A green light-responsive polymer nano drug carrier
A nano-drug carrier and polymer technology, applied in the field of biomedical materials, can solve the problems of limiting the clinical application of polymer nano-drug carriers, and achieve the effects of avoiding light damage, large drug loading, and realizing release.
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Embodiment 1
[0029] (1) Preparation of furan derivatives: Dissolve 1.51g of Michaelis acid or 1,3-dimethylbarbituric acid and 0.961g of furfural in 30mL of water, react at room temperature for 16h; after the reaction is completed, filter and wash with water, A yellow solid was obtained; the yellow solid was redissolved in dichloromethane, washed successively with saturated sodium bisulfite solution, ultrapure water, saturated sodium carbonate solution and saturated sodium chloride solution; finally dried over anhydrous magnesium sulfate, filtered and rotary evaporation treatment to obtain furan derivatives;
[0030] (2) Preparation of polyethylene glycol-b-poly(hexyl acrylate-co-pentafluorophenyl methacrylate): 1 part of 2-(dodecyltrithiocarbonate)-2-methyl Polyethylene glycol monomethyl ether propionate, 0.05 parts of azobisisobutyronitrile, 4 parts of pentafluorophenyl methacrylate, and 40 parts of hexyl acrylate were dissolved in 1 mL of dioxane, and reacted at 60 ° C for 2 h; After co...
Embodiment 2
[0035] (1) Preparation of furan derivatives: Dissolve 1.51g of Michaelis acid or 1,3-dimethylbarbituric acid and 0.961g of furfural in 30mL of water, and react at room temperature for 16h; after the reaction is completed, filter and wash with water. A yellow solid was obtained; the yellow solid was redissolved in dichloromethane, washed successively with saturated sodium bisulfite solution, ultrapure water, saturated sodium carbonate solution and saturated sodium chloride solution; finally dried over anhydrous magnesium sulfate, filtered and rotary evaporation treatment to obtain furan derivatives;
[0036](2) Preparation of polyethylene glycol-b-poly(hexyl acrylate-co-pentafluorophenyl methacrylate): 5 parts of 2-(dodecyltrithiocarbonate group)-2-methyl Polyethylene glycol monomethyl ether propionate, 0.1 part of azobisisobutyronitrile, 5 parts of pentafluorophenyl methacrylate, and 60 parts of hexyl acrylate were dissolved in 5 mL of dioxane, and reacted at 75 ° C for 15 h; ...
Embodiment 3
[0041] (1) Preparation of furan derivatives: Dissolve 1.51g of Michaelis acid or 1,3-dimethylbarbituric acid and 0.961g of furfural in 30mL of water, react at room temperature for 16h; after the reaction is completed, filter and wash with water, A yellow solid was obtained; the yellow solid was redissolved in dichloromethane, washed successively with saturated sodium bisulfite solution, ultrapure water, saturated sodium carbonate solution and saturated sodium chloride solution; finally dried over anhydrous magnesium sulfate, filtered and rotary evaporation treatment to obtain furan derivatives;
[0042] (2) Preparation of polyethylene glycol-b-poly(hexyl acrylate-co-pentafluorophenyl methacrylate): 10 parts of 2-(dodecyltrithiocarbonate group)-2-methyl Polyethylene glycol monomethyl ether propionate, 0.2 parts of azobisisobutyronitrile, 8 parts of pentafluorophenyl methacrylate, and 80 parts of hexyl acrylate were dissolved in 10 mL of dioxane, and reacted at 90 ° C for 30 h; ...
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