Vertical alveolar ridge augmentation with beta-tricalcium phosphate and autologous osteoblasts in canine mandible

Biomaterials. 2009 May;30(13):2489-98. doi: 10.1016/j.biomaterials.2008.12.067. Epub 2009 Jan 14.

Abstract

A tissue-engineered bone has become a viable alternative to autologous bone for bone augmentation in atrophy alveolar ridge. The aim of the present study was to evaluate porous beta-tricalcium phosphate (beta-TCP) combined with autologous osteoblasts to augment edentulous alveolar ridge in a canine model. Autologous osteoblasts were expanded and combined with beta-TCP scaffold to fabricate a tissue-engineered bone. 12 bilateral alveolar ridge augmentation surgeries were carried out in 6 beagle dogs with the following 3 groups: beta-TCP/osteoblasts, beta-TCP alone and autogenous iliac bone control (n=4 per group). Sequential fluorescent labeling and radiographs were used to compare new bone formation and mineralization in each group. 24 weeks later, animals were sacrificed and non-decalcified and decalcified sections were evaluated histologically and histomorphometrically. Results indicated that the tissue-engineered bone dramatically enhanced new bone formation and mineralization, increase the new bone area, and maintain the height and thickness of the augmented alveolar ridge when compared with beta-TCP alone group. More importantly, the tissue-engineered bone achieved an elevated bone height and thickness comparable to that of autogenous iliac bone graft. This study demonstrated the potential of porous beta-TCP as a substrate for autogenous osteoblasts in bone tissue engineering for alveolar ridge augmentation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alveolar Ridge Augmentation*
  • Animals
  • Bone and Bones / cytology
  • Bone and Bones / metabolism
  • Calcium Phosphates* / metabolism
  • Cell Adhesion
  • Cells, Cultured
  • Dogs
  • Mandible / cytology*
  • Mandible / metabolism*
  • Mandible / surgery
  • Microscopy, Electron, Scanning
  • Osteoblasts / cytology*
  • Osteoblasts / metabolism*
  • Phenotype

Substances

  • Calcium Phosphates
  • beta-tricalcium phosphate