Evidence map›Paper›PMID 42222561›Full record

ArticleChemical & biomedical imaging2026

A New Class of Anionic Near-Infrared Fluorescent Dyes with 1,6-Diheterophenalene-2,5-dione End Groups.

Isaac Fuentes, Rui Tang, Megan S Michie, Christina Lin, Mikhail Y Berezin, Vladimir B Birman

Abstract read
In one paragraph

Article in Chemical & biomedical imaging, 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

6 authors.

Isaac FuentesDepartment of Chemistry, Washington University, St. Louis, Missouri 63130, United States.
Rui TangDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri 63110, United States.ORCID https://orcid.org/0000-0002-2734-1003
Megan S MichieDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri 63110, United States.ORCID https://orcid.org/0000-0001-8749-4063
Christina LinDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri 63110, United States.
Mikhail Y BerezinDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri 63110, United States.ORCID https://orcid.org/0000-0002-2670-2487
Vladimir B BirmanDepartment of Chemistry, Washington University, St. Louis, Missouri 63130, United States.ORCID https://orcid.org/0000-0003-0299-358X

Funding

Mapping Neural Recovery: Visualizing Peripheral Nerve Regeneration and Brain Plasticity Post-Peripheral Nerve InjuryR01NS139461 · NINDS · WASHINGTON UNIVERSITY · PI Mikhail Y. Berezin · 2025 to 2026
$1.1M
Molecular and cellular imaging of bone biopsies using AI augmented deep UV Raman microscopyR21CA269099 · NCI · TEXAS ENGINEERING EXPERIMENT STATION · PI BEREZIN, MIKHAIL Y., YAKOVLEV, VLADISLAV V. · 2022 to 2024
$577k
In vivo Visualization of Delayed Wallerian Degeneration in Peripheral Nerve InjuryR21NS135646 · NINDS · WASHINGTON UNIVERSITY · PI BEREZIN, MIKHAIL Y. · 2024 to 2025
$421k
NCI NIH HHS R21 CA269099NINDS NIH HHS R01 NS139461NINDS NIH HHS R21 NS135646
6 · The paper itself

Abstract

We describe the synthesis and evaluation of oxonol-based near-infrared (NIR) dyes designed for in vivo optical imaging applications. These small-molecule anionic dyes, dubbed FROGs (Fiercely Radiant Oxonol Green), exhibit strong NIR absorption and emission, high molar absorptivity, and good photostability. In vitro studies revealed distinct cellular uptake profiles: whereas compound FROG-1 displayed minimal cellular internalization, FROG-2 showed robust accumulation in cancer cells. Fluorescence lifetime imaging microscopy (FLIM) further revealed that FROG-2 produced a uniform and prolonged lifetime signal within cancer cells, indicative of stable intracellular localization. Both representative compounds were administered to nude mice and monitored using multispectral fluorescence imaging across a broadband excitation/emission channel combinations between 500 and 840 nm. Principal component analysis of the imaging data revealed distinct temporal and spatial distribution patterns: FROG-1 demonstrated renal clearance with minimal off-target accumulation, while FROG-2 showed mixed renal and hepatic clearance and spectral heterogeneity at early time points, suggesting differential stability or interaction with tissue microenvironments. Ex vivo organ imaging at 24 h confirmed these clearance routes. These findings highlight the potential of tailored oxonol dyes as versatile NIR probes and provide insight into the structure-biodistribution relationship critical for biomedical imaging probe development.

Indexed as

anionic polymethine dyesfluorescence lifetime imaging (FLIM)multispectral in vivo imagingnear-infrared fluorescent dyesoxonol fluorophores

Identifiers

PMID42222561
PMCPMC13217353

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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.