Method for preparing hemostatic sponge from oxidized bletilla striata modified collagen fibers
A technology of collagen fibers and hemostatic sponges, which is applied in the field of biomedical materials, can solve problems such as poor bonding, poor mutual bonding ability, and poor degradation resistance, and achieve the effects of improving collagen stability, thermal stability, and hemostatic performance
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Embodiment 1
[0036] (1) Purification of Bletilla striata polysaccharide: Weigh 20 parts by weight of Bletilla striata polysaccharide, dissolve it in 1000 parts by weight of deionized water, and stir it magnetically for 1 hour to completely dissolve it; accurately weigh 1 part by weight of papain (enzyme activity: 800,000 u / g), added to the crude polysaccharide solution of Bletilla striata, stirred by magnetic force for 1h, after it was completely dissolved, 1mol / L NaOH was added to it to make the pH to 7; under the condition of 48℃ water bath, enzymatic hydrolysis for 2h; after the reaction, add 1000 parts by weight of absolute ethanol, allowing Bletilla striata polysaccharide to precipitate out in flocculent form; centrifuge at 8000r / min for 5min, collect the precipitate, redissolve in water, remove insolubles by suction filtration and collect the filtrate; centrifuge at 8000r / min again, Repeat 4-5 times, place the final product in a constant temperature drying oven and dry to constant we...
Embodiment 2
[0040] (1) Purification of Bletilla striata polysaccharide: Weigh 20 parts by weight of Bletilla striata polysaccharide, dissolve it in 400 parts by weight of deionized water, and stir it magnetically for 0.5 h to dissolve it completely; weigh 0.5 part by weight of papain (enzyme activity 100,000 u / g), added to the crude polysaccharide solution of Bletilla striata, stirred by magnetic force for 0.5h, after it was completely dissolved, 1mol / L NaOH was added to it to make the pH to 6; Add 1000 parts by weight of absolute ethanol to allow Bletilla striata polysaccharide to precipitate in flocculent form; centrifuge at 6000r / min for 5min, collect the precipitate, redissolve it in water, remove insoluble matter by suction filtration and collect the filtrate; centrifuge again at 6000r / min , repeated 4-5 times, the final product was placed in a constant temperature drying oven and dried to a constant weight to obtain purified Bletilla striata polysaccharide;
[0041] (2) Preparation...
Embodiment 3
[0044] (1) Purification of Bletilla striata polysaccharide: Weigh 20 parts by weight of Bletilla striata polysaccharide, dissolve it in 1200 parts by weight of deionized water, and stir it magnetically for 2 hours to completely dissolve it; accurately weigh 1.5 parts by weight of papain (enzyme activity: 800,000 u / g), added to the crude polysaccharide solution of Bletilla striata, stirred magnetically for 2 hours, after it was completely dissolved, 1mol / L NaOH was added to it to make the pH 8; under the condition of 65℃ water bath, enzymatic hydrolysis for 3 hours, after the reaction, add 1000 parts by weight of absolute ethanol, allowing Bletilla striata polysaccharide to precipitate out in flocculent form; centrifuge at 10000r / min for 5min, collect the precipitate, redissolve in water, remove insolubles by suction filtration and collect the filtrate; centrifuge again at 10000r / min, Repeat 4-5 times, place the final product in a constant temperature drying oven and dry to con...
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