A kind of decellularized dermal matrix tissue engineering scaffold and preparation method thereof
A technology of decellularized dermis and matrix tissue, applied in tissue regeneration, medical science, prosthesis, etc., can solve the problems of long enzyme treatment time, cumbersome process, and difficulty in satisfying rapid cell growth, and achieves a simple and easy preparation method, Effect of promoting tissue repair and excellent biocompatibility
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[0028] The invention provides a preparation method of an acellular dermal matrix tissue engineering scaffold, comprising the following steps:
[0029] (1) Immersing heterogeneous or allogeneic skin in saline solution to remove epidermal tissue to obtain dermal tissue;
[0030] (2) sequentially inactivating and decellularizing the dermal tissue to obtain a dermal matrix;
[0031] (3) drying and thinning the obtained dermis matrix sequentially to obtain dermis matrix fibers;
[0032] (4) The dermal matrix fibers are mixed with the dispersion liquid, followed by freeze-drying and cross-linking treatment in sequence to obtain the decellularized dermal matrix tissue engineering scaffold.
[0033] In the present invention, in the preparation method of the acellular dermal matrix tissue engineering scaffold, it is preferable to first scrape off the heterogeneous or allogeneic skin and hair with a blade, and then use a drum skin harvester to take the skin, and the thickness is prefer...
Embodiment 1
[0058] (1) Take the skin: scrape off the hair of the pigskin with a blade, take the skin with a drum skin machine, and cut the thickness of the dermal matrix (including the epidermis) to 1 mm.
[0059] (2) Peel off the skin: cut the heterogeneous or allogeneic skin into a size of 1cm×3cm, soak it in 1.5mol / L sodium chloride solution according to the ratio of 1g:5ml, shake it on the shaker for 12 hours, and gently peel off the skin with tweezers , to obtain dermal tissue.
[0060] (3) Virus inactivation: first wash the dermis tissue with purified water for 30 minutes, then soak the dermis tissue with 75% alcohol according to the ratio of 1g:5ml for 2 hours, and rinse with deionized water for 30 minutes.
[0061] (4) Decellularization: soak the dermal tissue in 1mol / L sodium hydroxide solution, the ratio of solid to liquid is 1g:5mL, and the soaking time is 12h; then soak the dermal tissue in 0.1% polyethylene glycol octylphenyl In an aqueous ether solution, the ratio of solid ...
Embodiment 2
[0065] (1) Take the skin: scrape off the hair of the pigskin with a blade, take the skin with a drum skin machine, and cut the thickness of the dermal matrix (including the epidermis) to 1 mm.
[0066] (2) Peeling off the skin: Cut the heterogeneous or allogeneic skin into a size of 1cm×3cm, immerse it in 1mol / L sodium chloride solution according to the ratio of 1g:4ml, shake it on the shaker for 12 hours, and gently peel off the skin with tweezers. Get dermal tissue.
[0067] (3) Virus inactivation: first wash the dermis tissue with purified water for 30 minutes, then soak the dermis tissue with 70% alcohol according to the ratio of 1g:4ml for 2 hours, and rinse with deionized water for 30 minutes.
[0068] (4) Decellularization: soak the dermal tissue in 0.5mol / L sodium hydroxide solution, the ratio of solid to liquid is 1g:4mL, and the soaking time is 6h; then soak the dermal tissue in 0.05% polyethylene glycol octylbenzene In the base ether aqueous solution, the ratio of ...
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