Biomineralized hydroxyapatite nanoclay composite scaffolds with polycaprolactone for stem cell-based bone tissue engineering

J Biomed Mater Res A. 2015 Jun;103(6):2077-101. doi: 10.1002/jbm.a.35342. Epub 2014 Oct 21.

Abstract

Nanoclay modified with unnatural amino acid was used to design a nanoclay-hydroxyapatite (HAP) hybrid by mineralizing HAP in the nanoclay galleries mimicking biomineralization. This hybrid (in situ HAPclay) was used to fabricate polycaprolactone (PCL)/in situ HAPclay films and scaffolds for bone regeneration. Cell culture assays and imaging were used to study interactions between human mesenchymal stem cells (hMSCs) and PCL/in situ HAPclay composites (films and scaffolds). SEM imaging indicated MSC attachment, formation of mineralized extracellular (ECM) on PCL/in situ HAPclay films, and infiltration of MSCs to the interior of PCL/in situ HAPclay scaffolds. Mineralized ECM was formed by MSCs without use of osteogenic supplements. AFM imaging performed on this in vitro generated mineralized ECM on PCL/in situ HAPclay films revealed presence of components (collagen and mineral) of hierarchical organization reminiscent of natural bone. Cellular events observed during two-stage seeding experiments on PCL/in situ HAPclay films indicated similarities with events occurring during in vivo bone formation. PCL/in situ HAPclay films showed significantly increased (100-595% increase in elastic moduli) nanomechanical properties and PCL/in situ HAPclay scaffolds showed increased degradation. This work puts forth PCL/in situ HAPclay composites as viable biomaterials for bone tissue engineering.

Keywords: biomineralization; bone tissue engineering; hydroxyapatite composite; mesenchymal stem cell; nanoclay.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Aluminum Silicates / pharmacology
  • Bone and Bones / drug effects
  • Bone and Bones / physiology*
  • Calcification, Physiologic / drug effects*
  • Cell Differentiation / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Clay
  • Compressive Strength / drug effects
  • Durapatite / pharmacology*
  • Extracellular Matrix / drug effects
  • Extracellular Matrix / metabolism
  • Humans
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / ultrastructure
  • Nanoparticles / chemistry*
  • Nanoparticles / ultrastructure
  • Polyesters / pharmacology*
  • Porosity
  • Spectroscopy, Fourier Transform Infrared
  • Staining and Labeling
  • Tissue Engineering / methods*
  • Tissue Scaffolds / chemistry*

Substances

  • Aluminum Silicates
  • Polyesters
  • polycaprolactone
  • Durapatite
  • Alkaline Phosphatase
  • Clay