Magnetic resonance imaging guided targeting metal organic framework drug carrier preparation method
A metal-organic framework and magnetic resonance imaging technology, which is applied in the direction of drug combinations, pharmaceutical formulations, preparations for in vivo tests, etc., can solve the problems of lack of targeting and imaging orientation, and achieve great development potential and application value. The effect of cheap raw materials and simple process
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Embodiment 1
[0024] A method for preparing a magnetic resonance imaging-guided targeted metal-organic framework drug carrier, comprising the following steps:
[0025] 1) Preparation of magnetic balls: Add 0.54 g of ferric chloride hexahydrate and 21.6 g of ethylene glycol into a 50 mL round-bottomed flask, and dissolve with ultrasonic stirring. Under magnetic stirring, add 0.2g of polyacrylic acid, 1.5g of water, and 1.2g of urea to the above solution in sequence. After the mixture is stirred for 15 to 30 minutes, transfer it to a 30mL hydrothermal reaction kettle, seal it, and react it in a blast drying oven at 200°C. 12 hours. After the reaction, the reaction kettle is naturally cooled to room temperature, the reactant is magnetically sucked by ethanol for three to five times, and then vacuum-dried for 12 to 24 hours to obtain black magnetic balls.
[0026] 2) Preparation of magnetic sphere dispersion: Take 25 mg of magnetic spheres in a 25 mL vial, add 10 mL of N,N-dimethylformamide, a...
Embodiment 2
[0031]A method for preparing a magnetic resonance imaging-guided targeted metal-organic framework drug carrier, comprising the following steps:
[0032] 1) Preparation of magnetic spheres: Add 0.81 g of ferric chloride hexahydrate and 32.4 g of ethylene glycol into a 100 mL round-bottomed flask, and dissolve with ultrasonic stirring. Under magnetic stirring, add 0.3g of polyacrylic acid, 2.25g of water, and 1.8g of urea to the above solution in sequence. After the mixture is stirred for 15 to 30 minutes, transfer it to a 50mL hydrothermal reactor, seal it, and react in a blast drying oven at 220°C. 8 hours. After the reaction, the reaction kettle is naturally cooled to room temperature, the reactant is magnetically sucked by ethanol for three to five times, and then vacuum-dried for 12 to 24 hours to obtain black magnetic balls.
[0033] 2) Preparation of magnetic sphere dispersion: Take 50 mg of magnetic spheres in a 25 mL vial, add 5 mL of methanol, and sonicate for 30 minu...
Embodiment 3
[0038] A method for preparing a magnetic resonance imaging-guided targeted metal-organic framework drug carrier, comprising the following steps:
[0039] 1) Preparation of magnetic spheres: Add 1.62 g of ferric chloride hexahydrate and 64.8 g of ethylene glycol into a 250 mL round bottom flask, and dissolve them with ultrasonic stirring. Under magnetic stirring, add 0.6g of polyacrylic acid, 4.5g of water, and 3.6g of urea to the above solution in sequence. After the mixture is stirred for 15 to 30 minutes, transfer it to a 100mL hydrothermal reactor, seal it, and react in a blast drying oven at 210°C. 10 hours. After the reaction, the reaction kettle is naturally cooled to room temperature, the reactant is magnetically sucked by ethanol for three to five times, and then vacuum-dried for 12 to 24 hours to obtain black magnetic balls.
[0040] 2) Preparation of magnetic sphere dispersion: Take 75 mg of magnetic spheres in a 25 mL vial, add 10 mL of N,N-dimethylformamide, and s...
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