探究钛颗粒大小和浓度对人类成骨细胞成骨反应的影响--体外研究

S. Sheela, Waad Kheder, Rani Samsudin
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引用次数: 0

摘要

目的:本研究旨在探讨钛颗粒的大小和浓度与人成骨细胞(HOB)成骨反应之间的相关性。材料与方法:制备不同浓度的纳米和微米二氧化钛颗粒,并采用 XTT 法分析其对 HOB 的生物相容性。共聚焦激光扫描显微镜研究了肌动蛋白细胞骨架组织的变化。使用 ROS 分析法分析了 HOBs 暴露于二氧化钛颗粒后细胞内活性氧(ROS)的生成情况。此外,还分析了以碱性磷酸酶活性、骨蛋白激酶、巨噬细胞集落刺激因子水平和生物矿化为代表的成骨潜能:结果:二氧化钛纳米颗粒和微颗粒的短期相互作用不会对 HOBs 产生毒性。然而,与对照组相比,用 100 微克/毫升的纳米二氧化钛和微颗粒处理的细胞会产生更多的 ROS。此外,与二氧化钛微颗粒相比,用 100 微克/毫升二氧化钛纳米颗粒处理的细胞显示出更高的碱性磷酸酶活性、骨保护素、巨噬细胞集落刺激因子水平和生物矿化度。结论总之,该研究发现二氧化钛纳米颗粒比微颗粒更具生物相容性,从而深入了解了纳米结构支持成骨细胞分化的能力及其在生物医学应用中的可行性。
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Investigating the influence of titanium particle size and concentration on osteogenic response of human osteoblasts – in vitro study
Purpose: The purpose of this study was to investigate the correlation between the size and concentration of titanium particles and the osteogenic response of human osteoblasts (HOB).  Materials and Methods: Different concentrations of titanium dioxide nano- and micro-particles were prepared and their biocompatibility on HOBs was analyzed using XTT assay. The changes in the actin cytoskeletal organization were studied by confocal laser scanning microscopy. The generation of intracellular reactive oxygen species (ROS) by HOBs after exposure to titanium dioxide particles was analyzed using ROS assay. Besides, the osteogenic potential represented by alkaline phosphatase activity, osteoprotegerin, macrophage colony stimulating factor levels, and biomineralization were analyzed. Results: Short-term interaction of titanium dioxide nano- and micro-particles did not induce toxicity to HOBs. However, cells treated with 100 μg/mL titanium dioxide nano- and micro-particles demonstrated higher ROS generation compared to control. Besides, cells treated with 100 µg/mL titanium dioxide nanoparticles showed higher alkaline phosphatase activity, osteoprotegerin, macrophage colony stimulating factor levels and biomineralization compared to titanium dioxide microparticles.  Conclusion: Collectively, the study found titanium dioxide nanoparticles to be more biocompatible than microparticles providing an insight into the capability of nanostructures in supporting osteoblast differentiation and its plausibility in biomedical applications.
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