Preparation method of animal skin acellular matrix dressing and dressing obtained
An acellular matrix and decellularization technology, which is applied in the preparation of animal skin acellular matrix dressings, and in the field of acellular matrix dressings, can solve the adverse effects on the structure and performance of collagen fibers in the acellular dermal matrix, and the removal of DNA/RNA has not attracted enough attention , easy to produce immune rejection and other problems, to achieve the effect of allowing cell repopulation, reducing the risk of transmission, and completely removing antigens
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[0033] In one embodiment of the preparation method according to the present invention, the animal skin is preferably common mammalian skin, such as human cadaver skin, pig skin, cowhide, etc., more preferably low-cost pig skin.
[0034] In one embodiment of the preparation method according to the present invention, the decellularization solution comprises trypsin with a mass concentration of 0.01% to 0.09%, ammonium sulfate with a mass concentration of 0.5% to 1.0%, and ammonium sulfate with a mass concentration of 0.5% to 0.15% % degreaser.
[0035] In one embodiment of the preparation method according to the present invention, the degreasing agent can be any type used in the field, including but not limited to Pingpinga, Triton X-100, sodium laurylalanine, fatty alcohol poly Oxyethylene ether etc.
[0036] In one embodiment of the preparation method according to the present invention, the split skin piece is soaked in the decellularization solution for 10-60 minutes, which ...
Embodiment 1
[0090] A cadaver skin slice with a thickness of 0.6 mm was taken with a skin extractor, the external fat was scraped off bluntly, and washed 5 times in purified water for 10 minutes each time. After being washed with purified water, it was placed in a -80°C ultra-low temperature refrigerator for deep freezing for 5 hours. Take out the skin slices from the ultra-low temperature refrigerator, put them into a container filled with purified water at room temperature and soak them until they are completely thawed, and a freeze-thaw process is completed at this time. The thawed skin slices were then frozen in a -80°C refrigerator for 5 hours, and so repeated freezing and thawing 4 times. Then add 5% acetic acid solution and soak for 20 minutes, take it out and then wash it thoroughly with purified water, scrape off the epidermis bluntly, and retain the basement membrane. Put the above cadaver skin slices into a combined solution of 0.06% peracetic acid and 0.5% sodium chloride for ...
Embodiment 2
[0092] Healthy pigs were selected, and after slaughter, a skin slice with a thickness of 0.3 mm was taken with a skinning machine, the external fat was bluntly scraped off, and washed three times in purified water, each time for 15 minutes. After being washed with purified water, it was placed in a -80°C ultra-low temperature refrigerator for deep freezing for 15 hours. Take out the skin slices from the ultra-low temperature refrigerator, put them into a container filled with purified water at room temperature and soak them until they are completely thawed, and a freeze-thaw process is completed at this time. The thawed skin slices were then frozen in a -80°C refrigerator for 15 hours, and so repeated freezing and thawing 3 times. Then add 2% acetic acid solution and soak for 30 minutes, take it out and then wash it thoroughly with purified water, scrape off the epidermis bluntly, and retain the basement membrane. Put the above pigskin into a combined solution of 0.05% perace...
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