Glucose-primed PEEK orthopedic implants for antibacterial therapy and safeguarding diabetic osseointegration

被引:31
作者
He, Miaomiao [1 ]
Wang, Hao [1 ,2 ]
Han, Qiuyang [1 ]
Shi, Xiuyuan [3 ]
He, Shuai [1 ]
Sun, Jiyu [1 ]
Zhu, Zhuoli [1 ]
Gan, Xueqi [1 ,2 ,6 ]
Deng, Yi [1 ,4 ,5 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, Coll Biomed Engn, Sch Chem Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, West China Hosp Stomatol, Natl Ctr Stomatol, Natl Clin Res Ctr Oral Dis,State Key Lab Oral Dis, Chengdu 610041, Sichuan, Peoples R China
[3] Imperial Coll London, Dept Mat, London SW7 2AZ, England
[4] Sichuan Univ, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
[5] Univ Hong Kong, Dept Mech Engn, Hong Kong, Peoples R China
[6] Sichuan Univ, West China Hosp Stomatol, State Key Lab Oral Dis, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
PEEK; Implant-associated infection; Antibacterial; Osteogenicity; Diabetic osseointegration; BONE; COPPER; POLYETHERETHERKETONE; SCAFFOLDS;
D O I
10.1016/j.biomaterials.2023.122355
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Diabetic infectious microenvironment (DIME) frequently leads to a critical failure of osseointegration by virtue of its main peculiarities including typical hyperglycemia and pathogenic infection around implants. To address the plaguing issue, we devise a glucose-primed orthopedic implant composed of polyetheretherketone (PEEK), Cu-chelated metal-polyphenol network (hauberk coating) and glucose oxidase (GOx) for boosting diabetic osseointegration. Upon DIME, GOx on implants sostenuto consumes glucose to generate H2O2, and Cu liberated from hauberk coating catalyzes the H2O2 to highly germicidal center dot OH, which massacres pathogenic bacteria through photo-augmented chemodynamic therapy. Intriguingly, the catalytic efficiency of the coating gets greatly improved with the turnover number (TON) of 0.284 s-1. Moreover, the engineered implants exhibit satisfactory cytocompatibility and facilitate osteogenicity due to the presence of Cu and osteopromotive polydopamine coating. RNA-seq analysis reveals that the implants enable to combat infections and suppress proinflammatory phenotype (M1). Besides, in vivo evaluations utilizing infected diabetic rat bone defect models at week 4 and 8 authenticate that the engineered implants considerably elevate osseointegration through pathogen elimination, inflammation dampening and osteogenesis promotion. Altogether, our present study puts forward a conceptually new tactic that arms orthopedic implants with glucose-primed antibacterial and osteogenic capacities for intractable diabetic osseointegration.
引用
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页数:21
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