Amylase modified product for co-delivery of genes and antitumor drugs as well as preparation method and application thereof
An anti-tumor drug, amylose technology, applied in the field of biomedical engineering materials, to achieve selectivity, reduce product cytotoxicity, and improve water solubility
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Embodiment 1
[0037] Mix 0.48g of dry amylose and 8mL of 1-azido-propylene oxide and dissolve in 20mL of aqueous sodium hydroxide (aqueous solution of sodium hydroxide formed by adding 0.4g of sodium hydroxide to 100ml of water), at 30°C Stir in the dark for 24 hours; after the reaction, dialyze the reaction product with a 14,000 cut-off dialysis bag for 48 hours, filter, and freeze-dry to obtain azide-containing amylose with a yield of 85%.
Embodiment 2
[0039] Mix 0.48g of dry amylose and 4mL of 1-azido-propylene oxide and dissolve in 20mL of aqueous sodium hydroxide solution (aqueous sodium hydroxide solution formed by adding 0.8g of sodium hydroxide to 100ml of water), at 40°C Stir in the dark for 36 hours; after the reaction, the reaction product was dialyzed for 72 hours, filtered, and freeze-dried to obtain amylose containing azide groups with a yield of 81%.
Embodiment 3
[0041] Mix 0.50g of the 3rd generation alkyne-containing dendritic polylysine with 50mg of the azide-group-containing amylose obtained in Example 1 and dissolve in 30mL of anhydrous dimethyl sulfoxide; 2 Protect for 15 minutes, then add 33.6mg copper sulfate pentahydrate and 53.2mg sodium ascorbate, heat up to 50°C and react for 48 hours; Amylose Modifications for Co-delivery of Antineoplastic Drugs. The yield was 79%, and the result of elemental analysis showed that the dendritic amylose derivative contained 9.05% N.
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