Evidence map›Paper›PMID 41123269›Full record

ArticleAnalytical chemistry2025

Multiplexed Fiber-Optic Fluorescence for Functional Monitoring of Perfused Hearts.

Jianrong Qiu, Edward Waters, Emily Lupton, Friedrich Baark, Antoine L D Wallabregue, Stuart J Conway, Richard Southworth, Mads S Bergholt

Abstract read
In one paragraph

Article in Analytical chemistry, 2025. 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

8 authors.

Jianrong QiuCentre for Craniofacial and Regenerative Biology, King's College London, London SE1 9RT, U.K.
Edward WatersSchool of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, U.K.
Emily LuptonSchool of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, U.K.
Friedrich BaarkSchool of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, U.K.
Antoine L D WallabregueDepartment of Chemistry, University of Oxford, Oxford OX1 3TA, U.K.
Stuart J ConwayDepartment of Chemistry & Biochemistry, UCLA, Los Angeles, California 90095-1569, United States.ORCID 0000-0002-5148-117X
Richard SouthworthSchool of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, U.K.
Mads S BergholtCentre for Craniofacial and Regenerative Biology, King's College London, London SE1 9RT, U.K.ORCID 0000-0003-3986-8942

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monitoring molecular dynamics in the heart is essential for advancing our understanding of cardiac physiology and biochemistry in both healthy and diseased states, as well as for guiding the development and evaluation of novel cardiac therapies. We present a multiexcitation, ratiometric fiber-optic spectroscopic platform for noninvasive, real-time monitoring of biochemical and physiological processes in isolated Langendorff-perfused rat hearts. The system employs a fiber-optic balloon probe capable of concurrent optical measurements and intraventricular pressure sensing, thereby providing complementary physiological data. A multiedge bandpass filter enables parallel fluorescence spectroscopy, allowing simultaneous detection and analysis of both exogenous and endogenous fluorophores. Coupled with multivariate regression analysis, we demonstrate the accurate quantification of fluorophore concentrations, facilitating comprehensive assessment of cardiac biochemical and functional dynamics. To mitigate geometric variability and motion artifacts, we developed a robust ratiometric approach using paired fluorescence agents. We demonstrate the system's capability by employing the fluorescent lipophilic cation tetramethylrhodamine ethyl ester (TMRE) as a noninvasive biomarker for mitochondrial membrane potential, extracting physiologically relevant metrics. This platform enables sensitive assessment of cardiac function with established fluorescent probes and holds promising potential as a versatile tool for investigating the dynamics of novel fluorophores.

Indexed as

Fiber Optic TechnologyFluorescent DyesHeartAnimalsMaleMembrane Potential, MitochondrialPerfusionRatsRats, Sprague-DawleyRhodaminesSpectrometry, FluorescenceFluorescent DyesRhodamines

Identifiers

PMID41123269
PMCPMC12590462

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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.