Method for preparing peripheral nerve conduit by salt-induced phase transition
A peripheral nerve, nerve conduit technology, applied in the field of biomedical materials
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Embodiment 1
[0032] Using temperature-sensitive chitosan solution with a concentration of 0.4% as raw material, prepare a nerve conduit with an inner diameter of 0.5 mm and a length of 1 mm. After the solution forms a gel and has a certain strength, the mandrel is taken out together with the gel and placed in a 0.5% (w / v) NaCl solution to shrink for 12 hours. After the samples were taken out and pre-frozen at -20°C, they were freeze-dried for 12 hours. Remove mandrel 60 The temperature-sensitive chitosan nerve guide was prepared by Co irradiation sterilization.
Embodiment 2
[0034] Using temperature-sensitive chitosan solution with a concentration of 0.8% as raw material, prepare a nerve conduit with an inner diameter of 1 mm and a length of 10 mm. After the gel is formed and has a certain strength, the core rod is taken out together with the gel and placed in 2.5% (w / v) CH 3 COONH 4 Shrinkage in the solution for 48h. After the samples were taken out and pre-frozen at -30°C, they were freeze-dried for 18 hours. Remove mandrel 60 The temperature-sensitive chitosan nerve guide was prepared by Co irradiation sterilization.
Embodiment 3
[0036] Using temperature-sensitive chitosan solution with a concentration of 1% as raw material, prepare a nerve conduit with an inner diameter of 3mm and a length of 40mm. After the gel is formed and has a certain strength, the core rod is taken out together with the gel and placed in 5% (w / v) Na 2 HPO 4 and CH 3 Shrink in COONa solution for 24h. After the samples were taken out and pre-frozen at -40°C, they were freeze-dried for 24 hours. Remove the mandrel and sterilize it with 60Co radiation to form a temperature-sensitive chitosan nerve guide.
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