Active oxygen free radical sensitive cyclodextrin material as drug delivery carrier and preparation method thereof
A delivery carrier and cyclodextrin technology, which is applied in the direction of non-active components of polymer compounds, can solve the problems of material shortage and limitation, and achieve the effects of simple preparation method, easy large-scale synthesis, and good in vivo biocompatibility
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Embodiment 1
[0038] Under the protection of nitrogen, 10mmol 3-hydroxymethylphenylboronic acid and 15mmol pinacol are reacted in 60mL anhydrous tetrahydrofuran to obtain 3-hydroxymethylphenylboronic acid pinacol ester; 5mmol 3-hydroxymethylphenylboronic acid pinacol ester and 10mmolN, N'-carbonyldiimidazole was reacted in 20mL anhydrous chloroform to obtain 3-imidazolecarbonyloxy-phenylboronic acid pinacol ester; in the presence of 4mmol 4-dimethylaminopyridine, 0.3mmol α-cyclodextrin and 4mmol 3-imidazolecarbonyl The oxy-phenylboronic acid pinacol ester was reacted in 15 mL of dimethyl sulfoxide at 20°C. After 8 hours, the cyclodextrin material was obtained by precipitation in water, centrifugal collection, and drying.
Embodiment 2
[0040] Under the protection of nitrogen, 10mmol 4-hydroxymethylphenylboronic acid and 20mmol pinacol are reacted in 50mL anhydrous dioxane to obtain 4-hydroxymethylphenylboronic acid pinacol ester; 5mmol 4-hydroxymethylphenylboronic acid pinacol ester React with 15mmolN,N'-carbonyldiimidazole in 30mL anhydrous dichloromethane to obtain 4-imidazolecarbonyloxy-phenylboronic acid pinacol ester; in the presence of 4mmolN,N'-dicyclohexylcarbodiimide, 0.15mmolβ -Cyclodextrin and 4mmol 4-imidazolecarbonyloxy-phenylboronic acid pinacol ester were reacted in 12mL N,N-dimethylformamide at 30°C. After 12 hours, it was precipitated in water, collected by centrifugation, and dried. The cyclodextrin material is obtained.
Embodiment 3
[0042] Under the protection of nitrogen, 10mmol 3-hydroxymethylphenylboronic acid and 25mmol pinacol are reacted in 60mL anhydrous acetonitrile to obtain 3-hydroxymethylphenylboronic acid pinacol ester; 8mmol 3-hydroxymethylphenylboronic acid pinacol ester and 20mmolN, N'-carbonyldiimidazole was reacted in 25mL of anhydrous ethyl acetate to obtain 3-imidazolecarbonyloxy-phenylboronic acid pinacol ester; in the presence of 4.8mmol N,N'-diisopropylcarbodiimide, 0.1mmolγ- Cyclodextrin was reacted with 4.8mmol of 3-imidazolecarbonyloxy-phenylboronic acid pinacol ester in 10mL N,N-dimethylacetamide at 40°C. After 24 hours, it was precipitated in water, collected by centrifugation, and dried. The cyclodextrin material is obtained.
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