Solution a

The heat of reaction accelerates the setting reaction of zinc phosphate cement, thereby causing the working time to decrease. Mixing the cement with incremental additions of powder and over a large area of a cool slab will reduce the temperature rise and allow a longer working time.

Solution b

Too much powder incorporated into a mix as it approaches secondary consistency decreases the working time and causes the cement base to be weak and friable because of insufficient matrix to bind the powder together. The base should be slightly tacky after it is rolled in powder at the completion of mixing.

Problem 7

A properly mixed zinc phosphate cement base became contaminated with saliva during placement. Should there be any deleterious effect expected from the contamination?

Solution

Yes, a soft, friable surface results from the dilution of acid and leaching of the matrix of a setting cement base by saliva.

Problem 8

A calcium hydroxide base appeared to disintegrate when acid came into contact with it during an acid-etching procedure. Are there bases that can be used in conjunction with acid-etching procedures for a composite?

Solution a

Yes, acid-resistant calcium hydroxide bases containing disalicylates are available.

Solution b

Glass ionomer bases can be etched to enhance the bond between the base and the composite.

Solution c

Use hybrid ionomer cement. Its bond to composite is not affected by etching.

Problem 9

When an amalgam is placed over a ZOE base, the cement sometimes crumbles and becomes incorporated into the amalgam mass. Should a thicker layer of ZOE cement or a different cement base be placed to provide better support?

Solution a

The ZOE base is a material with a low rigidity. Increasing its thickness will result in less rather than more support. Maintain the thickness of a low-strength base at less than 0.5 mm.

Solution b

A more rigid cement base, such as zinc phosphate cement, should be placed over the ZOE

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base to provide additional support for condensation and for the amalgam from occlusal forces.

Problem 10

A paste-primer (one-step) composite orthodontic cement failed shortly after the appliance was activated. Composite remained on the tooth and the metal bracket. What factors might explain these observations, and how can the problem be corrected?

Solution a

The bond strength of a one-step composite cement can be very low if too thick a layer of the paste is placed on the bracket. The primer cannot diffuse through the thick layer of paste, causing insufficient polymerization of the cement. Keep the thickness of the cement paste to less than 0.25 mm.

Solution b

The enamel primer of a one-step cement remaining in the warm, humid environment of the mouth too long before the bracket is placed will cause a decrease in the cohesive strength of the cement. Apply the brackets to the teeth within 1 minute after applying the primer.

General

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Barakat MM, Powers JM: In vitro bond strength of cements to treated teeth, Aust Dent J 3 l : 415, 1986.

Craig RG, Peyton FA: Thermal conductivity of tooth structure, dental cements, and amalgam, J Dent Res 40:411, 1961.

Craig RG, Peyton FA, Johnson DW: Compressive properties of enamel, dental cements, and gold, J Dent Res 40936, 1961.

Chapter 20 CEMENTS

629

Dennison JB, Powers JM: A review of dental cements used for permanent retention of restorations. I. Composition and manipulation, Mich Dent AssocJ 56:116, 1974.

McCabe JF, Wilson HJ: The use of differential scanning calorimetry for the evaluation of dental materials. I. Cements, cavity lin-

ing materials and anterior restorative materials, J Oral Rehabil7:103, 1980.

Mesu FP: Degradation of luting cements measured in vitro, J Dent Res 61:655, 1982.

Mitchem JC, Gronas DG: Clinical evaluation of cement solubility, J Prosthet Dent 40:453, 1978.

Myers ML, Staffanou RS, Hembree JH Jr et al: Marginal leakage of contemporary cementing agents, J Prosthet Dent 50:513, 1983.

Norman RD, Swam ML, Phillips RW: Studies on film thickness, solubility, and marginal leakage of dental cements, J Dent Res 42950, 1963.

Norman RD, Swartz ML, Phillips RW: Direct pH determinations of setting cements. I. A test method and the effects of storage time

and media, J Dent Res 45:136, 1966. Norman RD, Swartz ML, Phillips RW: Direct pH

determinations of setting cements. 11. The effects of prolonged storage time, powder/ liquid ratio, temperature, and dentin, J Dent Res 45:1214, 1966.

