Porous biological material using modified gelatin as crosslinking agent and preparation method of porous biological material
A technology of biomaterials and porosity, applied in the field of biomedical materials
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Embodiment 1
[0026] Add 0.2 g of methacrylamide-modified gelatin with an amino substitution degree of 35% into a 20 mL stoppered glass bottle, then add 1.0 g of acrylamide monomer and 10 mL of deionized water, blow in nitrogen, and stir for 15 minutes until a homogeneous clear solution is formed. Then add 100 μL of N,N,N',N'-tetramethylethylenediamine solution with a concentration of 10% by mass, mix well and continue to pass nitrogen gas for 5 minutes, then add 200 μL of persulfuric acid with a concentration of 4% by mass Ammonium solution, then quickly sealed, placed in 20 o After reacting in C water bath for 12 hours, the reactants were taken out and soaked in 20 o C deionized water for 48 hours, changing the deionized water every 8 hours, and then freeze-drying for 24 hours to obtain a porous biomaterial with good biocompatibility.
Embodiment 2
[0028] Add 0.2 g of methacrylamide-modified gelatin with an amino substitution degree of 60 % and 0.2 g of inorganic nanoclay Laponite into a 20 mL stoppered glass bottle, then add 1.0 g of acrylamide monomer and 10 mL of deionized water , nitrogen gas was introduced, and stirred for 30 minutes until a uniform and transparent solution was formed. Then add 100 μL of N,N,N',N'-tetramethylethylenediamine solution with a concentration of 10% by mass, mix well and continue to pass nitrogen gas for 5 minutes, then add 200 μL of persulfuric acid with a concentration of 4% by mass ammonium solution, then quickly sealed and placed at -20 o After reacting in C refrigerator for 24 hours, the reactants were taken out and soaked in 20 o C deionized water for 48 hours, changing the deionized water every 8 hours, and then freeze-drying for 24 hours to obtain a porous biomaterial with good biocompatibility and rapid swelling.
Embodiment 3
[0030]Add 0.1 g of methacrylamide-modified gelatin with an amino substitution degree of 90% and 0.1 g of inorganic nanoclay Laponite into a 20 mL stoppered glass bottle, then add 1.0 g of N-isopropylacrylamide monomer and 10 mL of deionized water was blown with nitrogen, and stirred for 20 minutes until a uniform and transparent solution was formed. Then add 100 μL of N,N,N,N-tetramethylethylenediamine solution with a concentration of 10% by mass, mix well and continue to blow nitrogen gas for 5 minutes, then add 200 μL of ammonium persulfate solution with a concentration of 4% by mass , then quickly sealed and placed at -30 o After reacting in C refrigerator for 24 hours, the reactants were taken out and soaked in 20 o C deionized water for 48 hours, change the deionized water every 8 hours, and then freeze-dry for 24 hours to obtain a temperature-sensitive and fast-swelling porous biomaterial.
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