Department of Electrical and Computer Engineering, University of Virginia, Charlottesville, VA, 22904, USA.
CytoRecovery, Inc., Blacksburg, VA, 24060, USA.
Anal Bioanal Chem. 2020 Jun;412(16):3881-3889. doi: 10.1007/s00216-020-02667-9. Epub 2020 May 5.
The trapping and deflection of biological cells by dielectrophoresis (DEP) at field non-uniformities in a microfluidic device is often conducted in a contactless dielectrophoresis (cDEP) mode, wherein the electrode channel is in a different layer than the sample channel, so that field penetration through the interceding barrier causes DEP above critical cut-off frequencies. In this manner, through physical separation of the electrode and sample channels, it is possible to spatially modulate electric fields with no electrode-induced damage to biological cells in the sample channel. However, since this device requires interlayer alignment of the electrode to sample channel and needs to maintain a thin interceding barrier (~ 15 μm) over the entire length over which DEP is needed (~ 1 cm), variations in alignment and microstructure fidelity cause wide variations in cDEP trapping level and frequency response across devices. We present a strategy to eliminate interlayer alignment by fabricating self-aligned electrode and sample channels, simultaneously with the interceding barrier layer (14-μm width and 50-μm depth), using a single-layer imprint and bond process on cyclic olefin copolymer. Specifically, by designing support structures, we preserve fidelity of the high aspect ratio insulating posts in the sample channel and the interceding barrier between the sample and electrode channels over the entire device footprint (~ 1 cm). The device operation is validated based on impedance measurements to quantify field penetration through the interceding barrier and by DEP trapping measurements. The presented fabrication strategy can eventually improve cDEP device manufacturing protocols to enable more reproducible DEP performance. Graphical abstract.
在微流控装置中,通过非均匀电场的介电泳(DEP)来捕获和偏转生物细胞通常采用非接触式介电泳(cDEP)模式,其中电极通道位于与样品通道不同的层中,因此电场通过中间隔离层的穿透会导致介电泳超过临界截止频率。通过电极和样品通道的物理分离,可以对电场进行空间调制,而不会对样品通道中的生物细胞造成电极诱导的损伤。然而,由于这种设备需要对电极和样品通道进行层间对准,并需要在需要DEP 的整个长度上保持薄的中间隔离层(15μm)(1cm),因此对准和微结构保真度的变化会导致 cDEP 捕获水平和频率响应在设备之间产生很大的差异。我们提出了一种通过在环状烯烃共聚物上使用单层压印和键合工艺同时制造自对准电极和样品通道以及中间隔离层(14μm 宽和 50μm 深)来消除层间对准的策略。具体来说,通过设计支撑结构,我们保留了样品通道中高纵横比绝缘柱和样品与电极通道之间中间隔离层的保真度,跨越整个设备足迹(~1cm)。通过阻抗测量来量化中间隔离层的电场穿透,并通过 DEP 捕获测量来验证设备的操作。所提出的制造策略最终可以改进 cDEP 设备制造协议,以实现更可重复的 DEP 性能。