Lecture 5 Glass Ionomer Cements Flashcards

1
Q

What are Glass Ionomer cements?

A
  • Developed 30 years ago by Alan Wilson and John McClean as extension of silicate based cements.
  • Also known as glass polyalkenoate
  • Acid-base reaction concept: Acid + Base -> Salt + water
  • Water soluble polymer system poly-(acrylic acid)
  • Base is composed of fluoro-alumino-silicate (FAS).
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2
Q

Describe Glass composition

A
  • Fluoro-alumino-silicate (FAS) based glasses
  • Glass composition melted then quenched into water to retain glass and to prevent crystallisation also to assist with crushing.
  • Typical composition: silicon dioxide 30%, aluminium oxide 20%, calcium fluoride 33%, sodium fluoride 4%, aluminium fluoride 3%, aluminium phosphate 10% (by weight%)
  • Some companies replace calcium fluoride with strontium fluoride (same ionic radius) that is with strontium fluoride. More radio-opaque.

Strontium fluoride stops growth of bacteria.

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3
Q

Describe the polymer component

A
  • Water soluble polymer originally poly-(acrylic acid)
  • Currently copolymer of acrylic acid with itaconic or maleic acid
  • Referred to as poly-alkenoic acid. These are long chain polymers of a few thousand units. If too long then too viscous.
  • All contain carboxyl group - COOH
  • Inclusion of tartaric acid delays the setting reaction before the viscosity of the mix rises.
  • Allows for faster setting once the viscosity increases.
  • the tartrate ions sequester the first metal released from the glass and prevent cross-linking of the poly-acid chains.
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4
Q

Describe setting reaction of GIC

A
  • Two main metal ions are released from glass (powder) by acids (in the mixing liquid): calcium and aluminium.
  • Calcium initially has faster setting -> no hydrolysis of covalent bonds.
  • Aluminium much slower -> hydrolysis of covalent bonds.
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5
Q

Describe acid-base reaction

A
  • Poly-(acrylic acid) is the acid component that ionises into hydrogen ions and polyalkenoate anions.

Glass + H+ => calcium ion + SiO4(4-)

  • Formation of the silica gel and the calcium ion are chelated by the polyacid chains.
  • The set cement consists of an agglomeration of unreacted powder surrounded by a silica gel in an amorphous matrix of hydrated calcium and aluminium polysalts.
  • The FAS glass is the source of the base. The outer layer of the glass particles are decomposed releasing calcium ions, aluminium ions and fluoride ions etc.
  • Residual silica gel layer on glass particles.
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6
Q

Describe setting reactions

A
  • Release of anions from the glass
  • Initially release of calcium ions. This is followed by aluminium and fluoride ions.
  • Release of ions determines the reaction kinetics with the polyalkenoic anions.
  • Rate of the reaction also determined by the size of glass particles. Smaller particles are more reactive and can promote a faster set.
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7
Q

Describe bonding to enamel and dentine

A
  • Two chemical reactions possible with enamel and mineral component of dentine.
  • Hydrogen bonding and ionic bonding. The latter via calcium ions in the apatite.
  • This suggests that hard etching with phosphoric acid is not required. Simply conditions the surface with polyalkenoic acid to achieve bonding prior to placing GIC mass.
  • Some suggestions that bonding with collagen is possible but this has not been proven yet.
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8
Q

Describe GIC’s water and shrinkage

A
  • Water plays a critical role with acid-base systems as it is the medium for ion transport.
  • Volumetric shrinkage for conventional GIC’s is small provided they are kept moist. If the humidity drops below 80%, if they lose water and crazing of the material occurs. Prevent with sealing varnish.
  • Too much water initially leaches out the ions (aluminium and calcium) which cross-link the poly-alkenoic chains thus strength reduces.
  • The setting cement should be protected from water (saliva).
  • The set cement should be protected from loss of water (isolated outside rubber dam for too long, mouth breathers).
  • Generally GICs are not advised to cement ceramic crowns since slight absorption of water may create high stress.
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9
Q

Describe GIC materials

A
  • Wide range of material system are available for GIC’s
  • Luting cement
  • Fissure sealant
  • Occlusal surface in primary dentition
  • Cermet-GIC’s, which contain silver or amalgam (5 to 10 um diameter) particles.
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10
Q

Describe Resin-modified GIC

A
  • Strength of conventional GIC somewhat low, hence the wish to include resin to increase strength and also to command set with lamp.
  • Typical resins include hydroxyethyl methacrylate (HEMA) or Bis-GMA together with a photo-initiator such as camphorquinone.
  • Alternative is polyalkenoic acid with pendant methacrylate group.
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11
Q

Compare the mechanical properties of GIC’s with composite resins

A

Compressive strength (MPa):

  • GIC 200-220
  • RMGIC 250
  • Composite 250-350

Tensile strength (MPa):

  • GIC 10-20
  • RMGIC 30-40
  • Composite 50-60

Tooth bonded conventional GIC’s often fail in a cohesive manner.

