Repair of rat calvarial defects using Si-doped hydroxyapatite scaffolds loaded with a bone morphogenetic protein-2-related peptide

J Orthop Res. 2016 Nov;34(11):1874-1882. doi: 10.1002/jor.23208. Epub 2016 Mar 14.

Abstract

Tissue engineering promises therapies ideal for treating conventional large bone injuries and defects. In the present study, we developed a novel Si-HA scaffold loaded with a synthetic BMP-2-related peptide, P28, and tested its ability to repair a critical-sized calvarial defect. We created a calvarial defect (5 mm in diameter) in the parietal bone of 32 rats and implanted one of the following biomaterials: No implant (control), Si-HA, P28/Si-HA, or rhBMP-2/Si-HA. As assessed by micro CT imaging and histological evaluations, the P28/Si-HA scaffold promoted bone recovery to a similar degree as the rhBMP-2/Si-HA scaffold. In addition, both P28/Si-HA and rhBMP-2/Si-HA promoted recovery better than Si-HA alone. The novel P28/Si-HA scaffold might represent a promising biomaterial for future bone tissue engineering applications. © 2016 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:1874-1882, 2016.

Keywords: BMP-2; bone regeneration; hydroxyapatite; silicon; synthetic peptide.

Publication types

  • Evaluation Study

MeSH terms

  • Animals
  • Bone Morphogenetic Protein 2 / administration & dosage
  • Bone Morphogenetic Protein 2 / pharmacokinetics*
  • Bone Regeneration / drug effects*
  • Durapatite
  • Male
  • Random Allocation
  • Rats, Sprague-Dawley
  • Silicon
  • Tissue Scaffolds*
  • X-Ray Microtomography

Substances

  • BMP2 protein, human
  • Bone Morphogenetic Protein 2
  • Durapatite
  • Silicon