Although
ferroptosis therapy has been proven to be a promising
strategy for cancer treatment, its efficacy still might be limited
by insufficient H2O2 supply in tumor tissue.
Herein, we designed a cancer cell membrane-cloaked cascade nanoreactor
based on ferric metal–organic frameworks (MOF) and glucose
oxidase (GOx) decoration for synergistic ferroptosis–starvation
anticancer therapy. The GOx can catalyze glucose to generate sufficient
H2O2 for ferroptosis therapy, and the glucose
consumption caused by GOx can be utilized as another attractive cancer
treatment strategy called starvation therapy. When the nanoreactor
reached tumor sites, high concentration of GSH reduced Fe3+ to trigger structure collapse of MOF and release Fe2+ and GOx catalyzed the oxidation of glucose to generate H2O2. Then Fenton reaction happened between H2O2 and Fe2+ to produce hydroxyl radicals (•OH) and promoted ferroptosis therapy. With these cascade
reactions, the synergistic ferroptosis–starvation anticancer
therapy was realized. Furthermore, the cancer cell membrane endows
the nanoreactor homologous targeting and immune escaping ability,
which facilitated the nanoreactor to accumulate into tumor site with
high efficiency. The nanoreactor exhibits high efficiency for tumor
suppression with the in situ consumed and produced
compounds, which can promote the development of precise cooperative
cancer therapy with spatiotemporal controllability.
Photothermal therapy effectively ablate tumor by the hyperthermia (>50 °C), which was caused by laser irradiation. However, the hyperthermia may inevitably diffuse to the surrounding healthy tissues and induce additional...
A porphyrin containing covalent organic frameworks (COF) is synthesized as the substrate to decorate selenium nanoparticles (Se NPs) via in situ reduction, which could employ Se NPs mediated therapy (SeT)...
An iodine‐promoted one‐pot cascade oxidative annulation reaction has been developed for the synthesis of [1,2,3]triazolo[1,5‐a]quinolines from methyl azaarenes and N‐tosylhydrazines. The reaction has a broad substrate scope and can be easily scaled up to gram‐scale. 1,2,3‐Triazoles are an important skeletal structure for the construction of C−C and C−P bonds, 2‐cyclopropylquinolines and imidazo[1,5‐a]quinolines, for which different synthetic applications were explored.
An aerobic copper-catalyzed oxidative domino cyclization of methyl azaarenes with 6-amino-pyrimidine-2,4-diones and pyrazol-5-amines has been developed, which enables access to dipyrazolo/dipyrimidine-fused pyridines. Cu(OTf)2 is used as a transition-metal catalyst. The...
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