Orderly porous polymer thin film, preparation method and application in capture and controllable glucose-responsive release of insulin
A porous film and polymer technology, applied in the capture and release of insulin in response to controllable sugar, in the field of polymer ordered porous film materials, can solve the problems of less attention to the film system, and achieve simple and convenient equipment and high release efficiency , the effect of mild conditions
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Embodiment 1
[0031] Dissolve 30mg PS (purchased from Sigma-Aldrich, molecular weight: 350,000) and 2.5mg DDA in 5mL dichloromethane solution to prepare polymer organic solution, take 50μL deionized water into 1mL volumetric flask, and then add polymer Take the organic solution to the marked line, shake it for about 1 min to obtain a microemulsion, and pour the microemulsion on a clean glass substrate under the conditions of humidity of 35% and temperature of 27°C. After the organic solvent and water were completely volatilized, an ordered porous film with a pore diameter of about 2 μm, a pore depth of 1 μm, and a film thickness of 35 μm was obtained.
[0032] The obtained ordered porous film was immersed in a 3wt% PAA solution for 30 minutes, the film was taken out, washed three times in deionized aqueous solution, and then placed in the air to dry naturally.
[0033] Soak the PAA-loaded porous film in a mixed solution of 7.5mM APBA and 12.5mM EDC for 3h, remove the film, wash it three tim...
Embodiment 2
[0040] As shown in Example 1, with other conditions unchanged, the mass of DDA was changed to 1.5 mg, and an ordered porous film with a pore diameter of about 2 μm, a pore depth of 1 μm, and a film thickness of 20 μm was prepared.
[0041] Then according to the steps of Example 1, the modification of PAA, APBA and Alg in the hole, the positioning assembly of insulin aggregates, and the in situ release study in the hole were respectively realized. Under this condition, the insulin release efficiency was 95%.
Embodiment 3
[0043] As shown in Example 1, with other conditions unchanged, the surfactant DDA was replaced by DDAB, and an ordered porous film with a pore diameter of about 4 μm, a pore depth of 2 μm, and a film thickness of 50 μm was prepared.
[0044] Then according to the steps of Example 1, the modification of PAA, APBA and Alg in the hole, the positioning assembly of insulin aggregates, and the in situ release study in the hole were respectively realized. In this case, the insulin release efficiency was 95%.
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