Osteoconduction in keratin-hydroxyapatite composite bone-graft substitutes

J Biomed Mater Res B Appl Biomater. 2017 Oct;105(7):2034-2044. doi: 10.1002/jbm.b.33735. Epub 2016 Jul 8.

Abstract

Reconstituted keratin-hydroxyapatite (K-HA) composites have shown potential as nonload-bearing bone graft substitute material. This in vivo study investigated the bone regeneration response of keratin plus 40% HA composite materials in comparison to collagen counterparts and an unfilled defect site. The implantation site was a noncritical size defect created in the long bones (tibia) of sheep, with observations made at 1, 2, 4, 6, 8, and 12 weeks postimplantation. Porous K-HA materials displayed an excellent biocompatibility similar to collagen counterparts; however, the rate of bone regeneration at K-HA implantation sites was markedly slower than that of the collagen or unfilled defect sites. While collagen materials were undetectable by 4 weeks implantation, K-HA composite remnants were present at 12 weeks. However, there is evidence that K-HA implants participated in the natural remodelling process of bone, with bone regeneration occurring via a creeping substitution mechanism. Observations imply that the rate of bone ingrowth into the K-HA defect site was matched with the rate of K-HA resorption. These results suggest that K-HA materials may offer significant benefits as nonload-bearing bone graft substitutes where it is desirable that the degradation of the scaffolding material be well matched with the rate of bone regeneration. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 2034-2044, 2017.

Keywords: bone graft substitute; creeping substitution; keratin; keratin-hydroxyapatite; osteoconduction.

MeSH terms

  • Animals
  • Bone Regeneration / drug effects*
  • Bone Substitutes / chemistry
  • Bone Substitutes / pharmacology*
  • Durapatite / chemistry
  • Durapatite / pharmacology*
  • Female
  • Keratins / chemistry
  • Keratins / pharmacology*
  • Sheep
  • Tibia* / injuries
  • Tibia* / metabolism
  • Tibia* / pathology

Substances

  • Bone Substitutes
  • Keratins
  • Durapatite