Evidence map›Paper›PMID 40772668›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2026

Universal Method for Covalent Attachment of Hydrogels to Diverse Polymeric Surfaces for Biomedical Applications.

Masoud Zhianmanesh, Azin Khodaei, Matthew Crago, Oliver Lotz, Sina Naficy, Fariba Dehghani, Marcela Bilek, Saber Amin Yavari, Behnam Akhavan

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

9 authors.

Masoud ZhianmaneshSchool of Biomedical Engineering, The University of Sydney, Sydney, NSW, 2006, Australia.
Azin KhodaeiDepartment of Orthopedics, Utrecht, 3584, The Netherlands.
Matthew CragoSchool of Chemical and Biomolecular Engineering, The University of Sydney, Sydney, NSW, 2006, Australia.
Oliver LotzSchool of Biomedical Engineering, The University of Sydney, Sydney, NSW, 2006, Australia.
Sina NaficySchool of Chemical and Biomolecular Engineering, The University of Sydney, Sydney, NSW, 2006, Australia.
Fariba DehghaniSchool of Chemical and Biomolecular Engineering, The University of Sydney, Sydney, NSW, 2006, Australia.
Marcela BilekSchool of Biomedical Engineering, The University of Sydney, Sydney, NSW, 2006, Australia.
Saber Amin YavariDepartment of Orthopedics, Utrecht, 3584, The Netherlands.
Behnam AkhavanSchool of Biomedical Engineering, The University of Sydney, Sydney, NSW, 2006, Australia.ORCID 0000-0002-1599-658X

Funding

Australian Research Council DE210100662Australian Research Council FL190100216Australian Research Council LP210100437
6 · The paper itself

Abstract

Hydrogels, renowned for their biocompatibility and capacity to mimic biological tissues, are integral to many biomedical applications, such as implantable devices and wound dressings. However, their poor mechanical strength and the challenge of achieving durable adhesion to polymeric surfaces have hindered their broader utility. Current methods of creating hybrid solid-hydrogel (HSH) structures often rely on complex chemical linkers, adding steps, cytotoxic risks, and scalability issues. Here, a novel, reagent-free method that covalently bonds hydrogels to polymeric substrates directly via reactive oxygen species (ROS) generated by an atmospheric pressure plasma jet (APPJ) is introduced. Through an evaporation-induced enhanced concentration (EIEC) approach, robust hydrogel layers are formed on ROS-functionalized surfaces, eliminating the need for silane-based linkers and achieving up to 60 kPa adhesion strength in wet conditions. This strategy offers robust hydrogel adhesion, reduces processing complexity, and preserves cytocompatibility, as demonstrated by the culture of human mesenchymal stem cells (hMSCs) and THP-1 derived macrophages with minimal immune response. Applicable across various hydrogels, such as gelatin methacryloyl (GelMA), chitosan, and polymeric substrates, including Teflon, polyethylene, and polycaprolactone (PCL), this dry process holds substantial promise for integration into advanced biomanufacturing systems, such as 3D bioprinters, unlocking new potentials in tissue engineering and biomedical device fabrication.

Indexed as

Biocompatible MaterialsHydrogelsPolymersCell AdhesionHumansMacrophagesMesenchymal Stem CellsPolyestersReactive Oxygen SpeciesSurface PropertiesTHP-1 CellsBiocompatible MaterialsHydrogelspolycaprolactonePolyestersPolymersReactive Oxygen Specieshydrogel coatingshydrogel immobilizationplasma surface functionalizationsolid‐hydrogel constructs

Identifiers

PMID40772668
PMCPMC12759228

What OpenQuestion holds

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LicenceCC BY
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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.