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CERAMICS
INTRODUCTION
Greek term "keramos" which means pottery.
an article having a glazed or unglazed body of crystalline or
partly crystalline structure, or of glass, which body is produced
from essentially inorganic, non-metallic substances and either is
formed from a molten mass which solidifies on cooling, or is
formed and simultaneously or subsequently matured by the
action of the heat.
BIOCERAMICS.
I GENERATION BIOCERAMICS
In 1960’s
BIO-INERTNESS
Interaction with the living tissue as low as possible.
Alumina & Zirconia
II GEN BIOCERAMICS
1980’s
BIOACTIVE or BIO-RESORBABLE
Favorable interaction with body
Able to form strong interaction with living tissue
crystalline calcium phosphates, bioactive glasses and glass-ceramics
bone tissue augmentation, bone cements or the coating of metallic
implants
III GEN BIOCERAMICS
Start of 21st
century
concept replacement of tissues is been substituted with
regeneration of tissues.
Able to induce regeneration and repair of living tissues based
on genes
porous second generation bioceramics
Organic & inorganic hybrids, mesoporous of silica, stargels,
templated glasses.
CERAMICS IN ARTHROPLASTYoxide ceramics
formed by closely packed crystals of Very small and very pure
crystals oxides of aluminum or zirconium metals
Sliding ceramics
1930 Rock, 1st
person to consider the possibility of ceramics in
A’plasty.
1970 French surgeon Boutin implanted the first ceramic-on-
ceramic cemented total hip joint in France
MANUFACTURING PROCESS
 Particulates of C. + H20 + organic binder
 Moulding
 Hot isostatic pressure.
 Evaporation of water, burning the binder by thermal
treatment
 Sintering with Cao / Mgo
 Final ceramic structure.
MATERIAL PROPERTIES
Hardness
Wettability
Biocompatiblity
Excellent tribological properties
Chemical & corrosion resistant
Good surface finish
HARDNESS:
very resistant to scratches from the tiny particles
harder the surfaces coupled together, the less wear the coupling
system produces
WETTABILITY:
 Self lubricating, because of ionic structure which produces
hydrophilic surface.
Synovial fluids gets attracted & spreads out  which minimizes
adhesive wear.
BIO-COMPATABILITY
 Exist in highly oxidative state
 Chemically inert, resistant to oxidative degradation.
 Insoluble in water, hydrative degradation not possible.
Results in less wear, smaller wear particle size, decreased
cytotoxity & osteolysis.
TRIBOLOGICAL PROPERTY
 wear rate of alumina-alumina bearing coupling is extremely
low (0.001 mm/year). If compared with metal-polyethylene
(0.2 mm/ yr)
 4000 times less
 fluid film lubrification - reduces the coefficient of clutch.
Evaluation
 I GENERATION:
1974-1988
Grain size – 4.5 micrometers
burst strength of 46 KN
Impurities
high rate of #
II GENERATION:
1990-1993
Grain size – 3.2 micro
burst strength – 58
 III GENERATION:
From 1994
grain size – 1.8 micro
burst strength – 65 KN
Improved mech, HIP, Laser etching.
ALUMINA
Old A. ceramic materials the crystals of aluminum oxides
were large, not assembled closely; there were many
impurities and voids between them [5%].
impurities - weak points for propagation of fracture cracks.
The coarse structure and impurities were the cause of the
frequent fractures
Modern alumina [0.5% impurity]: HIPing process extrudes
impurities out off the material and packs the crystals very close
together.
very tough structure, tougher than the metallic stem on which it is
seated, and even more tough then the natural thighbone.
disadvantage of the modern alumina ceramic is lower toughness
high alumina ceramics : materials that have the minimal
content of 97% of alumina.
high purity alumina ceramics: percentage of minimal alumina
is of 99%.
 HPA: commonly used for arthroplasty.
Biolax forte.
Zirconia Toughened Alumina
(ZTA) ceramic
Mixed-oxide ceramics.
