声动力疗法
生物膜
材料科学
金黄色葡萄球菌
骨髓炎
微生物学
化学
医学
细菌
活性氧
生物
免疫学
生物化学
遗传学
作者
Yijie Cheng,Yufei Zhang,Zhe Zhao,Gang Li,Jie Li,Anran Li,Yun Xue,Baolin Zhu,Zhongming Wu,Xinge Zhang
标识
DOI:10.1002/adma.202206646
摘要
Abstract Osteomyelitis caused by methicillin‐resistant Staphylococcus aureus (MRSA) biofilm infection is difficult to eradicate and can even be life‐threatening. Given that the infection is persistent and deep‐seated in the bone tissue, controlled and efficient treatment of osteomyelitis remains challenging. Herein, an activatable nanostructure (Au/TNT@PG) is presented for synergistic sonodynamic‐catalytic therapy of MRSA‐infected osteomyelitis. The Au/TNT@PG backbone is obtained by conjugating a guanidinium‐rich polymer (PG), a component that penetrates the biofilm matrix, onto ultrasound (US)‐absorbing gold‐doped titanate nanotubes (Au/TNTs). Under deep‐penetrating US irradiation, the nanocomposite generates 1 O 2 for sonodynamic therapy and catalyzes the decomposition of endogenous H 2 O 2 into toxic •OH in the acidic infection microenvironment for catalytic therapy, leading to bacterial cell death. Its robust antibacterial effectiveness is attributable to its bacteria‐capturing ability, the biofilm penetrability of positively charged guanidinium, and the subsequent synergistic effect of sonodynamic‐catalytic action of Au/TNT. Such a remotely controlled approach potentiates the polarization of macrophages to M2‐type while suppressing the M1‐type, leading to topical inflammation resolution and enhanced osteoblast proliferation and differentiation to inhibit bone loss. Therefore, this study provides a generic nanotherapeutic approach for efficient sonodynamic‐catalytic therapy with respect to osteomyelitis.
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