TY - JOUR
T1 - In-Depth Investigation of Electrostatic Interaction-Based Hydrogel Shrinking for Volumetric Printing and Tissue Engineering Applications
AU - Iudin, Dmitrii
AU - Gerridzen, Léon J J A
AU - N Bernal, Paulina
AU - Schuurmans, Carl C L
AU - Neumann, Myriam
AU - Nguyen, Lam
AU - van Steenbergen, Mies J
AU - Hak, Jaimie
AU - Li, Wanlu
AU - Casadidio, Cristina
AU - van Genderen, Anne Metje
AU - Masereeuw, Rosalinde
AU - Levato, Riccardo
AU - Zhang, Yu Shrike
AU - van Ravensteijn, Bas G P
AU - Vermonden, Tina
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society.
PY - 2025/7/14
Y1 - 2025/7/14
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/105008969007
U2 - 10.1021/acs.biomac.5c00117
DO - 10.1021/acs.biomac.5c00117
M3 - Article
C2 - 40518730
SN - 1525-7797
VL - 26
SP - 4108
EP - 4123
JO - Biomacromolecules
JF - Biomacromolecules
IS - 7
ER -