In vitro degradation and cell response of calcium carbonate composite ceramic in comparison with other synthetic bone substitute materials

Mater Sci Eng C Mater Biol Appl. 2015 May:50:257-65. doi: 10.1016/j.msec.2015.02.019. Epub 2015 Feb 16.

Abstract

The robust calcium carbonate composite ceramics (CC/PG) can be acquired by fast sintering calcium carbonate at a low temperature (650 °C) using a biocompatible, degradable phosphate-based glass (PG) as sintering agent. In the present study, the in vitro degradation and cell response of CC/PG were assessed and compared with 4 synthetic bone substitute materials, calcium carbonate ceramic (CC), PG, hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP) ceramics. The degradation rates in decreasing order were as follows: PG, CC, CC/PG, β-TCP, and HA. The proliferation of rat bone mesenchymal stem cells (rMSCs) cultured on the CC/PG was comparable with that on CC and PG, but inferior to HA and β-TCP. The alkaline phosphatase (ALP) activity of rMSCs on CC/PG was lower than PG, comparable with β-TCP, but higher than HA. The rMSCs on CC/PG and PG had enhanced gene expression in specific osteogenic markers, respectively. Compared to HA and β-TCP, the rMSCs on the CC/PG expressed relatively lower level of collagen I and runt-related transcription factor 2, but showed more considerable expression of osteopontin. Although CC, PG, HA, and β-TCP possessed impressive performances in some specific aspects, they faced extant intrinsic drawbacks in either degradation rate or mechanical strength. Based on considerable compressive strength, moderate degradation rate, good cell response, and being free of obvious shortcoming, the CC/PG is promising as another choice for bone substitute materials.

Keywords: Calcium carbonate; Calcium phosphate; Cell response; In vitro degradation; Phosphate-based glass.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / drug effects
  • Actin Cytoskeleton / metabolism
  • Alkaline Phosphatase / metabolism
  • Animals
  • Bone Substitutes / pharmacology*
  • Calcium Carbonate / pharmacology*
  • Calcium Phosphates / pharmacology
  • Cell Adhesion / drug effects
  • Cell Proliferation / drug effects
  • Cell Shape / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Ceramics / pharmacology*
  • Compressive Strength
  • Gene Expression Regulation / drug effects
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / enzymology
  • Rats
  • X-Ray Diffraction

Substances

  • Bone Substitutes
  • Calcium Phosphates
  • beta-tricalcium phosphate
  • Alkaline Phosphatase
  • Calcium Carbonate