Bacterial cellulose skin regeneration material with density structure and preparation method thereof
A technology of bacterial cellulose and bacterial cellulose film, which is applied in the field of bacterial cellulose skin repair materials with dense structure and its preparation, can solve the problems of high preparation cost, prolonging the treatment period, wound scars, etc., and achieve good air permeability The effect of water holding capacity, reduction of scar hyperplasia, and good biocompatibility
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Embodiment 1
[0060] 1) Preparation of fermentation medium;
[0061] Components of the fermentation medium, 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, and amount of water;
[0062] The pH of the fermentation broth is 4.0;
[0063] 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;
[0064] 2) Bacteria expansion;
[0065] The fermentation culture liquid is inoculated and expanded; the degree of expansion: the number of strain cells is 2×10 5 individual / mL.
[0066] 3) Static cultivation;
[0067] 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;
[0068] By adju...
Embodiment 2
[0078] 1) Preparation of fermentation medium;
[0079] Components of the fermentation medium, in mass percent, in wt%: 5 glucose, fructose, sucrose or mannitol, 0.5 peptone, 0.5 yeast extract, 0.1 citric acid, 0.2 disodium hydrogen phosphate, 0.1 potassium dihydrogen phosphate, and amount of water;
[0080] The pH of the fermentation broth is 6.0;
[0081] 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;
[0082] 2) Bacteria expansion;
[0083] The fermentation culture liquid is inoculated and expanded; the degree of expansion: the number of strain cells is 2×10 7 individual / mL.
[0084] 3) Static cultivation;
[0085] 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;
[0086] By adjusting...
Embodiment 3
[0096] 1) Preparation of fermentation medium;
[0097] Components of the fermentation medium, in mass percent, in wt%: 3 glucose, fructose, sucrose or mannitol, 0.3 peptone, 0.3 yeast extract, 0.05 citric acid, 0.1 disodium hydrogen phosphate, 0.05 potassium dihydrogen phosphate, and amount of water;
[0098] The pH of the fermentation broth is 5.0;
[0099] 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;
[0100] 2) Bacteria expansion;
[0101] The fermentation culture liquid is inoculated and expanded; the degree of expansion: the number of strain cells is 2×10 7 individual / mL.
[0102] 3) Static cultivation;
[0103] 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;
[0104] By adjusti...
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