Patel Yogesh M, Jain Sanidhya, Singh Abhishek Kumar, Khare Kedar, Ahlawat Sarita, Bahga Supreet Singh
Department of Mechanical Engineering, Indian Institute of Technology Delhi, New Delhi 110016, India.
Department of Physics, Indian Institute of Technology Delhi, New Delhi 110016, India.
Biomicrofluidics. 2020 Dec 14;14(6):064110. doi: 10.1063/5.0033291. eCollection 2020 Nov.
We present design, characterization, and testing of an inexpensive, sheath-flow based microfluidic device for three-dimensional (3D) hydrodynamic focusing of cells in imaging flow cytometry. In contrast to other 3D sheathing devices, our device hydrodynamically focuses the cells in a single-file near the bottom wall of the microchannel that allows imaging cells with high magnification and low working distance objectives, without the need for small device dimensions. The relatively large dimensions of the microchannels enable easy fabrication using less-precise fabrication techniques, and the simplicity of the device design avoids the need for tedious alignment of various layers. We have characterized the performance of the device with 3D numerical simulations and validated these simulations with experiments of hydrodynamic focusing of a fluorescently dyed sample fluid. The simulations show that the width and the height of the 3D focused sample stream can be controlled independently by varying the heights of main and side channels of the device, and the flow rates of sample and sheath fluids. Based on simulations, we also provide useful guidelines for choosing the device dimensions and flow rates for focusing cells of a particular size. Thereafter, we demonstrate the applicability of our device for imaging a large number of RBCs using brightfield microscopy. We also discuss the choice of the region of interest and camera frame rate so as to image each cell individually in our device. The design of our microfluidic device makes it equally applicable for imaging cells of different sizes using various other imaging techniques such as phase-contrast and fluorescence microscopy.
我们展示了一种用于成像流式细胞术中细胞三维(3D)流体动力学聚焦的廉价、基于鞘流的微流控装置的设计、表征和测试。与其他3D鞘流装置不同,我们的装置通过流体动力学将细胞聚焦在微通道底壁附近的单列中,这使得能够使用高倍率和低工作距离物镜对细胞进行成像,而无需小尺寸的装置。微通道相对较大的尺寸使得使用不太精确的制造技术就能轻松制造,并且装置设计的简单性避免了对各层进行繁琐对准的需要。我们通过3D数值模拟对装置的性能进行了表征,并用荧光染色样品流体的流体动力学聚焦实验验证了这些模拟。模拟结果表明,通过改变装置主通道和侧通道的高度以及样品和鞘流的流速,可以独立控制3D聚焦样品流的宽度和高度。基于模拟,我们还提供了选择装置尺寸和流速以聚焦特定大小细胞的有用指导。此后,我们展示了我们的装置在使用明场显微镜对大量红细胞成像方面的适用性。我们还讨论了感兴趣区域和相机帧率的选择,以便在我们的装置中单独对每个细胞进行成像。我们微流控装置的设计使其同样适用于使用各种其他成像技术(如相差显微镜和荧光显微镜)对不同大小的细胞进行成像。