Evidence map›Paper›PMID 42683595›Full record

ArticleMacromolecular bioscience2026

Gelatin Methacrylate as a Mesenchymal Stem Cell Delivery Vehicle: Experimental and Semi-Quantitative Evaluation Under Metabolic Stress.

Pratima Yadav, Anwesha Mukherjee, Bodhisatwa Das

Abstract read
In one paragraph

Article in Macromolecular bioscience, 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

3 authors.

Pratima YadavDepartment of Biomedical Engineering, Indian Institute of Technology Ropar, Rupnagar, Punjab, India.
Anwesha MukherjeeDepartment of Biomedical Engineering, Indian Institute of Technology Ropar, Rupnagar, Punjab, India.
Bodhisatwa DasDepartment of Biomedical Engineering, Indian Institute of Technology Ropar, Rupnagar, Punjab, India.ORCID https://orcid.org/0000-0002-1447-9089

Funding

Department of Biotechnology, Government of IndiaIndian Institute of Technology RoparMinistry of Human Resource and Development (MHRD), Government of India
6 · The paper itself

Abstract

Stem cell-based therapies derived from various sources hold significant potential in regenerative medicine due to their unique properties, particularly their ability to differentiate, self-renew, and modulate the immune system. A polymer-encapsulated Mesenchymal stem cell (MSC) approach can create protective environments for stem cells, enhancing overall therapeutic efficacy. Gelatin Methacrylate (GelMA) is used as a model extracellular matrix to encapsulate MSCs for potential applications in cell-based therapy and bioprinting. This study aims to understand the limitations of GelMA-encapsulation-based cell therapy for an injured tissue. Due to the harsh microenvironment at the implantation site, directly injected stem cells for treatment are affected by factors such as nutrient and oxygen deprivation, immune rejection, reduced cell retention, and inflammatory cytokines. In the current study, we tried to mimic this system. We optimized the GelMA hydrogel cell-encapsulation composition from synthesis through physicochemical characterization, and then tested its cytocompatibility with MSCs. We have further performed numerical modeling to understand and control the behavior of MSCs within the 3D GelMA hydrogel construct under varying metabolic and immunological stress microenvironmental conditions, thereby optimizing the boundary conditions of GelMA-based cell delivery systems.

Indexed as

GelatinMesenchymal Stem CellsMesenchymal Stem Cell TransplantationMethacrylatesStress, PhysiologicalAnimalsHumansHydrogelsGelatinHydrogelsMethacrylatesencapsulationGelMAgrowth kineticsmesenchymal stem cellsmicro‐environment

Identifiers

PMID42683595
PMCPMC13535904

What OpenQuestion holds

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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.