Evidence map›Paper›PMID 42649995›Full record

ArticleCancers2026

High-Throughput Discovery of Near-Infrared Oxazine Probes for Fluorescence-Guided Glioblastoma Surgery.

Vince Cataldi, Dhanir Tailor, Antonio R Montano, Syed Zaki Husain Rizvi, Samrat Chakraborty, Joshua C Saldivar, Sanjay V Malhotra, Lei G Wang, Summer L Gibbs, Adam W G Alani

Abstract read
In one paragraph

Article in Cancers, 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

10 authors.

Vince CataldiDepartment of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Portland, OR 97201, USA.ORCID 0000-0002-6369-0534
Dhanir TailorCenter for Experimental Therapeutics, Oregon Health & Science University, Portland, OR 97239, USA.ORCID 0000-0002-8138-4469
Antonio R MontanoBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97239, USA.
Syed Zaki Husain RizviDepartment of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Portland, OR 97201, USA.
Samrat ChakrabortyDepartment of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Portland, OR 97201, USA.
Joshua C SaldivarCenter for Experimental Therapeutics, Oregon Health & Science University, Portland, OR 97239, USA.
Sanjay V MalhotraCenter for Experimental Therapeutics, Oregon Health & Science University, Portland, OR 97239, USA.ORCID 0000-0003-4056-5033
Lei G WangBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97239, USA.
Summer L GibbsBiomedical Engineering Department, Oregon Health & Science University, Portland, OR 97239, USA.ORCID 0000-0001-8077-1582
Adam W G AlaniDepartment of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Portland, OR 97201, USA.ORCID 0000-0002-9214-9317

Funding

Oregon Health & Science University College of Pharmacy and the OHSU Center for Experimental Therapeutics for the 2023 PHACET grantOregon State University Debra Larson O'Leary Research Fund in Pharmacy at Oregon State University
6 · The paper itself

Abstract

BACKGROUND/

objectivesGlioblastoma (GBM) is the most aggressive primary malignant brain tumor in adults, characterized by highly infiltrative growth and poorly defined margins that hinder complete surgical resection. Fluorescence-guided surgery (FGS) can enhance intraoperative tumor visualization; however, currently available fluorophores often exhibit limited tumor specificity and inconsistent labeling. This study aimed to identify near-infrared (NIR) probes with improved glioblastoma selectivity using a high-throughput discovery approach.

methodsA chemically diverse library of 127 NIR oxazine probes was screened using automated fluorescence imaging across four GBM cell lines and a sarcoma control line. Top-performing probes were further evaluated in an orthotopic U251MG-GFP glioblastoma mouse model to assess blood-brain barrier penetration and tumor localization in vivo.

resultsFive candidate probes exhibited strong, selective NIR fluorescence in GBM cells. In vivo imaging revealed that the lead probe, LGW01-44, achieved the highest tumor-to-brain contrast with minimal background signal. Ex vivo analysis of brain sections confirmed preferential accumulation of LGW01-44 within intracranial tumor tissue.

conclusionsThese findings establish a scalable high-throughput platform for the discovery of tumor-selective NIR imaging agents and identify the oxazine probe LGW01-44 as a promising candidate for fluorescence-guided glioblastoma surgery.

Indexed as

fluorescence-guided surgeryglioblastomahigh-throughput screeningmolecular imaging probesnear-infrared imagingoxazine fluorophores

Identifiers

PMID42649995
PMCPMC13510431

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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.