Instituto de Cerámica y Vidrio, CSIC, C/Kelsen 5, 28049 Madrid, Spain.
Acta Biomater. 2010 Jun;6(6):2254-63. doi: 10.1016/j.actbio.2009.12.027. Epub 2009 Dec 21.
This study concerns the preparation and in vitro characterization of an apatite-wollastonite-2M bioactive glass ceramic which is intended to be used for the regeneration of hard tissue (i.e. in dental and craniomaxillofacial surgery). This bioglass ceramic has been obtained by appropriate thermal treatment through the devitrification (crystallization) of a glass with a stoichiometric eutectic composition within the Ca(3)(PO(4))(2)-CaSiO(3) binary system. Crack-free specimens of the bioglass ceramic were immersed in human bone marrow cell cultures for 3, 7, 14 and 21days, in order to study biocompatibility. Cell morphology, proliferation and colonization were assessed by scanning electron microscopy and confocal laser scanning microscopy. A total protein content assay was used to evaluate the viability and proliferation of cultured bone marrow cells. The results showed that the cells were able to adhere and proliferate on the designed material due to the essentiality of silicon and calcium as accessory factors for cell activity stimulation.
本研究涉及一种磷灰石-硅灰石-2M 生物活性玻璃陶瓷的制备和体外特性研究,该生物活性玻璃陶瓷拟用于硬组织(即牙科和颅面外科)的再生。该生物玻璃陶瓷是通过适当的热处理,通过在 Ca(3)(PO(4))(2)-CaSiO(3) 二元系统内具有化学计量共晶组成的玻璃进行析晶(结晶)而获得的。无裂纹的生物玻璃陶瓷标本在人骨髓细胞培养物中浸泡 3、7、14 和 21 天,以研究其生物相容性。通过扫描电子显微镜和共聚焦激光扫描显微镜评估细胞形态、增殖和定植。总蛋白含量测定用于评估培养骨髓细胞的活力和增殖。结果表明,由于硅和钙作为细胞活性刺激的辅助因子的必要性,细胞能够在设计的材料上附着和增殖。