Cytotoxicity Evaluation and Crystallochemical Analysis of a Novel and Commercially Available Bone Substitute Material
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 grea...
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Veröffentlicht in: | Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2015-05, Vol.24 (3), p.511-516 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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.
The objective was to evaluate the biological and chemical properties of an experimental bone substitute material.
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.
The tested materials showed a close resemblance in chemical composition and a considerable differentiation in cytotoxic response.
The novel composite demonstrated a high degree of cytocompatibility, which is promising in future clinical trials. |
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ISSN: | 1899-5276 |
DOI: | 10.17219/acem/22599 |