Evidence map›Paper›PMID 41618075›Full record

ArticlePharmaceutical research2026

Naringenin Loaded Hydrogel Supports Wound Repair in a Cell Model of Diabetic Skin.

Mandeep Kaur Marwah, Yukta Sameer Hindalekar, Karan Rana, Hala Shokr, Mohamad Anas Al Tahan, Lissette Sanchez-Aranguren, Maymunah Sarr, Rosie Kainth, Parmida Babaei, Humaa Asif and 2 more

Abstract read
In one paragraph

Article in Pharmaceutical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Mandeep Kaur MarwahAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK. m.marwah1@aston.ac.uk.ORCID http://orcid.org/0000-0003-4881-003X
Yukta Sameer HindalekarAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Karan RanaSchool of Biosciences, College of Health and Life Sciences, Aston University, Birmingham, UK.
Hala ShokrPharmacy Division, School of Health Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Mohamad Anas Al TahanAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Lissette Sanchez-ArangurenAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Maymunah SarrChemical Engineering and Biotechnologies, College of Engineering and Physical Sciences, Aston University, Aston Triangle, Birmingham, B4 7ET, UK.
Rosie KainthAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Parmida BabaeiAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Humaa AsifSchool of Biosciences, College of Health and Life Sciences, Aston University, Birmingham, UK.
Shakil AhmadAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Anisa MahomedChemical Engineering and Biotechnologies, College of Engineering and Physical Sciences, Aston University, Aston Triangle, Birmingham, B4 7ET, UK. a.mahomed2@aston.ac.uk.ORCID http://orcid.org/0000-0002-3719-7543

Funding

Breakthrough T1D UK 1-SGA-2024-0002
6 · The paper itself

Abstract

introductionDiabetic foot ulcers are a major complication of diabetes, driven by inflammation, oxidative stress, and poor vascular function. Naringenin, a citrus flavonoid, addresses these factors but has low solubility and stability. We developed a Na-AMPS hydrogel dressing to enhance its delivery under diabetic-like conditions.

methodsA Na-AMPS hydrogel containing 0.02%(w/w) naringenin was formulated and assessed for rheological and adhesive properties, drug release, and biological activity in HUVEC and HDFa cells. Cytotoxicity (XTT), reactive oxygen species (ROS), mitochondrial membrane potential (TMRM), cytokine levels (IL-6, IL-8, MMP-9, TGF-β), and wound closure (scratch assay) were measured. RESULTS/DISCUSSION: Naringenin modestly reduced the hydrogel elastic modulus (15,791.5 ± 1965 Pa at 30 Hz) without affecting adhesion. Release studies showed rapid drug release from solution but sustained release from hydrogels (17.88 ± 2.61% over 24 h). Under hyperglycaemic and pro-inflammatory conditions, naringenin significantly decreased ROS in HUVECs (41,030.58 ± 2737 to 31,778.74 ± 1822 AU; p < 0.001) and HDFa cells (38,188.13 ± 4593 to 29,950.94 ± 1426 AU; p < 0.05). Naringenin improved mitochondrial membrane potential in both cell types (p < 0.05-0.01) and attenuated pro-inflammatory cytokines. IL-6 decreased in HUVECs (39.40 ± 5.02 to 27.15 ± 3.10 pg/mL; p < 0.01) and HDFa cells (40.05 ± 2.23 to 16.41 ± 1.27 pg/mL; p < 0.0001). In HDFa's, MMP-9 was reduced (403.43 ± 18.70 to 195.33 ± 11.02 pg/mL; p < 0.0001), while in HUVECs, wound closure was enhanced.

conclusionNaringenin-loaded Na-AMPS hydrogels demonstrated sustained release, suitable mechanical properties, and significant antioxidant, anti-inflammatory, and wound healing effects. These findings highlight their therapeutic potential for diabetic wounds treatment.

Indexed as

FlavanonesHydrogelsSkinWound HealingCell LineCytokinesDrug LiberationFibroblastsHumansHuman Umbilical Vein Endothelial CellsMembrane Potential, MitochondrialOxidative StressReactive Oxygen SpeciesCytokinesFlavanonesHydrogelsnaringeninReactive Oxygen SpeciesControlled-releaseDiabetic wound healingHydrogelInflammationNaringenin biological activityTopical drug delivery

Identifiers

PMID41618075
PMCPMC13076458

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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.