Zein and glycopolypeptide graft and its preparation method and application
A technology of zein and grafts, which is applied in the field of chemical modification of natural protein and its medical application, can solve the problems of unseen research work, and achieve good cell growth, good biocompatibility and degradability , Good adhesion and growth effect
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Embodiment 1
[0044] Example 1 Preparation of zein and glycopolypeptide graft (ZG-1) and its 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 h, it was slowly poured into ice water (100 mL), and extracted three times with ethyl acetate. The obtained organic phase was washed with saturated NaHCO 3 The solution was washed until no gas was generated, and then washed with water and concentrated brine three times in sequence. 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] Galactose pentaacetate (10.00g) and 3-butyn-1-ol (2.3mL) were dissolved in 50mL of dry dichloromethane, and Et was added dropwise at 0°C under nitrogen protection ...
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 h, it was slowly poured into ice water (100 mL), and extracted three times with ethyl acetate. The obtained organic phase was washed with saturated NaHCO 3 The solution was washed until no gas was generated, and then washed with water and concentrated brine three times in sequence. 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] Galactose pentaacetate (10.00g) and 3-butyn-1-ol (2.3mL) were dissolved in 50mL of dry dichloromethane, and Et was added dropwise at 0°C under nitrogen protection ...
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