TY - JOUR
T1 - Self-Degradation of Digital Light 3D Printed Covalent Cross-Linked Hydrogel at Ambient Temperature
AU - Liang, Chen
AU - Chu, Ang
AU - Lu, Zhe
AU - Feng, Shiwei
AU - Liu, Fukang
AU - Cui, Jingjing
AU - Guo, Yunlong
AU - Gao, Weizi
AU - Zhang, Biao
N1 - Publisher Copyright:
© 2025 American Chemical Society
PY - 2025/7/28
Y1 - 2025/7/28
N2 - Photocuring-based three-dimensional (3D) printed hydrogels have versatile applications in various fields. However, the heterogeneous network with nanogel cross-linking points during free radical polymerization (FRP) often results in hydrogels that are unable to degrade or be reprocessed, significantly limiting their applications. Herein, a UV-curable reversible addition–fragmentation chain transfer (RAFT)-mediated hydrogel system compatible with digital light processing (DLP) 3D printing is reported, enabling the fabrication of complex hydrogel structures with rapid, controlled degradation and self-degradation capabilities at ambient temperature. The enhanced degradability stems from the synergistic combination of the hydrolyzable bonds and RAFT chemistry. The hydrogel precursors exhibit optimal rheological properties, while the mechanical properties of the resulting hydrogels are precisely tunable by adjusting the cross-linker content and water content. Degradation kinetics can be systematically controlled by adjusting the cross-linker content, water content, and the treatment temperature. Hydrogels containing 50 wt % water content demonstrate complete degradation into molecular chain segments and/or molecules within 6 h at 37 °C. Furthermore, the 3D printed RAFT-mediated hydrogels can self-degrade at ambient temperature. After self-degradation, the resulting solution exhibits the unsaturated acrylic functional molecules with the characteristic of high viscosity, which can be directly used for UV-assisted direct ink writing (DIW) to refabricate new 3D hydrogel structures.
AB - Photocuring-based three-dimensional (3D) printed hydrogels have versatile applications in various fields. However, the heterogeneous network with nanogel cross-linking points during free radical polymerization (FRP) often results in hydrogels that are unable to degrade or be reprocessed, significantly limiting their applications. Herein, a UV-curable reversible addition–fragmentation chain transfer (RAFT)-mediated hydrogel system compatible with digital light processing (DLP) 3D printing is reported, enabling the fabrication of complex hydrogel structures with rapid, controlled degradation and self-degradation capabilities at ambient temperature. The enhanced degradability stems from the synergistic combination of the hydrolyzable bonds and RAFT chemistry. The hydrogel precursors exhibit optimal rheological properties, while the mechanical properties of the resulting hydrogels are precisely tunable by adjusting the cross-linker content and water content. Degradation kinetics can be systematically controlled by adjusting the cross-linker content, water content, and the treatment temperature. Hydrogels containing 50 wt % water content demonstrate complete degradation into molecular chain segments and/or molecules within 6 h at 37 °C. Furthermore, the 3D printed RAFT-mediated hydrogels can self-degrade at ambient temperature. After self-degradation, the resulting solution exhibits the unsaturated acrylic functional molecules with the characteristic of high viscosity, which can be directly used for UV-assisted direct ink writing (DIW) to refabricate new 3D hydrogel structures.
KW - Controlled Degradation
KW - Digital Light 3D Printing
KW - Hydrogels
KW - RAFT
KW - Refabrication
KW - Self-Degradation
UR - https://www.scopus.com/pages/publications/105010639667
U2 - 10.1021/acssuschemeng.5c02690
DO - 10.1021/acssuschemeng.5c02690
M3 - 文章
AN - SCOPUS:105010639667
SN - 2168-0485
VL - 13
SP - 11315
EP - 11323
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 29
ER -