Evidence map›Paper›PMID 39987852›Full record

ArticleBiomaterials2025

Matrix-designed bright near-infrared fluorophores for precision peripheral nerve imaging.

Antonio R Montaño, Anas Masillati, Dani A Szafran, Nourhan A Shams, Grace E Hubbell, Connor W Barth, Summer L Gibbs, Lei G Wang

Abstract read
In one paragraph

Article in Biomaterials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  5. Article
  6. Uridine-Based PET/NIRF Dual-Modality imaging for precision tumor diagnosis and surgery.European journal of nuclear medicine and molecular imaging · 2026
    Article
  7. Advancements in Intraoperative Imaging for Enhanced Surgical Precision.Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer · 2026
    Review
  8. Review
  9. Article
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

8 authors.

Antonio R MontañoBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97201, USA.
Anas MasillatiBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97201, USA.
Dani A SzafranBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97201, USA.
Nourhan A ShamsBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97201, USA.
Grace E HubbellBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97201, USA.
Connor W BarthBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97201, USA.
Summer L GibbsBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97201, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97201, USA. Electronic address: gibbss@ohsu.edu.
Lei G WangBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97201, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97201, USA. Electronic address: wanglei@ohsu.edu.

Funding

Multichannel Fluorescence Guided Surgery Tools Enabling Simultaneous Cancer Margin and Nerve Visualization in ProstatectomyR01CA271532 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Summer Lynne Gibbs · 2022 to 2026
$3.1M
NCI NIH HHS R01 CA271532
6 · The paper itself

Abstract

The FDA's recent approval of pafolacianine, the first molecular targeted contrast agent for fluorescence-guided surgery (FGS), signifies a remarkable milestone in precision medicine. This advance offers new hope for cancer patients by enabling guided removal of cancerous tissues, where completed surgical removal remains a consistent challenge without real-time intraoperative guidance. For optimal surgical outcomes, delicate nerve tissues must be preserved to maintain patient quality of life. Despite advances in the clinical translation pipeline, the development of clinically viable nerve-specific contrast agents for FGS remains a significant challenge. Herein, a medicinal chemistry-based matrix design strategy was applied to effectively generate a synthetic roadmap permitting management of nerve-specificity within the near-infrared (NIR) oxazine fluorophore family. Many of these newly developed fluorophores demonstrated robust nerve-specificity and superior safety profiles, while also offering spectral profiles that are compatible with the clinical surgical FGS infrastructure. Notably, improving observed brightness in vivo enabled exceptional visibility of buried nerve tissue, a priority during surgical procedures. Critically, the lead probe showed a large dosage safety window capable of generating substantial contrast at doses 100x lower than the maximum tolerated dose. Following clinical translation, such NIR nerve-specific fluorophores stand poised to significantly improve outcomes for surgical patients by improving identification and visualization of surface and buried nerve tissues in real time within the surgical arena.

Indexed as

Fluorescent DyesOptical ImagingPeripheral NervesAnimalsContrast MediaHumansMiceSpectroscopy, Near-InfraredContrast MediaFluorescent DyesFluorescence-guided surgery (FGS)Fluorescence imagingNear-infrared (NIR)Nerve-specific imagingOxazine

Identifiers

PMID39987852
PMCPMC11932071

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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.