TY - JOUR
T1 - Highly Strong and Transparent Hydrogel Elastomers Microfabricated for 3D Microphysiological Systems
AU - Li, Wenxiu
AU - Li, Lianxin
AU - He, Huimin
AU - Peng, Wang
AU - Zhou, Zhengdong
AU - Wu, Wanqing
AU - Lv, Dong
AU - Chen, Yaqing
AU - Pan, Wending
AU - Zhou, Xiaoyu
AU - Yin, Jun
AU - Yang, Mengsu
PY - 2025/7/23
Y1 - 2025/7/23
N2 - 3D microarchitected hydrogels have recently been exploited to establish microphysiological systems for preclinical studies. However, promising hydrogels, unlike anhydrous elastomers, which have been widely adopted for device microfabrication, are still scarce for biodevice engineering due to their limitations in mechanical properties and manufacturability. Here, we leverage temperature-controlled physical cross-linking of a polymer network to generate highly strong, elastic, and transparent hydrogels, which can be further readily microfabricated into elaborate constructs for diverse device designs. Specifically, with the addition of a good solvent of dimethyl sulfoxide, poly(vinyl alcohol) dissolved in the mixed solvent of dimethyl sulfoxide/water (4:1) shows extensive physical cross-links of nanosized polymeric crystallites upon one single freeze-thaw cycle, leading to the resulting hydrogels (similar to 80% water content) with superior mechanical properties and optical transparency, comparable to or even exceeding the anhydrous elastomer of polydimethylsiloxane. Furthermore, the simple processing technologies enable the patterning of hydrogels (high resolution of 20 μm) customized for various in vitro models, as exemplified by hydrogel microwell arrays supporting efficient tumor-spheroid generation and hydrogel microchannels lined with a confluent endothelial monolayer. This approach to fabricating microphysiological systems on hydrogel platforms will provide new avenues for technological innovation in disease models, organ-on-a-chip, and personalized medicine. © 2025 The Authors. Published by American Chemical Society
AB - 3D microarchitected hydrogels have recently been exploited to establish microphysiological systems for preclinical studies. However, promising hydrogels, unlike anhydrous elastomers, which have been widely adopted for device microfabrication, are still scarce for biodevice engineering due to their limitations in mechanical properties and manufacturability. Here, we leverage temperature-controlled physical cross-linking of a polymer network to generate highly strong, elastic, and transparent hydrogels, which can be further readily microfabricated into elaborate constructs for diverse device designs. Specifically, with the addition of a good solvent of dimethyl sulfoxide, poly(vinyl alcohol) dissolved in the mixed solvent of dimethyl sulfoxide/water (4:1) shows extensive physical cross-links of nanosized polymeric crystallites upon one single freeze-thaw cycle, leading to the resulting hydrogels (similar to 80% water content) with superior mechanical properties and optical transparency, comparable to or even exceeding the anhydrous elastomer of polydimethylsiloxane. Furthermore, the simple processing technologies enable the patterning of hydrogels (high resolution of 20 μm) customized for various in vitro models, as exemplified by hydrogel microwell arrays supporting efficient tumor-spheroid generation and hydrogel microchannels lined with a confluent endothelial monolayer. This approach to fabricating microphysiological systems on hydrogel platforms will provide new avenues for technological innovation in disease models, organ-on-a-chip, and personalized medicine. © 2025 The Authors. Published by American Chemical Society
KW - poly(vinyl alcohol)hydrogel
KW - mechanical robustness
KW - transparency
KW - microfabrication
KW - microphysiologicalsystems
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:001526027600001
UR - http://www.scopus.com/inward/record.url?scp=105010184692&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-105010184692&origin=recordpage
U2 - 10.1021/acsami.5c07880
DO - 10.1021/acsami.5c07880
M3 - RGC 21 - Publication in refereed journal
C2 - 40637032
SN - 1944-8244
VL - 17
SP - 42394
EP - 42406
JO - ACS Applied Materials & Interfaces
JF - ACS Applied Materials & Interfaces
IS - 29
ER -