TY - JOUR
T1 - Bioactive anti-inflammatory, antibacterial, conductive multifunctional scaffold based on MXene@CeO2 nanocomposites for infection-impaired skin multimodal therapy
AU - Zheng, Hua
AU - Wang, Shenqiang
AU - Cheng, Fang
AU - He, Xiaowei
AU - Liu, Zongxu
AU - Wang, Wenyan
AU - Zhou, Li
AU - Zhang, Qiuyu
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/11/15
Y1 - 2021/11/15
N2 - Overcoming multidrug-resistant (MDR) bacterial infection and simultaneously enhancing wound healing/skin reconstruction are still critical challenges for both clinic practice and fundamental research. The single modal therapy strategy is usually inefficient. Herein, for the first time, multifunctional MXene@CeO2 nanocomposites were prepared by combining the 2D antibacterial conductive Ti3C2Tx MXenes and antioxidant CeO2 and applied in developing multifunctional hydrogel scaffold (FOM) for MDR infection-impaired skin multimodal therapy. FOM scaffold was fabricated by incorporating MXene@CeO2 nanocomposites in a dynamic Schiff-based chemical crosslinked hydrogel of polyethylenimine grafted Pluronic F127 (F127-PEI) and oxidized sodium alginate (OSA). FOM scaffold possessed multifunctional properties including injectable self-healing behavior, efficient anti-inflammatory, antibacterial, and antioxidative abilities, conductive bioactivities, tissue-adhesive ability and fast hemostatic capacity. FOM scaffold could promote fibroblasts migration and cell proliferation with electrical stimulation. Additionally, FOM scaffold demonstrated the significant anti-inflammatory and multidrug resistant infection therapy, meanwhile promoting fibroblasts proliferation, granulation tissue formation, collagen deposition, re-epithelialization to accelerate MDR-infected wound healing. This work firstly demonstrated the important role of multifunctional MXene@CeO2 nanocomposites in infected-wound healing/skin reconstruction. This study provided an efficient multimodal therapy on MDR infection-impaired skin via the optimization of the structure and multifunctional properties of biomaterials.
AB - Overcoming multidrug-resistant (MDR) bacterial infection and simultaneously enhancing wound healing/skin reconstruction are still critical challenges for both clinic practice and fundamental research. The single modal therapy strategy is usually inefficient. Herein, for the first time, multifunctional MXene@CeO2 nanocomposites were prepared by combining the 2D antibacterial conductive Ti3C2Tx MXenes and antioxidant CeO2 and applied in developing multifunctional hydrogel scaffold (FOM) for MDR infection-impaired skin multimodal therapy. FOM scaffold was fabricated by incorporating MXene@CeO2 nanocomposites in a dynamic Schiff-based chemical crosslinked hydrogel of polyethylenimine grafted Pluronic F127 (F127-PEI) and oxidized sodium alginate (OSA). FOM scaffold possessed multifunctional properties including injectable self-healing behavior, efficient anti-inflammatory, antibacterial, and antioxidative abilities, conductive bioactivities, tissue-adhesive ability and fast hemostatic capacity. FOM scaffold could promote fibroblasts migration and cell proliferation with electrical stimulation. Additionally, FOM scaffold demonstrated the significant anti-inflammatory and multidrug resistant infection therapy, meanwhile promoting fibroblasts proliferation, granulation tissue formation, collagen deposition, re-epithelialization to accelerate MDR-infected wound healing. This work firstly demonstrated the important role of multifunctional MXene@CeO2 nanocomposites in infected-wound healing/skin reconstruction. This study provided an efficient multimodal therapy on MDR infection-impaired skin via the optimization of the structure and multifunctional properties of biomaterials.
KW - Bioactive multifunctional scaffold
KW - Infected-wound healing
KW - MXene@CeO nanocomposites
KW - Multimodal Therapy
UR - http://www.scopus.com/inward/record.url?scp=85107640900&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2021.130148
DO - 10.1016/j.cej.2021.130148
M3 - 文章
AN - SCOPUS:85107640900
SN - 1385-8947
VL - 424
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 130148
ER -