首页> 外国专利> PHARMACEUTICAL COMPOSITION OF ENTEROSORBENT AND PREBIOTICS, MEDICAL FORMS AND METHOD OF PREVENTION AND TREATMENT OF DISEASES OF THE GASTROINTESTINAL TRACT

PHARMACEUTICAL COMPOSITION OF ENTEROSORBENT AND PREBIOTICS, MEDICAL FORMS AND METHOD OF PREVENTION AND TREATMENT OF DISEASES OF THE GASTROINTESTINAL TRACT

机译:肠溶菌和药物的药物成分,医学形式以及预防和治疗胃肠道疾病的方法

摘要

The pharmaceutical composition consists in the fact that it contains hydrolysis lignin with a moisture content of 55-65%, consisting of particles with a size of 0.15-0.55 mm, a 45-55% aqueous solution of lactulose and a 50-55% aqueous solution of oligosaccharides , in the following ratio of components, wt.%: aqueous solution of lactulose - 10-60; oligosaccharides - 10-50; hydrolytic lignin - the rest. The hydrolysis of lignin with lactulose and fructooligosaccharides is successively added and mixed using a rotary mixer. The composition is prescribed orally, for at least 14 and no more than 30 days, with a 2-4-fold daily intake, depending on the weight and age of the patient. The composition is used as a medicine for the treatment of diseases of the gastrointestinal tract, including intestinal infections of bacterial, viral and protozoal etiology; food poisoning and intoxication, acute and chronic hepatitis and cirrhosis, diarrhea, gastric and duodenal ulcer, Crohn's disease, ulcerative colitis, irritable bowel syndrome; disorders of mineral metabolism with a deficiency of Ca and Mg, including osteoporosis and other disorders of bone formation; as an immunomodulator in atopic dermatitis and immunodeficiency states; to protect and restore intestinal microflora after antibiotic therapy, chemotherapy and radiation therapy. The result consists in accelerating the achievement of results and increasing the effectiveness of the impact on the state of intestinal microbiocenosis, as well as the effectiveness of the treatment of hepatitis and cirrhosis, eliminating undesirable side effects when used in medical practice, and expanding the indications of medical use, i.e.
机译:该药物组合物的事实在于其包含水分含量为55-65%的水解木质素,其由尺寸为0.15-0.55mm的颗粒,45-55%的乳果糖水溶液和50-55%的水组成。寡糖溶液,按以下组分的重量百分比计:乳果糖水溶液-10-60;寡糖-10-50;水解木质素-其余。依次添加木质素与乳果糖和低聚果糖的水解,并使用旋转混合器混合。根据患者的体重和年龄,口服该组合物的处方时间为至少14天且不超过30天,每天摄入量为2-4倍。该组合物被用作治疗胃肠道疾病的药物,包括细菌,病毒和原生动物病因的肠道感染。食物中毒和中毒,急慢性肝炎和肝硬化,腹泻,胃和十二指肠溃疡,克罗恩病,溃疡性结肠炎,肠易激综合症;缺乏钙和镁的矿物质代谢疾病,包括骨质疏松症和其他骨形成疾病;作为特应性皮炎和免疫缺陷状态的免疫调节剂;在抗生素治疗,化学疗法和放射治疗后保护和恢复肠道菌群。结果包括加快结果的实现并提高对肠道微生物菌群状态的影响的有效性,以及治疗肝炎和肝硬化的有效性,消除在医学实践中使用时的不良副作用,并扩大适应症医疗用途,即

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