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Manganese carbonate nanoparticles‐mediated mitochondrial dysfunction for enhanced sonodynamic therapy

Sonodynamic therapy (SDT) has attracted widespread attention due to its non‐invasiveness and deep tissue penetration. However, the development of efficient sonodynamic nanoplatforms to improve the therapeutic efficiency is still one of the main challenges of current research. In this work, a new typ...

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Detalles Bibliográficos
Autores principales: Zhang, Haoyuan, Pan, Xueting, Wu, Qingyuan, Guo, Juan, Wang, Chaohui, Liu, Huiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10190974/
https://www.ncbi.nlm.nih.gov/pubmed/37323218
http://dx.doi.org/10.1002/EXP.20210010
Descripción
Sumario:Sonodynamic therapy (SDT) has attracted widespread attention due to its non‐invasiveness and deep tissue penetration. However, the development of efficient sonodynamic nanoplatforms to improve the therapeutic efficiency is still one of the main challenges of current research. In this work, a new type of sonosensitizer prepared by a simple method, manganese carbonate nanoparticles (MnCO(3) NPs), is used for enhanced SDT. MnCO(3) NPs could generate large amounts of (1)O(2) and •OH under ultrasound irradiation. At the same time, CO(2) and Mn ions could be released in a weak acid environment due to the excellent degradability of MnCO(3) NPs. The CO(2) bubbles caused cell necrosis by ultrasonic cavitation and used for ultrasound imaging. And Mn ions activated the mitochondrial cell apoptosis pathway. In vivo experiments proved that this sonosensitizer with mitochondrial regulatory capacity showed high tumor inhibition rates for enhanced sonodynamic tumor therapy.