Improved osteogenesis in rat femur segmental defects treated with human allograft and zinc adjuvants

Exp Biol Med (Maywood). 2021 Aug;246(16):1857-1868. doi: 10.1177/15353702211019008. Epub 2021 May 26.

Abstract

Bone allograft is widely used to treat large bone defects or complex fractures. However, processing methods can significantly compromise allograft osteogenic activity. Adjuvants that can restore the osteogenic activity of processed allograft should improve clinical outcomes. In this study, zinc was tested as an adjuvant to increase the osteogenic activity of human allograft in a Rag2 null rat femoral defect model. Femoral defects were treated with human demineralized bone matrix (DBM) mixed with carboxy methyl cellulose containing ZnCl2 (0, 75, 150, 300 µg) or Zn stearate (347 µg). Rat femur defects treated with DBM-ZnCl2 (75 µg) and DBM-Zn stearate (347 µg) showed increased calcified tissue in the defect site compared to DBM alone. Radiograph scoring and µCT (microcomputed tomography) analysis showed an increased amount of bone formation at the defects treated with DBM-Zn stearate. Use of zinc as an adjuvant was also tested using human cancellous bone chips. The bone chips were soaked in ZnCl2 solutions before being added to defect sites. Zn adsorbed onto the chips in a time- and concentration-dependent manner. Rat femur defects treated with Zn-bound bone chips had more new bone in the defects based on µCT and histomorphometric analyses. The results indicate that zinc supplementation of human bone allograft improves allograft osteogenic activity in the rat femur defect model.

Keywords: Rag2; Zinc; allograft; bone regeneration; rat.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allografts / immunology*
  • Animals
  • Bone Matrix / transplantation
  • Bone Transplantation / methods
  • Cancellous Bone / cytology*
  • Cancellous Bone / immunology
  • Femur / metabolism
  • Humans
  • Osteogenesis / physiology*
  • Rats
  • Transplantation, Homologous / methods
  • Zinc / metabolism*

Substances

  • Zinc