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.
Authors
- Zunming Zhang (ORCID: https://orcid.org/0000-0002-1002-4036)
- Adam de la Zerda (ORCID: https://orcid.org/0000-0002-5617-0194)
- M Zhou (ORCID: https://orcid.org/0009-0006-4229-853X)
- Ziqi Zhou
- Xinyu Chen (ORCID: https://orcid.org/0000-0002-9507-5835)
- Jingjing Zhao (ORCID: https://orcid.org/0000-0002-0324-2940)
- Zhaoyu Lai
Institutions
- University of California San Diego (US)
- Huazhong University of Science and Technology (CN)
- Stanford University (US)
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
Funders
- National Science Foundation
- National Institutes of Health
- Division of Electrical, Communications and Cyber Systems