Functionalized mesoporous silicon tumor targeted transport and controlled release system and preparation method thereof
A tumor-targeting, mesoporous silicon technology, applied in anti-tumor drugs, drug delivery, powder delivery, etc., can solve the inaccurate evaluation of the carrier system, the difficulty of clinical trials, and the inability of the drug delivery system to achieve targeting, etc. problems, to achieve excellent biocompatibility, promote cell uptake, and high loading capacity
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Embodiment 1
[0056] 1. Preparation of p-toluenesulfonyl-β-cyclodextrins (β-CD-OTs)
[0057] Weigh 25g of β-CD and dissolve it in 300mL of 0.4M NaOH solution, and stir in an ice-water bath until the cyclodextrin is completely dissolved. 18 g of p-toluenesulfonyl chloride (TsCl) was weighed and slowly added dropwise to the β-CD solution. After stirring and reacting in an ice-water bath for 90 min, suction filtration was performed. The filtrate was taken, and the pH was adjusted to 8.5 with HCl. The mixture was stirred and reacted at room temperature for 2 h, and the reactant was placed in the refrigerator (4° C.) overnight, and suction filtered the next day, and the filter residue was washed three times with deionized water. The final product was dried at 60 °C to obtain β-CD-OTs.
[0058] 2. Preparation of nitrogenated cyclodextrin (β-CD-N3)
[0059] Weigh 10g of β-CD-OTs and dissolve in 100mL of deionized water, heat to 80°C, then add 2.54g of sodium azide (NaN3), and stir for 18h. The...
Embodiment 2
[0084] 1. Preparation of p-toluenesulfonyl-β-cyclodextrins (β-CD-OTs)
[0085] Weigh 25g of β-CD and dissolve it in 350mL of 0.4M NaOH solution, and stir in an ice-water bath until the cyclodextrin is completely dissolved. 20 g of p-toluenesulfonyl chloride (TsCl) was weighed and slowly added dropwise to the β-CD solution. After stirring and reacting in an ice-water bath for 90 min, suction filtration was performed. The filtrate was taken, and the pH was adjusted to 8.5 with HCl. The mixture was stirred and reacted at room temperature for 2 h, and the reactant was placed in the refrigerator (4° C.) overnight, and suction filtered the next day, and the filter residue was washed three times with deionized water. The final product was dried at 60 °C to obtain β-CD-OTs.
[0086] 2. Preparation of nitrogenated cyclodextrin (β-CD-N3)
[0087] Weigh 10g of β-CD-OTs and dissolve in 100mL of deionized water, heat to 80°C, then add 3.22g of sodium azide (NaN3), and stir for 18h. The...
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