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The role of temperature of sintering of tricalcium phosphate ceramic on the adhesion rate of human monocyte and monocyte derived macrophages

机译:磷酸三钙陶瓷的烧结温度对人单核细胞和单核细胞衍生巨噬细胞黏附率的影响

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The objective of this study was to investigate the effect of temperature of sintering of tricalcium phosphate ceramic (TCP) on the adherence and viability of monocyte and monocyte derived macrophages. The monocytes were isolated from human peripheral blood, biotin labeled and seeded at a density of 5/spl times/10/sup 5/ cells/well according to standard laboratory procedures. Cells were considered macrophages after remaining in culture for 24 hours. Cells were then plated in each microtiter well preloaded with TCP of different sintering temperatures (400, 800 and 1150/spl deg/C). At the end of 1, 2, 3 and 7 days the viability and cell number of monocyte or monocyte derived macrophages were determined using an established assay (biotin-labeled-macrophages). Cell number was determined in control wells with known amounts of cell number, a standard curve was generated by plotting absorbance units versus cell number. At the end of each phase, the blocks were collected and prepared for SEM evaluation. The data from this experiment suggest that: (i) monocytes and macrophages are capable of surviving on all different types of blocks tested over a 7 day period, (ii) SEM evaluation of the ceramic blocks showed an increase in the size and number of micro and macropores with time in blocks sintered at 400 and 800/spl deg/C. In contrast, the size and number of pores calculated from representative views of TCP blocks sintered at 1150/spl deg/C were significantly lower than the other two groups. The mechanism of action of these cells toward the aforementioned bioceramic surfaces has to be investigated in a larger scale. Information obtained from this study provided new insights on the interrelationship between bioceramics, temperature of sintering effect, incubation time and the possible cell response during chronic inflammation at the site of implantation.
机译:这项研究的目的是调查烧结三磷酸钙陶瓷(TCP)的温度对单核细胞和单核细胞衍生的巨噬细胞的粘附和生存能力的影响。从人外周血中分离单核细胞,用生物素标记并按照标准实验室程序以5 / spl×10 / sup 5 /细胞/孔的密度接种。保留培养24小时后,将细胞视为巨噬细胞。然后将细胞铺在预先装有不同烧结温度(400、800和1150 / spl deg / C)的TCP的每个微量滴定孔中。在第1、2、3和7天结束时,使用已建立的测定法(生物素标记的巨噬细胞)确定单核细胞或单核细胞衍生的巨噬细胞的生存力和细胞数。用已知数量的细胞数在对照孔中确定细胞数,通过绘制吸光度单位对细胞数作图来产生标准曲线。在每个阶段结束时,收集块并准备进行SEM评估。来自该实验的数据表明:(i)单核细胞和巨噬细胞能够在7天的测试时间内在所有不同类型的块上存活,(ii)陶瓷块的SEM评价表明,微块的大小和数量增加了和大孔随时间的变化以400和800 / spl deg / C的速度烧结。相反,从以1150 / spl deg / C烧结的TCP块的代表性视图计算的孔的大小和数量显着低于其他两组。这些细胞对上述生物陶瓷表面的作用机理必须进行大规模研究。从这项研究中获得的信息为生物陶瓷之间的相互关系,烧结效果的温度,孵育时间以及植入部位的慢性炎症过程中可能的细胞反应提供了新的见解。

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