Method for simultaneously loading zif-8 nanospheres with AuNPs and Fe3O4NPs
A technology of nanospheres and reduction method, which is applied in the direction of pharmaceutical formulas, medical preparations with non-active ingredients, medical preparations containing active ingredients, etc. It can solve the problems of simultaneous loading of zif-8 nanospheres that have not been disclosed, and achieve high yield High, high loading capacity, uniform and stable particle size
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Embodiment 1
[0032] (1) Synthesize 13nm Au NPs by the sodium citrate reduction method described in the literature. Simply put 0.01%, 300mL chloroauric acid in a 500mL round bottom flask with a reflux condenser, stir vigorously and add 1% , 9mL trisodium citrate aqueous solution, react for 20min, until the solution turns red, quickly cool the obtained Au NPs solution with ice water, and set aside;
[0033] (2) Take the Au NPs in (1), add 50mL polyethylene glycol mPEG-SH, react for 2h, collect the precipitate by centrifugation at 16000rpm, wash with deionized water for 3 times, and disperse in methanol to obtain polyethylene glycol-stabilized Au NPs;
[0034] (3) Configure 100mL oleic acid-ethanol solution, the volume ratio of oleic acid to ethanol is 3:47, and take another 5mmol Fe(acac) 3 Add oleic acid-ethanol solution, mix and stir for 10 minutes, transfer to a 200mL steel-lined high-pressure reactor, and react at 180 degrees Celsius for 12 hours. times of washing to obtain oleic acid-...
Embodiment 2
[0038] (1) Synthesize 13nm Au NPs by the sodium citrate reduction method described in the literature. Simply put 0.01%, 300mL chloroauric acid in a 500mL round bottom flask with a reflux condenser, stir vigorously and add 1% , 9mL trisodium citrate aqueous solution, react for 20min, until the solution turns red, quickly cool the obtained Au NPs solution with ice water, and set aside;
[0039] (2) Take the Au NPs in (1), add 50mL polyethylene glycol mPEG-SH, react for 2h, collect the precipitate by centrifugation at 16000rpm, wash with deionized water for 3 times, and disperse in methanol to obtain polyethylene glycol-stabilized Au NPs;
[0040] (3) Configure 100mL oleic acid-ethanol solution, the volume ratio of oleic acid to ethanol is 3:47, and take another 1mmol Fe(acac) 3 Add oleic acid-ethanol solution, mix and stir for 10 minutes, transfer to a 200mL steel-lined high-pressure reactor, and react at 180 degrees Celsius for 12 hours. times of washing to obtain oleic acid-...
Embodiment 3
[0044] (1) Synthesize 13nm Au NPs by the sodium citrate reduction method described in the literature. Simply put 0.01%, 300mL chloroauric acid in a 500mL round bottom flask with a reflux condenser, stir vigorously and add 1% , 9mL trisodium citrate aqueous solution, react for 20min, until the solution turns red, quickly cool the obtained Au NPs solution with ice water, and set aside;
[0045] (2) Take the Au NPs in (1), add 50mL polyethylene glycol mPEG-SH, react for 2h, collect the precipitate by centrifugation at 16000rpm, wash with deionized water for 3 times, and disperse in methanol to obtain polyethylene glycol-stabilized Au NPs;
[0046] (3) Configure 100mL oleic acid-ethanol solution, the volume ratio of oleic acid to ethanol is 3:47, and take another 3mmol Fe(acac) 3 Add oleic acid-ethanol solution, mix and stir for 10 minutes, transfer to a 200mL steel-lined high-pressure reactor, and react at 180 degrees Celsius for 12 hours. times of washing to obtain oleic acid-...
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