Evidence map›Paper›PMID 40694341›Full record

ArticleACS applied materials & interfaces2025

Scalable Biofabrication of Functional 3D Scaffolds via Synergy of Autopilot Single-Jet Electrospun 3D PCL Fiber Scaffolds and Cell-Laden Hydrogels.

Balchandar Navaneethan, Mehdi Salar Amoli, Yen-Ching Yang, Sarah Rezapourdamanab, Chiao-Yu Tseng, Yamini Singh, Chin-Lin Guo, Vahid Serpooshan, Chia-Fu Chou

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Balchandar NavaneethanInstitute of Physics, Academia Sinica, Taipei 11529, Taiwan, ROC.
Mehdi Salar AmoliWallace H. Coulter Department of Biomedical Engineering, Emory University School of Medicine and Georgia Institute of Technology, Atlanta, Georgia 30322, United States.
Yen-Ching YangInstitute of Physics, Academia Sinica, Taipei 11529, Taiwan, ROC.
Sarah RezapourdamanabWallace H. Coulter Department of Biomedical Engineering, Emory University School of Medicine and Georgia Institute of Technology, Atlanta, Georgia 30322, United States.
Chiao-Yu TsengInstitute of Physics, Academia Sinica, Taipei 11529, Taiwan, ROC.
Yamini SinghWallace H. Coulter Department of Biomedical Engineering, Emory University School of Medicine and Georgia Institute of Technology, Atlanta, Georgia 30322, United States.
Chin-Lin GuoInstitute of Physics, Academia Sinica, Taipei 11529, Taiwan, ROC.
Vahid SerpooshanWallace H. Coulter Department of Biomedical Engineering, Emory University School of Medicine and Georgia Institute of Technology, Atlanta, Georgia 30322, United States.ORCID 0000-0002-5304-095X
Chia-Fu ChouInstitute of Physics, Academia Sinica, Taipei 11529, Taiwan, ROC.ORCID 0000-0003-0070-5556

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

3D bioprinting enables cell-laden hydrogel construct fabrication in a layer-by-layer fashion but faces scalability challenges due to the mechanical weakness of hydrogels. Matrix reinforcement compromises cellular activity, creating a scalability-functionality trade-off that remains unresolved as sophisticated strategies including sequential and embedded printing fail to effectively overcome these limitations. This study presents an alternative approach by integrating autopilot single-jet electrospun (AJ-3D ES) 3D PCL fiber scaffolds with hydrogels, achieving anatomical precision, mechanical robustness, and enhanced cell function. Hydrogel dip-coating of anatomically structured PCL scaffolds enabled organ-scale cellular constructs. By providing an ECM-mimicking porous fiber network, embedded cells mitigated the limitations of hydrogel stiffness (even ∼50 kPa) and facilitated cell-cell interactions, supporting epithelialization, fibroblast clustering, and 3D phase-separated HepG2-HUVEC co-cultures. Contour 3D bioprinting along PCL fiber scaffold topographies facilitated endothelial patterning for vascularization and native-tissue mimicking complexity. Volumetric scalability was demonstrated through hydrogel casting, embedded bioprinting, and modular stacking within 3D PCL fiber scaffolds, ensuring hydrogel integrity while maintaining medium diffusion for sustained cell survival and function. In vivo studies confirmed the proangiogenic nature of PCL fiber scaffolds with tissue bridging via cell infiltration and ECM collagen deposition, underscoring clinical translational potential. By integrating topographic and volumetric flexibility, this approach advances biofabrication strategies for functional tissue and organ constructs.

Indexed as

BioprintingHydrogelsPolyestersPrinting, Three-DimensionalTissue ScaffoldsAnimalsHep G2 CellsHumansHuman Umbilical Vein Endothelial CellsMiceTissue EngineeringHydrogelspolycaprolactonePolyesters3D bioprintingBiofabricationcell-laden hydrogelselectrospinningfunctional constructsPCL fiber

Identifiers

PMID40694341
PMCPMC12400274

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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.