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BIOACTIVE CONCENTRATE, THEIR PRODUCTION PROCESS AND CERTAIN MEDICINES THAT ALSO CONTAIN CHONDROITIN SULFATE

机译:生物活性浓缩物,其生产过程和某些药物,其中还含有硫酸软骨素

摘要

PCT No. PCT/RO96/00003 Sec. 371 Date Oct. 3, 1997 Sec. 102(e) Date Oct. 3, 1997 PCT Filed Mar. 14, 1996 PCT Pub. No. WO96/32117 PCT Pub. Date Oct. 19, 1996This bioactive concentrate is an active substance-aqueous solution or lyophilized powder-consisting of anti-hyaluronidase and antiinflammatory mucopolysaccharide polymers and an addition of restitutive and anti-hyaluronidase chondroitinsulphate, which has a pH=4-6 and antihyaluronidase activity. The bioactive concentrate producing method consists in a two-phased treatment of animal-originated connective cartilaginous tissues such as bovine and sheep trachea, umbilical cord, young animal tendons, bowels, testicles or sea organisms, with phenol solution and the solution resulted is concentrated by vacuum evaporation and then defatted; after filtering, the supernatant obtained is treated for deproteinization, the ion excess is removed by passing through ion exchanger column, the alcohol solution is concentrated to remove alcohol until reaching a volume of 70% as against the aqueous solution subject to proteinzation. Drug compsitions contain the bioactive concentrate-solution or in lyophilized state-associated with synergic substances such as: heparin, sodium or lysin acetylsallicylate, ascorbic acid, vitamin E,"I"-like structured water, benzyl alcohol, propylene glycocou, plant extracts (Achillea, Calendula, Matricaria, Plantago, Hypericum) and usual excipients, being conditioned in the form of intramuscular or intraarticular injections, ointment, gel and suppositories. Finally the histamines are removed and chondroitin sulphate is added up to the concentration required.
机译:PCT号PCT / RO96 / 00003秒371日期1997年10月3日102(e),1997年10月3日,PCT,1996年3月14日提交,PCT Pub。 WO96 / 32117 PCT公开号日期:1996年10月19日,该生物活性浓缩物是一种活性物质水溶液或冻干粉剂,由抗透明质酸酶和抗炎性粘多糖聚合物组成,并添加具有pH = 4-6和抗透明质酸酶活性的恢复性和抗透明质酸酶软骨硫酸盐。 。生物活性浓缩物的生产方法包括用酚溶液对动物起源的结缔软骨组织(例如牛和羊气管,脐带,幼小动物腱,肠,睾丸或海洋生物)进行两阶段处理,然后将所得溶液浓缩真空蒸发然后脱脂;过滤后,将获得的上清液进行脱蛋白处理,通过离子交换柱除去过量的离子,浓缩醇溶液以去除醇,直到相对于要进行蛋白化的水溶液达到70%的体积。药物组合物包含生物活性浓缩液或处于冻干状态,并具有协同作用,例如:肝素,乙酰水杨酸钠或溶血素,抗坏血酸,维生素E,“ I”型结构化水,苯甲醇,丙二醇,植物提取物(阿喀琉,金盏花,母菊,车前子,金丝桃)和通常的赋形剂,以肌内或关节内注射,软膏,凝胶和栓剂的形式进行处理。最后,除去组胺,加入硫酸软骨素至所需浓度。

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