Preparation method of EMPLGA/Gel-HA hydrogel-microsphere bionic composite support
A composite scaffold and hydrogel technology, applied in the field of preparation of biomimetic composite scaffolds, can solve the problems of low mechanical strength, difficult disinfection, and poor shape retention ability of hydrogel porous materials, achieve superior biological properties, and expand the scope of regulation. , the effect of high mechanical strength
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Embodiment 1
[0033] Add 78.0g of dried D,L-lactide and 22.0g of glycolide into the dried ampoule, and then add 0.015g of dehydrated stannous octoate (Sn(Oct) 2 ); After vacuum drying for 12 h, seal the tube with an alcohol blowtorch under the condition of 4.0 Pa. Put the sealed ampoule into a thermostat, react at 140°C for 24 hours, break the ampoule, and take out the crude product PLGA. Product M w =1.76×10 5 Da, M w / M n =1.21.
[0034] The crude product was dissolved in trichloromethane to prepare a 2.0 wt% solution, dropped into 3 times the volume of ethanol and precipitated 3 times, and dried in vacuum. The purified PLGA was mixed with 6.0 g of maleic anhydride and 0.20 g of dibenzoyl peroxide, placed in a three-necked flask, and reacted for 24 hours at a pressure of 0.084 MPa and 100° C. to obtain a crude MPLGA polymer. The grafted crude polymer was placed in a Soxhelt extractor, and chloroform was used as a solvent to extract for 8 hours. The extracted residue was vacuum dried and dis...
Embodiment 2
[0041] Add 76.0g of dried D,L-lactide and 24.0g of glycolide into the dried ampoule, and add 0.022g of dehydrated stannous octoate (Sn(Oct) 2 ); After vacuum drying for 12 h, seal the tube with an alcohol blowtorch under the condition of 5.0Pa. Put the sealed ampoule into a thermostat and react for 36 h at 120°C. Break the ampoule to obtain the crude product PLGA. Product M w =1.45×10 5 Da, M w / M n =1.31.
[0042] The crude product was dissolved in chloroform to prepare a 3.0wt% solution, dropped into 4 times the volume of ethanol and precipitated 4 times, and dried in vacuum. The purified PLGA was mixed with 6.5g maleic anhydride and 0.25g dibenzoyl peroxide, placed in a three-necked flask, and reacted for 24h under the conditions of a pressure of 0.065MPa and 100°C to obtain a crude MPLGA polymer. Place the grafted crude polymer in a Soxhelt extractor and extract with chloroform as a solvent for 8 hours. The residue after extraction is vacuum dried and dissolved in chloroform...
Embodiment 3
[0049] Add 73.0g of dried D,L-lactide and 27.0g of glycolide into the dried ampoule, and then add 0.025g of dehydrated stannous octoate (Sn(Oct) 2 ); After vacuum drying for 12 h, seal the tube with an alcohol blowtorch under the condition of 6.0 Pa. Put the sealed ampoule in a thermostat, react at 130°C for 36 h, break the ampoule, and take out the crude product PLGA. Product M w =1.85×10 5 Da, M w / M n =1.23.
[0050] The crude product was dissolved in chloroform to prepare a 4.0wt% solution, dropped into 5 times the volume of ethanol and precipitated 5 times, and dried in vacuum. The purified PLGA was mixed with 6.8 g maleic anhydride and 0.18 g dibenzoyl peroxide, placed in a three-necked flask, and reacted for 24 hours at a pressure of 0.076 MPa and 100° C. to obtain a crude MPLGA polymer. The grafted crude polymer was placed in a Soxhelt extractor, and chloroform was used as a solvent to extract for 8 hours. The residue was vacuum dried and dissolved in chloroform to prepa...
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