ETH Zurich, Department of Biosystems Science and Engineering (D-BSSE), Bio Engineering Laboratory (BEL), Basel, Switzerland.
Lab Chip. 2012 Mar 7;12(5):906-15. doi: 10.1039/c2lc20911j. Epub 2011 Dec 22.
We present a microfluidic cell-culture chip that enables trapping, cultivation and release of selected individual cells. The chip is fabricated by a simple hybrid glass-SU-8-PDMS approach, which produces a completely transparent microfluidic system amenable to optical inspection. Single cells are trapped in a microfluidic channel using mild suction at defined cell immobilization orifices, where they are cultivated under controlled environmental conditions. Cells of interest can be individually and independently released for further downstream analysis by applying a negative dielectrophoretic force via the respective electrodes located at each immobilization site. The combination of hydrodynamic cell-trapping and dielectrophoretic methods for cell releasing enables highly versatile single-cell manipulation in an array-based format. Computational fluid dynamics simulations were performed to estimate the properties of the system during cell trapping and releasing. Polystyrene beads and yeast cells have been used to investigate and characterize the different functions and to demonstrate biological compatibility and viability of the platform for single-cell applications in research areas such as systems biology.
我们提出了一种微流控细胞培养芯片,能够捕获、培养和释放选定的单个细胞。该芯片通过简单的混合玻璃-SU-8-PDMS 方法制造,可产生完全透明的微流控系统,适用于光学检查。使用温和的吸力在定义的细胞固定孔中捕获微流道中的单个细胞,在受控的环境条件下培养它们。通过在每个固定点的相应电极上施加负介电泳力,可以将感兴趣的细胞单独且独立地释放出来,以进行进一步的下游分析。基于流体力的细胞捕获和介电泳方法的细胞释放相结合,可在基于阵列的格式中实现高度通用的单细胞操作。进行了计算流体动力学模拟,以估计细胞捕获和释放过程中的系统特性。聚苯乙烯珠和酵母细胞已被用于研究和表征不同的功能,并证明了该平台在系统生物学等单细胞应用研究领域中的生物相容性和生存能力。