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Real-time, label-free monitoring of cell viability based on cell adhesion measurements with an atomic force microscope

机译:基于原子力显微镜的细胞粘附力测量,实时,无标签地监测细胞活力

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The adhesion of cells to an oscillating cantilever sensitively influences the oscillation amplitude at a given frequency. Even early stages of cytotoxicity cause a change in the viscosity of the cell membrane and morphology, both affecting their adhesion to the cantilever. We present a generally applicable method for real-time, label free monitoring and fast-screening technique to assess early stages of cytotoxicity recorded in terms of loss of cell adhesion. We present data taken from gold nanoparticles of different sizes and surface coatings as well as some reference substances like ethanol, cadmium chloride, and staurosporine. Measurements were recorded with two different cell lines, HeLa and MCF7 cells. The results obtained from gold nanoparticles confirm earlier findings and attest the easiness and effectiveness of the method. The reported method allows to easily adapt virtually every AFM to screen and assess toxicity of compounds in terms of cell adhesion with little modifications as long as a flow cell is available. The sensitivity of the method is good enough indicating that even single cell analysis seems possible.
机译:细胞对振荡悬臂的粘附会敏感地影响给定频率下的振荡幅度。甚至细胞毒性的早期阶段也会引起细胞膜粘度和形态的改变,这都会影响它们与悬臂的粘附。我们提出了一种普遍适用的实时,无标签监测和快速筛选技术的方法,以评估在细胞粘附丧失方面记录的早期细胞毒性。我们提供的数据取自具有不同尺寸和表面涂层的金纳米颗粒以及一些参考物质,例如乙醇,氯化镉和星形孢菌素。用两种不同的细胞系HeLa和MCF7细胞记录测量结果。从金纳米颗粒获得的结果证实了较早的发现,并证明了该方法的简便性和有效性。只要有流通池,所报道的方法几乎可以轻松地使几乎每种原子力显微镜适应筛选和评估化合物在细胞粘附方面的毒性,而无需进行任何改动。该方法的灵敏度足够好,表明甚至单细胞分析似乎也是可能的。

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