Instant adhesive tissue patch and preparation method thereof
A tissue and patch technology, applied in tissue regeneration, medical science, prosthesis, etc., can solve problems such as greater inflammatory response, insufficient softness of materials, erosion of abdominal wall organs, etc., to avoid nerve damage and save operation time Effect
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Embodiment 1
[0043] 1. Preparation of fibrinogen mixed solution
[0044] Fibrinogen is dissolved in phosphate buffer, and XIII factor, fibronectin, polyethylene glycol (PEG), glycerol and aprotinin solution are added, and the concentration of fibrinogen in the prepared mixed solution is 110 mg / ml, and the concentration of XIII factor The concentration is 40U / ml, the concentration of fibronectin is 6mg / ml, the concentration of polyethylene glycol is 50mg / ml, the concentration of glycerol is 300mg / ml, and the concentration of aprotinin is 300KU / ml. Adjust the pH of the solution to 7.0.
[0045] 2. Extraction and purification of prothrombin
[0046] Take an appropriate amount of fresh pig blood and centrifuge for 10 minutes at 3°C and 5500r / min to remove blood cells. Next, the collected plasma was diluted with 10-fold deionized water and stirred, and then the pH of the solution was adjusted to 5.0 with 2 mol / L acetic acid. Then the solution was transferred to a refrigerator, and stood at...
Embodiment 2
[0056] 1. Preparation of fibrinogen mixed solution
[0057] Dissolve fibrinogen in phosphate buffer, add XⅢ factor, fibronectin, polyethylene glycol (PEG), glycerol and aprotinin solution, the concentration of fibrinogen in the prepared mixed solution is 200mg / ml, XⅢ factor The concentration is 80U / ml, the concentration of fibronectin is 10mg / ml, the concentration of polyethylene glycol is 100mg / ml, the concentration of glycerol is 100mg / ml, and the concentration of aprotinin is 200KU / ml. Adjust the pH of the solution to 6.5.
[0058] 2. Extraction and purification of prothrombin
[0059] Take an appropriate amount of fresh pig blood and centrifuge for 10 minutes at 3°C and 5500r / min to remove blood cells. Next, the collected plasma was diluted with 10-fold deionized water and stirred, and then the pH of the solution was adjusted to 5.0 with 2 mol / L acetic acid. Then the solution was transferred to a refrigerator, and stood at 4° C. for 12 hours, and the precipitate was c...
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