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GSH-Triggered/Photothermal-Enhanced H(2)S Signaling Molecule Release for Gas Therapy

Traditional treatment methods for tumors are inefficient and have severe side effects. At present, new therapeutic methods such as phototherapy, chemodynamic therapy, and gasodynamic therapy have been innovatively developed. High concentrations of hydrogen sulfide (H(2)S) gas exhibit cancer-suppress...

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Detalles Bibliográficos
Autores principales: Liang, Xinqiang, Kurboniyon, Mekhrdod S., Zou, Yuanhan, Luo, Kezong, Fang, Shuhong, Xia, Pengle, Ning, Shufang, Zhang, Litu, Wang, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610203/
https://www.ncbi.nlm.nih.gov/pubmed/37896203
http://dx.doi.org/10.3390/pharmaceutics15102443
Descripción
Sumario:Traditional treatment methods for tumors are inefficient and have severe side effects. At present, new therapeutic methods such as phototherapy, chemodynamic therapy, and gasodynamic therapy have been innovatively developed. High concentrations of hydrogen sulfide (H(2)S) gas exhibit cancer-suppressive effects. Herein, a Prussian blue-loaded tetra-sulfide modified dendritic mesoporous organosilica (PB@DMOS) was rationally constructed with glutathione (GSH)-triggered/photothermal-enhanced H(2)S signaling molecule release properties for gas therapy. The as-synthesized nanoplatform confined PB nanoparticles in the mesoporous structure of organosilica silica due to electrostatic adsorption. In the case of a GSH overexpressed tumor microenvironment, H(2)S gas was controllably released. And the temperature increases due to the photothermal effects of PB nanoparticles, further enhancing H(2)S release. At the same time, PB nanoparticles with excellent hydrogen peroxide catalytic performance also amplified the efficiency of tumor therapy. Thus, a collective nanoplatform with gas therapy/photothermal therapy/catalytic therapy functionalities shows potential promise in terms of efficient tumor therapy.