Evidence map›Paper›PMID 42842138›Full record

ArticlePhotochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology2026

Singlet oxygen phosphorescence detection in living adherent cells in vitro.

Steffen Hackbarth, Muriel Kabus, Xiuli Zheng, Tong Mu, Ronald Sroka, Weimin Liu

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Article in Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Steffen HackbarthInstitute of Physics, Photobiophysics, Humboldt-Universität zu Berlin, Newtonstr. 15, 12489, Berlin, Germany. hacky@physik.hu-berlin.de.ORCID https://orcid.org/0000-0003-2611-5976
Muriel KabusLaser Research Laboratory and Laboratory of Tumor Immunology, LIFE Center, LMU University Hospital, LMU Munich, Fraunhoferstr. 20, 82152, Planegg, Germany.ORCID http://orcid.org/0009-0007-4427-4459
Xiuli ZhengTechnical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Tong MuTechnical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Ronald SrokaLaser Research Laboratory and Laboratory of Tumor Immunology, LIFE Center, LMU University Hospital, LMU Munich, Fraunhoferstr. 20, 82152, Planegg, Germany.
Weimin LiuTechnical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.

Funding

Bundesministerium für Ernährung und Landwirtschaft #28N203402Chinese Academy of Science PIFI Program #2024PVA0082LMU-FöFoLe-Progamm #45/2023
6 · The paper itself

Abstract

objectiveOptical detection of singlet oxygen in cells affects the investigated cells and potentially, photosensitization skews the observed results, since the generated singlet oxygen undergoes chemical reactions with cellular quenchers. For this reason, the illumination intensity has to be kept low during a measurement to avoid killing and destruction of the investigated cells. The scope of this paper is to show, that scanning detection can meet both, sufficient sensitivity and low illumination dose, for adherent cells in 6-well plates. MATERIAL AND

methodsThe individual illumination dose for cells under investigation is reduced by distributing it among a large number of adherent growing cells. Adherent cell lines were investigated with regard to singlet oxygen production by means of simultaneous fiber-coupled irradiation at 635 nm and singlet oxygen phosphorescence detection. Singlet oxygen kinetics could be measured in two different cell types incubated with different photosensitizers, by scanning a major part of the area of a confluent layer of cells in a well.

resultIn each case, singlet oxygen signals kinetics could be observed and analyzed. Incubation with increasing amounts of photosensitizer did correlate to the determined signal amplitude and photosensitizer triplet decay times.

conclusionFocused excitation and observation in combination with scanning across the whole well results in successful determination of singlet oxygen kinetics from incubated adherent cells without detaching them. Further development is required to reduce artifacts, likely originating from scattered excitation light.

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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.