Three-dimensional forward-scattering imaging flow cytometry system for single-cell analysis

Label-free single-cell 3D imaging is essential for accurate phenotyping by minimizing perturbations to native cellular states and facilitating downstream molecular analyses. Among the available modalities, 3D forward-scattering (dark-field) imaging offers the richest subcellular details but faces challenges from strong transmitted-beam interference. We present a high-throughput 3D forward-scattering imaging flow cytometry system employing optical needle-beam illumination, linear micro-mirror arrays for axial scatter detection, and spatiotemporal deconvolution algorithms. Experimental validations with microstructures, hydrogel beads, and HEK-293 cells confirm the method's capability for robust subcellular resolution at ∼400 cells/s, enabling advanced label-free cellular diagnostics and analysis. This platform enables label-free, high-content cellular analysis and is readily adaptable to integrated cell sorting and AI-driven classification, offering broad potential for biomedical research and diagnostics.

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Publication Details

Journal
APL Photonics
Published
2025-12-01
DOI
https://doi.org/10.1063/5.0301435
Primary Topic
Cell Image Analysis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Three-dimensional forward-scattering imaging flow cytometry system for single-cell analysis

Zunming Zhang, Adam de la Zerda, M Zhou, Ziqi Zhou et al.
APL Photonics
Cell Image Analysis Techniques
article

Three-dimensional forward-scattering imaging flow cytometry system for single-cell analysis

Zunming Zhang, Adam de la Zerda, M Zhou, Ziqi Zhou, Xinyu Chen, Jingjing Zhao, Zhaoyu Lai
article en

Abstract

Label-free single-cell 3D imaging is essential for accurate phenotyping by minimizing perturbations to native cellular states and facilitating downstream molecular analyses. Among the available modalities, 3D forward-scattering (dark-field) imaging offers the richest subcellular details but faces challenges from strong transmitted-beam interference. We present a high-throughput 3D forward-scattering imaging flow cytometry system employing optical needle-beam illumination, linear micro-mirror arrays for axial scatter detection, and spatiotemporal deconvolution algorithms. Experimental validations with microstructures, hydrogel beads, and HEK-293 cells confirm the method's capability for robust subcellular resolution at ∼400 cells/s, enabling advanced label-free cellular diagnostics and analysis. This platform enables label-free, high-content cellular analysis and is readily adaptable to integrated cell sorting and AI-driven classification, offering broad potential for biomedical research and diagnostics.

APL PhotonicsVol. 10(12)
University of California San Diego (US), Huazhong University of Science and Technology (CN), Stanford University (US)
National Science Foundation, National Institutes of Health, Division of Electrical, Communications and Cyber Systems
Openalex Percentile: Top 73%
Cell Image Analysis Techniques
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