Evidence map›Paper›PMID 42431294›Full record

ArticleExperimental eye research2026

Understanding the effects of ciprofloxacin on corneal epithelial cells: a study using electric cell-substrate impedance sensing (ECIS) technology.

Loveleen Banga, Mohamed Shawky, Faazeela Ebrahim, Raisa Chowdhury, Alyssa Kuhl, Abdul Shukkur Ebrahim, Elizabeth Berger

Abstract read
In one paragraph

Article in Experimental eye research, 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

7 authors.

Loveleen BangaDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: loveleen.banga@med.wayne.edu.
Mohamed ShawkyDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: mohamedshawky@wayne.edu.
Faazeela EbrahimDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: fa6180@wayne.edu.
Raisa ChowdhuryDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: raisac0923@gmail.com.
Alyssa KuhlDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: alyssaakuhl@gmail.com.
Abdul Shukkur EbrahimDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: eabdulsh@med.wayne.edu.
Elizabeth BergerDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: eberger@med.wayne.edu.

Funding

VISION RESEARCH--COREP30EY004068 · NEI · WAYNE STATE UNIVERSITY · PI LINDA D HAZLETT · 1985 to 2026
$13.2M
Thymosin beta-4 as an Adjunct Treatment for Bacterial KeratitisR01EY029836 · NEI · WAYNE STATE UNIVERSITY · PI BERGER, ELIZABETH · 2019 to 2023
$1.9M
The Role of Eosinophils in Modulating the Corneal Response to InfectionR01EY036697 · NEI · WAYNE STATE UNIVERSITY · PI Elizabeth Berger · 2025 to 2026
$1.2M
NEI NIH HHS P30 EY004068NEI NIH HHS R01 EY029836NEI NIH HHS R01 EY036697
6 · The paper itself

Abstract

Ciprofloxacin (CPFX) is a widely used ocular antibiotic, but its effects on ocular surface cells remain unclear. Mechanistic investigations into the efficacy of thymosin beta-4 (Tβ4) as an adjunct to CPFX in treating Pseudomonas aeruginosa keratitis revealed off-target effects of the antibiotic. Subsequently, an in vitro approach was used to elucidate the impact of CPFX on corneal epithelial cells, both alone and in combination with Tβ4. Electric cell-substrate impedance sensing (ECIS) was used to directly analyze cell behavior. CPFX demonstrated biphasic effects, characterized by early alterations in impedance (<24 h), followed by significant disruption of the cell monolayer thereafter. Although Tβ4 improved wound healing and barrier function, the disruptive effects of CPFX were not fully mitigated. The negative impact of the antibiotic was concentration-dependent and mirrored by its concentration-dependent toxicity. Western blot analysis demonstrated concentration-dependent alterations in apoptotic signaling that paralleled reductions in cell viability. Collectively, these findings indicate that CPFX exerts concentration-dependent cytotoxic effects accompanied by altered apoptotic signaling on corneal epithelial cells, with early stress-related changes preceding cellular damage. These findings highlight the importance of cautious interpretation of early time points and careful consideration of CPFX use in contexts where epithelial integrity and wound healing are paramount.

Indexed as

Anti-Bacterial AgentsCiprofloxacinEpithelium, CornealEye Infections, BacterialAnimalsApoptosisBlotting, WesternCells, CulturedCell SurvivalElectric ImpedanceHumansPseudomonas aeruginosaPseudomonas InfectionsThymosin beta(4)Wound HealingAnti-Bacterial AgentsCiprofloxacinThymosin beta(4)CiprofloxacinCorneal epithelial cellsECIS

Identifiers

PMID42431294
PMCPMC13477596

What OpenQuestion holds

Textmetadata
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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.