Bone formation of middle ear cavity using biphasic calcium phosphate lyophilized with Escherichia coli-derived recombinant human bone morphogenetic protein 2 using animal model

Int J Pediatr Otorhinolaryngol. 2013 Sep;77(9):1430-3. doi: 10.1016/j.ijporl.2013.05.035. Epub 2013 Jul 3.

Abstract

Objective: The aim of the study was to analyze the value of Escherichia coli-derived recombinant human bone morphogenetic protein-2 (ErhBMP-2) coated biphasic calcium phosphate (BCP) for the obliteration of middle ear bone defect after mastoid surgery.

Methods: Twenty-four specific pathogen-free Sprague-Dawley rats were randomly assigned to the BCP group (n=12) and BCP-ErhBMP-2 group (n=12; in which BCP scaffold of the granular type was coated with ErhBMP-2). In both groups, BCP scaffold was used to surgically fill the middle ear bulla. New bone formation was evaluated by measuring bone density (%) after 4 and 8 weeks in all rats in both groups.

Results: At 4 weeks, new bone was visible at the periphery and center of the middle ear cavity in both groups. In the BCP group, a moderate amount of fibrous tissue had infiltrated into the interspace of the scaffolds. New bone almost totally filled the interspace in the BCP-ErhBMP-2 group. At 8 weeks, copious new bone formation had occurred. Histometric measurements showed that bone density in the BCP group was smaller than in the BCP-ErhBMP-2 group at 4 weeks (25.10% and 38.43%, respectively; p<0.05) and 8 weeks (25.54% and 34.18%, respectively; p<0.05).

Conclusions: New bone formation was greater in the presence of BCP-ErhBMP-2 scaffolds. ErhBMP-2 coated BCP scaffolds is a potentially useful material for middle ear obliteration after mastoidectomy.

Keywords: Bone morphogenetic protein; Mastoid obliteration; Otitis media; Scaffold.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Morphogenetic Protein 2 / pharmacology*
  • Bone Regeneration / drug effects
  • Bone Substitutes / pharmacology*
  • Disease Models, Animal
  • Ear, Middle / surgery
  • Escherichia coli
  • Humans
  • Hydroxyapatites / pharmacology*
  • Male
  • Mastoid / surgery
  • Osteogenesis / drug effects*
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / pharmacology
  • Sensitivity and Specificity
  • Tissue Scaffolds
  • Transforming Growth Factor beta / pharmacology*

Substances

  • Bone Morphogenetic Protein 2
  • Bone Substitutes
  • Hydroxyapatites
  • Recombinant Proteins
  • Transforming Growth Factor beta
  • hydroxyapatite-beta tricalcium phosphate
  • recombinant human bone morphogenetic protein-2