75% of alumina and the rest are zirconium, Yttrium and chrome
oxides.
superior strength and resistance to wear.
Biolax delta
bending strength around 1000 MPa, more than the double of the
alumina standard (400 MPa).
Burst strength - 100 KN
Zirconia ceramic
one of the stronger ceramics
 introduced to reduce the risk of fracture.
Pure zirconia is an unstable
material showing three different crystalline phases
Stabilisation of zirconia by adding oxides to maintain the tetragonal
phase
Smaller Femoral heads [22 mm]
More smoother finish
Zirconia femoral heads should articulate only against
polyethylene sockets
It ages in the body’s temperature and the surface of the
zirconia ball roughens
Advantages as bearing material
Smoother surface & less co-efficient of friction & wear.
Superior lubrication property.
Harder & less susceptible to third body wear
Inert with no ion release.
best used in young and active patients who have a high risk of
loosening and osteolysis in the mid to long term.
Oxinium materials
Zirconium is a strong and biocompatible metal similar to
titanium
Thin layer of zirconium oxide is coated on the surface of the
solid zirconium metal
femoral head made out of Oxinium that articulates with a
polyethylene cup
combines the benefits of metals and ceramics.
It offers superior wear resistance on its surface
zirconium metal itself, with characteristics close to titanium, is a
material without the risk of brittle fracture.
oxidized zirconium is black
Ceramics for total knees
The total knee joints doesn’t have congruent joint surfaces.
Thus, in a total knee joint with both joint surfaces made from
ceramic materials, there would appear large localized stresses that
would destroy components made from the contemporary ceramics
difficult to fabricate such a large yet thin ceramic component as is
the form of the femoral component
Oxinium total knee prosthesis
Bioactive ceramics
Osteoconductive property
acting as a scaffold to enhance bone formation on their surface
used either as a coating on various substrates or to fill bone defects.
Calcium phosphate ceramics.
hydroxyapatite (HA) and tricalcium phosphate (TCP).
In solid form, neither of these materials exhibits adequate fatigue
resistance for use as a load-bearing implant
Hydroxyapatite (Ca10(PO4)6(OH)2)
Synthetic apatite
Most similar material from structural & chemical point of view to
the mineral component of bone.
bone-graft substitute, HA coating to prosthesis.
bonding mechanism - attachment at the surface of the HA of
osteogenically-competent cells which differentiate into osteoblasts
A cellular bone matrix is then formed at the surface of the HA.
An amorphous area is present between the surface and the bone
tissue containing thin apatite crystals.
As maturation occurs, this bonding zone shrinks HA becomes
attached to bone through a thin epitaxial layer, resulting in a strong
interface with no layer of fibrous tissue interposed between the
bone and HA.
Such integration rarely, if ever, occurs with porous or smooth
metal implants
hot plasma spray technique.
optimal thickness of the coating- 50 microns
Thinner coatings may not supply sufficient Ca and P long enough to
be effective,
Thicker layers can experience sufficient stress under implant cyclic
bending and shear and tensile loads to be subject to fatigue failure
Tricalcium phosphate (Ca3(PO4)2)
exists in either alpha or beta crystalline forms.
The beta form is the most stable.
The rate of biodegradation is higher when compared with HA.
Degradation occurs by combined dissolution and osteoclastic
resorption.
to stimulate early bone in-growth into porous surfaces.
Bone graft substitutes
Porous coraline ceramics
Chiroff et al, first recognised that, corals made from marine
invertebrates have a structure similar to both cortical & cancellous
bone.
Exoskeleton of genus porite [ICF- 190mm], structure similar to
cortical bone.
Genus gonipora – similar to cancellous bone
Hydrothermal exchange process converts delicate coral
carbonate in to hydroxyapatite without altering the internal
structure.
Invaded & converted to mature lamellar B.
Only surface resorption & no remodeling.
Reconstruct metaphyseal defects.
Bioactive glasses.
