Droplet-based microfluidics has been demonstrated to offer the advantage of high precision control, high throughput, and material savings. Traditional fabrication methods of droplet generation involve soft lithography, molding, etching, and embossing process, relying on expensive equipment, tedious operations, and even requiring a cleanroom fabrication environment. Recently, 3D printing with the characteristics of low cost, easy reprinting, and well-achieved microstructure in three dimensions has been suggested as a promising technology to improve the fabrication of microfluidics. In this study, we combined 3D printing technology and microfluidics to design a microfluidic device that enables the continuous generation of droplets, which can be utilized to encapsulate single particles and cells. The digital model of the microfluidic device was designed and edited by software, and then uploaded to a stereolithography 3D printer with a resolution of 10 μm for printing. To verify the feasibility of the device to generate droplets, the mineral oil and water were used as the continuous phase and the dispersed phase, respectively. The diameters of droplets ranging from about 70 μm to 240 μm and the product rate about 1500/min can be achieved. The result of encapsulation probability of microspheres is around 55% with that of the single-microspheres about 30%, which verifies the ability of droplet device for encapsulating single particles. The droplet microfluidics is applied for cell imaging to monitor the cell viability for a long time. The result presents the viability changes from the living state to death of MDA-MB-231 breast cancer cells.
In this manuscript, we aim to develop the dynamic light scattering imaging (DLSI) method to investigate the difference between triple negative breast cancer (TNBC) and human epidermal growth factor receptor-2 (HER-2) positive breast cancer. The experimental device with the capability to obtain time-series light scattering images was well designed and built. The breast cancer cell lines of MDA-MB-231 and HER-2 enriched SKBR3 were prepared and used for experiments. The autocorrelation functions of the light intensity fluctuation were calculated to characterize both types of breast cancer cells. The dynamic light scattering images were further analyzed to establish a DLSI-based approach for automatic classification of the two types of cells. The results show that the proposed DLSI-based model achieved better classification performance compared to the conventional static light scattering-based model.
In this manuscript, we develop a 3D-printing based microfluidic device for light scattering imaging of single cells. A rapid fabrication method to make microfluidic device that enables 3D-hydrodynamic focusing by utilizing 3D printing technique is proposed. The focusing effect of the microfluidic cytometer was measured and shows the ability to confine the cells to flow near the center stream along the channel. Also, the standard beads with 9.51 μm in diameter were used to test the reliability of the device. The collected light scattering images are in good agreement with simulation results. We suggest that the 3D-printing based light scattering microfluidic device is in principle applicable for fast, label-free detection of single cells.
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