Composite nerve conduit and preparation method thereof
A nerve conduit and catheter technology, applied in the field of biomedical tissue engineering, can solve the problems of unfavorable surface morphology for nerve cell adhesion and growth, failure to provide biochemical clues for nerve cell regeneration and growth neurotrophic factors, etc., to achieve excellent mechanical properties, preparation The method is simple and the effect of uniform wall thickness
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Embodiment 1
[0042] Embodiment 1, preparation composite nerve guide
[0043] Prepare the composite nerve guide as follows:
[0044] (1) Prepare the outer catheter:
[0045] 1) Under room temperature conditions, a certain amount of chitosan was dissolved in 2wt% acetic acid to prepare a solution with a mass fraction of 6wt%. Dissolve a certain amount of polyvinyl alcohol in acetic acid of the same concentration, heat in a water bath at 95°C for 1 hour, and prepare a solution with a mass fraction of 12 wt%. Mix the above two solutions in different proportions, stir evenly, and centrifuge to remove air bubbles before use. The mass ratio of chitosan and polyvinyl alcohol in the mixture is 1:2.
[0046] 2) Using catheter forming equipment, dip the chitosan-polyvinyl alcohol mixture on a mold with a length of 5cm and a diameter of 4mm, fix the stainless steel mold on the brushless motor, and control the mold at a speed of 700rpm through the motor controller Horizontal rotation. After the so...
Embodiment 2
[0054] Embodiment 2, performance test
[0055] 1. Mechanical properties
[0056] The mechanical properties of the outer catheter prepared in step (1) in Example 1 were tested by a universal mechanical tensile testing machine, the calibration distance was 30 mm, and the tensile rate was 5 mm / min. The results show( image 3 ), the outer conduit has superior mechanical properties, with a maximum load of 19N.
[0057] 2. Biological activity
[0058] Taking E8 chick embryo dorsal root ganglion (DRG) as the test object, the biological activity of the composite nerve conduit prepared in Example 1 was verified by the chick embryo dorsal root ganglion (DRG) culture method. The specific operation is as follows:
[0059] Chicken dorsal root ganglia extracted from 8-day-old chicken embryos were placed in the composite nerve conduit, and the composite nerve was co-cultured with the conduit for 48 hours, then the composite nerve conduit was cut, and the dorsal root ganglion was observed...
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