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CERABONE |
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Cerabone®
is a hydroxylapatite ceramic made of purely anorganic material. It can
be supplied as a molding block in different sizes and as granules of
differing dimensions.
The osteoconductive
properties of Cerabone® make it suitable as a bone replacement material
for permanent filling in or reconstruction of congenital or acquired
bone defects and for increasing volume in spongiosaplasty.
Cerabone® has a range of advantages compared with other hydroxylapatite
ceramics:
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Spongiosa structure, with interconnecting macroporous and microporous
pore system, is largely identical to that of human bone.
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Low porosity fluctuation and highly uniform spongy structure make
for higher stability (pressure and shear resistance) and greater load-bearing
capacity than comparable ceramics. This is increased still further
once the bone has built through.
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Optimal pore width (100–1,500 µm). The literature gives a pore
width of at least 50 µm for problem-free integration of implant
and bone. With Cerabone®, complete bone building throughout and
integration is possible.
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Particularly high degree of purity of the hydroxylapatite structure.
For example, almost complete reduction of out of phase calcium oxide
content. This also improves the material’s mechanical stability considerably.
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Cerabone® molding blocks are available in larger sizes than other
hydroxylapatite ceramics (up to 20x20x40 mm). So even elongated bone
defects can be bridged or treated with one continuous molding block
instead of with two or more molding blocks placed next to each other.
Easy intraoperative working (molding) of the molding block. Cerabone®
can be adjusted optimally to the particular bone defect using common
surgical instruments (e. g. files, pincers).
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Cerabone® is reasonably priced.
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Cerabone® has excellent biocompatibility.
The
source material for the production of Cerabone® is bovine spongy
bone. However, there is no risk of immunological reactions or of transmission
of pathogens because as a result of high-temperature treatment during
the manufacture of Cerabone® there is no residual protein in the
finished product. The chemical composition of Cerabone® is to a
very great extent identical with that of the mineral stage of human
bone.
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Forms
supplied and pack sizes |
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Cerabone® L80
Molding block 20x20x40 mm, |
Cerabone®
Granules F
Granule size 0.5-1.6 mm
Packs of 3x2 ml |
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Cerabone®
L40
Molding block 20x20x20 mm, |
Cerabone® Granules M
Granule size 1.6-3.15 mm
Packs of 3x5 ml |
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Cerabone®
L20
Molding block 20x20x10 mm |
Cerabone® Granules G
Granule size 3.15-6.3 mm
Packs of 3x5 ml |
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tolerance of +2mm/-1mm in each case)
Each pack contains one sterile
molding block. |
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Areas of application
For
permanent filling or reconstruction of aseptic bone defects:
1 In accident surgery and orthopedics, e. g. for
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filling in bone defects in the case of depressed fractures close
to joints
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filling in bone defects in the acetabulum when changing prostheses
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filling
in resection defects in the case of benign bone tumors
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filling
in substance defects in the case of cartilage or bone transplants
- filling
in bone defects after autologous spongiosa removal
2 In orthodontic and facial surgery, e. g. for
- filling
in resection defects in the case of benign bone tumors or cysts
- filling
in bone defects after radiculectomy
- filling
in alveolar defects after tooth extraction
- filling
in defects after jaw osteotomy
3 For plastic reconstruction, e. g.
- improving
contours in the facial skeleton
To increase
volume in the case of autogenous spongiosa transplants in a wide range
of surgical specialisms.
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