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Non-invasive measurement of cell viability in 3-dimensional cell culture construct

机译:3维细胞培养构建物中细胞活力的无创测量

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In this work, a non-invasive measurement technique for the quantitative determination of cell viability in a three-dimensional (3D) cell culture construct is proposed. This technique is based on on-site electrical impedance measurement. A microfluidic chip with a 3D culture chamber is fabricated to demonstrate this technique. In vitro 3D cell culture has been interpreted for faithfully representation of the in vivo cellular responses in 3D cell culture construct is normally time-consuming and labor-intensive. In this study, the microfluidic chip consists of a culture chamber, in which a pair of vertical electrodes at its opposite sidewalls was embedded, and a fluidic channel for drug perfusion. Cancer cells encapsulated in agarose gel were loaded into the culture chamber to perform 3D cell culture under the perfusion of culture medium and anti-cancer drug in different concentrations (6, 12, 18, and 24 µg/ml) for 2 days. Since higher drug concentration led to more cell damage or death, the total impedance magnitude of the culture construct was shown to be reasonably proportional to the anti-cancer drug concentration. Moreover, cell proliferation can be also monitored using this technique. The proposed measurement method can determine cell viability without affecting the cellular behaviors during culture. It has a high potential to develop a fast and easy measurement compared with the conventional cellular analysis techniques.
机译:在这项工作中,提出了一种用于定量确定三维(3D)细胞培养构建物中细胞活力的非侵入性测量技术。该技术基于现场电阻抗测量。带有3D培养室的微流控芯片被制造出来以证明该技术。体外3D细胞培养已被解释为能忠实地代表3D细胞培养构建物中的体内细胞反应,通常耗时且费力。在这项研究中,微流控芯片由一个培养室和一个用于药物灌注的流体通道组成,该培养室在其相对侧壁上嵌入了一对垂直电极。将封装在琼脂糖凝胶中的癌细胞装入培养室,以在不同浓度(6、12、18和24 µg / ml)的培养基和抗癌药灌注下进行3D细胞培养。由于较高的药物浓度导致更多的细胞损伤或死亡,因此显示培养物构建体的总阻抗幅度与抗癌药物浓度成正比。此外,还可以使用该技术监测细胞增殖。所提出的测量方法可以确定细胞活力而不影响培养过程中的细胞行为。与传统的细胞分析技术相比,它具有开发快速简便的测量的巨大潜力。

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