Transcript Document

BIOCERAMICS
- Alumina
- Zirconia
- Carbon
- Hydroxyapatite
- glasses (vetroceramics, bioglasses)
PROPERTIES
- INERT: No reaction; fibrotic tissues may
form
- BIOACTIVE: Bond between implant and
tissue
- BIOREABSORBABLE: Dissolution and
substitution with healthy tissue
- Alumina
- Zirconia
- Carbon
- Hydroxyapatite
- glasses (vetroceramics, bioglasses)
Dense, high purity (>99,5%) alumina is
used for femur heads, joints components
and dental implants because of:
¨
excellent resistance to corrosion
¨
good biocompatibility
¨
high resistance to wear
¨
high resistance to fracture
For biomedical applications alumina is sintered at
1600-1800°C.
Additives: used to inhibit the growth of grain (highest
density)
• MgO <0,5%
• SiO2 and alkaline oxides <0,1%
• CaO <0,1%
Mechanical properties depend sizably on grain
dimensions (density), i.e. on percentage of additives
Grain dimension above 7 micron may cause a decrease
mechanical features by 20%.
Reasonable compromise: grain < 4 micron and purity >
99,7%
Advantages in joint replacement
Due to the high surface energy (as measured
through contact angle), it is easy to prepare very
smooth surfaces.
With flat surfaces, roughness is concave (not
protruding), only of the order of 0,01 micron.
Revolving surfaces with high congruency
(uncertainty in curvature radius between 0,1
and 1 micron).
Fragment formation in couplings Al2O3 /Al2O3 is
much less than with other couplings
The friction coefficient in joints Al2O3 /Al2O3
decreases with time approaching that of the
natural joint
Because of adsorption of biological molecules,
a layer liquid-like is formed which brings
about lubrication of components, by avoiding
the direct contact of the two surfaces.
However, friction and wear of the two surfaces
may lead to mobilization of the acetabular
component
- Alumina
- Zirconia
- Carbon
- Hydroxyapatite
- glasses (vetroceramics, bioglasses)
Al2O3 has high biocompatibility and
marked resistance to wear (excellent
tribological
properties),
but
poor
tenacity and bending strength, so that
femur heads larger than 32 mm are not
fabricated.
ZrO2 has higher tensile strength and
bending strength, together with a lower
Young modulus
Two materials actually used: tetragonal zirconia partially
stabilized with yttria (TZP) and the same partially
stabilized with MgO (Mg – PSZ).
Zirconia has as natural contaminants Fe2O3,
SiO2, TiO2 and sometimes ThO2 and uranium
compounds: to be removed, in particular the
radioactive ones (though present in 0,5 ppm).
γ and α radioactivity present. γ activity is about
the natural threshold, α is higher.
α rays are dangerous (high ionizing power, and
are said to destroy cells both of hard and soft
tissues adjacent to implants.
A problem with long-term implants.
Alumina and zirconia: a comparison
Both exceptionally biocompatible, because of their
stability in physiological media (higher in alumina).
Zirconia has the drawback of radioactivity (under
control)
Zirconia has better mechanical properties but worse
tribological properties.
Both ceramics are OK for implants suffering mostly
compression loads.
These ceramics are never used for implants with direct
interface with the bone, but for mobile parts of joints, the
surface of which is in contact with a mobile prosthetic
component.
Young modulus (much lower in zirconia) is in
both cases much higher than that of the bone:
trabecular bone: 0,05-0,5 GPa
7-25
“
ZrO2:
150-208
“
Al2O3 :
 400
“
Compact bone:
A marked difference in implants between the
bone and the material is not acceptable
(distribution of loads)
- Alumina
- Zirconia
- Carbon
- Hydroxyapatite
- glasses (vetroceramics, bioglasses)
Carbon may exist in several forms, some of
which show:
• good chemical inertness
• excellent biocompatibility
• practically
no
(HEMOCOMPATIBILITY)
thrombogenicity
 carbon
is the material of choice in all
implantable devices in contact with blood
Most applications as coatings of different nature
Three forms of carbon:
• amorphous
• pyrolytic
• vapor deposited
All forms are characterized by a disordered
structure (general terminology: “turbostratic
carbon”)
Allotropic forms of Carbon
Diamond
Three-dimensional continuous covalent network of
tetrahedrally linked atoms in sp3 hybridization
Graphite
Atoms in sp2 hybridization regularly arranged in
planes, made of hexagons
Stacking sequence is ABABAB (i.e. considering 3
planes, adjacent two are offset, while the first and third
coincide
Planes held together by weak van der Waals forces:
easy sliding of adjacent planes  excellent solid
lubricant
Turbostratic Carbon (TC)
Microstructure without long range order,
though not very different from the ordered
graphitic form.
Disorder introduced into the stacking sequence
of graphite by casual rotations or slips of the
layers.
TC has a high degree of isotropy at the
macroscopic level and low degree of order
The distance between hexagonal layers is
much shorter than in graphite.
Atom vacancies in the layers causes point
defects, where a covalent bond between
adjacent layers can establish.
Mechanical properties are closer to those of
diamond than to those of graphite
Crystalline graphite: average diameter of
crystals or the order of 100 nm
TC: very small crystallites, not larger than 10
nm.
Graphite
Turbostratic
Carbon
Amorphous Carbon (AC)
Prepared through the thermal degradation of
organic polymers (e.g. phenol-formaldehyde).
The object to be made is formed through the
techniques of plastics technology
Gas evolution during thermal treatment:
• control of the heating rate, to allow the evolved
gases to permeate through the bulk of the
polymer
• limitation to the size of objects fabricated
(few mm)
AC (hardness Mohs 7, density 1,47) is made of
disordered crystallites not larger than 5
micron.
Non
porous
(despite
the
preparation
procedure and the low density), and with
permeability to gases of 13 orders of
magnitude lower than graphite
 Non interconnected porosity
Pyrolytic Carbon (PC)
Prepared by thermal decomposition
vacuum of gaseous hydrocarbons.
in
Originally produced for nuclear reactors (high
temperatures) for its stability
Later, its high antithrombogenic power was
noted, as well as its biocompatibility with
bloood and soft tissues
These features, together with excellent
resistance to wear, cyclic fatigue and
degradation, has made it the material of
election for mechanical heart valves
Cardiac valves: PC as coating
Coating with PC of objects
• Vertical
fluidized-bed reactor, containing the
objects and zirconia particles (catalyst for
cracking and pyrolysis)
• a gas mixture of propane (C source) and
methyl-chlorosilane (source of Si), transport
gas (He)
• elevated temperatures (1000-1500°C)
Reactions
occurring
Scheme of
the
fluidizedbed reactor
Solid Products: Carbon and Silicon carbide,
which coat any object present
Silicon content is at least 10%. Being
immiscible with C, Si is present as sub-micron
SiC particles, dispersed in the carbon matrix
SiC increases resistance to fracture, to wear,
hardness and elastic modulus
Vapor deposited Carbon
Complex forms and flexible materials may be obtained
by coating of metal or polymeric substrates by a thin
layer deposited via vapor (at the most 0,1-1,0 micron
thickness, but higher density than in other cases).
This coating (a version of classical CVD, Chemical
Vapor Deposition) is made under vacuum, by means
of a catalyst and a gaseous carbon precursor
Cooling of the substrate during deposition allows
coating of low-melting materials (e.g. Dacron, Teflon,
polyurethanes).
Critical the adhesion to substrate, in particular when
flexible