Evidence map›Paper›PMID 40518730›Full record

ArticleBiomacromolecules2025

In-Depth Investigation of Electrostatic Interaction-Based Hydrogel Shrinking for Volumetric Printing and Tissue Engineering Applications.

Dmitrii Iudin, Léon J J A Gerridzen, Paulina N Bernal, Carl C L Schuurmans, Myriam Neumann, Lam Nguyen, Mies J van Steenbergen, Jaimie Hak, Wanlu Li, Cristina Casadidio and 6 more

Abstract read
In one paragraph

Article in Biomacromolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Dmitrii Iudin
Léon J J A GerridzenORCID 0009-0002-4485-2187
Paulina N BernalDepartment of Orthopedics, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.
Carl C L SchuurmansDivision of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, Massachusetts 02139, United States.
Lam Nguyen
Mies J van Steenbergen
Jaimie Hak
Wanlu LiDivision of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, Massachusetts 02139, United States.
Cristina CasadidioSchool of Pharmacy, ChIP Research Center, University of Camerino, Via Madonna delle Carceri, 62032 Camerino, MC, Italy.ORCID 0000-0002-3925-7087
Anne Metje van Genderen
Rosalinde MasereeuwORCID 0000-0002-1560-1074
Riccardo LevatoDepartment of Orthopedics, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.
Yu Shrike ZhangDivision of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, Massachusetts 02139, United States.ORCID 0000-0002-0045-0808
Bas G P van RavensteijnORCID 0000-0001-9024-3927

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Three-dimensional printing of hydrogels enables the fabrication of complex structures for tissue engineering. Postprinting shrinking via electrostatic interactions offers a promising strategy to better replicate the size and intricacy of native tissues. This study explores hyaluronic acid (HA)-based hydrogels that undergo shrinking upon polycation penetration and complexation focusing on the influence of the HA macromer concentration, molecular weight, cross-linking density, hydrogel initial volume, and polycation properties on shrinking efficiency. To support cell adhesion, RGD peptides were incorporated into the HA network. The polycation concentration strongly affected cell viability: a high concentration of 1 wt % resulted in reduced viability, while 0.1 wt % preserved it with effective shrinkage. Volumetrically printed structures were reduced up to 9 times in volume, achieving features as small as 42 ± 6 μm. This shrinking approach enables the fabrication of hydrogel structures with significantly reduced dimensions, making it a powerful tool for developing high-precision hydrogel structures for tissue engineering.

Indexed as

Hyaluronic AcidHydrogelsPrinting, Three-DimensionalTissue EngineeringAnimalsCell AdhesionCell SurvivalHumansOligopeptidesStatic Electricityarginyl-glycyl-aspartic acidHyaluronic AcidHydrogelsOligopeptides

Identifiers

PMID40518730
PMCPMC12273623

What OpenQuestion holds

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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.