Oilo G, Espevik S: Stresdstrain behavior of some dental luting cements, Acta Odonto1 Scand 36:45, 1978.

Osborne JW, Swartz ML, Goodacre CJ et al:

A method for assessing the clinical solubility and disintegration of luting cements,

J Prosthet Dent 40:413, 1978.

Paddon JM, Wilson AD: Stress relaxation studies on dental materials. I. Dental cements, J Dent 4:183, 1976.

Phillips LJ, Schnell RJ, Phillips RW: Measurement of electric conductivity of dental cement. 111. Effect of increased contact area and thickness; values for resin, calcium hydroxide, zinc oxide-eugenol, J Dent Res 34597, 1955.

630

Chapter 20 CEMENTS

Powers JM, Craig RG: A review of the composition and properties of endodontic filling materials, Mich Dent Assoc J 61:523, 1979.

Powers JM, Farah JW, Craig RG: Modulus of elasticity and strength properties of dental cements, J A m Dent Assoc 92:588, 1976.

Richter WA, Ueno H: Clinical evaluation of dental cement durability, J Prosthet Dent 33:294, 1975.

Tanizaki K, Inoue K: Effect of tannin-fluoride preparation on the reduction of secondary caries, J Osaka Univ Dent Sch

19:129, 1979.

Vermilyea S, Powers JM, Craig RG: Rotational viscometry of a zinc phosphate and a zinc polyacrylate cement, J Dent Res

56:762, 1977.

Walls AW, McCabe JF, Murray JJ: An erosion test for dental cements, J Dent Res 64:1100, 1985.

Watts DC, Smith R: Thermal diffusion in some polyelectrolyte dental cements: the effects of powder/liquid ratio, J Oral Rehabil

11:285, 1984.

Wilson AD: The chemistry of dental cements, Chem Soc Rev 7:265, 1978.

Zinc Phosphate Cements

Crisp S, Jennings MA, Wilson AD: A study of temperature changes occurring in the setting dental cements, J Oral Rehabil 5139, 1978.

Kendziar GM, Leinfelder KF, Hershey HG: The effect of cold temperature mixing on the properties of zinc phosphate cement, Angle Orthod 46:345, 1976.

Mitchem JC, Gronas DG: Clinical evaluation of cement solubility, J Prosthet Dent 40:453, 1978.

Muhler JC (Indiana Univ Foundation, Bloomington, Ind): Dental cement. Canadian Patent 912,026 (C1 6-36), Oct 17, 1972; Appl July 20, 1970, 23 pp.

Servais GE, Cartz L: Structure of zinc phosphate dental cement, J Dent Res 50:613, 1971.

Wilson AD: Specification test for the solubility and disintegration of dental cements: a critical evaluation, J Dent Res 55:721, 1976.

Zinc Oxide-Eugenol Cements

Brauer GM: A review of zinc oxide-eugenol type filling materials and cements, Rev Belg Med Dent 20:323, 1965.

Brauer GM, McLaughlin R, Huget EF: Aluminum oxide as a reinforcing agent for zinc oxide-eugenol-o-ethoxy-benzoic acid cements, J Dent Res 47:622, 1968.

Civjan S, Brauer GM: Physical properties of cements, based on zinc oxide, hydrogenated rosin, o-ethoxybenzoic acid, and euge-

nol, J Dent Res 43:281, 1964.

Civjan S, Brauer GM: Clinical behavior of o-ethoxy-benzoic acid-eugenol-oxide cements, J Dent Res 4430, 1965.

Civjan S, Huget EF, Wolfhard G et al: Characterization of zinc oxide-eugenol cements reinforced with acrylic resin, J Dent Res

51:107, 1972.

El-Tahawi HM, Craig RG: Thermal analysis of zinc oxide-eugenol cements during setting, J Dent Res 50:430, 1971.

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Gilson TD, Myers GE: Clinical studies of dental cements. I. Five zinc oxide-eugenol cements, J Dent Res 47:737, 1968.

Gilson TD, Myers GE: Clinical studies of dental cements. 11. Further investigation of two zinc oxide-eugenol cements for temporary restorations, J Dent Res 48366, 1969.

