Material for promoting operation wound heal and preparation method thereof
A healing material and wound technology, applied in the field of medical materials, can solve problems such as heavy metal allergy, itching, and limited application range, and achieve the effect of promoting repair speed and effect, promoting healing, and promoting wound repair
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Embodiment 1
[0038] Take 200 g of fresh porcine small intestinal submucosa (SIS), cut it and wash it thoroughly with clean water. First, soak in 300ml of 8% (v / v) hydrogen peroxide solution for 8 hours for degreasing treatment, after thorough cleaning, soak in 500ml of chloroform and methanol mixed solution (ratio: 1:1) for 5 hours to remove cells. After thoroughly washing with clean water, use 400ml of trypsin solution with a concentration of 0.1% (g / ml) and a pH of 8.0 for 2 hours to remove the protein, thoroughly wash until the product is clean, and finally pre-freeze and freeze-dry the product at -80°C . It is pulverized to a size of 0.01mm-1mm in diameter with an ultra-low temperature pulverizer, and packed and sealed.
Embodiment 2
[0040] Take 200g of fresh amniotic membrane, cut it and wash it thoroughly with water. First soak 200ml of hydrogen peroxide solution with a concentration of 12% (v / v) for 5h for degreasing treatment, after thorough cleaning, then soak 400ml with a mixed solution of chloroform and methanol (ratio 1:2) for 15 to remove cells. After thoroughly washing with water, use 200ml of trypsin with a concentration of 0.25% (g / ml) and a pH of 8.4 for deproteinization treatment for 1 hour, thoroughly wash until the product is clean, and finally pre-freeze and freeze-dry the product at -80°C. It is pulverized to a size of 0.01mm-1mm in diameter with an ultra-low temperature pulverizer, and packed and sealed.
Embodiment 3
[0042] Take 300 g of fresh porcine small intestinal submucosa (SIS), cut it and wash it thoroughly with water. First, use 300ml of 15% (v / v) hydrogen peroxide solution for degreasing treatment for 1h, after thorough cleaning, soak in 900ml of chloroform and methanol mixed solution (ratio: 1:1) for 2h to remove cells. After thoroughly washing with clean water, use 1000ml of trypsin with a concentration of 0.1% for deproteinization treatment. The treatment time is 28 hours. It was dissolved for 3 days, and the suspended solution was separated into a supernatant. The electrospinning equipment is used to spin and form a flat film-like material. The pressure is 20kV, and the inner diameter of the spinneret is 0.5mm. The distance between the spinneret and the collecting plate is 28cm. Among them, the content of soluble protein in extracellular matrix reaches 81%.
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