Bioglass 45S5
bonding mechanism to bone - series of surface reactions ultimately
leading to the formation of a hydroxycarbonate apatite layer at the
glass surface.
Greater production of bone, compared with HA.
poor mechanical properties
wollastonite (CaOSiO2)
glass ceramic developed by Kokubo et al
osteoconductive properties similar to Bioglass 45S5
increased mechanical strength.
It has been used as a spacer at the iliac crest, for vertebral
prostheses and as a shelf in procedures about the shoulder
Bioactive bone cement
Explored in order to avoid complications related to PMMA debris
and to enhance fixation of the prosthesis.
calcium-phosphate based bone cement and glass-ceramic bone
cement.
Calcium phosphate cements
Biocompatible & resorbable cement
Injectable cements
Replaced by creeping substitution with host bone.
As bone void fillers with uniform & predictable drug eluding
property.
Deliver the antibiotics.
N-SRS, ETEX alpha - BSM
Norian SRS
N. skeletal repair system.
Augmentation of fracture repair.[DHS, pedicle screw]
Combination of monocalcium phosphate, tricalcium
phosphate, calcium carbonate & a sodium phosphate solution
in to inj. Paste
Hardens with in minutes into dahllite [carbonated HA] in a
nonexothermic reaction.
ETEX alpha BSM
Calcium orthophosphate cement
Dicalciumphosphate dihydrate, octocalcium P & many
precipitating apatites.
Poorly crystalline apatite which will mimic bone, aiming
superior resorption & osteointegration.
Easy intraop handling characteristics..
OSTEOSETMedical grade calcium sulphate
High tech processing [retains all biological adv & consistent mech /
resorption profile]
Provide structural support & is bioabsorbable and biocompatible.
Resorption profile matches with the rate at which host
environment can lay down bone around the compound.
Available as pellets
Antibiotic delivery – aminoglycosides/ ideal.
FUTURE
Scaffold fabricated with a synthetic bioceramic which after
being supplemented with moieties of biological activity is
implanted in a living organism to induce tissue regeneration,

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Ceramics (2)

  • 2. INTRODUCTION Greek term "keramos" which means pottery. an article having a glazed or unglazed body of crystalline or partly crystalline structure, or of glass, which body is produced from essentially inorganic, non-metallic substances and either is formed from a molten mass which solidifies on cooling, or is formed and simultaneously or subsequently matured by the action of the heat. BIOCERAMICS.
  • 3. I GENERATION BIOCERAMICS In 1960’s BIO-INERTNESS Interaction with the living tissue as low as possible. Alumina & Zirconia
  • 4. II GEN BIOCERAMICS 1980’s BIOACTIVE or BIO-RESORBABLE Favorable interaction with body Able to form strong interaction with living tissue crystalline calcium phosphates, bioactive glasses and glass-ceramics bone tissue augmentation, bone cements or the coating of metallic implants
  • 5. III GEN BIOCERAMICS Start of 21st century concept replacement of tissues is been substituted with regeneration of tissues. Able to induce regeneration and repair of living tissues based on genes porous second generation bioceramics Organic & inorganic hybrids, mesoporous of silica, stargels, templated glasses.
  • 6. CERAMICS IN ARTHROPLASTYoxide ceramics formed by closely packed crystals of Very small and very pure crystals oxides of aluminum or zirconium metals Sliding ceramics 1930 Rock, 1st person to consider the possibility of ceramics in A’plasty. 1970 French surgeon Boutin implanted the first ceramic-on- ceramic cemented total hip joint in France
  • 7. MANUFACTURING PROCESS  Particulates of C. + H20 + organic binder  Moulding  Hot isostatic pressure.  Evaporation of water, burning the binder by thermal treatment  Sintering with Cao / Mgo  Final ceramic structure.
