Scaffold material for clinical dural reconstruction and preparation method thereof
A dura mater, physical method technology, applied in the direction of tissue regeneration, can solve the problems of hard and difficult to adhere materials, easy to cause adhesion and other problems
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Embodiment 1
[0009] Take 1.0 g of commercially available type I collagen and 0.5 g of commercially available chitin, and dissolve them in 100 ml of 0.2 mol / L glacial acetic acid solution. After completely dissolving, the mixture was poured into a mold tray, placed on an automatic shaker, and shaken automatically for 60 minutes, and finally the obtained biofilm was dehydrated to make its water content 40.0%. Sterilized by irradiation after sealing the package. The mass ratio of type I collagen: chitosan is 2:1.
Embodiment 2
[0011] Take 10.0 g of commercially available type I collagen and 3.0 g of commercially available chitin, and dissolve them in 100 ml of 0.05 mol / L glacial acetic acid solution. After completely dissolving, pour the mixed liquid into the mold tray, put it on an automatic shaker, shake it automatically for 120 minutes, and finally dehydrate the obtained biofilm to make its water content 10.0%. Sterilized by irradiation after sealing the packaging. The mass ratio of type I collagen: chitosan is 10:3.
Embodiment 3
[0013] Take 2.0 g of commercially available type I collagen and 0.5 g of commercially available chitin, and dissolve them in 100 ml of 0.01 mol / L glacial acetic acid solution. After completely dissolving, pour the mixed liquid into the mold tray, put it on an automatic shaker, and shake it automatically for 30 minutes, and finally dehydrate the obtained biofilm to make its water content 1.0%. Sterilized by irradiation after sealing the packaging. The mass ratio of type I collagen: chitosan is 4:1.
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