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Updated: Aug 7, 2026

Calvarial Model of Bone Augmentation in Rabbit for Assessment of Bone Growth and Neovascularization in Bone Substitution Materials
Published on: August 13, 2019
Comparing ectopic bone growth induced by rhBMP-2 on an absorbable collagen sponge in rat and rabbit models
H-P Hsu1, J M Zanella, S M Peckham
1Tissue Engineering, VA Boston Healthcare System, Boston Campus, Room D1-152, Mail Stop: 151 Research, 150 S. Huntington Ave., Boston, Massachusetts 02130, USA.
Recombinant human Bone Morphogenetic Protein-2 (rhBMP-2) delivered via absorbable collagen sponge (ACS) effectively induces bone growth. Fluid released from the rhBMP-2/ACS implant retains over 95% of the protein, with implants demonstrating significant bone formation in vivo.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Orthopedic Surgery
Background:
- Recombinant human Bone Morphogenetic Protein-2 (rhBMP-2) is a bone morphogen used as an autograft substitute for spinal fusion.
- It is typically incorporated onto an absorbable collagen sponge (ACS) carrier in the operating room.
- While rhBMP-2/ACS effectiveness is established, further understanding of its performance is needed.
Purpose of the Study:
- To determine if fluid released from rhBMP-2/ACS implants can induce bone growth at ectopic sites.
- To quantify protein retention in ACS under simulated intraoperative conditions.
- To compare in vivo bone formation by rhBMP-2 solution versus rhBMP-2/ACS implants.
Main Methods:
- In vitro assessment of rhBMP-2 protein retention in ACS after varying soak times and compression.
- In vivo ectopic implantation of rhBMP-2/ACS constructs and rhBMP-2 solution in rat and rabbit models.
- Histological evaluation of ossicle formation at 4 and 12 weeks post-implantation.
Main Results:
- Over 95% of rhBMP-2 protein was retained by ACS in simulated intraoperative conditions (15-min soak, compression).
- rhBMP-2 solution alone did not induce bone formation in rats or rabbits.
- rhBMP-2/ACS implants induced significant ossicle formation in rats (22/24 sites), with no significant changes in size/shape over time. Rabbits showed a lower ossification rate.
Conclusions:
- The rhBMP-2/ACS carrier effectively retains the morphogen, preventing significant loss during handling.
- rhBMP-2 requires a carrier like ACS for effective in vivo bone induction at ectopic sites.
- rhBMP-2/ACS is a viable option for promoting bone formation, though species-dependent responses may occur.
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