Photothermal Catalytic Reduction and Bone Tissue Engineering Towards a Three‐in‐One Therapy Strategy for Osteosarcoma

Author:

Lu Hengli1,Li Zihua1,Duan Zhengwei1,Liao Yuxin1,Liu Kaiyuan2,Zhang Yiwei1,Fan Lin1,Xu Tianyang1,Yang Dong1,Wang Sen1,Fu Yuesong1,Xiang Huijing3,Chen Yu345ORCID,Li Guodong1

Affiliation:

1. Department of Orthopaedics Shanghai Tenth People's Hospital School of Medicine Tongji University Shanghai 200072 P. R. China

2. Department of Bone Tumor Surgery Shanghai General Hospital Shanghai Jiaotong University School of Medicine Shanghai 200025 P. R. China

3. Materdicine Lab School of Life Sciences Shanghai University Shanghai 200444 P. R. China

4. Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine Vision and Brain Health) Wenzhou Institute of Shanghai University Wenzhou Zhejiang 325088 P. R. China

5. Shanghai Institute of Materdicine Shanghai 200051 P. R. China

Abstract

AbstractOsteosarcoma is one of the most dreadful bone neoplasms in young people, necessitating the development of innovative therapies that can effectively eliminate tumors while minimizing damage to limb function. An ideal therapeutic strategy should possess three essential capabilities: antitumor effects, tissue‐protective properties, and the ability to enhance osteogenesis. In this study, self‐assembled Ce‐substituted molybdenum blue (CMB) nanowheel crystals are synthesized and loaded onto 3D‐printed bioactive glass (CMB@BG) scaffolds to develop a unique three‐in‐one treatment approach for osteosarcoma. The CMB@BG scaffolds exhibit outstanding photothermally derived tumor ablation within the near‐infrared‐II window due to the surface plasmon resonance properties of the CMB nanowheel crystals. Furthermore, the photothermally synergistic catalytic effect of CMB promotes the rapid scavenging of reactive oxygen species caused by excessive heat, thereby suppressing inflammation and protecting surrounding tissues. The CMB@BG scaffolds possess pro‐proliferation and pro‐differentiation capabilities that efficiently accelerate bone regeneration within bone defects. Altogether, the CMB@BG scaffolds that combine highly efficient tumor ablation, tissue protection based on anti‐inflammatory mechanisms, and enhanced osteogenic ability are likely to be a point‐to‐point solution for the comprehensive therapeutic needs of osteosarcoma.

Funder

National Natural Science Foundation of China

Shanghai Rising-Star Program

Publisher

Wiley

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