Cytotoxicity Evaluation and Crystallochemical Analysis of a Novel and Commercially Available Bone Substitute Material

Adv Clin Exp Med. 2015 May-Jun;24(3):511-6. doi: 10.17219/acem/22599.

Abstract

Background: Alloplastic biomaterials are an alternative for autologous transplants and xenografts in oral surgery and dental implantology. These non-immunogenic and resorbable materials are becoming the basis for complete and predictable guided bone regeneration in many cases. The chemical composition of a great majority of them is based on calcium phosphate salts. In vivo performance is often variable.

Objectives: The objective was to evaluate the biological and chemical properties of an experimental bone substitute material.

Material and methods: The present research focuses on the cytotoxicity comparison and physiochemical characterization of two biomaterials: a novel chitosan/tricalcium phosphate/alginate composite (CH/TCP/Ag) and a commercially available synthetic bone graft made of HA (60%) and βTCP (40%) (HA/TCP). The materials were evaluated according to PN-EN ISO 10993 Biological evaluation of medical devices i.e. cytotoxicity on mouse fibroblasts (L929) and, in addition, tests on human osteoblasts (hFOB1.19) and human osteosarcoma (MG-63) were conducted. The crystallochemical analysis was performed using the X-ray powder diffraction method. The Bruker-AXS D8 Advance diffractometer (Karlsruhe, Germany) was used to collect diffractograms.

Results: The tested materials showed a close resemblance in chemical composition and a considerable differentiation in cytotoxic response.

Conclusions: The novel composite demonstrated a high degree of cytocompatibility, which is promising in future clinical trials.

MeSH terms

  • Animals
  • Bone Neoplasms / pathology*
  • Bone Substitutes / chemistry
  • Bone Substitutes / toxicity*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Crystallization
  • Crystallography, X-Ray
  • Fibroblasts / drug effects*
  • Fibroblasts / pathology
  • Humans
  • Mice
  • Osteoblasts / drug effects*
  • Osteoblasts / pathology
  • Osteosarcoma / pathology*
  • Powder Diffraction
  • Risk Assessment
  • Time Factors

Substances

  • Bone Substitutes