An anti-infection electrospinning degradable hernia prosthesis and preparation method thereof
An electrospinning and anti-infection technology, which is applied in the direction of electrospinning, filament/thread forming, textiles and papermaking, etc., can solve the problems of easy shedding of antibacterial substances, poor anti-infection effect, unfavorable growth of new capillaries and wounds Repair and other issues
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[0030] The invention provides a preparation method of an anti-infection electrospinning degradable hernia patch, comprising the following steps:
[0031] mixing polyurethane solution, gallic acid and polyvinyl alcohol to obtain a spinning solution;
[0032] Electrospinning the spinning solution to obtain a spun film;
[0033] The spinning film is soaked in water, and the polyvinyl alcohol is dissolved to obtain an anti-infection electrostatic spinning degradable hernia patch.
[0034] The invention mixes polyurethane solution, gallic acid and polyvinyl alcohol to obtain spinning solution. In the present invention, the preparation method of the polyurethane solution preferably includes the following steps: mixing diisocyanate, polycaprolactone and an organic solvent to carry out polycondensation reaction to obtain a prepolymer; Mixed with organic tin catalyst, a chain extension reaction occurs to obtain a polyurethane solution.
[0035] In the present invention, it is prefer...
Embodiment 1
[0052] 10g of polycaprolactone with a number average molecular weight of 30000, 0.758g of diphenylmethane diisocyanate and 21.952g of dimethylformamide were put into a machine equipped with mechanical stirring, reflux condenser and N 2 In the three-necked flask with inlet and outlet, magnetically stir until dissolved, and in N 2 Polycondensation reaction at 80°C for 3 hours under protection to obtain a prepolymer;
[0053] Add 0.218g of 1,4-butanediol to the above prepolymer, drop 2 to 3 drops of dibutyltin dilaurate, and conduct a chain extension reaction at 110°C for 9 hours to obtain a transparent polyurethane solution with a solid content of 25%. ;
[0054] Mix 3 g of the polyurethane solution, 0.009 g of gallic acid and 0.5 g of a 10 wt % polyvinyl alcohol aqueous solution, homogenize under ultrasonic conditions (ultrasonic power is 60 W, time is 2 h), to obtain a spinning solution;
[0055] Set up the spray table, put the spinning solution into a 5mL syringe in the spr...
Embodiment 2
[0059] Put 10g of polycaprolactone with a number average molecular weight of 20000, 0.758g of dicyclohexylmethane diisocyanate and 21.952g of tetrahydrofuran into a device equipped with mechanical stirring, reflux condenser and N 2 In the three-necked flask with inlet and outlet, magnetically stir until dissolved, and in N 2 Polycondensation reaction at 70°C for 4 hours under protection to obtain a prepolymer;
[0060] Add 0.218g of 1,4-butanediol to the above prepolymer, drop 2 to 3 drops of dibutyltin dilaurate, and conduct a chain extension reaction at 90°C for 10 hours to obtain a transparent, high-viscosity, solid content of 25%. Polyurethane solution;
[0061] Mix 3 g of the polyurethane solution, 0.027 g of gallic acid and 0.7 g of a 10 wt % polyvinyl alcohol aqueous solution, homogenize under ultrasonic conditions (ultrasonic power is 80 W, time is 1 h), to obtain a spinning solution;
[0062] Set up the spray table, put the spinning solution into a 5mL syringe in th...
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