Bionic eyelid scaffold having double-layer composite structure and construction method thereof
A double-layer composite, eyelid technology, applied in the field of bionic eyelid stent and its preparation, can solve the problems of different antigenicity, difficult to adhere well to the ocular surface, non-biodegradable, etc., and achieves good biocompatibility and good biocompatibility. Application prospect, simple preparation method effect
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Embodiment 1
[0036] 1) Add gelatin particles with a thickness of 1mm and a particle size of 180-280μm into the polyethylene template, then inject an ethanol solution with a volume concentration of 85%, put it in an oven at a temperature of 40°C, and wait until the solution is completely dried to form gelatin particles After bonding, a gelatin template sheet with a thickness of 1 mm was taken out to form a gelatin template.
[0037] Then a blend of polytrimethylene fumarate (PPF) and hydroxyethyl methacrylate (HEMA) at a mass ratio of 1:2 (containing 1% benzoyl peroxide as an initiator) was used as a degradable elastic polyester The blend was introduced into a gelatin template, cross-linked at 85°C for 4 hours, then soaked in a constant temperature water bath at 37°C, and the gelatin template was removed to obtain porous polytrimethylene fumarate / hydroxyethyl methacrylate The elastic support is a porous elastic polyester support.
[0038] 2) Using the porous elastic polyester scaffold prep...
Embodiment 2
[0042] The preparation method is the same as that in Example 1, the difference is that the 0.5% type I collagen solution in step 2) is replaced with a 40 mg / mL fibrinogen solution, and thrombin with a working concentration of 25 U / mL is added, and the mixture is exchanged at a temperature of 37°C. Combined for 1 hour, freeze-dried, and the smaller surface pores were obtained after removal, and the denser polytrimethylene fumarate / fibrin glue double-layer scaffold was obtained.
Embodiment 3
[0044] The preparation method is the same as in Example 1, the difference is that the particle size of the gelatin particles in step 1 is changed to 280-450 μm, and the freezing at -20°C for 2 hours in step 2 is changed to -80°C for 1 hour, by changing the size of the porogen , the freezing temperature to regulate the pore size and porosity of the scaffold.
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