Quantifying uncertainty in phasor-based time-domain fluorescence lifetime imaging microscopy

The phasor approach to time-domain fluorescence lifetime imaging microscopy (FLIM) offers a powerful, fit-free method for analyzing complex fluorescence decay signals. However, its quantitative accuracy is fundamentally limited by noise-particularly photon shot noise-which introduces variability and deviations in lifetime estimation and fluorophore unmixing. In this study, we present a theoretical uncertainty model for phasor-based time-domain FLIM that analytically captures the propagation of shot noise and quantifies its impact on phasor coordinates and fluorophore weight estimation. We validate the model using Monte Carlo simulations and experimental data acquired from standard fluorescent dyes and biological tissue samples. Our model improves the overall reliability and efficiency of phasor-based time-domain FLIM, particularly in photon-limited imaging applications.

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Publication Details

Journal
Biomedical Optics Express
Published
2025-06-16
DOI
https://doi.org/10.1364/boe.565990
Citations
3
Primary Topic
Photoacoustic and Ultrasonic Imaging
Type
article
Field-Weighted Citation Impact
2.02
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article

Quantifying uncertainty in phasor-based time-domain fluorescence lifetime imaging microscopy

Qinyi Chen, Liang Gao, Jongchan Park, Siyu Mu
3 citations
Biomedical Optics Express
Photoacoustic and Ultrasonic Imaging
2.02
article

Quantifying uncertainty in phasor-based time-domain fluorescence lifetime imaging microscopy

Qinyi Chen, Liang Gao, Jongchan Park, Siyu Mu
article en
3 citations

Abstract

The phasor approach to time-domain fluorescence lifetime imaging microscopy (FLIM) offers a powerful, fit-free method for analyzing complex fluorescence decay signals. However, its quantitative accuracy is fundamentally limited by noise-particularly photon shot noise-which introduces variability and deviations in lifetime estimation and fluorophore unmixing. In this study, we present a theoretical uncertainty model for phasor-based time-domain FLIM that analytically captures the propagation of shot noise and quantifies its impact on phasor coordinates and fluorophore weight estimation. We validate the model using Monte Carlo simulations and experimental data acquired from standard fluorescent dyes and biological tissue samples. Our model improves the overall reliability and efficiency of phasor-based time-domain FLIM, particularly in photon-limited imaging applications.

Biomedical Optics ExpressVol. 16(8)
California NanoSystems Institute (US), University of California, Los Angeles (US), University of California System (US)
Affordable and clean energy
Openalex Percentile: Top 14%
Photoacoustic and Ultrasonic Imaging
2.02
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