Porous bacterial cellulose skin repair material with density structure and preparation method thereof
A technology of bacterial cellulose and bacterial cellulose membrane, which is applied in the field of porous bacterial cellulose skin repair material with a sparse and dense structure and its preparation, can solve the problem of high preparation cost, prolonging the treatment period and affecting the connectivity between the epidermis and the dermis. and other problems, to shorten the wound healing cycle, reduce the proliferation of scars, and achieve good structural continuity.
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Embodiment 1
[0061] 1) Preparation of fermentation medium;
[0062] Components of the culture solution, in mass percent, in wt%: glucose, fructose, sucrose or mannitol 2, peptone 0.05, yeast extract 0.05, citric acid 0.01, disodium hydrogen phosphate 0.02, potassium dihydrogen phosphate 0.01;
[0063] The pH of the culture solution is 4.0;
[0064] The above components are mixed, sterilized by high pressure steam, irradiated with ultraviolet light and cooled to room temperature, and passed through pure oxygen to obtain the fermentation culture solution;
[0065] 2) Bacteria expansion;
[0066] The fermentation culture liquid is inoculated and expanded; the degree of expansion: the number of strain cells is 2×10 5 individual / mL.
[0067] 3) Static cultivation;
[0068] Transfer the expanded bacterial solution to a culture container filled with fermentation broth, place it in a constant temperature incubator, and culture it statically at 28°C;
[0069] The double-layer structure of the ...
Embodiment 2
[0079] 1) Preparation of fermentation medium;
[0080] Components of the culture solution, in mass percent, in wt%: glucose, fructose, sucrose or mannitol 5, peptone 0.5, yeast extract 0.5, citric acid 0.1, disodium hydrogen phosphate 0.2, potassium dihydrogen phosphate 0.1;
[0081] The pH of the culture solution is 6.0;
[0082] The above components are mixed, sterilized by high pressure steam, irradiated with ultraviolet light and cooled to room temperature, and passed through pure oxygen to obtain the fermentation culture solution;
[0083] 2) Bacteria expansion;
[0084] The fermentation culture liquid is inoculated and expanded; the degree of expansion: the number of strain cells is 2×10 7 individual / mL.
[0085] 3) Static cultivation;
[0086] Transfer the expanded bacterial solution to a culture container filled with fermentation broth, place it in a constant temperature incubator, and culture it statically at 32°C;
[0087] The double-layer structure of the bacte...
Embodiment 3
[0097] 1) Preparation of fermentation medium;
[0098] Components of the fermentation broth, in mass percent, in wt%: glucose, fructose, sucrose or mannitol 3, peptone 0.3, yeast extract 0.3, citric acid 0.05, disodium hydrogen phosphate 0.1, potassium dihydrogen phosphate 0.05;
[0099] The pH of the fermentation broth is 5.0;
[0100] The above components are mixed, sterilized by high pressure steam, irradiated with ultraviolet light and cooled to room temperature, and passed through pure oxygen to obtain the fermentation culture solution;
[0101] 2) Bacteria expansion;
[0102] The fermentation culture liquid is inoculated and expanded; the degree of expansion: the number of strain cells is 2×10 7 individual / mL.
[0103] 3) Static cultivation;
[0104] Transfer the expanded bacterial solution to a culture container filled with fermentation broth, place it in a constant temperature incubator, and culture it statically at 30°C;
[0105] The double-layer structure of the b...
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Abstract
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