Cu2MoS4 nano-enzyme as well as preparation method, nano-drug and application thereof
A nanozyme, a selected technology, applied in the field of nanomaterials, can solve problems such as difficult to cure cancer, achieve efficient chemical kinetic therapy, relieve hypoxia, and inhibit cancer metastasis
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[0034] The present invention also provides a kind of above-mentioned Cu 2 MoS 4 The preparation method of the nanozyme comprises: mixing cuprous oxide, an organic carbon source, an inorganic molybdenum source and an organic sulfur source in an organic solvent, and calcining at a high temperature to obtain a hollow Cu 2 MoS 4 nanozyme.
[0035] Wherein, the present invention does not have special limitation to the source of all raw materials and can be commercially available or self-made.
[0036] In the present invention, the cuprous oxide is preferably prepared according to the following method: mix the inorganic copper salt and the polymer surfactant in water, adjust the pH value of the mixed solution to strong alkalinity, then add a reducing agent, and after the reaction, obtain Cuprous oxide.
[0037]Mixing an inorganic copper salt and a polymer surfactant in water, the inorganic copper salt is preferably one or more of copper chloride, copper nitrate and copper sulfat...
Embodiment 1
[0053] Preparation of Cu 2 O precursor: 0.171g CuCl 2 ·H 2 O and 3.333 g of polyvinylpyrrolidone were dispersed in 100 mL of deionized water. After stirring for 10 min, 2mol·L -1 , 10mL of sodium hydroxide solution and 0.6mol·L -1 , 10mL of ascorbic acid solution was added to the above solution one after another. After stirring at room temperature for 1 h, the product was centrifuged (10000rpmmin -1 , 5min), washed with deionized water and ethanol three times respectively, and the product was dried overnight at 60°C in a vacuum oven to obtain Cu 2 O precursor.
Embodiment 2
[0055] Preparation of hollow CMS nanozyme: 40mg Cu 2 The O precursor and 120 mg of glucose were sonicated in 20 mL of ethylene glycol. Then, 70mg Na 2 MoO 4 2H 2 O and 120mg of thioacetamide were added to the above solution, and ultrasonicated for 30min (power 250W). The above mixed solution was transferred to a 45mL polytetrafluoroethylene autoclave, calcined at 200°C for 24h, and then cooled to room temperature. Subsequently, the product was centrifuged (10000 rpm, 5 min), and washed three times with deionized water and ethanol respectively.
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