Evidence map›Paper›PMID 38681843›Full record

ArticleRSC advances2024

Engineering peptide-modified alginate-based bioinks with cell-adhesive properties for biofabrication.

Emine Karakaya, Luisa Gleichauf, Lisa Schöbel, Ahmed Hassan, Anahita Ahmadi Soufivand, Joerg Tessmar, Silvia Budday, Aldo R Boccaccini, Rainer Detsch

Abstract read
In one paragraph

Article in RSC advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  4. Review
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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

9 authors.

Emine KarakayaDepartment of Material Science and Engineering, Institute for Biomaterials, Friedrich-Alexander University Erlangen-Nuremberg Germany rainer.detsch@fau.de.
Luisa GleichaufDepartment of Material Science and Engineering, Institute for Biomaterials, Friedrich-Alexander University Erlangen-Nuremberg Germany rainer.detsch@fau.de.
Lisa SchöbelDepartment of Material Science and Engineering, Institute for Biomaterials, Friedrich-Alexander University Erlangen-Nuremberg Germany rainer.detsch@fau.de.
Ahmed HassanDepartment of Material Science and Engineering, Institute for Biomaterials, Friedrich-Alexander University Erlangen-Nuremberg Germany rainer.detsch@fau.de.
Anahita Ahmadi SoufivandDepartment of Mechanical Engineering, Institute of Continuum Mechanics and Biomechanics, Friedrich-Alexander-University Erlangen-Nuremberg Germany.
Joerg TessmarDepartment for Functional Materials in Medicine and Dentistry, University of Würzburg Germany.ORCID https://orcid.org/0000-0001-7057-5369
Silvia BuddayDepartment of Mechanical Engineering, Institute of Continuum Mechanics and Biomechanics, Friedrich-Alexander-University Erlangen-Nuremberg Germany.ORCID https://orcid.org/0000-0002-7072-8174
Aldo R BoccacciniDepartment of Material Science and Engineering, Institute for Biomaterials, Friedrich-Alexander University Erlangen-Nuremberg Germany rainer.detsch@fau.de.ORCID https://orcid.org/0000-0002-7377-2955
Rainer DetschDepartment of Material Science and Engineering, Institute for Biomaterials, Friedrich-Alexander University Erlangen-Nuremberg Germany rainer.detsch@fau.de.ORCID https://orcid.org/0000-0001-9383-428X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alginate (ALG) and its oxidised form alginate-dialdehyde (ADA) are highly attractive materials for hydrogels used in 3D bioprinting as well as drop-on-demand (DoD) approaches. However, both polymers need to be modified using cell-adhesive peptide sequences, to obtain bioinks exhibiting promising cell-material interactions. Our study explores the modification of ALG- and ADA-based bioinks with the adhesive peptides YIGSR (derived from laminin), RRETEWA (derived from fibronectin) and IKVAV (derived from laminin) for 3D bioprinting. Two coupling methods, carbodiimide and Schiff base reactions, were employed to modify the polymers with peptides. Analytical techniques, including FTIR and NMR were used to assess the chemical composition, revealing challenges in confirming the presence of peptides. The modified bioinks exhibited decreased stability, viscosity, and stiffness, particularly-ADA-based bioinks in contrast to ALG. Sterile hydrogel capsules or droplets were produced using a manual manufacturing process and DoD printing. NIH/3T3 cell spreading analysis showed enhanced cell spreading in carbodiimide-modified ADA, Schiff base-modified ADA, and PEG-Mal-modified ADA. The carbodiimide coupling of peptides worked for ADA, however the same was not observed for ALG. Finally, a novel mixture of all used peptides was evaluated regarding synergistic effects on cell spreading which was found to be effective, showing higher aspect ratios compared to the single peptide coupled hydrogels in all cases. The study suggests potential applications of these modified bioinks in 3D bioprinting approaches and highlights the importance of peptide selection as well as their combination for improved cell-material interactions.

Identifiers

PMID38681843
PMCPMC11046382

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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 OpenQuestion graph.