Enhanced osteogenicity of bioactive composites with biomimetic treatment

Biomed Res Int. 2014:2014:207676. doi: 10.1155/2014/207676. Epub 2014 Apr 9.

Abstract

Purpose: This study aimed to explore if initiation of biomimetic apatite nucleation can be used to enhance osteoblast response to biodegradable tissue regeneration composite membranes.

Materials and methods: Bioactive thermoplastic composites consisting of poly(ε-caprolactone/DL-lactide) and bioactive glass (BAG) were prepared at different stages of biomimetic calcium phosphate deposition by immersion in simulated body fluid (SBF). The modulation of the BAG dissolution and the osteogenic response of rat mesenchymal stem cells (MSCs) were analyzed.

Results: SBF treatment resulted in a gradual calcium phosphate deposition on the composites and decreased BAG reactivity in the subsequent cell cultures. Untreated composites and composites covered by thick calcium phosphate layer (14 days in SBF) expedited MSC mineralization in comparison to neat polymers without BAG, whereas other osteogenic markers--alkaline phosphatase activity, bone sialoprotein, and osteocalcin expression--were initially decreased. In contrast, surfaces with only small calcium phosphate aggregates (five days in SBF) had similar early response than neat polymers but still demonstrated enhanced mineralization.

Conclusion: A short biomimetic treatment enhances osteoblast response to bioactive composite membranes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Animals
  • Biocompatible Materials / pharmacology*
  • Biomimetic Materials / pharmacology*
  • Calcification, Physiologic / drug effects
  • Calcium / analysis
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Gene Expression Regulation / drug effects
  • Glass
  • Integrin-Binding Sialoprotein / genetics
  • Integrin-Binding Sialoprotein / metabolism
  • Male
  • Osteoblasts / cytology
  • Osteoblasts / drug effects
  • Osteoblasts / metabolism
  • Osteoblasts / ultrastructure
  • Osteocalcin / genetics
  • Osteocalcin / metabolism
  • Osteogenesis / drug effects*
  • Rats, Sprague-Dawley
  • Silicon Dioxide / analysis
  • Spectrometry, X-Ray Emission

Substances

  • Biocompatible Materials
  • Integrin-Binding Sialoprotein
  • Osteocalcin
  • Silicon Dioxide
  • Alkaline Phosphatase
  • Calcium