Evidence map›Paper›PMID 33171883›Full record

ArticleBioengineering (Basel, Switzerland)2020

Advanced Bioink for 3D Bioprinting of Complex Free-Standing Structures with High Stiffness.

Yawei Gu, Benjamin Schwarz, Aurelien Forget, Andrea Barbero, Ivan Martin, V Prasad Shastri

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Double-Network Polysaccharide-Collagen Hybrid Bioink.ACS applied materials & interfaces · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Effective and new technologies in kidney tissue engineering.Frontiers in bioengineering and biotechnology · 2024
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Double-interpenetrating nanostructured networks of marine polysaccharides possessing properties comparable to synthetic polymers.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Review
  18. 3D Printed Solutions for Spheroid Engineering and Cancer Research.International journal of molecular sciences · 2022
    Article
  19. Article
  20. Review
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

6 authors.

Yawei GuInstitute for Macromolecular Chemistry, University of Freiburg, 79104 Freiburg, Germany.ORCID 0000-0002-0597-861X
Benjamin SchwarzInstitute for Macromolecular Chemistry, University of Freiburg, 79104 Freiburg, Germany.
Aurelien ForgetInstitute for Macromolecular Chemistry, University of Freiburg, 79104 Freiburg, Germany.ORCID 0000-0002-3305-3980
Andrea BarberoTissue Engineering Laboratory, Department of Biomedicine, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.
Ivan MartinTissue Engineering Laboratory, Department of Biomedicine, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.ORCID 0000-0001-6493-0432
V Prasad ShastriInstitute for Macromolecular Chemistry, University of Freiburg, 79104 Freiburg, Germany.

Funding

China Scholarship Council Not applicableDeutsche Forschungsgemeinschaft EXC 294
6 · The paper itself

Abstract

One of the challenges in 3D-bioprinting is the realization of complex, volumetrically defined structures, that are also anatomically accurate and relevant. Towards this end, in this study we report the development and validation of a carboxylated agarose (CA)-based bioink that is amenable to 3D printing of free-standing structures with high stiffness at physiological temperature using microextrusion printing without the need for a fugitive phase or post-processing or support material (FRESH). By blending CA with negligible amounts of native agarose (NA) a bioink formulation (CANA) which is suitable for printing with nozzles of varying internal diameters under ideal pneumatic pressure was developed. The ability of the CANA ink to exhibit reproducible sol-gel transition at physiological temperature of 37 °C was established through rigorous characterization of the thermal behavior, and rheological properties. Using a customized bioprinter equipped with temperature-controlled nozzle and print bed, high-aspect ratio objects possessing anatomically-relevant curvature and architecture have been printed with high print reproducibility and dimension fidelity. Objects printed with CANA bioink were found to be structurally stable over a wide temperature range of 4 °C to 37 °C, and exhibited robust layer-to-layer bonding and integration, with evenly stratified structures, and a porous interior that is conducive to fluid transport. This exceptional layer-to-layer fusion (bonding) afforded by the CANA bioink during the print obviated the need for post-processing to stabilize printed structures. As a result, this novel CANA bioink is capable of yielding large (5-10 mm tall) free-standing objects ranging from simple tall cylinders, hemispheres, bifurcated 'Y'-shaped and 'S'-shaped hollow tubes, and cylinders with compartments without the need for support and/or a fugitive phase. Studies with human nasal chondrocytes showed that the CANA bioink is amenable to the incorporation of high density of cells (30 million/mL) without impact on printability. Furthermore, printed cells showed high viability and underwent mitosis which is necessary for promoting remodeling processes. The ability to print complex structures with high cell densities, combined with excellent cell and tissue biocompatibility of CA bodes well for the exploitation of CANA bioinks as a versatile 3D-bioprinting platform for the clinical translation of regenerative paradigms.

Indexed as

3D printingbioinkcarboxylated agaroseclinical translationalfree-standinghuman nasal chondrocytes

Identifiers

PMID33171883
PMCPMC7711998

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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.