Xenogeneic acellular dermis and preparation method thereof
An acellular and dermis technology, applied in the field of acellular xenogeneic dermis and its preparation, can solve problems such as collagen damage and unfavorable wound recovery, and achieve the effects of reducing negative effects, facilitating recovery as soon as possible, and avoiding acute immune response of the human body.
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Embodiment 1
[0045] see figure 1 and figure 2 , a method for preparing decellularized heterogeneous dermis, comprising the following steps in sequence,
[0046] Step A: Prepare pig dermis slices. The specific operation is to clean the back skin of the mature large white pig (Yorkshire pig breed), and after removing the hair with the depilator, use the skin drum to cut a piece of skin with a thickness of 0.25 mm and discard it (function: remove the epidermis, hair and hair follicles). Then use the skin drum to take a 0.50-0.75 mm thick dermis for later use. Those skilled in the art should know that the raw materials are not limited by the breed and age of pigs, and the back skin of mature large white pigs is only a preferred method. The preferred reason is that it is convenient to obtain materials and there are many available raw materials.
[0047] Step B: Disinfect the pig dermis slices. The specific operation is to put the pig dermis slices into a sterile bottle, add 0.5% peracetic ...
Embodiment 2
[0055] see figure 1 , figure 2 and image 3 , on the basis of embodiment 1, this embodiment also has the following steps in sequence after step G,
[0056] Step H: Add the ribonuclease solution, and carry out thorough mixing and reaction, the ribonuclease in the ribonuclease solution is synthesized by artificial recombination or directly extracted from animal tissue, and the ribonuclease solution is 4-hydroxyethyl Piperazineethanesulfonic acid buffer, each liter of 4-hydroxyethylpiperazineethanesulfonic acid buffer contains 20 mmol 4-hydroxyethylpiperazineethanesulfonic acid, 2.5 mmol magnesium chloride, 0.5 mmol calcium chloride and 0.5 Gram ribonuclease, its pH value is 8, and the ratio of ribonuclease solution volume and pig dermis sheet volume is 20:1.
[0057] Step I: Aspirate the ribonuclease solution, then add phosphate buffered saline to fully wash the pig dermis slices. The specific operation is to suck out the ribonuclease solution, wash with phosphate-buffered ...
Embodiment 3
[0060] see figure 1 , figure 2 , image 3 and Figure 4 , present embodiment is on the basis of embodiment 2, also has following steps successively after step 1,
[0061] Step J: adding alpha-galactosidase solution for thorough mixing and reaction, said alpha-galactosidase solution is prepared by adding alpha-galactosidase to citrate buffer solution. The specific operation is to shake on a shaker for 10 hours.
[0062] Step K: Aspirate the alpha-galactosidase solution, then add phosphate-buffered saline to thoroughly wash the porcine dermal slices. The specific operation is aspirating the alpha-galactosidase solution, washing with phosphate-buffered saline three times, and shaking on a shaker for 30 minutes each time.
[0063] In this embodiment, steps J~K are alpha-galactose removal methods. The alpha-galactose referred to in this example is Galactose-alpha-1,3-galactose, and the alpha-galactosidase referred to is galactose-alpha-1,3-galactosidase. Galactose-alpha-1,3...
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