Presentation + Paper
15 March 2023 High-throughput parallel 3D imaging flow cytometry
Masashi Ugawa, Sadao Ota
Author Affiliations +
Abstract
Imaging flow cytometry has enabled high-throughput morphology-based analysis of large cell populations at the singlecell level. However, most of these systems were based on 2D imaging, and with the loss of the spatial information in the depth direction, its accuracy was limited, especially when performing analysis based on subcellular structures. Efforts to develop 3D imaging flow cytometry have been undertaken, but the throughput was limited because of the slow 3D imaging systems. Even by adopting light-sheet microscopy, the throughput was limited to less than 100 cells/s, due to the camera frame rate. To overcome this limitation, we combined oblique-plane microscopy with 1D acoustofluidic particle focusing to image multiple cells in parallel. With this, we were able to overcome the throughput limitation by the camera frame rate and achieve a detection throughput of 2,300 cells/s, the highest to our knowledge for 3D imaging flow cytometry. Furthermore, with such high throughput, we were able to capture 3D images of 4×105 cells in an acquisition time of less than five min and perform subcellular-structure-based analysis of mitotic cells, demonstrating practical 3D imaging flow cytometry for the first time to our knowledge. Result show, that with 3D imaging flow cytometry, we can capture structural information that would be overlooked with its 2D imaging counterpart.
Conference Presentation
© (2023) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Masashi Ugawa and Sadao Ota "High-throughput parallel 3D imaging flow cytometry", Proc. SPIE 12383, Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XXI, 1238309 (15 March 2023); https://doi.org/10.1117/12.2648669
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KEYWORDS
Flow cytometry

3D image processing

Imaging systems

Cameras

Microscopy

3D acquisition

Particles

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