Zein and glycopolypeptide grafted copolymer and preparation method and application thereof
A zein and graft technology, which is applied in the field of chemical modification of natural protein and its medical application, can solve problems such as no research work, and achieves favorable cell growth, good biocompatibility and degradability. , the effect of low price
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Embodiment 1
[0044] Example 1 Preparation of Zein and Glycopolypeptide Graft (ZG-1) and Electrospun Membrane
[0045] (1) Preparation of galactose pentaacetate
[0046] D-galactose (5.00 g) was dissolved in 15 mL of pyridine, and acetic anhydride (27 mL) was added at 0°C under nitrogen protection. After reacting for 24 hours, it was slowly poured into ice water (100 mL), and extracted three times with ethyl acetate. Use saturated NaHCO for the organic phase 3 The solution is cleaned until no gas is generated, and then washed with water and brine for 3 times. The organic phase was dried with anhydrous magnesium sulfate and then rotary evaporated to obtain an oily product with a yield of 97%.
[0047] (2) Preparation of 3-ynbutyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside
[0048] Dissolve galactose pentaacetate (10.00 g) and 3-butyn-1-ol (2.3 mL) in 50 mL of dry dichloromethane, add Et dropwise at 0°C under nitrogen protection 2 O·BF 3 (4.8mL), react at room temperature for 2h. Dilute with dic...
Embodiment 2
[0066] Example 2 Preparation of Zein and Glycopolypeptide Graft (ZG-2) and its Electrospun Membrane
[0067] (1) Preparation of galactose pentaacetate
[0068] D-galactose (5.00 g) was dissolved in 15 mL of pyridine, and acetic anhydride (27 mL) was added at 0°C under nitrogen protection. After reacting for 24 hours, it was slowly poured into ice water (100 mL), and extracted three times with ethyl acetate. Use saturated NaHCO for the organic phase 3 The solution is cleaned until no gas is generated, and then washed with water and brine for 3 times. The organic phase was dried with anhydrous magnesium sulfate and then rotary evaporated to obtain an oily product with a yield of 97%.
[0069] (2) Preparation of 3-ynbutyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside
[0070] Dissolve galactose pentaacetate (10.00 g) and 3-butyn-1-ol (2.3 mL) in 50 mL of dry dichloromethane, add Et dropwise at 0°C under nitrogen protection 2 O·BF 3 (4.8mL), react at room temperature for 2h. Dilute with...
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