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Tumor Microenvironment-Responsive Magnetotactic Bacteria-Based Multi-Drug Delivery Platform for MRI-Visualized Tumor Photothermal Chemodynamic Therapy.
Feng, Feng; Li, Qilong; Sun, Xuefei; Yao, Li; Wang, Xiuyu.
Afiliação
  • Feng F; Institute of Process Equipment, College of Energy Engineering, Zhejiang University, Hangzhou 310027, China.
  • Li Q; Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, China.
  • Sun X; Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, China.
  • Yao L; Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, China.
  • Wang X; Institute of Process Equipment, College of Energy Engineering, Zhejiang University, Hangzhou 310027, China.
Biology (Basel) ; 13(9)2024 Aug 25.
Article em En | MEDLINE | ID: mdl-39336086
ABSTRACT
Cancer cells display elevated reactive oxygen species (ROS) and altered redox status. Herein, based on these characteristics, we present a multi-drug delivery platform, AMB@PDAP-Fe (APPF), from the magnetotactic bacterium AMB-1 and realize MRI-visualized tumor-microenvironment-responsive photothermal-chemodynamic therapy. The Fe3+ in PDAP-Fe is reduced by the GSH at the tumor site and is released in the form of highly active Fe2+, which catalyzes the generation of ROS through the Fenton reaction and inhibits tumor growth. At the same time, the significant absorption of the mineralized magnetosomes in AMB-1 cells in the NIR region enables them to efficiently convert near-infrared light into heat energy for photothermal therapy (PTT), to which PDAP also contributes. The heat generated in the PTT process accelerates the process of Fe2+ release, thereby achieving an enhanced Fenton reaction in the tumor microenvironment. In addition, the magnetosomes in AMB-1 are used as an MRI contrast agent, and the curing process is visualized. This tumor microenvironment-responsive MTB-based multi-drug delivery platform displays the potency to combat tumors and demonstrates the utility and practicality of understanding the cooperative molecular mechanism when designing multi-drug combination therapies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biology (Basel) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biology (Basel) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Suíça