TY - JOUR
T1 - A Janus hydrogel with thermostatic photothermal regulation and temperature-responsive drug release for infected wound management
AU - Lyu, Chen
AU - Wang, Haibo
AU - Zhang, Chunyang
AU - Liu, Kuilong
AU - Zhou, Hao
AU - Gou, Xinyin
AU - Chen, Binling
AU - Wang, Xiaoyue
AU - Ma, Guiping
N1 - Publisher Copyright:
© 2026 Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
PY - 2026/6/18
Y1 - 2026/6/18
N2 - In this study, we developed a Janus-structured hydrogel that integrates a thermostatic photothermal system with a temperature-responsive drug delivery system. The photothermal hydrogel contains phase-change-regulated core–shell microspheres, enabling specific thermostatic photothermal temperature (TPT)-triggered drug release for synergistic antibacterial treatment. The adhesive layer, composed of lipoic acid/sodium lipoate acid, methacrylated gelatin, N-isopropylacrylamide, and poly(ethylene glycol) diacrylate, provided temperature-responsive shrinkage, controllable drug release, and reduced adhesion at elevated temperature. Owing to chemical integration at the bilayer interface, the hydrogel showed good mechanical stability. Under near-infrared (NIR) laser, it demonstrated over 99% bactericidal efficiency against E. coli and S. aureus, with a biofilm clearance rate exceeding 90%. Moreover, the hydrogel significantly promoted wound healing in a rat model with S. aureus-infected wounds, achieving a healing rate of 98.33% after 14 days healing, compared to 73.82% in the control group. This study presents a promising strategy for designing wound dressings for infected wounds, combining photothermal therapy, drug delivery, and adhesion control.
AB - In this study, we developed a Janus-structured hydrogel that integrates a thermostatic photothermal system with a temperature-responsive drug delivery system. The photothermal hydrogel contains phase-change-regulated core–shell microspheres, enabling specific thermostatic photothermal temperature (TPT)-triggered drug release for synergistic antibacterial treatment. The adhesive layer, composed of lipoic acid/sodium lipoate acid, methacrylated gelatin, N-isopropylacrylamide, and poly(ethylene glycol) diacrylate, provided temperature-responsive shrinkage, controllable drug release, and reduced adhesion at elevated temperature. Owing to chemical integration at the bilayer interface, the hydrogel showed good mechanical stability. Under near-infrared (NIR) laser, it demonstrated over 99% bactericidal efficiency against E. coli and S. aureus, with a biofilm clearance rate exceeding 90%. Moreover, the hydrogel significantly promoted wound healing in a rat model with S. aureus-infected wounds, achieving a healing rate of 98.33% after 14 days healing, compared to 73.82% in the control group. This study presents a promising strategy for designing wound dressings for infected wounds, combining photothermal therapy, drug delivery, and adhesion control.
KW - Antibacterial
KW - Photothermal
KW - Programmable drug delivery
KW - Temperature-dependent adhesion
UR - https://www.scopus.com/pages/publications/105038825357
U2 - 10.1016/j.eurpolymj.2026.114795
DO - 10.1016/j.eurpolymj.2026.114795
M3 - Article
AN - SCOPUS:105038825357
SN - 0014-3057
VL - 254
JO - European Polymer Journal
JF - European Polymer Journal
M1 - 114795
ER -