An inexpensive microfluidic device for three-dimensional hydrodynamic focusing in imaging flow cytometry

• Published in: Biomicrofluidics 2020-11, Vol.14 (6), p.064110-064110
• Main Authors: Patel, Yogesh M., Jain, Sanidhya, Singh, Abhishek Kumar, Khare, Kedar, Ahlawat, Sarita, Bahga, Supreet Singh
• Format: Article
• Language: English
• Subjects: Computational fluid dynamics; Flow cytometry; Flow velocity; Fluid flow; Fluorescence; Imaging; Imaging techniques; Microchannels; Microfluidic devices; Microscopy; Regular; Sheathing; Sheaths; Simulation
• ISSN: 1932-1058; 1932-1058
• DOI: 10.1063/5.0033291

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.