Core@paratroopers Nanoassemblies with Catalytic Cascade for Efficient Tumor Starvation Therapy

The catalytic therapy based on the nanozymes has received increasing interest in cancer treatment. However, the catalytic capabilities of standalone nanozymes are relatively limited, necessitating the development of a nano‐bio composite system that integrates both nanozymes and natural enzymes. This...

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Veröffentlicht in:Advanced functional materials 2024-09, Vol.34 (36), p.n/a
Hauptverfasser: Lu, Qianqian, Hou, Mengmeng, Huang, Xirui, Yu, Hongyue, Li, Xingjin, Jia, Jia, Zhou, Qiaoyu, Lv, Kexin, Ren, Tingting, Liu, Minchao, Zhan, Yating, Kou, Yufang, Dong, Lingkai, Zhao, Tiancong, Li, Xiaomin
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container_issue 36
container_start_page
container_title Advanced functional materials
container_volume 34
creator Lu, Qianqian
Hou, Mengmeng
Huang, Xirui
Yu, Hongyue
Li, Xingjin
Jia, Jia
Zhou, Qiaoyu
Lv, Kexin
Ren, Tingting
Liu, Minchao
Zhan, Yating
Kou, Yufang
Dong, Lingkai
Zhao, Tiancong
Li, Xiaomin
description The catalytic therapy based on the nanozymes has received increasing interest in cancer treatment. However, the catalytic capabilities of standalone nanozymes are relatively limited, necessitating the development of a nano‐bio composite system that integrates both nanozymes and natural enzymes. This construction often inevitably leads to interference between natural enzyme and nanozymes, resulting in reduced synergistic performance. Herein, a cascade catalysis system featuring the “core@paratroopers” structure is proposed, wherein hollow manganese dioxide (HMnO2) serves as “core” and ultra‐small hybrid single‐micelle (H‐micelle) encapsulated with glucose oxidase (GOx) as “paratroopers” (H‐micelle‐GOx). The outer SiO2 layer of the H‐micelle can effectively protect the GOx. Under hypoxic conditions, HMnO2 reacts with endogenous H2O2 to produce O2, thereby enhancing the catalytic efficiency of GOx for starvation therapy. Simultaneously, the generated H2O2 boosts the catalytic efficiency of HMnO2, accelerating local O2 generation and alleviating tumor hypoxia. Additionally, this system exhibits rapid degradation in the tumor microenvironment characterized by high glutathione (GSH) expression, facilitating the release and deep penetration of the ultra‐small H‐micelle‐GOx “paratroopers” within the solid tumor. A cascade catalysis system with a “core@paratroopers” structure is proposed. Hollow MnO2 (HMnO2) acts as the “core” and H‐micelle‐GOx acts as the “paratroopers”. HMnO2 reacts with endogenous H2O2 to enhance GOx's catalytic efficiency for starvation therapy, reducing tumor hypoxia. This system degrades rapidly in the tumor microenvironment with high glutathione expression, releasing and penetrating the ultra‐small H‐micelle‐GOx “paratroopers” within the tumor.
doi_str_mv 10.1002/adfm.202401328
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However, the catalytic capabilities of standalone nanozymes are relatively limited, necessitating the development of a nano‐bio composite system that integrates both nanozymes and natural enzymes. This construction often inevitably leads to interference between natural enzyme and nanozymes, resulting in reduced synergistic performance. Herein, a cascade catalysis system featuring the “core@paratroopers” structure is proposed, wherein hollow manganese dioxide (HMnO2) serves as “core” and ultra‐small hybrid single‐micelle (H‐micelle) encapsulated with glucose oxidase (GOx) as “paratroopers” (H‐micelle‐GOx). The outer SiO2 layer of the H‐micelle can effectively protect the GOx. Under hypoxic conditions, HMnO2 reacts with endogenous H2O2 to produce O2, thereby enhancing the catalytic efficiency of GOx for starvation therapy. Simultaneously, the generated H2O2 boosts the catalytic efficiency of HMnO2, accelerating local O2 generation and alleviating tumor hypoxia. Additionally, this system exhibits rapid degradation in the tumor microenvironment characterized by high glutathione (GSH) expression, facilitating the release and deep penetration of the ultra‐small H‐micelle‐GOx “paratroopers” within the solid tumor. A cascade catalysis system with a “core@paratroopers” structure is proposed. Hollow MnO2 (HMnO2) acts as the “core” and H‐micelle‐GOx acts as the “paratroopers”. HMnO2 reacts with endogenous H2O2 to enhance GOx's catalytic efficiency for starvation therapy, reducing tumor hypoxia. 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Additionally, this system exhibits rapid degradation in the tumor microenvironment characterized by high glutathione (GSH) expression, facilitating the release and deep penetration of the ultra‐small H‐micelle‐GOx “paratroopers” within the solid tumor. A cascade catalysis system with a “core@paratroopers” structure is proposed. Hollow MnO2 (HMnO2) acts as the “core” and H‐micelle‐GOx acts as the “paratroopers”. HMnO2 reacts with endogenous H2O2 to enhance GOx's catalytic efficiency for starvation therapy, reducing tumor hypoxia. 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Additionally, this system exhibits rapid degradation in the tumor microenvironment characterized by high glutathione (GSH) expression, facilitating the release and deep penetration of the ultra‐small H‐micelle‐GOx “paratroopers” within the solid tumor. A cascade catalysis system with a “core@paratroopers” structure is proposed. Hollow MnO2 (HMnO2) acts as the “core” and H‐micelle‐GOx acts as the “paratroopers”. HMnO2 reacts with endogenous H2O2 to enhance GOx's catalytic efficiency for starvation therapy, reducing tumor hypoxia. This system degrades rapidly in the tumor microenvironment with high glutathione expression, releasing and penetrating the ultra‐small H‐micelle‐GOx “paratroopers” within the tumor.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/adfm.202401328</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-1995-2274</orcidid><orcidid>https://orcid.org/0000-0001-6056-6928</orcidid></addata></record>
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subjects cascade catalysis system
Catalysis
core@paratroopers structure
Glucose oxidase
Glutathione
glutathione expression
hollow MnO2
Hydrogen peroxide
H‐micelle‐GOx
Manganese dioxide
Micelles
Silicon dioxide
Therapy
Tumors
title Core@paratroopers Nanoassemblies with Catalytic Cascade for Efficient Tumor Starvation Therapy
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