Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ, USA.
Electrophoresis. 2011 Sep;32(18):2550-8. doi: 10.1002/elps.201100066. Epub 2011 Aug 23.
Trapping of individual cells at specific locations in a microfluidic lab-on-a-chip platform is essential for single cell studies, especially those requiring individual stimulation followed by downstream analysis. To this aim, we have designed microdevices based on direct current (DC) insulator-based dielectrophoresis (iDEP) acting as individual single cell traps. We present both the design of a negative iDEP trap and a positive iDEP trap using insulating posts integrated at microchannel intersections. We obtained electric field distributions via numerical simulations adapted to the intersection and trap geometry with which we predict single particle pathlines. With polystyrene particles of 10 μm diameter, we demonstrated an effective design for a single particle trap in the case of negative dielectrophoresis. The onset trapping voltage shows an inverse relation to the buffer conductivity, thus indicating the influence of electrokinetic effects on the trapping behavior. Additionally, we demonstrated the proof-of-principle of single MCF-7 breast cancer cell trapping in a positive iDEP trap. Our single particle trapping experiments were further in very good agreement with numerical simulations. To ensure that no significant damage occurred to the cells during the experiment, we further optimized medium conditions to ensure viability of the cells for at least 1 h, more than sufficient for microfluidic trapping experiments. Our results thus indicated the successful design of DC iDEP traps, which can easily be integrated into a variety of microchip operations for single cell analysis.
在微流控芯片实验室平台上将单个细胞捕获到特定位置对于单细胞研究至关重要,特别是那些需要单独刺激然后进行下游分析的研究。为此,我们设计了基于直流(DC)基于电介质的介电泳(iDEP)的微器件,用作单个单细胞陷阱。我们展示了使用集成在微通道交叉处的绝缘柱设计的负 iDEP 陷阱和正 iDEP 陷阱。我们通过数值模拟获得了电场分布,该模拟适应了交叉点和陷阱的几何形状,我们可以通过该模拟预测单个粒子的轨迹。使用 10μm 直径的聚苯乙烯粒子,我们在负介电泳的情况下证明了单个粒子陷阱的有效设计。起始捕获电压与缓冲液电导率呈反比关系,表明电泳动力学对捕获行为的影响。此外,我们在正 iDEP 陷阱中证明了单个 MCF-7 乳腺癌细胞捕获的原理验证。我们的单粒子捕获实验与数值模拟非常吻合。为了确保细胞在实验过程中不受任何显著损伤,我们进一步优化了介质条件,以确保细胞的活力至少为 1 小时,这对于微流控捕获实验来说已经足够了。因此,我们的结果表明成功设计了 DC iDEP 陷阱,该陷阱可以轻松集成到各种微芯片操作中,用于单细胞分析。