A rechargeable coating with temporal-sequence antibacterial activity and soft tissue sealing

被引:2
作者
Wang, Fang [1 ,2 ]
Guan, Shiwei [1 ,2 ]
Xing, Min [3 ]
Qian, Wenhao [3 ]
Qiu, Jiajun [1 ]
Liu, Xuanyong [1 ,2 ,4 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine M, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] Shanghai Xuhui Dist Dent Ctr, Shanghai 200032, Peoples R China
[4] Donghua Univ, Coll Biol Sci & Med Engn, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金;
关键词
Polyimides; Medical titanium; Transcutaneous implants; Antibacterial; Soft tissue sealing; MITOCHONDRIAL ELECTRON-TRANSPORT; TITANIUM; INHIBITION; BEHAVIOR;
D O I
10.1016/j.bioactmat.2024.05.029
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Transcutaneous implants that penetrate through skin or mucosa are susceptible to bacteria invasion and lack proper soft tissue sealing. Traditional antibacterial strategies primarily focus on bacterial eradication, but excessive exposure to bactericidal agents can induce noticeable tissue damage. Herein, a rechargeable model (HPI-Ti) was constructed using perylene polyimide, an aqueous battery material, achieving temporal-sequence regulation of bacterial killing and soft tissue sealing. Charge storage within HPI-Ti is achieved after galvanostatic charge, and chemical discharge is initiated when immersed in physiological environments. During the early discharge stage, post-charging HPI-Ti demonstrates an antibacterial rate of 99.96 +/- 0.01 % for 24 h, preventing biofilm formation. Contact-dependent violent electron transfer between bacteria and the material causes bacteria death. In the later discharge stage, the attenuated discharging status creates a gentler electron-transfer microenvironment for fibroblast proliferation. After discharge, the antibacterial activity can be reinstated by recharge against potential reinfection. The antibacterial efficacy and soft tissue compatibility were verified in vivo. These results demonstrate the potential of the charge-transfer-based model in reconciling antibacterial efficacy with tissue compatibility.
引用
收藏
页码:224 / 238
页数:15
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