Evaluation of implants coated with recombinant human bone morphogenetic protein-2 and vacuum-dried using the critical-size supraalveolar peri-implant defect model in dogs

J Periodontol. 2010 Dec;81(12):1839-49. doi: 10.1902/jop.2010.100220. Epub 2010 Jul 14.

Abstract

Background: Endosseous implants coated with recombinant human bone morphogenetic protein-2 (rhBMP-2) in a laboratory bench setting and air-dried induce relevant bone formation but also resident bone remodeling. Thus, the objective of this study is to evaluate the effect of implants fully or partially coated with rhBMP-2 and vacuum-dried using an industrial process on local bone formation and resident bone remodeling.

Methods: Twelve male adult Hound Labrador mongrel dogs were used. Critical-size, supraalveolar, peri-implant defects received titanium porous oxide surface implants coated in their most coronal aspect with rhBMP-2 (coronal-load, six animals), or by immersion of the entire implant in a rhBMP-2 solution (soak-load, six animals) for a total of 30 μg rhBMP-2 per implant. All implants were vacuum-dried. The animals were sacrificed at 8 weeks for histometric evaluation.

Results: Clinical healing was unremarkable. Bone formation was not significantly affected by the rhBMP-2 application protocol. New bone height and area averaged (± SE) 3.2 ± 0.5 versus 3.6 ± 0.3 mm, and 2.3 ± 0.5 versus 2.6 ± 0.8 mm(2) for coronal-load and soak-load implants, respectively (P >0.05). The corresponding bone density and bone-implant contact registrations averaged 46.7% ± 5.8% versus 31.6% ± 4.4%, and 28% ± 5.6% versus 36.9% ± 3.4% (P >0.05). In contrast, resident bone remodeling was significantly influenced by the rhBMP-2 application protocol. Peri-implant bone density averaged 72.2% ± 2.1% for coronal-load versus 60.6% ± 4.7% for soak-load implants (P <0.05); the corresponding bone-implant contact averaged 70.7% ± 6.1% versus 47.2% ± 6.0% (P <0.05).

Conclusions: Local application of rhBMP-2 and vacuum-drying using industrial process seems to be a viable technology to manufacture implants that support local bone formation and osseointegration. Coronal-load implants obviate resident bone remodeling without compromising local bone formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alveolar Bone Loss / surgery*
  • Alveolar Process / diagnostic imaging
  • Alveolar Process / pathology
  • Animals
  • Bone Density / drug effects
  • Bone Morphogenetic Protein 2
  • Bone Morphogenetic Proteins / therapeutic use*
  • Bone Remodeling / drug effects*
  • Coated Materials, Biocompatible / chemistry
  • Coated Materials, Biocompatible / therapeutic use*
  • Dental Implantation, Endosseous
  • Dental Implants*
  • Dental Prosthesis Design
  • Desiccation
  • Dogs
  • Humans
  • Immersion
  • Male
  • Mandible / diagnostic imaging
  • Mandible / pathology
  • Mandibular Diseases / surgery
  • Osseointegration / drug effects
  • Osteogenesis / drug effects*
  • Radiography
  • Recombinant Proteins / therapeutic use*
  • Surface Properties
  • Titanium / chemistry
  • Tooth Socket / surgery
  • Transforming Growth Factor beta / therapeutic use*
  • Vacuum

Substances

  • Bone Morphogenetic Protein 2
  • Bone Morphogenetic Proteins
  • Coated Materials, Biocompatible
  • Dental Implants
  • Recombinant Proteins
  • Transforming Growth Factor beta
  • recombinant human bone morphogenetic protein-2
  • titanium dioxide
  • Titanium