Evidence map›Paper›PMID 42454289›Full record

ArticleCellular and molecular bioengineering2026

Non-linear Characterization of Commercial and Decellularized Hydrogels: Statistical Framework Enhanced by Bayesian Optimization.

D E García-García, D Marques, H Amaveda, M Mora, J Asín, I Villaoslada, P M Baptista, M A Pérez, J M García-Aznar

Abstract read
In one paragraph

Article in Cellular and molecular bioengineering, 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
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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

9 authors.

D E García-GarcíaMultiscale in Mechanical and Biological Engineering, Instituto de Investigación en Ingeniería de Aragón (I3A), University of Zaragoza, 50014 Zaragoza, Spain.
D MarquesMultiscale in Mechanical and Biological Engineering, Instituto de Investigación en Ingeniería de Aragón (I3A), University of Zaragoza, 50014 Zaragoza, Spain.
H AmavedaInstituto de Nanociencia y Materiales de Aragón (INMA), CSIC-Universidad de Zaragoza, 50018 Zaragoza, Spain.
M MoraInstituto de Nanociencia y Materiales de Aragón (INMA), CSIC-Universidad de Zaragoza, 50018 Zaragoza, Spain.
J AsínDepartment of Statistical Methods, University Institute of Mathematics (IUMA), University of Zaragoza, 50009 Zaragoza, Spain.
I VillaosladaMultiscale in Mechanical and Biological Engineering, Instituto de Investigación en Ingeniería de Aragón (I3A), University of Zaragoza, 50014 Zaragoza, Spain.
P M BaptistaInstituto de Investigación Sanitaria de Aragón (IIS Aragón), 50009 Zaragoza, Spain.
M A PérezMultiscale in Mechanical and Biological Engineering, Instituto de Investigación en Ingeniería de Aragón (I3A), University of Zaragoza, 50014 Zaragoza, Spain.
J M García-AznarMultiscale in Mechanical and Biological Engineering, Instituto de Investigación en Ingeniería de Aragón (I3A), University of Zaragoza, 50014 Zaragoza, Spain.ORCID 0000-0002-9864-7683

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scope: Hydrogels are widely used in the design of tissue substitutes because of their ability to mimic the extracellular matrix (ECM). Their mechanical cues critically influence the cellular response, making accurate characterization essential. However, it remains challenging due to their intricate nature. This study computationally evaluates the hyperelastic properties of next-generation hydrogels of high biomedical interest, including basal membrane extract and decellularized liver matrices, as well as structural proteins. Methods: We present a combined framework based on Bayesian optimization and statistical analyses that go beyond classical least-squares fitting, leveraging rheological experimental data. It defines each hyperelastic strain-energy density function, and addresses both intra- and inter-sample variability. This approach quantifies uncertainty and reveals the natural variability that deterministic models overlook, and it also enables quantification of coefficient variation with composition. Results: Validation against experimental data shows computational fits of 5% error in most cases, and low calculation time. Analyses reveal that composition-collagen addition, fibrin concentration, and decellularized extracellular matrix (dECM) age-modulate initial stiffness, nonlinearity, and overall mechanical resistance of the hydrogels. Conclusion: Hydrogels derived from basal membrane extracts exhibit comparable non-linear mechanics, while collagen addition reduces stiffness and nonlinearity. In fibrin-based hydrogels with decellularized liver matrix, mechanical behavior is concentration and age-dependent. Such insights are highly relevant for mechanobiology, enabling prediction of how cells sense mechanical cues and scaffold composition influences in vivo interactions. Supplementary Information: The online version of this article (10.1007/s12195-026-00913-1) contains supplementary material, which is available to authorized users.

Indexed as

Bayesian optimizationComputational mechanical characterizationHyperelasticityInter- and intra-sample variabilityStatistical analysis

Identifiers

PMID42454289
PMCPMC13365100

What Socratic holds

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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 Socratic graph.