GSH-Triggered/Photothermal-Enhanced H2S Signaling Molecule Release for Gas Therapy

Author:

Liang Xinqiang1,Kurboniyon Mekhrdod2ORCID,Zou Yuanhan1,Luo Kezong1,Fang Shuhong1,Xia Pengle1,Ning Shufang1,Zhang Litu1,Wang Chen1ORCID

Affiliation:

1. Department of Research, Guangxi Cancer Molecular Medicine Engineering Research Center, Guangxi Medical University Cancer Hospital, Nanning 530021, China

2. National Academy of Sciences of Tajikistan, Dushanbe 734000, Tajikistan

Abstract

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 (H2S) 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 H2S 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, H2S gas was controllably released. And the temperature increases due to the photothermal effects of PB nanoparticles, further enhancing H2S 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.

Funder

National Natural Science Foundation

Key R&D Program of Scientific Research and Technology Development Project of Guangxi

Key R&D Program of Scientific Research and Technology Development Project of Nanning, Guangxi

Key R&D Program of Scientific Research and Technical Development Project of Qingxiu District

Youth Science Foundation of Guangxi Medical University

Publisher

MDPI AG

Subject

Pharmaceutical Science

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