Evidence map›Paper›PMID 42738082›Full record

ReviewMaterials (Basel, Switzerland)2026

Generation of Human Bioartificial Tissues Using Agarose-Derived Biomaterials.

Fernando Campos, Jesús Chato-Astrain, Miguel Ángel Martín-Piedra, Óscar Darío García-García, David Sánchez-Porras, Miguel Etayo-Escanilla, Paula Ávila-Fernández, Ingrid Garzón, Miguel Alaminos

Abstract readReview
In one paragraph

Review in Materials (Basel, Switzerland), 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

9 authors.

Fernando CamposTissue Engineering Group, Department of Histology, School of Medicine, University of Granada, E18016 Granada, Spain.ORCID 0000-0003-0034-9264
Jesús Chato-AstrainTissue Engineering Group, Department of Histology, School of Medicine, University of Granada, E18016 Granada, Spain.ORCID 0000-0002-2378-2696
Miguel Ángel Martín-PiedraTissue Engineering Group, Department of Histology, School of Medicine, University of Granada, E18016 Granada, Spain.ORCID 0000-0002-4639-3175
Óscar Darío García-GarcíaTissue Engineering Group, Department of Histology, School of Medicine, University of Granada, E18016 Granada, Spain.ORCID 0000-0002-4710-0733
David Sánchez-PorrasTissue Engineering Group, Department of Histology, School of Medicine, University of Granada, E18016 Granada, Spain.ORCID 0000-0002-4755-7741
Miguel Etayo-EscanillaTissue Engineering Group, Department of Histology, School of Medicine, University of Granada, E18016 Granada, Spain.ORCID 0009-0000-9205-7933
Paula Ávila-FernándezTissue Engineering Group, Department of Histology, School of Medicine, University of Granada, E18016 Granada, Spain.ORCID 0000-0002-0328-4112
Ingrid GarzónTissue Engineering Group, Department of Histology, School of Medicine, University of Granada, E18016 Granada, Spain.ORCID 0000-0001-5944-0578
Miguel AlaminosTissue Engineering Group, Department of Histology, School of Medicine, University of Granada, E18016 Granada, Spain.ORCID 0000-0003-4876-2672

Funding

Consejería de Universidad, Investigación e Innovación, Junta de Andalucía DGP_PIDI_2024_00361 and DGP_PIDI_2024_01347European UnionInstituto de Salud Carlos III FIS PI25/00002, FIS PI24/00006, and FIS PI23/00335
6 · The paper itself

Abstract

Agarose is a thermoreversible, highly biocompatible polysaccharide increasingly used in tissue engineering (TE). Its molecular architecture, optical clarity, tunable mechanics, and chemical inertness make agarose hydrogels attractive scaffolds for generating bioartificial tissues by TE. This review summarizes current knowledge on agarose extraction, purification, structural variants, and physicochemical properties regarding gelation behavior, stiffness, porosity, and bioactivity. We discuss how agarose type and concentration critically determine hydrogel biomechanical and optical performance, influencing cell behavior and in vivo suitability. Although biologically inert, agarose can be functionalized or combined with fibrin, collagen, chitosan, and other biomaterials to enhance cell adhesion, proliferation, and differentiation. Diverse biofabrication approaches-including micromolding, bead production, 3D bioprinting, and de novo assembly of cells, biomaterials and bioactive factors-have enabled the generation of microtissues, organoids, and complex multilayered constructs. Agarose-based biomaterials allowed for the successful generation of bioartificial substitutes of cartilage, bone, adipose tissue, skin, cornea, oral mucosa, and the peripheral nerve, with several fibrin-agarose advanced therapy medicinal products (ATMP) already reaching clinical application, including the skin substitute UGRSKIN, the artificial cornea NANOULCOR and the palate mucosa BIOCLEFT. Together, current evidence positions agarose as a versatile and translationally relevant biomaterial for next-generation TE, warranting further exploration of its potential in additional therapeutic contexts.

Indexed as

agarosebiomaterialstissue engineering

Identifiers

PMID42738082
PMCPMC13566688

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.