  • 8. MATERIAL PROPERTIES Hardness Wettability Biocompatiblity Excellent tribological properties Chemical & corrosion resistant Good surface finish
  • 9. HARDNESS: very resistant to scratches from the tiny particles harder the surfaces coupled together, the less wear the coupling system produces WETTABILITY:  Self lubricating, because of ionic structure which produces hydrophilic surface. Synovial fluids gets attracted & spreads out  which minimizes adhesive wear.
  • 10. BIO-COMPATABILITY  Exist in highly oxidative state  Chemically inert, resistant to oxidative degradation.  Insoluble in water, hydrative degradation not possible. Results in less wear, smaller wear particle size, decreased cytotoxity & osteolysis.
  • 11. TRIBOLOGICAL PROPERTY  wear rate of alumina-alumina bearing coupling is extremely low (0.001 mm/year). If compared with metal-polyethylene (0.2 mm/ yr)  4000 times less  fluid film lubrification - reduces the coefficient of clutch.
  • 12. Evaluation  I GENERATION: 1974-1988 Grain size – 4.5 micrometers burst strength of 46 KN Impurities high rate of #
  • 13. II GENERATION: 1990-1993 Grain size – 3.2 micro burst strength – 58  III GENERATION: From 1994 grain size – 1.8 micro burst strength – 65 KN Improved mech, HIP, Laser etching.
  • 14. ALUMINA Old A. ceramic materials the crystals of aluminum oxides were large, not assembled closely; there were many impurities and voids between them [5%]. impurities - weak points for propagation of fracture cracks. The coarse structure and impurities were the cause of the frequent fractures
  • 15. Modern alumina [0.5% impurity]: HIPing process extrudes impurities out off the material and packs the crystals very close together. very tough structure, tougher than the metallic stem on which it is seated, and even more tough then the natural thighbone. disadvantage of the modern alumina ceramic is lower toughness
  • 16.
  • 17. high alumina ceramics : materials that have the minimal content of 97% of alumina. high purity alumina ceramics: percentage of minimal alumina is of 99%.  HPA: commonly used for arthroplasty. Biolax forte.
  • 18. Zirconia Toughened Alumina (ZTA) ceramic Mixed-oxide ceramics. 75% of alumina and the rest are zirconium, Yttrium and chrome oxides. superior strength and resistance to wear. Biolax delta bending strength around 1000 MPa, more than the double of the alumina standard (400 MPa). Burst strength - 100 KN
  • 19. Zirconia ceramic one of the stronger ceramics  introduced to reduce the risk of fracture. Pure zirconia is an unstable material showing three different crystalline phases Stabilisation of zirconia by adding oxides to maintain the tetragonal phase Smaller Femoral heads [22 mm]
  • 20. More smoother finish Zirconia femoral heads should articulate only against polyethylene sockets It ages in the body’s temperature and the surface of the zirconia ball roughens
  • 21. Advantages as bearing material Smoother surface & less co-efficient of friction & wear. Superior lubrication property. Harder & less susceptible to third body wear Inert with no ion release. best used in young and active patients who have a high risk of loosening and osteolysis in the mid to long term.
  • 22. Oxinium materials Zirconium is a strong and biocompatible metal similar to titanium Thin layer of zirconium oxide is coated on the surface of the solid zirconium metal femoral head made out of Oxinium that articulates with a polyethylene cup
  • 23. combines the benefits of metals and ceramics. It offers superior wear resistance on its surface zirconium metal itself, with characteristics close to titanium, is a material without the risk of brittle fracture. oxidized zirconium is black
  • 24. Ceramics for total knees The total knee joints doesn’t have congruent joint surfaces. Thus, in a total knee joint with both joint surfaces made from ceramic materials, there would appear large localized stresses that would destroy components made from the contemporary ceramics difficult to fabricate such a large yet thin ceramic component as is the form of the femoral component
  • 25. Oxinium total knee prosthesis
  • 26. Bioactive ceramics Osteoconductive property acting as a scaffold to enhance bone formation on their surface used either as a coating on various substrates or to fill bone defects. Calcium phosphate ceramics. hydroxyapatite (HA) and tricalcium phosphate (TCP). In solid form, neither of these materials exhibits adequate fatigue resistance for use as a load-bearing implant
  • 27. Hydroxyapatite (Ca10(PO4)6(OH)2) Synthetic apatite Most similar material from structural & chemical point of view to the mineral component of bone. bone-graft substitute, HA coating to prosthesis. bonding mechanism - attachment at the surface of the HA of osteogenically-competent cells which differentiate into osteoblasts
  • 28. A cellular bone matrix is then formed at the surface of the HA. An amorphous area is present between the surface and the bone tissue containing thin apatite crystals. As maturation occurs, this bonding zone shrinks HA becomes attached to bone through a thin epitaxial layer, resulting in a strong interface with no layer of fibrous tissue interposed between the bone and HA.
