Schmidt Valentin, Polgár Beáta, Nemes Vanda Ágnes, Dergez Tímea, Janovák László, Maróti Péter, Rendeki Szilárd, Turzó Kinga, Patczai Balázs
Department of Traumatology and Hand Surgery, Faculty of Medicine, University of Pécs, Ifjúság Str. 13, H-7624 Pécs, Hungary.
Department of Medical Microbiology and Immunology, Faculty of Medicine, University of Pécs, Szigeti Str. 12, H-7624 Pécs, Hungary.
J Funct Biomater. 2025 Jul 29;16(8):275. doi: 10.3390/jfb16080275.
Bioactive glass materials have been used for decades in orthopedic surgery, traumatology, and oral and maxillofacial surgery to repair bone defects. This study aimed to evaluate in vitro the survival and proliferation of MG63 human osteosarcoma-derived cells on S53P4 bioactive glass (BonAlive granules). Microscopic visualization was performed to directly observe the interactions between the cells and the material. Osteoblast-like cells were examined on non-adherent test plates, on tissue culture (TC)-treated plates and on the surface of the bioglass to assess the differences. Cell survival and proliferation were monitored using a CCK-8 optical density assay. Comparing the mean OD of MG63 cells in MEM on TC-treated plates with cells on BG, we detected a significant difference ( < 0.05), over each time of observation. The sustained cell proliferation confirmed the non-cytotoxic property of the bioglass, as the cell number increased continuously at 48, 72, 96, and 168 h and even did not plateau after 168 h. Since the properties of bioglasses can vary significantly depending on their composition and environment, a thorough characterization of their biocompatibility is crucial to ensure their effective and appropriate application-for example, during hip and knee prosthesis insertion.
生物活性玻璃材料已在骨科手术、创伤学以及口腔颌面外科中用于修复骨缺损数十年。本研究旨在体外评估MG63人骨肉瘤来源细胞在S53P4生物活性玻璃(BonAlive颗粒)上的存活和增殖情况。进行显微镜观察以直接观察细胞与材料之间的相互作用。在非粘附测试板、组织培养(TC)处理的板以及生物玻璃表面上检查成骨样细胞,以评估差异。使用CCK-8光密度测定法监测细胞存活和增殖情况。比较TC处理板上MEM中MG63细胞的平均OD与生物玻璃上细胞的平均OD,我们在每次观察时均检测到显著差异(<0.05)。持续的细胞增殖证实了生物玻璃的无细胞毒性特性,因为细胞数量在48、72、96和168小时持续增加,甚至在168小时后仍未达到平台期。由于生物玻璃的特性会因其组成和环境的不同而有显著差异,因此对其生物相容性进行全面表征对于确保其有效和适当的应用至关重要——例如,在髋关节和膝关节假体植入过程中。