TY - JOUR
T1 - Macroporous hydrogel loaded with AIE-photosensitizer for enhanced antibacterial and wounds healing
AU - Liu, Yangkun
AU - Su, Gongmeiyue
AU - Lin, Jingsong
AU - Tan, Xudong
AU - Wu, Chaoying
AU - Shen, Qing'an
AU - Deng, Zishan
AU - Liu, Jiankai
AU - Han, Min
AU - Lai, Jian cheng
AU - Dai, Rongji
AU - Wang, Guixue
AU - Zang, Guangchao
AU - Li, Zhao
AU - Zhao, Hongyou
N1 - Publisher Copyright:
© 2025
PY - 2025/6
Y1 - 2025/6
N2 - Effective wound healing requires precise immune regulation, including infection clearance to prevent excessive immune cell activation and polarization of macrophages. Therapeutic systems with combined immunomodulatory effects are crucial. Photodynamic therapy (PDT) is a promising antimicrobial treatment(AIE), with photosensitizers (PSs) playing a central role. The PSs with aggregation-induced emission can efficiently generate reactive oxygen species (ROS) in the aggregated state, making them workable in high concentration. Introduction of a biocompatible carrier is beneficial for the PSs' immobilization and distribution and hydrogels are excellent candidates. It is pursuing to design a PS-hydrogel system with synergetic effect. Type II PSs can generate singlet oxygen under sufficient oxygen. Macroporous hydrogels (MPHs) own superiorities in matter transport and immune cell adhesion reduction. Herein, an AIE-PS, TCSPy+ was designed. With its nanoparticles (NPs), an MPH dressing was developed using a facile extrusion-sequential-photo-crosslinking method based on PEGDA and GelMA. In vitro and in vivo studies demonstrated that TCSPy+@MPH dressing exhibited superior antibacterial activity compared to non-porous hydrogel-based one, significantly inhibiting excessive immune cell activation and polarization of macrophages. The macroporous structure also facilitated inflammatory exudates removal. The synergetic effect with the combined immunomodulation ability allows the dressing to efficiently treat infected wounds, offering an effective strategy to design advanced therapeutic systems for tissue regeneration and immune regulation.
AB - Effective wound healing requires precise immune regulation, including infection clearance to prevent excessive immune cell activation and polarization of macrophages. Therapeutic systems with combined immunomodulatory effects are crucial. Photodynamic therapy (PDT) is a promising antimicrobial treatment(AIE), with photosensitizers (PSs) playing a central role. The PSs with aggregation-induced emission can efficiently generate reactive oxygen species (ROS) in the aggregated state, making them workable in high concentration. Introduction of a biocompatible carrier is beneficial for the PSs' immobilization and distribution and hydrogels are excellent candidates. It is pursuing to design a PS-hydrogel system with synergetic effect. Type II PSs can generate singlet oxygen under sufficient oxygen. Macroporous hydrogels (MPHs) own superiorities in matter transport and immune cell adhesion reduction. Herein, an AIE-PS, TCSPy+ was designed. With its nanoparticles (NPs), an MPH dressing was developed using a facile extrusion-sequential-photo-crosslinking method based on PEGDA and GelMA. In vitro and in vivo studies demonstrated that TCSPy+@MPH dressing exhibited superior antibacterial activity compared to non-porous hydrogel-based one, significantly inhibiting excessive immune cell activation and polarization of macrophages. The macroporous structure also facilitated inflammatory exudates removal. The synergetic effect with the combined immunomodulation ability allows the dressing to efficiently treat infected wounds, offering an effective strategy to design advanced therapeutic systems for tissue regeneration and immune regulation.
KW - Aggregation-induced emission photosensitizers
KW - Immunomodulatory
KW - Macroporous hydrogels
KW - Photodynamic therapy
UR - http://www.scopus.com/inward/record.url?scp=105004931415&partnerID=8YFLogxK
U2 - 10.1016/j.ijbiomac.2025.143977
DO - 10.1016/j.ijbiomac.2025.143977
M3 - Article
AN - SCOPUS:105004931415
SN - 0141-8130
VL - 312
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
M1 - 143977
ER -