| CPC A61F 2/06 (2013.01) [A61F 2/0077 (2013.01); A61F 2/062 (2013.01); B05D 1/002 (2013.01); D01D 5/003 (2013.01); D01D 5/0038 (2013.01); D01D 5/0061 (2013.01); D01D 5/0084 (2013.01); D04H 1/728 (2013.01); A61F 2002/0081 (2013.01); A61F 2210/0076 (2013.01); A61F 2240/001 (2013.01); A61F 2250/0058 (2013.01); A61L 2420/02 (2013.01); B05D 1/02 (2013.01); B05D 2254/02 (2013.01); B05D 2503/00 (2013.01); B05D 2518/00 (2013.01); B29C 48/151 (2019.02); D10B 2331/04 (2013.01); D10B 2331/041 (2013.01); D10B 2331/10 (2013.01); D10B 2509/00 (2013.01)] | 7 Claims |
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1. A preparation method for three-layer artificial blood vessel, including the following steps:
S1: dissolving a macromolecular compound into a solvent to obtain an electrospinning solution with a concentration of 5-30% w/v and an electric-spray solution with a concentration of 10-60% w/v;
S2: placing the electrospinning solution obtained in S1 over a mandrel device and performing electrospinning to obtain a porous electrospun inner layer, drying the inner layer to remove the residual solvent;
S3: with the inner layer obtained in S2 as a receiving surface, performing first electric spray, second electric spray, . . . nth electric spray with the electric-spray solution to obtain a dense middle layer, wherein a process of the first electric spray includes spraying, stopping, spraying, stopping, . . . repeated cycles, a time of the stopping in the process of the first electric spray is 5-20 min; and a time of each of the first electric spray, the second electric spray and the nth electric spray is 5-50 min; and
S4: with the dense middle layer obtained in S3 as a receiving surface, performing electrospinning, and then drying to obtain the three-layer artificial blood vessel.
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