Multi-nano transmission system and preparation method thereof
A delivery system and nanotechnology, which can be used in pharmaceutical formulations, medical preparations with non-active ingredients, amine active ingredients, etc., and can solve problems such as single function of materials
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Embodiment 1
[0055] In this embodiment, a multiple nano-delivery system and a preparation method thereof comprise the following steps:
[0056] (1) Accurately weigh 5.3mmol β-cyclodextrin and 34.1mmol 18-crown-6 under inert gas protection conditions, dissolve in 30mL anhydrous DMF, then add 42.0mmol KH and keep stirring to make it mix with cyclodextrin Hydroxyl fully reacted. Control the temperature at 50°C, and slowly add 13.4mL of glycidol dissolved in 10mL of anhydrous DMF into the above solution dropwise, and the dripping is completed in about 24h. Control the temperature at 80°C and continue the reaction for 16h to end. After the temperature of the system dropped to room temperature, a small amount of water was added to terminate the reaction, dialyzed against water (MWCO=1000), and freeze-dried to obtain a pale yellow β-CD-HPG solid.
[0057](2) 8 mmol CDI dissolved in 10 mL of anhydrous DMF was slowly added dropwise into the solution of 4 mmol β-CD-HPG (dissolved in anhydrous DMF)...
Embodiment 2
[0062] In this embodiment, a multiple nano-delivery system and a preparation method thereof comprise the following steps:
[0063] (1) Accurately weigh 5.3mmol β-cyclodextrin and 34.1mmol 18-crown-6 under inert gas protection conditions, dissolve in 30mL anhydrous DMF, then add 42.0mmol KH and keep stirring to make it mix with cyclodextrin Hydroxyl fully reacted. Control the temperature at 50°C, and slowly add 26.8 mL of glycidol dissolved in 20 mL of anhydrous DMF into the above solution dropwise, and the drop will be completed in about 24 hours. Control the temperature at 80°C and continue the reaction for 16h to end. After the temperature of the system dropped to room temperature, a small amount of water was added to terminate the reaction, dialyzed against water (MWCO=1000), and freeze-dried to obtain the host molecule β-CD-HPG solid with a higher degree of polymerization.
[0064] Steps (2)-(5) are the same as in Example 1.
Embodiment 3
[0066] In this embodiment, a multiple nano-delivery system and a preparation method thereof comprise the following steps:
[0067] Steps (1), (2), (4), and (5) in Example 1 are retained, and the step of targeting the mannose-modified host molecule is removed to obtain a non-targeting multiple nano-delivery system.
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