4.8 Article

Bone healing by sterilizable calcium phosphate tetrapods eluting osteogenic molecules

Journal

BIOMATERIALS
Volume 34, Issue 22, Pages 5530-5537

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2013.03.089

Keywords

Bone regeneration; Bone healing; Osteogenesis; Calcium phosphate

Funding

  1. Japan Society for the Promotion of Science (JSPS)
  2. Center for NanoBio Integration (CNBI)
  3. Center for Medical System Innovation (CMSI)
  4. Japan Science and Technology Agency (JST)
  5. Core-to-Core Program, A. Advanced Research Networks
  6. Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST program)
  7. Nakatomi Health Foundation
  8. Grants-in-Aid for Scientific Research [23390459, 23390460, 25670851] Funding Source: KAKEN

Ask authors/readers for more resources

Although bone grafts and prosthetic implants have shown some clinical success in the treatment of bone defects, the graft availability, biocompatibility, function, and longevity still remain to be improved. One possible solution to these problems is to develop bone implants acting on host cells to induce rapid bone regeneration. Here, we demonstrate bone healing by means of a sterilizable and osteogenic molecule-eluting implant system in which two small molecules, a smoothened agonist (SAG) and a helioxanthin derivative (TH), are loaded onto tetrapod-shaped calcium phosphate granules (Tetrabone). We succeeded in directing progenitor cells toward mature osteoblasts with the combined application of the two small molecules acting on different stages of osteogenesis. Tetrabone released SAG and TH for prolonged periods when loaded with these molecules. EOG sterilization did not affect the osteogenic activity of the SAG- and TH-loaded Tetrabones. The combinatorial use of SAG- and TH-loaded Tetrabones achieved bone healing without cell transplantation in a rat femur bone defect model within two weeks. This system will allow us to vary the combination rate of implants loaded with different osteogenic factors depending on the types and sizes of defects, potentially allowing full temporal and spatial control of the bone regeneration. (C) 2013 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available