Evidence map›Paper›PMID 39295849›Full record

ArticleFrontiers in bioengineering and biotechnology2024

Enabling 3D bioprinting of cell-laden pure collagen scaffolds via tannic acid supporting bath.

Sara Palladino, Francesco Copes, Pascale Chevallier, Gabriele Candiani, Diego Mantovani

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 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.

Sara PalladinoLaboratory for Biomaterials and Bioengineering, CRC-Tier I, Department of Mining, Metallurgy and Materials Engineering and Regenerative Medicine CHU de Québec, Laval University, Quebec City, QC, Canada.
Francesco CopesLaboratory for Biomaterials and Bioengineering, CRC-Tier I, Department of Mining, Metallurgy and Materials Engineering and Regenerative Medicine CHU de Québec, Laval University, Quebec City, QC, Canada.
Pascale ChevallierLaboratory for Biomaterials and Bioengineering, CRC-Tier I, Department of Mining, Metallurgy and Materials Engineering and Regenerative Medicine CHU de Québec, Laval University, Quebec City, QC, Canada.
Gabriele CandianiGenT_LΛB, Department of Chemistry, Materials and Chemical Engineering 'G. Natta', Politecnico di Milano, Milan, Italy.
Diego MantovaniLaboratory for Biomaterials and Bioengineering, CRC-Tier I, Department of Mining, Metallurgy and Materials Engineering and Regenerative Medicine CHU de Québec, Laval University, Quebec City, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fabrication of cell-laden biomimetic scaffolds represents a pillar of tissue engineering and regenerative medicine (TERM) strategies, and collagen is the gold standard matrix for cells to be. In the recent years, extrusion 3D bioprinting introduced new possibilities to increase collagen scaffold performances thanks to the precision, reproducibility, and spatial control. However, the design of pure collagen bioinks represents a challenge, due to the low storage modulus and the long gelation time, which strongly impede the extrusion of a collagen filament and the retention of the desired shape post-printing. In this study, the tannic acid-mediated crosslinking of the outer layer of collagen is proposed as strategy to enable collagen filament extrusion. For this purpose, a tannic acid solution has been used as supporting bath to act exclusively as external crosslinker during the printing process, while allowing the pH- and temperature-driven formation of collagen fibers within the core. Collagen hydrogels (concentration 2-6 mg/mL) were extruded in tannic acid solutions (concentration 5-20 mg/mL). Results proved that external interaction of collagen with tannic acid during 3D printing enables filament extrusion without affecting the bulk properties of the scaffold. The temporary collagen-tannic acid interaction resulted in the formation of a membrane-like external layer that protected the core, where collagen could freely arrange in fibers. The precision of the printed shapes was affected by both tannic acid concentration and needle diameter and can thus be tuned. Altogether, results shown in this study proved that tannic acid bath enables collagen bioprinting, preserves collagen morphology, and allows the manufacture of a cell-laden pure collagen scaffold.

Indexed as

3D printing supporting bathbioinkcollagenextrusion bioprintingtannic acid

Identifiers

PMID39295849
PMCPMC11408190

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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.