Evidence mapPaperPMID 40462549Full record

ArticleACS applied materials & interfaces2025

Combating Reactive Oxygen Species (ROS) with Antioxidant Supramolecular Polymers.

Penelope E Jankoski, Zacchaeus M Wallace, Loria R DiMartino, Jessica Shrestha, Ashe M Davis, Iyanuoluwani Owolabi, Alex S Flynt, Tristan D Clemons

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Cell-Laden Supramolecular and Covalent Polymer Hydrogels for High-Shear Delivery: A Design of Experiments Approach.Chemistry of materials : a publication of the American Chemical Society · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
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.

Penelope E JankoskiSchool of Polymer Science and Engineering, University of Southern Mississippi, Hattiesburg, Mississippi 39406, United States.
Zacchaeus M WallaceSchool of Polymer Science and Engineering, University of Southern Mississippi, Hattiesburg, Mississippi 39406, United States.
Loria R DiMartinoSchool of Polymer Science and Engineering, University of Southern Mississippi, Hattiesburg, Mississippi 39406, United States.
Jessica ShresthaSchool of Polymer Science and Engineering, University of Southern Mississippi, Hattiesburg, Mississippi 39406, United States.
Ashe M DavisSchool of Polymer Science and Engineering, University of Southern Mississippi, Hattiesburg, Mississippi 39406, United States.
Iyanuoluwani OwolabiCenter for Molecular and Cellular Biosciences, University of Southern Mississippi, Hattiesburg, Mississippi 39406, United States.
Alex S FlyntDepartment of Biomedical Engineering, University of Mississippi, Oxford, Mississippi 38677, United States.
Tristan D ClemonsSchool of Polymer Science and Engineering, University of Southern Mississippi, Hattiesburg, Mississippi 39406, United States.ORCID 0000-0001-8042-0141

Funding

Mississippi INBREP20GM103476 · UNIVERSITY OF SOUTHERN MISSISSIPPI · 2025 to 2025
$4.1M
Biology the initiator: Harnessing Reactive Oxygen Species for Biocompatible PolymerizationR21EB033533 · UNIVERSITY OF SOUTHERN MISSISSIPPI · 2025 to 2025
$222k
NIBIB NIH HHS R03 EB033704NIBIB NIH HHS R21 EB033533NIGMS NIH HHS P20 GM103476NIGMS NIH HHS R15 GM120716
6 · The paper itself

Abstract

Reactive oxygen species (ROS) are highly damaging biological molecules significantly upregulated following major injuries or diseases such as heart attack, burn injury, and stroke. Despite promising preclinical results, traditional small-molecule antioxidant therapies have had limited success in clinical applications. In this study, we employed a macromolecular approach to combat ROS, demonstrating that tethering the potent biological antioxidant, glutathione, to a peptide amphiphile effectively consumes harmful extracellular radicals while preserving antioxidant and polymeric functionality. By neutralizing these radical species, we can protect vulnerable cells from acute ROS toxicity. This was validated by assessing cellular oxidative damage and survival in cell lines stimulated with tert-butyl hydroperoxide (tBHP) to induce ROS production. The antioxidant nanofibers achieved cell rescue at concentrations an order of magnitude lower than molecular glutathione, a direct result of the extracellular localization and enhancement in the proximal concentration of the glutathione moieties along the supramolecular polymer. These antioxidant supramolecular polymers offer proof of principle for a macromolecular strategy to combat the damaging effects of extracellular ROS associated with disease and injury, showcasing their efficacy at low concentrations and maintaining antioxidant capabilities when in the gelled state, providing for the potential of an antioxidant tissue regenerative scaffold.

Indexed as

AntioxidantsGlutathionePolymersReactive Oxygen SpeciesAnimalsCell LineCell SurvivalHumansMiceNanofibersOxidative Stresstert-ButylhydroperoxideAntioxidantsGlutathionePolymersReactive Oxygen Speciestert-Butylhydroperoxideantioxidantoxidative stresspeptide amphiphilesreactive oxygen speciestissue regeneration

Identifiers

PMID40462549
PMCPMC12186237

What Socratic holds

Textmetadata
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 Socratic graph.