Gilson TD, Myers GE: Clinical studies of dental cements. 111. Seven zinc oxide-eugenol cements used for temporarily cementing completed restorations, J Dent Res

4914, 1970.

Gilson TD, Myers GE: Clinical studies of dental cements. IV. A preliminary study of a zinc oxide-eugenol cement for final cementation, J Dent Res 49:75, 1970.

Grossman LI: Physical properties of root canal cements, J Endodont 2:166, 1976.

Harvey W, Petch NJ: Acceleration of the setting of zinc oxide cements, Br Dent J 8O:l, 1946.

Higginbotham TL: A comparative study of the physical properties of five commonly used root canal sealers, Oral Surg Oral Med Oral Path01 24:89, 1967.

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McComb D, Smith DC: Comparison of physical properties of polycarboxylate-based and conventional root canal sealers,J Endodont 2:228, 1776.

Molnar EJ, Skinner EW: Study of zinc oxiderosin cements. I. Some variables which affect the hardening time, J A m Dent

Assoc 29744, 1942.

Nielsen TH: Sealing ability of chelate root filling cements. Part I. Device for measuring linear changes of setting chelate cements, J Endodont 6:731, 1780.

Powers JM, Craig RG: A review of the composition and properties of endodontic filling materials, Mich Dent Assoc J 61:523, 1979.

Silvey RG, Myers GE: Clinical studies of dental cements. V. Recall evaluation of restorations cemented with a zinc oxide-eugenol cement and a zinc phosphate cement, J Dent Res 55:287, 1776.

Silvey RG, Myers GE: Clinical studies of dental cements. VI. A study of zinc phosphate, EBA reinforced zinc oxide-eugenol and polyacrylic acid cements as luting agents in fixed prostheses, J Dent Res 56:1215, 1777.

Silvey RG, Myers GE: Clinical studies of dental cements. VII. A study of bridge retainers luted with three different dental cements, J Dent Res 57:703, 1778.

Vermilyea SG, Huget EF, DeSimon LB: Extrusion rheometry of fluid materials, J Dent Res 58:1691, 1779.

Wilson AD, Mesley RJ: Chemical nature of cementing matrixes of cements formed from zinc oxide and 2-ethoxy benzoic acideugenol liquids, J Dent Res 53:146, 1774.

Zinc Polyacrylate Cements

Ady AB, Fairhurst CW: Bond strength of two types of cements to gold casting alloy,

JProsthet Dent 27:217, 1973.

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Bertenshaw BW, Combe EC: Studies on polycarboxylate and related cements. 11. Analysis of cement powders, J Dent 1:65, 1772.

Chapter 20 CEMENTS

631

Brannstrom M, Nyborg H: Pulpal reaction to polycarboxylate and zinc phosphate cements used with inlays in deep cavity preparations, J Am Dent Assoc 74:308, 1777.

Chamberlain BB, Powers JM: Physical and mechanical properties of three zinc polyacrylate dental cements, Mich Dent Assoc J 58474, 1776.

Crisp S, Lewis BG, Wilson AD: Zinc polycarboxylate cements: a chemical study of erosion and its relationship to molecular structure, J Dent Res 55:277, 1976.

Crisp S, Prosser HJ, Wilson AD: An infra-red spectroscopic study of cement formation between metal oxides and aqueous solutions of poly(acry1ic acid), J Mater Sci 11:36, 1976.

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28:264, 1972.

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McLean JW: Polycarboxylate cements-five years' experience in general practice, Br Dent J 132:7, 1772.

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Oilo G: Linear dimensional changes during setting of two polycarboxylate cements, J Oral Rehabil3:161, 1976.

Plant CB: The effect of polycarboxylate cement on the dental pulp-a study, BY Dent J 129424, 1970.

Powers JM, Johnson ZG, Craig RG: Physical and mechanical properties of zinc polyacrylate dental cements, J A m Dent Assoc 88:380, 1774.

Smith DC: A new dental cement, Br Dent J 125:381, 1768.

Truelove EL, Mitchell DG, Phillips RW: Biologic evaluation of a carboxylate cement, J Dent Res 50:166, 1771.