Bojar Witold, Ciach Tomasz, Kucharska Martyna, Maurin Jan, Gruber Beata M, Krzysztoń-Russjan Jolanta, Bubko Irena, Anuszewska Elżbieta L
Medical Devices, National Medicines Institute, Warszawa, Poland.
Biomedical Engineering Laboratory, Faculty of Chemical and Process Engineering, Warsaw University of Technology, Poland.
Adv Clin Exp Med. 2015 May-Jun;24(3):511-6. doi: 10.17219/acem/22599.
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.
在口腔外科和牙种植学中,异体生物材料可替代自体移植和异种移植。这些非免疫原性且可吸收的材料在许多情况下正成为完全且可预测的引导性骨再生的基础。它们中的绝大多数化学成分基于磷酸钙盐。其体内性能往往存在差异。
评估一种实验性骨替代材料的生物学和化学性质。
本研究聚焦于两种生物材料的细胞毒性比较和理化特性:一种新型壳聚糖/磷酸三钙/藻酸盐复合材料(CH/TCP/Ag)和一种市售的由60% HA和40% βTCP制成的合成骨移植材料(HA/TCP)。根据PN-EN ISO 10993《医疗器械生物学评价》对材料进行评估,即对小鼠成纤维细胞(L929)的细胞毒性,此外,还对人成骨细胞(hFOB1.19)和人骨肉瘤(MG-63)进行了测试。使用X射线粉末衍射法进行晶体化学分析。采用布鲁克-艾克斯D8 Advance衍射仪(德国卡尔斯鲁厄)收集衍射图。
测试材料在化学成分上表现出相似性,但在细胞毒性反应上有显著差异。
这种新型复合材料表现出高度的细胞相容性,在未来临床试验中具有前景。