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Ultrasound-controlled MXene-based Schottky heterojunction improves anti-infection and osteogenesis properties

Background: The current clinical treatment of osteomyelitis is limited by the emergence of drug-resistant bacteria, which often leads to the failure of traditional antibiotic treatment and large bone defects. Sonodynamic therapy (SDT) is a new strategy that is widely used to overcome the problem of...

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Detalles Bibliográficos
Autores principales: Wang, Hongchuan, Mu, Na, He, Yaqi, Zhang, Xiaoguang, Lei, Jie, Yang, Cao, Ma, Liang, Gao, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086208/
https://www.ncbi.nlm.nih.gov/pubmed/37056559
http://dx.doi.org/10.7150/thno.81511
Descripción
Sumario:Background: The current clinical treatment of osteomyelitis is limited by the emergence of drug-resistant bacteria, which often leads to the failure of traditional antibiotic treatment and large bone defects. Sonodynamic therapy (SDT) is a new strategy that is widely used to overcome the problem of bacterial resistance to antibiotic therapy as well as poor tissue penetration using near-infrared light in photodynamic therapy (PDT). Therefore, it is necessary to develop a new sonosensitizer that can kill bacteria and promote bone repair. Methods: Herein, we developed a sonosensitizer, porphyrin metal-organic framework (HNTM), with a Schottky junction modified by Ti(3)C(2) nanosheets (HN-Ti(3)C(2)) for highly efficient sonodynamic therapy of osteomyelitis and bone regeneration. Results: Ti(3)C(2) greatly improves the acoustic catalytic performance by rapidly transferring the charge carriers generated by HNTM under ultrasound (US) irradiation, which killing drug-resistant bacteria through the generation of large amounts of reactive oxygen species (ROS). And HN-Ti(3)C(2) shows excellent 99.75% antibacterial effectiveness against MRSA. In addition, HN-Ti(3)C(2) generates a sonocurrent under low-intensity US to promote the repair of bone defects for a long time period. Mechanistic research using CCK-8 and RNA-seq showed that HN-Ti(3)C(2) nanocomposites can promote the proliferation of stem cells by regulating the cell cycle, DNA replication, and apoptosis. In addition, after low-intensity US irradiation, HN-Ti(3)C(2) promotes osteogenic differentiation via some key signaling pathways, including the calcium, Wnt, and TGF-beta signaling pathways, according to the Kyoto Encyclopedia of Genes and Genomes (KEGG). In a MRSA-infected rat tibial osteomyelitis model, HN-Ti(3)C(2) successfully eliminated the infection and significantly improved bone regeneration under US irradiation. Conclusion: This study indicates that engineered HN-Ti(3)C(2) is a distinctive nanocomposite for successful osteomyelitis treatment.