Biomimetic calcium phosphate coatings as bone morphogenetic protein delivery systems in spinal fusion

Spine J. 2011 Jun;11(6):560-7. doi: 10.1016/j.spinee.2009.12.006. Epub 2010 Jan 25.

Abstract

Background context: Use of recombinant human bone morphogenetic protein-2 (rhBMP-2) has been shown to enhance spinal fusion rates. Case reports of soft-tissue swelling, ectopic bone formation, and osteolysis have recently surfaced. It is hypothesized that incorporation of rhBMP-2 within a calcium phosphate (CaP) coating may help to localize delivery and mitigate these complications.

Purpose: To compare the characteristics of posterolateral fusion between rabbits receiving rhBMP-2 delivered via physical adsorption to a collagen sponge or rhBMP-2 incorporated within the physical structure of a CaP coating on a collagen sponge.

Study design/setting: New Zealand white rabbit model of posterolateral lumbar fusion at L5-L6.

Methods: Eighteen (18) New Zealand white rabbits underwent posterolateral spinal fusion at L5-L6. Rabbits received bilateral collagen sponges that were either coated with CaP (n=3), coated with CaP and dipped in rhBMP-2 (n=3), coated with a hybrid CaP-rhBMP-2 film (n=6), or coated with a hybrid CaP-rhBMP-2 film and dipped in rhBMP-2 (n=6). Animals were followed weekly with radiographs and were sacrificed at 6 weeks. Fusion masses were further characterized by manual palpation, computed tomography, and histology.

Results: Radiographic evaluation showed that animals in Group 3 (incorporated BMP) fused at 4 weeks, whereas animals in Group 2 (adsorbed BMP) and Group 4 (incorporated and adsorbed BMP) fused by 6 weeks. Animals that received rhBMP-2 physically adsorbed to the collagen sponge showed extension of the fusion mass beyond the L5-L6 level in 56% of cases and bone resorption in 78%. Histology of fusion masses showed mature bone formation in animals belonging to Groups 2, 3, and 4 and extensive osteoclast recruitment in animals belonging to Groups 2 and 4.

Conclusions: Delivery of rhBMP-2 via incorporation within CaP coatings results in increased rates of radiographic fusion. The burst release profile of rhBMP-2 adsorbed to surfaces, although effective in achieving fusion, may result in increased osteoclast recruitment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomimetic Materials / therapeutic use*
  • Bone Morphogenetic Protein 2 / administration & dosage*
  • Calcium Phosphates / administration & dosage*
  • Coated Materials, Biocompatible / therapeutic use*
  • Drug Delivery Systems / methods
  • Humans
  • Rabbits
  • Recombinant Proteins / administration & dosage
  • Spinal Fusion / methods*
  • Surgical Sponges*
  • Transforming Growth Factor beta / administration & dosage*

Substances

  • Bone Morphogenetic Protein 2
  • Calcium Phosphates
  • Coated Materials, Biocompatible
  • Recombinant Proteins
  • Transforming Growth Factor beta
  • recombinant human bone morphogenetic protein-2
  • calcium phosphate