Evidence map›Paper›PMID 41353453›Full record

ArticleAnalytical and bioanalytical chemistry2026

Engineering localized injury: a 3D microfluidic platform approach for ex vivo tissue interrogation.

Colby E Witt, Lauren M Delong, Maria K Kristinsdottir, Alexandra K Brooke, Ashley E Ross

Abstract read
In one paragraph

Article in Analytical and bioanalytical chemistry, 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

5 authors.

Colby E WittDepartment of Chemistry, University of Cincinnati, 312 College Dr., 404 Crosley Tower, Cincinnati, OH, 45221-0172, USA.ORCID http://orcid.org/0000-0002-7332-7632
Lauren M DelongDepartment of Chemistry, University of Cincinnati, 312 College Dr., 404 Crosley Tower, Cincinnati, OH, 45221-0172, USA.ORCID http://orcid.org/0000-0002-1266-3536
Maria K KristinsdottirDepartment of Chemistry, University of Cincinnati, 312 College Dr., 404 Crosley Tower, Cincinnati, OH, 45221-0172, USA.
Alexandra K BrookeDepartment of Chemistry, University of Cincinnati, 312 College Dr., 404 Crosley Tower, Cincinnati, OH, 45221-0172, USA.ORCID http://orcid.org/0000-0003-2440-4758
Ashley E RossDepartment of Chemistry, University of Cincinnati, 312 College Dr., 404 Crosley Tower, Cincinnati, OH, 45221-0172, USA. Ashley.ross@uc.edu.ORCID http://orcid.org/0000-0003-2456-3636

Funding

Monitoring rapid guanosine signaling during ischemiaR01NS121426 · NINDS · UNIVERSITY OF CINCINNATI · PI ROSS, ASHLEY E · 2021 to 2025
$1.9M
NINDS NIH HHS R01 NS121426NINDS NIH HHS R01NS121426
6 · The paper itself

Abstract

Over the years, interrogating and replicating biological events ex vivo and in vitro has proven to provide a breadth of knowledge into various mechanisms of diseases; however, there remains a challenge in understanding the onset of disease within tonic, localized environments over time. Microfluidics provides an alternative approach that can be coupled with many methods to better replicate specific localized and prolonged biological events. In this work, we introduce a novel 3D-printed device that significantly improves upon previous microfluidic approaches aimed at maintaining high spatial resolution and sustainment of delivery, ultimately enabling us to examine localized injuries within an ex vivo model with higher precision and control. This work focuses on focal ischemia; however, it should be noted that the device is applicable to any event that needs high spatial resolution and sustained fluidic delivery. We demonstrate that tissue remains viable on this platform and that we are capable of achieving exquisite fluidic control, not affordable from standard lithographic techniques. Additionally, we incorporate real-time neurochemical monitoring to demonstrate rapid and robust changes in dopamine signaling at the site of focal ischemia, further validating our platform for localized injury studies. This device fills a critical gap in the existing literature by significantly improving upon the capabilities of localized tissue stimulation and further enhances our understanding of local physiological changes during ischemic events, providing a critical advance in biomedical tools for measuring at localized regions within tissue.

Indexed as

Lab-On-A-Chip DevicesMicrofluidic Analytical TechniquesPrinting, Three-DimensionalAnimalsDopamineEquipment DesignDopamineIschemiaMicrofabricationMicrofluidicsNeurochemicalsTissue stimulation

Identifiers

PMID41353453
PMCPMC13388642

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.