Evidence map›Paper›PMID 42729346›Full record

ArticleFrontiers in bioengineering and biotechnology2026

Initial safe(r)-by-design assessment of printable konjac-agar-pectin hydrogels for future extrusion-based bioprinting applications.

Laura Mendoza-Cerezo, Francisco Iñesta-Vaquera, Antonio Macías-García, Alfonso C Marcos-Romero, Jesús M Rodríguez-Rego

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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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

5 authors.

Laura Mendoza-CerezoDepartamento de Expresión Gráfica, Escuela de Ingenierías Industriales, Universidad de Extremadura, Badajoz, Spain.
Francisco Iñesta-VaqueraDepartamento de Bioquímica, Biología Molecular y Genética, Facultad de Ciencias, Universidad de Extremadura, Badajoz, Spain.
Antonio Macías-GarcíaDepartamento de Expresión Gráfica, Escuela de Ingenierías Industriales, Universidad de Extremadura, Badajoz, Spain.
Alfonso C Marcos-RomeroDepartamento de Expresión Gráfica, Escuela de Ingenierías Industriales, Universidad de Extremadura, Badajoz, Spain.
Jesús M Rodríguez-RegoDepartamento de Expresión Gráfica, Escuela de Ingenierías Industriales, Universidad de Extremadura, Badajoz, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Natural polysaccharide-based hydrogels are promising materials for extrusion-based 3D bioprinting, although achieving an adequate balance between cellular response, extrudability and shape fidelity remains challenging. Methods: In this study, hydrogel formulations based on konjac glucomannan, agar and citrus pectin were developed and evaluated under an initial safe(r)-by-design approach for future extrusion-based bioprinting applications. The materials were combined at different concentrations to assess their rheological behaviour, direct-contact cellular response and printability-related performance. Results: Konjac glucomannan contributed to water retention and viscosity modulation, agar provided thermal gelation and structural reinforcement, and citrus pectin modified flow behaviour and polymer-network interactions. Rheological analysis showed shear-thinning flow for all formulations, while the four selected formulations showed G' values higher than G″ throughout the 0.1-20 Hz frequency range and re-established G' > G″ after large-amplitude deformation. Increasing agar concentration generally increased stiffness and extrusion resistance, whereas pectin reduced resistance to flow and was associated with lower mean relative pore-area values in the analysed grids. The direct-contact MTS assay was interpreted as a measure of apparent metabolic activity, rather than as an absolute quantification of viable cell number, due to the possible influence of hydrogel-assay interactions. Printability-related assays showed that the pectin-free formulations, particularly 2K0.1A and 2K0.2A, exhibited higher mean relative pore-area values in the analysed grids, whereas the pectin-containing formulations showed lower extrusion resistance and improved flowability but lower mean relative pore-area values. Discussion: Overall, 2K0.1A showed the most balanced behaviour among the evaluated formulations when considering extrusion resistance, collapse performance, relative self-supporting index and the descriptive pore-area results. These results support the potential of konjac-agar-pectin hydrogels as printable natural-material platforms, while highlighting the need for further optimisation and validation under cell-laden and tissue-specific conditions.

Indexed as

3D bioprintingbiochemistrycellular responsecharacterisationhydrogelsprintability

Identifiers

PMID42729346
PMCPMC13562252

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.