Biomimetic vascular network and devices using the same
US-9498320-B2 · Nov 22, 2016 · US
US9820846B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9820846-B2 |
| Application number | US-201514686262-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 14, 2015 |
| Priority date | Dec 12, 2014 |
| Publication date | Nov 21, 2017 |
| Grant date | Nov 21, 2017 |
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The present invention provides a reparation method of a tubular vascular graft, (a) immersing a tubular scaffold in a first light sensitivity gelatin solution, and irradiate the tubular scaffold by a first time period, to let surface of the tubular scaffold form a base layer; (b) immersing the tubular scaffold of the step (a) in a chitin gelatin solution, when the surface of the base layer form a film, then immersing the tubular scaffold into a sodium hydroxide solution to generate a middle layer of the surface of the base layer; (c) immersing the tubular scaffold of the step (b) in a second light sensitivity gelatin solution, wherein the second light sensitivity gelatin solution comprises a cell, the tubular scaffold is irradiated by a second time period to form a surface layer of the middle layer; (d) until the cell forms a tubular structure of the surface layer by the cell in the tubular scaffold of the step (c), heating the tubular scaffold by a temperature to solve the base layer into a solution, pulling out the tubular scaffold to get an artificial blood vessels.
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What is claimed is: 1. A method of preparing a tubular vascular graft, which comprises the steps: immersing a tubular scaffold in a first light sensitive gelatin solution, and irradiating the tubular scaffold by a first time period, to form a base layer on the surface of the tubular scaffold; immersing the tubular scaffold of the step (a) in a chitin gelatin solution, when the surface of the base layer form a film, then immersing the tubular scaffold into a sodium hydroxide solution to generate a middle layer on the surface of the base layer; immersing the tubular scaffold of the step (b) in a second light sensitivity gelatin solution, wherein the second light sensitivity gelatin solution comprises a plurality of cells, the tubular scaffold is irradiated by a second time period to form a surface layer on the surface of the middle layer; until the cells grow as a tubular structure within the surface layer of the step (c), heating the tubular scaffold by a temperature to dissolve the base layer into a solution, removing the tubular scaffold to get an artificial blood vessel. 2. The method of claim 1 , wherein the first sensitive gelatin solution and the second light sensitivity gelatin solution are dissolved in a phosphate solution comprising 10% gelatin and 1% photoinitiator. 3. The method of in claim 2 , wherein the gelatin solution is prepared from a 10 g gelatin solution, a 100 mL phosphate solution, and the 2-methyl-2-propenoic acid anhydride. 4. The method of in claim 3 , wherein the gelatin is extracted from collagen in animal connective tissue. 5. The method of in claim 1 , wherein if the light is ultraviolet, the first time period is 10 seconds. 6. The method of in claim 1 , wherein if the chitin gelatin solution is 1% (W/V), the chitin is dissolved in a 1% acetic acid solution. 7. The method of in claim 1 , wherein if the light is ultraviolet, the second time period is 12 seconds. 8. The method of in claim 1 , wherein the tubular scaffold is a transparent heat conducting material with a low biological toxicity.
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