A kind of oral membrane for attached gingiva reconstruction and its preparation method
An oral membrane and attached gingival technology, which is applied in the field of oral membrane for attached gingival reconstruction and its preparation, can solve the problems of affecting attached gingival reconstruction, damage penetration and the like, and achieve the effect of improving mechanical properties
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[0048] The present invention provides a method for preparing oral membranes for attached gingiva reconstruction, referring to figure 1 , the preparation method comprises the steps of:
[0049] (1) Dissolving atelopeptide type I collagen in acid solution to prepare collagen acid solution;
[0050] (2) defoaming and freeze-drying the collagen acid solution to obtain a sponge;
[0051] (3) The sponge is rolled, and the temperature of the roller is set at 30-40°C, more preferably at 35±2°C, to obtain the oral membrane.
[0052] In the present invention, the collagen sponge obtained after freeze-drying is rolled, and the temperature of the rollers is at 30 to 40°C (for example, 30°C, 31°C, 32°C, 33°C, 34°C, 35°C) during the controlled rolling. , 36°C, 37°C, 38°C, 39°C, 40°C, more preferably 35±2°C) the sponge can be pressed into a film, and the upper and lower surfaces of the film are smooth. The inventor found in research that if the temperature during rolling is too high (the te...
Embodiment 1
[0070] Step S-1: remove the fat and fascia on the Achilles tendon, wash and freeze;
[0071] Step S-2: cutting the frozen Achilles tendon into thin slices, the thickness of which is controlled at 0.8-1.0 mm;
[0072] Step S-3: Soak the slices cut in S-2 in 0.8wt% sodium bicarbonate solution for 24 hours for degreasing, and then wash them with purified water;
[0073] Step S-4: adding the degreased flakes to an acetic acid solution with a pH of 1, adding pepsin, and enzymatically hydrolyzing at 0° C. for 72 hours to remove telopeptides;
[0074] Step S-5: Centrifuge the enzymolysis solution obtained in step S-4 with a centrifuge, take the supernatant, and separate out collagen flocs with a sodium chloride solution;
[0075] Step S-6: Put the collagen flocs obtained in Step S-5 into a dialysis bag for dialysis, use gradient dialysis to perform dialysis, gradually reduce the concentration of acetic acid in the external fluid, and finally use purified water dialysis to complete t...
Embodiment 2
[0106] Step S-1: remove the fat and fascia on the Achilles tendon, wash and freeze;
[0107] Step S-2: cutting the frozen Achilles tendon into thin slices, the thickness of which is controlled at 0.8-1.0 mm;
[0108] Step S-3: Soak the slices cut in S-2 in 0.9wt% sodium bicarbonate solution for 18 hours for degreasing, and then wash them with purified water;
[0109] Step S-4: adding the defatted flakes to a citric acid solution with a pH of 3, adding pepsin, and enzymatically hydrolyzing at 14° C. for 72 hours to remove telopeptides;
[0110] Step S-5: Centrifuge the enzymolysis solution obtained in step S-4 with a centrifuge, take the supernatant, and use sodium carbonate solution to separate out collagen flocs;
[0111] Step S-6: Put the collagen flocs obtained in Step S-5 into a dialysis bag for dialysis, use gradient dialysis to perform dialysis, gradually reduce the concentration of acetic acid in the external fluid, and finally use purified water dialysis to complete t...
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