Evidence map›Paper›PMID 40432762›Full record

ArticleBio-protocol2025

Development of Polyethylene Glycol Diacrylate-Based Micropattern Substrate to Study the Interplay Between Surface Topography and Cellular Response for Tissue Engineering Applications.

Mohd Khairul Akma Darwis, Victoria Levario-Diaz, Sadaf Pashapour, Jonah Luka Voigt, Eloïse Lebaudy, Norhayati Sabani, Ahmad Shuhaimi Abu Bakar, Nihal Engin Vrana, Philippe Lavalle, Elisabetta Ada Cavalcanti-Adam and 1 more

Abstract read
In one paragraph

Article in Bio-protocol, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

11 authors.

Mohd Khairul Akma DarwisPresent address: Department of Biomedical Science, Advanced Medical and Dental Institute, Universiti Sains Malaysia, Kepala Batas, Penang, Malaysia.
Victoria Levario-DiazDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg, Germany.
Sadaf PashapourInstitute for Molecular Systems Engineering and Advanced Materials (IMSEAM), Heidelberg University, Heidelberg, Germany.
Jonah Luka VoigtDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg, Germany.
Eloïse LebaudyUMR_S 1121 Biomaterials and Bioengineering, Institut National de la Santé et de la Recherche Médicale, Biomedicine Research Center of Strasbourg, Strasbourg, France.
Norhayati SabaniFaculty of Electronic Engineering Technology, Universiti Malaysia Perlis, Pauh Putra Campus, Arau, Perlis, Malaysia.
Ahmad Shuhaimi Abu BakarLow Dimensional Materials Research Centre, Department of Physics, Faculty of Science, Universiti Malaya, Kuala Lumpur, Malaysia.
Nihal Engin VranaSpartha Medical, Biomedicine Research Center of Strasbourg, Strasbourg, France.
Philippe LavalleUMR_S 1121 Biomaterials and Bioengineering, Institut National de la Santé et de la Recherche Médicale, Biomedicine Research Center of Strasbourg, Strasbourg, France.
Elisabetta Ada Cavalcanti-AdamDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg, Germany.
Siti Hawa NgalimPresent address: Department of Biomedical Science, Advanced Medical and Dental Institute, Universiti Sains Malaysia, Kepala Batas, Penang, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A key goal in the bioengineering field is the development of surface patterning of proteins that guide and control cellular organization. To this end, we developed a method to create a microstructured hydrogel based on soft-lithography techniques using polydimethylsiloxane (PDMS) and polyethylene glycol diacrylate (PEGDA). This approach involves the design of microfluidic geometries using graphical software, employing PDMS as a mold and leaving PEGDA as a substrate for the fabrication of microstructures and, thus, patterning extracellular matrix (ECM) proteins to promote cell adhesion. The combination of these techniques allows the fabrication of hydrogel microstructures without following conventional photolithography methods, such as the use of a photomask, the alignment required to produce the patterns, and the associated expenses. This study highlights the versatility and potential of PEGDA-based hydrogels as platforms to advance tissue engineering strategies. Key features • This protocol focuses on investigating the feasibility of patterning PEGDA as a substrate for protein surface patterning and further tissue engineering applications. • Optimization of the fabrication of PEGDA hydrogels into simple shapes and angular patterns, ensuring a robust substrate capable of guiding cellular responses.

Indexed as

BiomaterialsMicropatternsPDMSPEGDAProtein patterning

Identifiers

PMID40432762
PMCPMC12104878

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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.