Self-assembled manganese phthalocyanine nanoparticles with enhanced peroxidase-like activity for anti-tumor therapy
Autor: | Wang Jinghan, Juewen Liu, Ren Xitong, Xiao Wang, Feng Bai, Haozhen Zhang, Shanqing Gao |
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Rok vydání: | 2021 |
Předmět: |
Ligand
Nanoparticle Enhanced permeability and retention effect Conjugated system Condensed Matter Physics Combinatorial chemistry Atomic and Molecular Physics and Optics Catalysis Active center chemistry.chemical_compound chemistry Phthalocyanine General Materials Science Self-assembly Electrical and Electronic Engineering |
Zdroj: | Nano Research. 15:2347-2354 |
ISSN: | 1998-0000 1998-0124 |
Popis: | The use of functional nanoparticles as peroxidase-like (POD-like) catalyst has recently become a focus of research in cancer therapy. Phthalocyanine is a macrocyclic conjugated metal ligand, which is expected to achieve a high POD-like catalytic activity, generating free radicals and inhibiting the proliferation of cancer cells. In this paper, we synthesized phthalocyanine nanocrystals with different structures through noncovalent self-assembly confined within micro-emulsion droplets, and manganese phthalocyanine (MnPc) possessing a metal-N-C active center was used as the building block. These nano-assemblies exhibit shape-dependent POD-like catalytic activities, because the emulsifier and MnPc co-mixed assembly reduced the close packing between MnPc molecules and exposed more active sites. The assembly had a water-dispersed nanostructure, which is conducive to accumulation at tumor sites through the enhanced permeability and retention effect (EPR). Because of a highly efficient microenvironmental response, the assembly showed higher catalytic activity only emerged under the acidic tumor-like microenvironment, but caused less damage to normal tissues in biomedical applications. In vivo and in vitro catalytic therapy tests showed excellent anti-tumor effects. This work explored a new way for the application of metal-organic macromolecules such as MnPc as nanozymes for catalytic tumor therapy. |
Databáze: | OpenAIRE |
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