Evidence map›Paper›PMID 42236802›Full record

ArticleScientific reports2026

Computational design of artificial supply networks for engineered human tissue.

Henning Bonart, Pramodt Srinivasula, Ulrike A Nuber, Steffen Hardt

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Henning BonartTechnische Universität Darmstadt, Department of Mechanical Engineering, Institute for Nano- and Microfluidics, Peter-Grünberg-Straße 10, 64287, Darmstadt, Germany.
Pramodt SrinivasulaTechnische Universität Darmstadt, Department of Mechanical Engineering, Institute for Nano- and Microfluidics, Peter-Grünberg-Straße 10, 64287, Darmstadt, Germany.
Ulrike A NuberTechnische Universität Darmstadt, Department of Biology and Department of Mechanical Engineering, Stem Cell and Developmental Biology, Schnittspahnstraße 13, 64287, Darmstadt, Germany. ulrike.nuber@tu-darmstadt.de.
Steffen HardtTechnische Universität Darmstadt, Department of Mechanical Engineering, Institute for Nano- and Microfluidics, Peter-Grünberg-Straße 10, 64287, Darmstadt, Germany. hardt@nmf.tu-darmstadt.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of large-scale, three-dimensional human tissues is crucial for various applications in therapeutic tissue engineering, disease modeling, and drug testing. However, due to the diffusion limit of oxygen, the lack of functional vascular networks is a significant limitation in maintaining these engineered tissues in the laboratory. To address this challenge, we present a systematic, model-based design process for artificial supply networks that can ensure a sufficient supply of oxygen and nutrients to engineered human tissue. Our approach combines mathematical models of fluid dynamics, cell metabolism, and network properties to identify key parameters influencing the supply performance. We demonstrate the applicability and possibilities of this design process by simulating different network structures, including cuboid and rhombic dodecahedral honeycombs, under various conditions. Our results show that the structure of the artificial supply network, oxygen concentration, and solute flow within the network strongly influence cellular metabolic activity and viability. We also examine the effects of non-uniform cell density, channel blockage, and long channel length on the oxygen distribution inside the cell-containing tissue compartment. Our findings highlight the importance of considering these factors in the design of artificial supply networks for large-scale engineered human tissues. This study provides a promising approach for quickly exploring the vast design space of possible network structures under different conditions for desired cell and tissue states, ultimately contributing to the development of more efficient and effective tissue engineering strategies.

Indexed as

Tissue EngineeringComputer SimulationHumansModels, BiologicalModels, TheoreticalOxygenOxygenArtificial supply networksCell metabolismComputational designSpecies transportTissue engineering

Identifiers

PMID42236802
PMCPMC13237089

What Socratic 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 Socratic graph.