Evidence map›Paper›PMID 41367193›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2026

Multi-scale Engineered Vasculature and Hierarchical Porosity via Volumetric Bioprinting-Guided Photopolymerization-Induced Phase Separation.

Oksana Y Dudaryeva, Maj-Britt Buchholz, Gabriel Größbacher, Sofia Amaral, Sammy Florczak, Camille Bonhomme, Alvaro Rojo Ferrer, Mark W Tibbitt, Riccardo Levato

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. In Situ Characterisation of Hydrogels via Dynamic Interface Printing.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  5. Review
  6. Article
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.

Oksana Y DudaryevaDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, 3584 CX, The Netherlands.
Maj-Britt BuchholzDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, 3584 CX, The Netherlands.
Gabriel GrößbacherDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, 3584 CX, The Netherlands.
Sofia AmaralDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, 3584 CX, The Netherlands.
Sammy FlorczakDepartment of Clinical Science, Faculty of Veterinary Medicine, Utrecht University, Utrecht, 3584CT, The Netherlands.
Camille BonhommeDepartment of Clinical Science, Faculty of Veterinary Medicine, Utrecht University, Utrecht, 3584CT, The Netherlands.
Alvaro Rojo FerrerDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, 3584 CX, The Netherlands.
Mark W TibbittMacromolecular Engineering Laboratory, Department of Mechanical and Process Engineering, ETH Zurich, Zurich, 8092, Switzerland.
Riccardo LevatoDepartment of Orthopaedics, University Medical Center Utrecht, Utrecht University, Utrecht, 3584 CX, The Netherlands.ORCID https://orcid.org/0000-0002-3795-3804

Funding

H2020 European Research Council 949806Horizon 2020 Framework Programme 96449Nederlandse Organisatie voor Wetenschappelijk Onderzoek OCENW.XS22.3.054Netherlands Organization for Scientific Research 024.003.013
6 · The paper itself

Abstract

Vascularization remains a major challenge in hydrogel-based engineered tissues due to the inherent nano-scale porosity of common synthetic and natural biomaterials. Critically, the confinement imposed by nanoscale networks inhibits blood vessels outgrowth, required for oxygen and nutrient delivery. Despite advancements in the biofabrication of small channels (0.1-1 mm), achieving vascularization (with capillaries down to 10 µm) throughout cm-scale bioprinted constructs remains a critical bottleneck. Herein, phase separating is integrated, cell-interactive gelatin-norbornene hydrogels with volumetric bioprinting to generate architecturally defined centimeter-scale constructs with 0.1-1mm scale printed channels and interpenetrating micron-scale porosity. This novel approach produced freeform construct designs with light-controllable micron-scale and hierarchical porosity. Importantly, this porosity enabled endothelial cell infiltration and microvessel outgrowth deep into the engineered tissue. Vascular structures formed in the pore spaces with feature sizes on the scale of capillaries (<10 µm), crucial to provide oxygen and nutrients to all regions of the hydrogel. The networks remained stable for over 14 days, outperforming classical nanoporous biomaterials. Vascular networks are perfusable in this custom-made bioreactor system and exhibited extended vessel outgrowth under perfused culture conditions. These complex hydrogel-based constructs with engineered multi-scale vascular networks have potential for generating actively perfusable advanced tissue models.

Indexed as

BioprintingTissue EngineeringAnimalsBiocompatible MaterialsGelatinHumansHuman Umbilical Vein Endothelial CellsHydrogelsNeovascularization, PhysiologicPhase SeparationPhotochemical ProcessesPolymerizationPorosityTissue ScaffoldsBiocompatible MaterialsGelatinHydrogels3D cell culturebioprintingcontrolled porosityhydrogelsperfusion

Identifiers

PMID41367193
PMCPMC12902586

What OpenQuestion holds

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LicenceCC BY
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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.