Evidence map›Paper›PMID 41622407›Full record

ArticleJournal of biophotonics2026

Enhancing Fluorescence Lifetime Imaging With Differential Transformer.

Ismail Erbas, Vikas Pandey, Navid Ibtehaj Nizam, Nanxue Yuan, Amit Verma, Tynan Young, John Williams, Margarida Barroso, Xavier Intes

Abstract read
In one paragraph

Article in Journal of biophotonics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ismail ErbasDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York, USA.ORCID 0000-0002-1104-8670
Vikas PandeyDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York, USA.
Navid Ibtehaj NizamDepartment of Biomedical Engineering, West Chester University, West Chester, Pennsylvania, USA.ORCID 0000-0002-8266-5254
Nanxue YuanDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York, USA.
Amit VermaDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, New York, USA.
Tynan YoungDepartment of Molecular Medicine, City of Hope, Beckman Research Institute, Duarte, California, USA.
John WilliamsDepartment of Molecular Medicine, City of Hope, Beckman Research Institute, Duarte, California, USA.ORCID 0000-0002-0522-384X
Margarida BarrosoDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, New York, USA.
Xavier IntesDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York, USA.

Funding

In vivo Macroscopic Fluorescence Lifetime Molecular Optical ImagingR01CA250636 · NCI · RENSSELAER POLYTECHNIC INSTITUTE · PI BARROSO, MARGARIDA, INTES, XAVIER · 2020 to 2023
$2.9M
Photon-counting X-ray and Optical Tomography for Preclinical Cancer ResearchR01CA237267 · NCI · RENSSELAER POLYTECHNIC INSTITUTE · PI BARROSO, MARGARIDA, INTES, XAVIER · 2019 to 2023
$2.9M
AI enhanced lifetime-based mesoscopic in vivo imaging of tissue molecular heterogeneityR01CA271371 · NCI · RENSSELAER POLYTECHNIC INSTITUTE · PI Margarida Barroso, Xavier Intes · 2023 to 2026
$2.7M
NCI NIH HHS R01 CA237267NCI NIH HHS R01 CA250636NCI NIH HHS R01 CA271371NIH HHS R01CA237267NIH HHS R01CA250636NIH HHS R01CA271371
6 · The paper itself

Abstract

Conventional analytical methods for fluorescence lifetime imaging (FLI) require the instrument response function (IRF) alongside temporal fluorescence decay to accurately estimate lifetime parameters. While the IRF remains spatially and temporally invariant in microscopy, it exhibits significant pixel-wise spatial variation and temporal offsets at mesoscopic and macroscopic scales due to sample size and surface topography. Existing deep learning approaches, trained on limited synthetic or simplified experimental datasets, often fail to generalize to complex biological or in vivo imaging. Here, we introduce MFliNet, a deep learning framework working in accordance with the physics of photon time-of-flight deconvolution for accurate multi-exponential decay parameter estimation. Utilizing a Differential Transformer encoder-decoder architecture, MFliNet jointly processes temporal fluorescence decay and corresponding IRF inputs to correct topographical distortions in photon arrival distributions. Validation with tissue-mimicking phantoms and preclinical tumor models demonstrates exceptional robustness and precision, enabling reliable, real-time macroscopic FLI for complex biological and intraoperative applications.

Indexed as

Optical ImagingAnimalsConvolutional Neural NetworksDeep LearningFluorescenceHumansImage Processing, Computer-AssistedMicePhantoms, ImagingTime Factorscancer imagingdeep learningdifferential transformerfluorescence lifetime imagingMFLI

Identifiers

PMID41622407
PMCPMC13063378

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.