首页> 外国专利> METHOD FOR OBTAINING INDIVIDUAL FRACTIONS OF MATRIX HYALURONATE OF VARIOUS MOLECULAR WEIGHTS OF HIGH FRACTIONAL AND CHEMICAL PURITY IN A SINGLE TECHNOLOGICAL CYCLE

METHOD FOR OBTAINING INDIVIDUAL FRACTIONS OF MATRIX HYALURONATE OF VARIOUS MOLECULAR WEIGHTS OF HIGH FRACTIONAL AND CHEMICAL PURITY IN A SINGLE TECHNOLOGICAL CYCLE

机译:在单一技术循环中获得高分和化学纯度的各种分子量的基质透明质酸盐的单个分数的方法

摘要

FIELD: polysaccharide chemistry.;SUBSTANCE: method for producing hyaluronate includes washing the byproduct with running water, grinding it, extracting, filtering and combining the extracts. As the raw material, frozen or fresh animal byproducts are used, selected from chicken comb, cattle skin and eyes. After washing, the byproduct is denatured by dehydrating it with a saturated solution of sodium chloride, decontaminated with a compound of active oxygen, and placed in distilled water to swell. The cycle of dehydration, decontamination and swelling is repeated at least once, after which the dehydration and decontamination are repeated. The denatured material is crushed and homogenized, and three-fold extraction is carried out from the crushed denatured material with 0.85-0.9% sodium chloride solution at a temperature of 35-40°C with the separation of the meal by vacuum filtration on metal grids. Then, the extracts are combined, and fermentolysis is carried out when vacuumed with an enzyme complex including the papain, pepsin, trypsin enzymes and phosphodiesterase at a temperature of 30-35°C for 24-36 hours at a pH of 6.5-7.2. The fermentation mixture is heated to 70-80°C, quickly cooled to 5-10°C, and the lipid membrane is separated. Then, sequential ultrafiltration is performed with a final membrane with a pore size of no more than 0.2 mcm. The hyaluronate is precipitated with cetylpyridinium chloride. The precipitate of cetylpyridinium hyaluronate is dissolved in 0.9-1.2% sodium chloride solution to a concentration of no more than 0.15%, and the solution is filtered through a membrane with a pore size of no more than 0.2 mcm. Then, a solution of hyaluronate with a concentration of no more than 0.15% is prepared, followed by purification and separation of the hyaluronate into fractions by cascade filtration in a continuous cycle by reverse osmosis, and the finished product is obtained. ;EFFECT: invention makes it possible to obtain substances of matrix hyaluronate of various molecular weights of high fractional and chemical purity from frozen or fresh animal byproducts, excluding its contamination with microbiological toxins with a maximum yield of hyaluronate of a wide molecular spectrum and the production of such related products as chondroitin sulfate, meal in a single technological cycle.;10 cl, 8 tbl, 7 ex
机译:田间:多糖化学。物质:制备透明质酸的方法包括用自来水洗涤副产物,研磨,提取,过滤和组合提取物。作为原料,使用冷冻或新鲜的动物副产品,选自鸡梳,牛皮和眼睛。洗涤后,通过用饱和氯化钠溶液将其脱水,用活性氧气净化,并置于蒸馏水中以溶胀以溶胀的副产物。重复脱水,去污和溶胀的循环,至少一次重复,重复脱水和净化。变性材料被挤压和均匀化,并在35-40℃的温度下用0.85-0.9%氯化钠溶液的碎变性材料进行三倍的萃取,通过在金属网格上的真空过滤分离膳食。然后,组合提取物,并在用蛋白质复合物在30-35℃的温度下在pH为6.5-7.2的温度下,用包括木瓜蛋白酶,百草素,胰蛋白酶酶和磷酸二酯酶的酶复合物真空,进行发酵溶解。将发酵混合物加热至70-80℃,快速冷却至5-10℃,分离脂质膜。然后,用最终膜进行顺序超滤,孔径不超过0.2mcm。透明质酸用十六烷基吡啶鎓沉淀。将十六烷吡啶鎓透明质酸盐的沉淀物溶于0.9-1.2%氯化钠溶液中,浓度不大于0.15%,并通过孔径的膜过滤溶液不超过0.2mcm的液体过滤。然后,制备浓度不超过0.15%的透明质酸盐的溶液,然后通过反渗透连续循环在连续循环中通过级联过滤纯化和分离级分,得到成品。 ;效果:发明使得可以从冷冻或新鲜动物副产物中获得各种分子量的各种分子量的基质透明质酸盐的物质,除了透明的微生物毒素的污染,透明质酸盐的透明质酸盐和生产将这种相关产品作为硫酸软骨素,在单一技术周期中的膳食。10 cl,8 tbl,7前

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