bioRxivBioengineeringPreprint
Confidence-supported label-free metabolic imaging with FPhaS phase autofluorescence microscopy
Hongming Fan, Jindou ShiiD, Zhongtian Yang, Alexander HoiD, Lingxiao YangiD, Kevin K. D. TaniD, Edita AksamitieneiD, Stephen A. BoppartiD
Abstract
Label-free optical redox imaging utilizes endogenous NAD(P)H and FAD autofluorescence to evaluate metabolism in living specimens. The conventional optical redox ratio collapses these two channels into a single value; however, it does not indicate whether a pixel has sufficient photon support or the cellular context necessary for quantitative aggregation. To address this limitation, we introduce FPhaS, a fixed-calibration phase- autofluorescence framework that integrates quantitative phase imaging (QPI) with simultaneous label-free autofluorescence multi-harmonic microscopy (SLAM), using fluorescence lifetime imaging (FLIM) solely for validation. Because QPI and SLAM are acquired with the same objective, a unified non-biological calibration aligns phase-derived structural data with the autofluorescence frame, yielding a residual error of 0.39 pixels. This calibration is maintained across all biological specimens. This shared geometric reference enables local evaluation of structural and metabolic information, rather than comparing approximately aligned images. FPhaS decomposes the data into cell presence, ratio credibility, and confidence-supported pooling. We validated FPhaS on A549 cells under high and low-photon conditions; the framework is designed to generalize to other cell and tissue types. Confidence-weighted intensity redox estimates were compared with lifetime-derived measurements within mask-locked cellular regions. Concordance improved exclusively when both the denominator photon support and an independent structural criterion were satisfied. The same reference layer generated cell-level descriptors of metabolic content, metabolic-structural organization, and measurement reliability, while also constraining the CombinedWLS reconstruction under diminished fluorescence acquisition. FPhaS redefines label-free metabolic imaging from producing comprehensive ratio maps to identifying regions where optical evidence substantiates quantitative inference.
- organism: human
- assay: imaging
- research focus: cell type annotation
- approach: microscopy & imaging analysis
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Label free multimodal optical imaging of metabolic heterogeneity and correlation in aging by integrating SRS, MPF, FLIM, and SHG
Hongje Jang, Shuang Wu, … Lingyan Shi·bioRxiv·Aug 22, 2026
- Assessing cellular metabolic dynamics with NAD(P)H fluorescence polarization imaging
Ling Lu, Jack C. Crowley, … Warren R. Zipfel·bioRxiv·Jul 28, 2025
- Bright Probes, Blurred Metabolism: Navigating Fluorescent Protein Cross-Excitation in NADH FLIM
Janielle Cuala, Oscar Alberto de la Fuente, … Falk Schneider·bioRxiv·May 29, 2026
- UVA hyperspectral light-sheet microscopy for volumetric metabolic imaging: application to pre-implantation embryo development
J. Morizet, D. Chow, … K. Dholakia·bioRxiv·Jun 21, 2023
- Multi-modal, Label-free, Optical Mapping of Cellular Metabolic Function and Oxidative Stress in 3D Engineered Brain Tissue Models
Yang Zhang, Maria G. Savvidou, … Irene Georgakoudi·Communications BiologyPeer-reviewed·Dec 2, 2025
- Formalin fixation and paraffin embedding interfere with preservation of optical metabolic assessments based on endogenous NAD(P)H and FAD two photon excited fluorescence
A. Sanchez-Hernandez, C. M. Polleys, I. Georgakoudi·bioRxiv·Jun 16, 2023