  • 29. Such integration rarely, if ever, occurs with porous or smooth metal implants hot plasma spray technique. optimal thickness of the coating- 50 microns Thinner coatings may not supply sufficient Ca and P long enough to be effective, Thicker layers can experience sufficient stress under implant cyclic bending and shear and tensile loads to be subject to fatigue failure
  • 30. Tricalcium phosphate (Ca3(PO4)2) exists in either alpha or beta crystalline forms. The beta form is the most stable. The rate of biodegradation is higher when compared with HA. Degradation occurs by combined dissolution and osteoclastic resorption. to stimulate early bone in-growth into porous surfaces.
  • 31. Bone graft substitutes Porous coraline ceramics Chiroff et al, first recognised that, corals made from marine invertebrates have a structure similar to both cortical & cancellous bone. Exoskeleton of genus porite [ICF- 190mm], structure similar to cortical bone. Genus gonipora – similar to cancellous bone
  • 32. Hydrothermal exchange process converts delicate coral carbonate in to hydroxyapatite without altering the internal structure. Invaded & converted to mature lamellar B. Only surface resorption & no remodeling. Reconstruct metaphyseal defects.
  • 33. Bioactive glasses. Bioglass 45S5 bonding mechanism to bone - series of surface reactions ultimately leading to the formation of a hydroxycarbonate apatite layer at the glass surface. Greater production of bone, compared with HA. poor mechanical properties
  • 34. wollastonite (CaOSiO2) glass ceramic developed by Kokubo et al osteoconductive properties similar to Bioglass 45S5 increased mechanical strength. It has been used as a spacer at the iliac crest, for vertebral prostheses and as a shelf in procedures about the shoulder
  • 35. Bioactive bone cement Explored in order to avoid complications related to PMMA debris and to enhance fixation of the prosthesis. calcium-phosphate based bone cement and glass-ceramic bone cement.
  • 36. Calcium phosphate cements Biocompatible & resorbable cement Injectable cements Replaced by creeping substitution with host bone. As bone void fillers with uniform & predictable drug eluding property. Deliver the antibiotics. N-SRS, ETEX alpha - BSM
  • 37. Norian SRS N. skeletal repair system. Augmentation of fracture repair.[DHS, pedicle screw] Combination of monocalcium phosphate, tricalcium phosphate, calcium carbonate & a sodium phosphate solution in to inj. Paste Hardens with in minutes into dahllite [carbonated HA] in a nonexothermic reaction.
  • 38. ETEX alpha BSM Calcium orthophosphate cement Dicalciumphosphate dihydrate, octocalcium P & many precipitating apatites. Poorly crystalline apatite which will mimic bone, aiming superior resorption & osteointegration. Easy intraop handling characteristics..
  • 39. OSTEOSETMedical grade calcium sulphate High tech processing [retains all biological adv & consistent mech / resorption profile] Provide structural support & is bioabsorbable and biocompatible. Resorption profile matches with the rate at which host environment can lay down bone around the compound. Available as pellets Antibiotic delivery – aminoglycosides/ ideal.
  • 40. FUTURE Scaffold fabricated with a synthetic bioceramic which after being supplemented with moieties of biological activity is implanted in a living organism to induce tissue regeneration,