Metal‐Organic Framework Functionalized Bioceramic Scaffolds with Antioxidative Activity for Enhanced Osteochondral Regeneration

Author:

Shu Chaoqin1,Qin Chen1,Chen Lei1,Wang Yufeng1,Shi Zhe1,Yu Jiangming2,Huang Jimin13,Zhao Chaoqian1,Huan Zhiguang13,Wu Chengtie13,Zhu Min4,Zhu Yufang13ORCID

Affiliation:

1. State Key Laboratory of High Performance Ceramics and Superfine Microstructure Shanghai Institute of Ceramics Chinese Academy of Sciences Shanghai 200050 P. R. China

2. Department of Orthopaedics Tongren Hospital Shanghai Jiaotong University Shanghai 200336 P. R. China

3. Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of Sciences Beijing 100049 P. R. China

4. School of Materials and Chemistry University of Shanghai for Science and Technology Shanghai 200093 P. R. China

Abstract

AbstractOsteoarthritis (OA) is a degenerative disease that often causes cartilage lesions and even osteochondral damage. Osteochondral defects induced by OA are accompanied by an inflammatory arthrosis microenvironment with overproduced reactive oxygen species (ROS), resulting in the exacerbation of defects and difficulty regenerating osteochondral tissues. Therefore, it is urgently needed to develop osteochondral scaffolds that can not only promote the integrated regeneration of cartilage and subchondral bone, but also possess ROS‐scavenging ability to protect tissues from oxidative stress. Herein, zinc‐cobalt bimetallic organic framework (Zn/Co‐MOF) functionalized bioceramic scaffolds are designed for repairing osteochondral defects under OA environment. By functionalizing Zn/Co‐MOF on the 3D‐printed beta‐tricalcium phosphate (β‐TCP) scaffolds, the Zn/Co‐MOF functionalized β‐TCP (MOF‐TCP) scaffolds with broad‐spectrum ROS‐scavenging ability are successfully developed. Benefiting from its catalytic active sites and degradation products, Zn/Co‐MOF endows the scaffolds with excellent antioxidative and anti‐inflammatory properties to protect cells from ROS invasion, as well as dual‐bioactivities of simultaneously inducing osteogenic and chondrogenic differentiation in vitro. Furthermore, in vivo results confirm that MOF‐TCP scaffolds accelerate the integrated regeneration of cartilage and subchondral bone in severe osteochondral defects. This study offers a promising strategy for treating defects induced by OA as well as other inflammatory diseases.

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Natural Science Foundation of Shanghai

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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