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On-chip ultrasonic sample preparation for cell based assays

机译:用于基于细胞的测定的片上超声样品制备

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摘要

We demonstrate an acoustophoresis method for size-based separation, isolation, up-concentration and trapping of cells that can be used for on-chip sample preparation combined with high resolution imaging for cell-based assays. The method combines three frequency-specific acoustophoresis functions in a sequence by actuating three separate channel zones simultaneously: zones for pre-alignment, size-based separation, and trapping. We characterize the mutual interference between the acoustic radiation forces between the different zones by measuring the spatial distribution of the acoustic energy density during different schemes of ultrasonic actuation, and use this information for optimizing the driving frequencies and voltages of the three utilized ultrasonic transducers attached to the chip, and the flow rates of the pumps. By the use of hydrodynamic defocusing of the pre-aligned cells in the separation zone, a cell population from a complex sample can be isolated and trapped with very high purity, followed by dynamic fluorescence analysis. We exemplify the method's potential by isolating A549 lung cancer cells from red blood cells with 100% purity, 92% separation efficiency, and 93% trapping efficiency resulting in a 130x up-concentration factor during 15 minutes of continuous sample processing through the chip. Furthermore, we demonstrate an on-chip fluorescence assay of the isolated cancer cells by monitoring the dynamic uptake and release of a fluorescence probe in individual trapped cells. The ability to combine isolation of individual cells from a complex sample with high-resolution image analysis holds great promise for applications in cellular and molecular diagnostics.
机译:我们展示了一种用于基于大小的分离,分离,向上浓缩和捕获细胞的声泳方法,可用于芯片上样品制备以及基于细胞的测定的高分辨率成像。该方法通过同时启动三个单独的通道区域:预对准区域,基于大小的分离区域和陷波,来依次组合三个特定频率的声泳功能。我们通过在超声激励的不同方案期间测量声能密度的空间分布来表征不同区域之间的声辐射力之间的相互干扰,并使用此信息来优化连接到三个超声换能器的驱动频率和电压芯片和泵的流速。通过使用分离区中预对准细胞的流体动力学离焦,可以分离并捕获来自复杂样品的细胞群,并获得很高的纯度,然后进行动态荧光分析。我们以100%的纯度,92%的分离效率和93%的捕获效率从红细胞中分离出A549肺癌细胞,从而在通过芯片进行连续样品处理的15分钟内产生了130倍的高浓缩因子,从而证明了该方法的潜力。此外,我们通过监测单个捕获细胞中荧光探针的动态摄取和释放,证明了分离出的癌细胞的芯片上荧光测定。将复杂样本中单个细胞的分离与高分辨率图像分析相结合的能力,在细胞和分子诊断中的应用前景广阔。

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