Preparation method of composite bacterial cellulose medical dressing
A technology of bacterial cellulose and composite membranes, applied in medical science, absorbent pads, bandages, etc., can solve the problem of wounds that cannot be used for dry wounds and wounds covered by hard necrotic tissue, biological dressings that cannot be used for dry wounds, inhibit In order to achieve the effect of promoting wound healing, improving mechanical properties and thermal stability, and low cost
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example 1
[0019]First measure 400mL of deionized water into the beaker, heat to boiling, then stop heating, then add 20g of green tea, soak for 40min, filter, collect the filtrate, then add 30g of sucrose, 8g of peptone, 10g of yeast powder, stir for 10min, and transfer to In a sterilizing tank, sterilize at 130°C for 20 minutes to prepare a seed medium for use; then weigh 200g of mashed potatoes, 20g of glucose and 15g of agar into a petri dish, then add 1000mL of deionized water, and stir evenly. Then add 5% acetic acid solution to adjust the pH to 6.8, then transfer it into a sterilization tank, and sterilize at 120°C for 30 minutes to obtain an activated medium; then add 5g of Saccharomyces cerevisiae, 5g of Acetobacter aceti and 8g of Gluconoacetobacter xylinum was inoculated into three activation media respectively, and then placed in a constant temperature incubator, cultured at 30°C for 3 days, and the activated strains were inoculated to the spare seeds at an inoculation amount ...
example 2
[0022] First measure 300mL of deionized water into the beaker, heat to boiling, then stop heating, then add 15g of green tea, soak for 30min, filter, collect the filtrate, then add 20g of sucrose, 5g of peptone, 8g of yeast powder, stir for 5min, and transfer to In a sterilizing tank, sterilize at 120°C for 10 minutes to prepare a seed medium for use; then weigh 100g of mashed potatoes, 10g of glucose and 10g of agar into a petri dish, then add 800mL of deionized water, and stir evenly. Then add 5% acetic acid solution to adjust the pH to 6.5, then transfer it into a sterilization tank, and sterilize it at 110°C for 20 minutes to obtain an activated medium; then add 3g of Saccharomyces cerevisiae, 3g of Acetobacter aceti and 6g of Gluconoacetobacter xylinum was inoculated into three activation media respectively, and then placed in a constant temperature incubator, cultured at 20°C for 2 days, and the activated strains were inoculated to spare seeds at an inoculation amount of ...
example 3
[0025] First measure 350mL of deionized water into the beaker, heat to boiling, then stop heating, then add 18g of green tea, soak for 35min, filter, collect the filtrate, then add 25g of sucrose, 7g of peptone, 9g of yeast powder, stir for 8min, and transfer to Sterilize the tank at 125°C for 15 minutes to prepare the seed culture medium for later use; then weigh 150g of mashed potatoes, 15g of glucose and 12g of agar into a petri dish, then add 900mL of deionized water, and stir evenly. Then add 5% acetic acid solution to adjust the pH to 6.6, then transfer it into a sterilization tank, and sterilize at 115°C for 25 minutes to obtain an activated medium; then add 4g of Saccharomyces cerevisiae, 4g of Acetobacter aceti and 7g of Gluconoacetobacter xylinum was inoculated into three activated media respectively, and then placed in a constant temperature incubator, cultured at 25°C for 2.5 days, and the activated strains were inoculated into spare seeds at an inoculation amount o...
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