  • Conventional GIC’s are cariostatic because of fluoride ions released but not anti-bacterial.
  • GIC’s have lower hardness and higher wear rate than filled composites. Thermal expansion of unconventional GIC’s lower (11x10^-6 /C), than composites (20 to 40 x10^-6/C). RMGIC is same as the composite.
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12
Q

Will GIC stabilise a carious lesion of a primary tooth? That is, will bacteria grow near the restoration?

A

Bacteria do not grow in high fluoride ion areas.

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13
Q

GIC provide an excellent prevention of secondary caries

A

True

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14
Q

Describe Cements

A

Intermediate restorative materials are agents for pulp protection.
Materials placed in dentine in close proximity to the pulp:
- Permanent placement, not a temporary filling material.
- Cavity varnishes, liners and bases (thicker)

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15
Q

Define working time vs setting time

A
  • Working time: time from the start of mixing until the time at which the viscosity of the mix is low enough to flow under pressure.
  • Setting time: time period during which the matrix formation has reached a point at which external physical forces will not cause permanent dimensional changes.
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16
Q

Describe cements’ outline

A
  • Calcium hydroxide cement
  • Zinc phosphate cement
  • Zinc oxide-eugenol cement
17
Q

Describe Calcium hydroxide

A
  • Calcium hydroxide is the chief ingredient (50%), and salicylate (40%) is the other main component.
  • In base cements, setting follows:
    1) Calcium hydroxide + salicylate = calcium disalicylate.
    2) Initially believed to supply calcium ions to form reparative dentine.
    3) Currently it is suggested that high pH (10) may prevent inflammation and bacterial action in the site.

Disadvantages:

  • Relatively low compressive strength
  • Partially soluble in pulpal fluid
  • Poor bonding to dentine.
18
Q

Describe base of calcium hydroxide and its applications

A

Base:

  • Glycol disalicylate (40%), reacts with Ca(OH)2 and ZnO
  • Calcium phosphate
  • Calcium tungstate
  • Iron oxide pigments

Base: catalyst does not affect setting time. Lower humidity and temperature will slow the reaction.

Applications - direct pulp capping (powder), pulp protection (deep dentine lesions)

19
Q

Describe setting, mechanism of action and disadvantage of calcium hydroxide

A

Setting: calcium hydroxide reacts with salicylate ester to form amorphous calcium disalicylate.

Mechanism of action:

  • Calcium hydroxide solubilises dentine matrix bioactive components - TGF-beta1 and glycosaminoglycans.
  • TGF-beta 1 is associated with signalling mechanisms triggering dentine bridge formation.

Disadvantages - relatively low compressive strength. Partially soluble in pulpal fluid. Poor bonding to dentine.

20
Q

Describe zinc phosphate cement

A
  • It is the oldest of the luting cements
  • Acid-base reaction -> powder + liquid
  • Powder - zinc oxide (90%) and magnesium oxide (10%)
  • Liquid - generally phosphoric acid, water aluminium phosphate and sometimes zinc phosphate.
  • Not a temporary cement.
  • Applications - metal crown, porcelain fused to metal.
21
Q

Describe setting reaction and set material of zinc phosphate cement

A

Setting reaction:

  • When mixed, phosphoric acid attacks the surface particles and released zinc ions into the liquid.
  • Aluminium reacts with zinc and forms a zinc aluminophosphate gel on the surface of the remaining particles.

Set material - unreacted zinc oxide particles embedded in a cohesive amorphous matrix of zinc aluminophosphate.

22
Q

Describe zinc oxide-eugenol

A

This material is very attractive for dental applications for a number of reasons. Often mixed with eugenol to assist setting and to ‘sedate’ tissue.
Acid + base -> salt + water.
2 (H-E ) + ZnO -> ZnE2 + H2O.

  • Reacts well with magnesium oxide and olive oil (improve viscosity or mixing ability and mask eugenol).
  • EBA (ortho-ethoxybenzoic acid) in higher concentration than eugenol plus aluminium oxide added to ZnO. Higher strength (2x) that of conventional ZnE cement.
23
Q

Composition of Zinc-oxide-eugenol

A

Composition:

  • Powder: zinc oxide, PMMA, pigments
  • Liquid: eugenol
  • Acetic acid

Applications - intermediate (temporary, less than 1 year) restoration and base under non-resin based materials.

24
Q

Advantages and disadvantages of zinc oxide-eugenol

A

Advantages:

  • Radio-opacity and low cost
  • Whiteness (colour)
  • Low toxicity, Zn is an essential component of human physiology
  • Reduced pain and calming effect of eugenol (oil of cloves) on the inflamed tissue.

Disadvantages:

  • Poor bond strength and weak adhesion to dentine. Strength improved in some recent formulations by adding resin (polystyrene or methyl methacrylate) or EBA.
  • Hydrolytic breakdown in oral cavity!