<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Iudin D</submitter><funding>European Research Council</funding><funding>Dutch Research Council (NWO)</funding><pagination>4108-4123</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12273623</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(7)</volume><pubmed_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 effectiv</pubmed_abstract><journal>Biomacromolecules</journal><pubmed_title>In-Depth Investigation of Electrostatic Interaction-Based Hydrogel Shrinking for Volumetric Printing and Tissue Engineering Applications.</pubmed_title><pmcid>PMC12273623</pmcid><funding_grant_id>022.006.003</funding_grant_id><funding_grant_id>18673</funding_grant_id><funding_grant_id>101115643</funding_grant_id><pubmed_authors>Iudin D</pubmed_authors><pubmed_authors>Levato R</pubmed_authors><pubmed_authors>Gerridzen LJJA</pubmed_authors><pubmed_authors>Neumann M</pubmed_authors><pubmed_authors>Nguyen L</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Casadidio C</pubmed_authors><pubmed_authors>van Genderen AM</pubmed_authors><pubmed_authors>Hak J</pubmed_authors><pubmed_authors>Masereeuw R</pubmed_authors><pubmed_authors>Vermonden T</pubmed_authors><pubmed_authors>N Bernal P</pubmed_authors><pubmed_authors>van Ravensteijn BGP</pubmed_authors><pubmed_authors>Schuurmans CCL</pubmed_authors><pubmed_authors>Zhang YS</pubmed_authors><pubmed_authors>van Steenbergen MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>In-Depth Investigation of Electrostatic Interaction-Based Hydrogel Shrinking for Volumetric Printing and Tissue Engineering Applications.</name><description>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 effectiv</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-03-18T14:01:12.538Z</modification><creation>2025-08-23T03:06:24.652Z</creation></dates><accession>S-EPMC12273623</accession><cross_references><pubmed>40518730</pubmed><doi>10.1021/acs.biomac.5c00117</doi></cross_references></HashMap>