Degradable meninx repairing material and preparing method thereof
A technology for repairing materials and meninges, which is applied in the field of natural biomedical materials, can solve the problems that the product cannot be degraded in the body, avoid side effects such as immune rejection or inflammation, prevent cerebrospinal fluid leakage, and facilitate removal
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Embodiment 1
[0079] Embodiment 1, preparation of degradable meningeal repair material
[0080] 1. Spread paraffin particles with a particle size of 100 μm on the lower layer of the culture container, and the spreading thickness is 1 mm, to prepare a scaffold layer for inducing tissue regeneration (thickness is 1 mm, pore diameter is 100 μm); the upper layer spreads 100 nm porogen paraffin (thickness 1mm, pore size 100nm), used to prepare the anti-adhesion layer. Insert the activated Acetobacter xylinum into the bacterial culture solution and mix it evenly, then add it into the culture container, the depth of the culture medium is about 2mm, and culture it at 20°C for 20 days, take out the BC membrane and place it at 50-70°C Heat in a water bath to remove the porogen paraffin. The bacterial culture solution is: mannitol 25g / L, tryptone 3g / L, yeast powder 5g / L, pH 5.0, sterilized at 121°C for 20min, cooled to 30°C before use.
[0081] 2. After the above-mentioned BC membrane was fully wash...
Embodiment 2
[0085] Embodiment 2, preparation of degradable meningeal repair material
[0086] 1. CaCO with particle size of 500 μm and 500 nm 3 Spread on the lower layer and upper layer of the culture container, respectively as the scaffold layer and anti-adhesion layer for inducing tissue regeneration, and the spreading thickness is 1.5mm. Insert the activated Acetobacter xylinum into the bacterial culture solution, mix it evenly, add it to the culture container, and culture it at 30°C for 14 days, then take out the BC membrane and soak it in 2% hydrochloric acid solution for 5 hours to remove the CaCO 3 porogen. The bacterial culture solution is: mannitol 25g / L, tryptone 3g / L, yeast powder 5g / L, pH 5.0, sterilized at 121°C for 20min, cooled to 30°C before use.
[0087] 2. The above BC membrane was fully washed with distilled water and dried by centrifugation, and then soaked in 8mol / L NaOH solution at 25°C and 6% Tween-40 solution at 30°C for 5h and 40h respectively. After immersion,...
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