To determine if recombinant human bone morphogenetic protein-2 (rhBMP-2) can be adsorbed onto porous ceramic hydroxyapatite (HA) and promote the integration of HA to host bone, 54 subperiosteal pockets were created on the skulls of 19 adult Pasteurella-free white rabbits. Fourteen HA implants were s
Prostaglandin E1 and recombinant bone morphogenetic protein effect on strength of hydroxyapatite implants
β Scribed by Ono, Ichiro ;Tateshita, Tohru ;Kuboki, Yoshinori
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 780 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0021-9304
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β¦ Synopsis
Although combinations of hydroxyapatite (HAP) and bone morphogenetic protein (BMP) are expected to provide potent alternatives to autogenous bone grafts, it is still anticipated that substances that act synergistically with BMP will be found because the inducing potential of purified BMP in bone is not strong enough. We already have shown that prostaglandin (PG) E 1 has a strong and dosedependent synergistic effect on the osteoinductive activity induced by recombinant human (rh) BMP and that it enhances osteoconduction even when used alone. In this study, porous HAP rods were treated as follows: (1) without PGE 1 or rhBMP (control group); (2) with varying concentrations of PGE 1 ; and (3) with varying concentrations of PGE 1 combined with 1 g of rhBMP-2. The rods were subperiosteally implanted on the cranial bone of rabbits to evaluate the effect of these treatments on the mechanical strength of the implanted HAP rods. The HAP rods were removed 3, 6, or 9 weeks after implantation and subjected to mechanical strength determinations. The control group (no addition of BMP to the rods) showed no significant increase in threepoint bending strength or in compression strength compared to pre-implantation. On the other hand, PGE 1 combined with rhBMP had a strong and dose-dependent effect on the mechanical strength of HAP, increasing it significantly, especially compression strength. PGE 1 also increased mechanical strength even when used alone. Histological examination revealed that PGE 1 , whether or not it was combined with rhBMP, increased bone formation into the pores of HAP and consequently increased the mechanical strength of porous HAP.
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