Evidence map›Paper›PMID 39291381›Full record

ArticleACS applied bio materials2024

3D Bioprinting Using Universal Fugitive Network Bioinks.

Hakan Arslan, Aneela Davuluri, Hiep H Nguyen, Byung Ran So, Juhyun Lee, Junha Jeon, Kyungsuk Yum

Abstract read
In one paragraph

Article in ACS applied bio materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Discrete 2D Material Programming for 3D Shaping and Morphogenesis-Inspired 4D Bioprinting.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Review
  4. 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

7 authors.

Hakan ArslanDepartment of Materials Science and Engineering, University of Texas at Arlington, Arlington, Texas 76019, United States.
Aneela DavuluriDepartment of Materials Science and Engineering, University of Texas at Arlington, Arlington, Texas 76019, United States.
Hiep H NguyenDepartment of Chemistry and Biochemistry, University of Texas at Arlington, Arlington, Texas 76019, United States.
Byung Ran SoDepartment of Chemistry and Biochemistry, University of Texas at Arlington, Arlington, Texas 76019, United States.ORCID 0000-0003-2171-1592
Juhyun LeeDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas 76019, United States.
Junha JeonDepartment of Chemistry and Biochemistry, University of Texas at Arlington, Arlington, Texas 76019, United States.ORCID 0000-0001-8632-8098
Kyungsuk YumDepartment of Materials Science and Engineering, University of Texas at Arlington, Arlington, Texas 76019, United States.ORCID 0000-0001-7516-7866

Funding

High spatiotemporal optical imaging to study dynamics of 3D cell motion and behavior in living organismsR35GM150947 · NIGMS · UNIVERSITY OF TEXAS ARLINGTON · PI Juhyun Lee · 2023 to 2026
$1.5M
NIGMS NIH HHS R35 GM150947
6 · The paper itself

Abstract

Three-dimensional (3D) bioprinting has emerged with potential for creating functional 3D tissues with customized geometries. However, the limited availability of bioinks capable of printing 3D structures with both high-shape fidelity and desired biological environments for encapsulated cells remains a key challenge. Here, we present a 3D bioprinting approach that uses universal fugitive network bioinks prepared by loading cells and hydrogel precursors (bioink base materials) into a 3D printable fugitive carrier. This approach constructs 3D structures of cell-encapsulated hydrogels by printing 3D structures using fugitive network bioinks, followed by cross-linking printed structures and removing the carrier from them. The use of the fugitive carrier decouples the 3D printability of bioinks from the material properties of bioink base materials, making this approach readily applicable to a range of hydrogel systems. The decoupling also enables the design of bioinks for the biological functionality of the final printed constructs without compromising the 3D printability. We demonstrate the generalizable 3D printability by printing self-supporting 3D structures of various hydrogels, including conventionally non-3D printable hydrogels and those with a low polymer content. We conduct preprinting screening of bioink base materials through 3D cell culture to select bioinks with high cell compatibility. The selected bioinks produce 3D constructs of cell-encapsulated hydrogels with both high-shape fidelity and high cell viability and proliferation. The universal fugitive network bioink platform could significantly expand 3D printable bioinks with customizable biological functionalities and the adoption of 3D bioprinting in diverse research and applied settings.

Indexed as

Biocompatible MaterialsBioprintingHydrogelsMaterials TestingPrinting, Three-DimensionalAnimalsCell SurvivalHumansInkParticle SizeTissue EngineeringTissue ScaffoldsBiocompatible MaterialsHydrogels3D bioprinting3D cell culture4D printingbioinksfugitive inkshydrogels

Identifiers

PMID39291381
PMCPMC13339714

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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.