TY - JOUR
T1 - Tunable Thermoshrinkable Hydrogels for 4D Fabrication of Cell-Seeded Channels
AU - Di Marco, Greta
AU - Falandt, Marc
AU - Neumann, Myriam
AU - Viola, Martina
AU - Sampon, Thibault
AU - Valverde, Marta G.
AU - van Genderen, Anne Metje
AU - Mihaila, Silvia M.
AU - van Nostrum, Cornelus F.
AU - van Ravensteijn, Bas G.P.
AU - Levato, Riccardo
AU - Masereeuw, Rosalinde
AU - Vermonden, Tina
N1 - Publisher Copyright:
© 2025 The Author(s). Advanced Functional Materials published by Wiley-VCH GmbH.
PY - 2025/8/28
Y1 - 2025/8/28
N2 - Fabricating hydrogel-based channels with diameters below 200 µm remains challenging in advanced in vitro modeling and tissue engineering. To address this challenge, thermoshrinkable hydrogels that undergo reversible isotropic dimensional changes with temperature are developed. A thermoresponsive polymer with methacrylate groups (PNH-MA) is synthesized from polyethylene glycol (PEG), N–isopropylacrylamide (NIPAM), and 2-hydroxyethyl acrylate (HEA), enabling photo-cross-linking and precise material tuning. PNH-MA hydrogels can shrink up to 90% in volume (50% in diameter) and remain transparent allowing cellular imaging. In a four-dimension (4D) fabrication strategy, channels seeded with proximal tubule epithelial cells are shrunk to reduce diameters. Using pin pull-out mold casting, channels of 120 and 410 µm diameters are shrunk to 65 and 200 µm, respectively. While needle injection is challenging for channels smaller than 200 µm, volumetric printing addresses this limitation. The shrinkage properties enable leak-proof perfusion, allowing cell seeding and continuous unilateral flow in channels as small as 100170 µm. PNH-MA polymers represent one of the few examples of low-viscosity resins successfully used for hydrogel volumetric printing of complex scaffolds. This study highlights the potential of PNH-MA hydrogels for scalable, high-precision tubular scaffold fabrication in advanced in vitro modeling.
AB - Fabricating hydrogel-based channels with diameters below 200 µm remains challenging in advanced in vitro modeling and tissue engineering. To address this challenge, thermoshrinkable hydrogels that undergo reversible isotropic dimensional changes with temperature are developed. A thermoresponsive polymer with methacrylate groups (PNH-MA) is synthesized from polyethylene glycol (PEG), N–isopropylacrylamide (NIPAM), and 2-hydroxyethyl acrylate (HEA), enabling photo-cross-linking and precise material tuning. PNH-MA hydrogels can shrink up to 90% in volume (50% in diameter) and remain transparent allowing cellular imaging. In a four-dimension (4D) fabrication strategy, channels seeded with proximal tubule epithelial cells are shrunk to reduce diameters. Using pin pull-out mold casting, channels of 120 and 410 µm diameters are shrunk to 65 and 200 µm, respectively. While needle injection is challenging for channels smaller than 200 µm, volumetric printing addresses this limitation. The shrinkage properties enable leak-proof perfusion, allowing cell seeding and continuous unilateral flow in channels as small as 100170 µm. PNH-MA polymers represent one of the few examples of low-viscosity resins successfully used for hydrogel volumetric printing of complex scaffolds. This study highlights the potential of PNH-MA hydrogels for scalable, high-precision tubular scaffold fabrication in advanced in vitro modeling.
KW - advanced in vitro modeling
KW - kidney engineering
KW - PNIPAM
KW - temperature-driven shrinking
KW - volumetric printing
UR - https://www.scopus.com/pages/publications/105002158614
U2 - 10.1002/adfm.202502042
DO - 10.1002/adfm.202502042
M3 - Article
AN - SCOPUS:105002158614
SN - 1616-301X
VL - 35
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 35
M1 - 2502042
ER -