无创介质电泳法评价细胞活性

Ryosuke Komai, K. Aritoshi, K. Taguchi
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引用次数: 0

摘要

生物技术的进步给我们的生活带来了各种各样的好处。使用光镊增加了细胞融合和培养的机会。虽然光镊是一种有用的技术,但激光照射会损伤细胞。因此,在我们的研究中,我们估计了Ar激光(514nm)和半导体激光(980nm)对细胞的损伤。在前期研究中,我们使用光镊在980nm激光和Ar激光下捕获细胞,并展示了聚合物微球和酵母细胞的操作数据。并根据操作数据计算了捕获功率和捕获效率。下一步,我们将重点研究利用双电泳(DEP)评价酵母细胞损伤的活性评价方法。利用光学镊子在980nm激光和Ar激光下捕获酵母细胞,观察细胞在不同照射时间下的运动情况。我们将初始值设置为电压1V,频率500kHz,并通过函数发生器(KENWOOD, FG-281)将这些参数设置应用到电极上。本实验证明了Ar激光光镊对酵母细胞有害,而980nm激光光镊对酵母细胞无害。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Cells Activity Using Non-invasive Dielectrophoresis Method
The advance of biotechnology has provided various benefits to our lives. There is an increase in the opportunity of cell fusion and cultivation for using optical tweezers. Although optical tweezers is useful technique, cells are damaged by laser irradiation. Therefore, in our study, we estimated the cells damage by Ar laser (514nm) and semiconductor laser at 980nm. As a preliminary stage to our study, we trapped cells using optical tweezers at 980nm laser and Ar laser and showed manipulation data of polymer microspheres and yeast cells. Furthermore we calculated trapping power and trapping efficiency from the results of manipulation data. In the next stage, we focused on activity evaluation method using Dielectrophoresis (DEP) as estimating yeast cells damage. We trapped yeast cells by optical tweezers at 980nm laser and Ar laser and observed the movement of cells while changing the time of irradiation. We set the initial value to voltage of 1V and frequency of 500kHz and applied such parameter settings to the electrode by function generator(KENWOOD, FG-281). This experiment proved that optical tweezers at Ar laser was harmful for yeast cells, while optical tweezers at 980nm laser was harmless for yeast cells.
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