Autofluorescence lifetime flow cytometry and single cell deposition
Autofluorescence lifetime imaging microscopy is sensitive to functional or treatment-induced metabolic changes in single cells. However, this label-free technique typically relies on laser-scanning microscopes that are not common for single-cell assessments in immunology. Here, we present a microfluidic lifetime-sensitive flow cytometer that measures time-domain decays of the metabolic co-enzyme NAD(P)H from single cells with picosecond temporal resolution using time-correlated single-photon counting (TCSPC) at a throughput of tens of cells per second. The system uses a picosecond-pulsed ultraviolet diode laser, alkali photomultiplier tubes, an FPGA-based time tagger, and provides real-time phasor-based classification (i.e., gating) of flowing cells for applications in immunology.
Authors
- Amani A. Gillette (ORCID: https://orcid.org/0000-0002-1470-3300)
- Kayvan Samimi (ORCID: https://orcid.org/0000-0002-2566-612X)
- Rupsa Datta (ORCID: https://orcid.org/0000-0002-6432-2389)
- Melissa C. Skala (ORCID: https://orcid.org/0000-0002-6320-7637)
- Ojaswi Pasachhe
- Wenxuan Zhao (ORCID: https://orcid.org/0009-0004-1952-6093)
- Meghana A. Kalluri
- Alex Sorenson
Publication Details
- Published
- 2025-03-19
- DOI
- https://doi.org/10.1117/12.3041767
- Primary Topic
- Advanced Biosensing Techniques and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00