A kind of palladium nanoparticles with pei-ciprofloxacin micelles as template and preparation method thereof
A nanotechnology of ciprofloxacin and palladium, which is applied in the field of nanomaterials, can solve the problems of palladium nanoparticles being unstable, prone to coagulation, and affecting catalytic performance, and achieve high stability, high catalytic efficiency, and broad-spectrum antibacterial effect Effect
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[0037] A preparation method of palladium nanoparticles using PEI-ciprofloxacin micelles as a template, comprising:
[0038] Step S1, prepare PEI-ciprofloxacin complex: mix polyethyleneimine, ciprofloxacin and 1-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride, dissolve In an aprotic solvent, hydrochloric acid is added, and after 60-84 hours of reaction, a PEI-ciprofloxacin complex is obtained.
[0039] As a polyelectrolyte dispersant, polyethyleneimine (PEI) can not only stabilize the space through the polymer chain, but also play an electrostatic stabilizing role through its own charge, making the system highly dispersible and stable. Ciprofloxacin is a third-generation quinolone antibacterial drug with broad-spectrum antibacterial activity and good bactericidal effect. The carboxyl group in the ciprofloxacin structure can react with the amino group in the PEI to form an amide bond to obtain a PEI-ciprofloxacin complex (the reaction principle is as follows: figure 1...
Embodiment 1
[0052] The present embodiment provides a kind of palladium nanoparticle with PEI-ciprofloxacin micelles as template, and its preparation method comprises:
[0053] (1) polyethyleneimine (PEI, Mw=600), ciprofloxacin, 1-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC·HCl), Dissolve in dimethylsulfoxide (DMSO) at a ratio of 1:1:2, and then add 1M hydrochloric acid (the dosage is one-third of DMSO). The reactant was sonicated for 30 minutes to fully dissolve it, protected in a nitrogen atmosphere for 30-40 minutes, and stirred at room temperature for 72 hours.
[0054] (2) Use a vacuum oven at 85°C to remove the solvent DMSO from the reacted mixture, then dissolve the solid substance removed from the solvent in 4 mL of methanol, dialyze the obtained methanol solution against water for three days, and change it every 8-12 hours water. After the dialysis is completed, the aqueous solution of the obtained product is lyophilized to obtain the pure final product PEI-cip...
Embodiment 2
[0067] The present embodiment provides a kind of palladium nanoparticle with PEI-ciprofloxacin micelles as template, and its preparation method comprises:
[0068] (1) polyethyleneimine (PEI, Mw=600), ciprofloxacin, 1-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC·HCl), Dissolve in dimethylsulfoxide (DMSO) at a ratio of 1:1:2, and then add 1M hydrochloric acid (the dosage is one-third of DMSO). The reactant was sonicated for 30 minutes to fully dissolve it, protected in a nitrogen atmosphere for 30-40 minutes, and stirred at room temperature for 72 hours.
[0069] (2) Use a vacuum oven at 85°C to remove the solvent DMSO from the reaction mixture, then dissolve the solvent-removed solid in 4 mL of methanol, dialyze the obtained methanol solution against water for three days, and change the water every 8-12 hours . After the dialysis is completed, the aqueous solution of the obtained product is lyophilized to obtain the pure final product PEI-ciprofloxacin.
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