Evidence map›Paper›PMID 32526699›Full record

ArticleRedox biology2020

Non-invasive real-time imaging of reactive oxygen species (ROS) using auto-fluorescence multispectral imaging technique: A novel tool for redox biology.

Abbas Habibalahi, Mahdieh Dashtbani Moghari, Jared M Campbell, Ayad G Anwer, Saabah B Mahbub, Martin Gosnell, Sonia Saad, Carol Pollock, Ewa M Goldys

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% of its field
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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Abbas HabibalahiARC Centre of Excellence Centre for Nanoscale Biophotonics, University of New South Wales, Kensington, 2052, NSW, Australia. Electronic address: a.habibalahi@unsw.edu.au.
Mahdieh Dashtbani MoghariSchool of Biomedical Engineering, Faculty of Engineering, Darlington Campus, The University of Sydney, NSW, 2006, Australia.
Jared M CampbellARC Centre of Excellence Centre for Nanoscale Biophotonics, University of New South Wales, Kensington, 2052, NSW, Australia.
Ayad G AnwerARC Centre of Excellence Centre for Nanoscale Biophotonics, University of New South Wales, Kensington, 2052, NSW, Australia.
Saabah B MahbubARC Centre of Excellence Centre for Nanoscale Biophotonics, University of New South Wales, Kensington, 2052, NSW, Australia.
Martin GosnellQuantitative Pty Ltd, ABN 17 165 684 186, Australia.
Sonia SaadKolling Institute of Medical Research, University of Sydney, Camperdown, 2006, NSW, Australia.
Carol PollockKolling Institute of Medical Research, University of Sydney, Camperdown, 2006, NSW, Australia.
Ewa M GoldysARC Centre of Excellence Centre for Nanoscale Biophotonics, University of New South Wales, Kensington, 2052, NSW, Australia.
UNSW Sydney · AUUniversity of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detecting reactive oxygen species (ROS) that play a critical role as redox modulators and signalling molecules in biological systems currently requires invasive methods such as ROS -specific indicators for imaging and quantification. We developed a non-invasive, real-time, label-free imaging technique for assessing the level of ROS in live cells and thawed cryopreserved tissues that is compatible with in-vivo imaging. The technique is based on autofluorescence multispectral imaging (AFMI) carried out in an adapted fluorescence microscope with an expanded number of spectral channels spanning specific excitation (365 nm-495 nm) and emission (420 nm-700 nm) wavelength ranges. We established a strong quantitative correlation between the spectral information obtained from AFMI and the level of ROS obtained from CellROX staining. The results were obtained in several cell types (HeLa, PANC1 and mesenchymal stem cells) and in live kidney tissue. Additioanly,two spectral regimes were considered: with and without UV excitation (wavelengths > 400 nm); the latter being suitable for UV-sensitive systems such as the eye. Data were analyzed by linear regression combined with an optimization method of swarm intelligence. This allowed the calibration of AFMI signals to the level of ROS with excellent correlation (R = 0.84, p = 0.00) in the entire spectral range and very good correlation (R = 0.78, p = 0.00) in the limited, UV-free spectral range. We also developed a strong classifier which allowed us to distinguish moderate and high levels of ROS in these two regimes (AUC = 0.91 in the entire spectral range and AUC = 0.78 for UV-free imaging). These results indicate that ROS in cells and tissues can be imaged non-invasively, which opens the way to future clinical applications in conditions where reactive oxygen species are known to contribute to progressive disease such as in ophthalmology, diabetes, kidney disease, cancer and neurodegenerative diseases.

Indexed as

BiologyOptical ImagingHumansMicroscopy, FluorescenceOxidation-ReductionReactive Oxygen SpeciesReactive Oxygen Species

Identifiers

PMID32526699
PMCPMC7287272
OpenAlexW3025741880

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.