Superparamagnetic iron oxide nano-particle-collagen-chitosan magnetic degradable nerve conduit and preparation method thereof
A technology of iron oxide nanometers and nerve conduits, which is applied in the fields of medical science and prostheses, can solve problems such as poor functional recovery of the innervation area, poor repair effect of nerve stents, and uncertain growth direction of regenerative nerves, etc., so as to improve the repair effect, Promotes the regeneration of damaged nerves and promotes secretion
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Embodiment 1
[0030] (1) Prepare 0.1mol / L Fe respectively 3+ and Fe 2+ solution, under nitrogen, according to Fe 3+ :Fe 2+ Mix at a molar ratio of 2:1, and mechanically stir for 3 hours to make it fully mixed. Under the condition of continuous nitrogen flow, 1 mol / L NaOH solution was added dropwise to the mixed solution until the pH of the mixed solution was 9, and a black precipitate was obtained. Then the water bath was heated for 2h, and then after standing for 5h, the supernatant was removed, the generated particles were filtered under reduced pressure, washed repeatedly with distilled water and absolute ethanol, and the impurity ions on the surface of the particles were washed away, and the obtained particles were obtained at 50 vacuum-dried at ℃, ground and sieved to obtain SPIONs.
[0031] (2) Weigh type I collagen and chitosan respectively, the masses of type I collagen and chitosan are 50 mg and 50 mg respectively, and weigh 5 mg of SPIONs prepared in (1).
[0032] (3) Add 1ml...
Embodiment 2
[0037] (1) Prepare 0.1mol / L Fe respectively 3+ and Fe 2+ solution, under nitrogen, according to Fe 3+ :Fe 2+ Mix at a molar ratio of 2:1, and stir mechanically for 3.5 hours to make it fully mixed. Under the condition of continuous nitrogen flow, 1 mol / L NaOH solution was added dropwise to the mixed solution until the pH of the mixed solution was 9.5, and a black precipitate was obtained. Then the water bath was heated for 2h, and then after standing for 5h, the supernatant was removed, the generated particles were filtered under reduced pressure, washed repeatedly with distilled water and absolute ethanol, and the impurity ions on the surface of the particles were washed away, and the obtained particles were obtained at 50 vacuum-dried at ℃, ground and sieved to obtain SPIONs.
[0038] (2) Weigh type I collagen and chitosan respectively. The masses of type I collagen and chitosan are 80 mg and 20 mg respectively, and weigh 10 mg of SPIONs prepared in (1).
[0039] (3) Ad...
Embodiment 3
[0044] (1) Prepare 0.1mol / L Fe respectively 3+ and Fe 2+ solution, under nitrogen, according to Fe 3+ :Fe 2+ Mix at a molar ratio of 2:1, and mechanically stir for 4 hours to make it fully mixed. Under the condition of continuous nitrogen flow, 1 mol / L NaOH solution was added dropwise to the mixed solution until the pH of the mixed solution was 10, and a black precipitate was obtained. Then the water bath was heated for 2h, and then after standing for 5h, the supernatant was removed, the generated particles were filtered under reduced pressure, washed repeatedly with distilled water and absolute ethanol, and the impurity ions on the surface of the particles were washed away, and the obtained particles were obtained at 50 vacuum-dried at ℃, ground and sieved to obtain SPIONs.
[0045] (2) Weigh type I collagen and chitosan respectively. The masses of type I collagen and chitosan are 20 mg and 80 mg respectively, and weigh 20 mg of SPIONs prepared in (1).
[0046] (3) Add 1...
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