Reconstruction of Segmental Bone Defect in Canine Tibia Model Utilizing Bi-Phasic Scaffold: Pilot Study

Author:

Haam Dae-Won1,Bae Chun-Sik2,Kim Jong-Min3,Hann Sung-Yun4ORCID,Yim Chang-Min Richard5,Moon Hong-Seok1ORCID,Oh Daniel S.6

Affiliation:

1. Department of Prosthodontics, College of Dentistry, Yonsei University, Seoul 03722, Republic of Korea

2. College of Veterinary Medicine, Chonnam National University, Gwangju 61186, Republic of Korea

3. College of Health and Medical Sciences, Cheongju University, Cheongju 28503, Republic of Korea

4. Department of Precision Mechanical Engineering, Kyungpook National University, Sangju 37224, Republic of Korea

5. School of Dental Medicine, Rutgers University, Newark, NJ 07102, USA

6. Department of Dental Biomaterials, College of Dentistry, Yonsei University, Seoul 03722, Republic of Korea

Abstract

The reunion and restoration of large segmental bone defects pose significant clinical challenges. Conventional strategies primarily involve the combination of bone scaffolds with seeded cells and/or growth factors to regulate osteogenesis and angiogenesis. However, these therapies face inherent issues related to immunogenicity, tumorigenesis, bioactivity, and off-the-shelf transplantation. The biogenic micro-environment created by implanted bone grafts plays a crucial role in initiating the bone regeneration cascade. To address this, a highly porous bi-phasic ceramic synthetic bone graft, composed of hydroxyapatite (HA) and alumina (Al), was developed. This graft was employed to repair critical segmental defects, involving the creation of a 2 cm segmental defect in a canine tibia. The assessment of bone regeneration within the synthetic bone graft post-healing was conducted using scintigraphy, micro-CT, histology, and dynamic histomorphometry. The technique yielded pore sizes in the range of 230–430 μm as primary pores, 40–70 μm as secondary inner microchannels, and 200–400 nm as tertiary submicron surface holes. These three components are designed to mimic trabecular bone networks and to provide body fluid adsorption, diffusion, a nutritional supply, communication around the cells, and cell anchorage. The overall porosity was measured at 82.61 ± 1.28%. Both micro-CT imaging and histological analysis provided substantial evidence of robust bone formation and the successful reunion of the critical defect. Furthermore, an histology revealed the presence of vascularization within the newly formed bone area, clearly demonstrating trabecular and cortical bone formation at the 8-week mark post-implantation.

Publisher

MDPI AG

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