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Gamma-globulin mfr. for intravenous injection to treat infections

机译:γ-球蛋白用于静脉注射以治疗感染

摘要

Prodn. of gamma-globulin, suitable for intravenous injection, comprises treating the gamma-globulin with the enzyme pepsin or uropepsin, at a pH of 6.0-7.5, pref. 6.5-7.0. Pref. both the gamma-globulin and the enzyme are of human origin. Therapeutic agents contg. a gamma-globulin and human uropepsin or uropepsinogen as stabiliser are also claimed. Pref. 0.01-5%, esp. 0.1-1%, of enzyme is used. Used for prophylactic and therapeutic treatment of bacterial and viral infections by intravenous injection of gamma-globulin. Gamma-globulin purified by known methods produces serious side-effects (sudden reduction of blood pressure, chilling, vomitting, pyrexia, cyanosis and shock) when administered intravenously. Treatment of the purified gamma-globulin by known methods (e.g. treatment with proteolytic enzymes (pepsin)) to avoid the side-effects due to complement activation give a product with a very short half-life. The present treatment, with pepin or uropepsin at neutral pH, gives a product suitable for intravenous injection, with a long circulatory half-life and with retention of the opsonic activity of the gamma globulin.
机译:产品适用于静脉内注射的γ-球蛋白的制备包括用胃蛋白酶或uropepsin酶在pH 6.0-7.5(优选)下处理γ-球蛋白。 6.5-7.0。首选γ-球蛋白和酶都是人类起源的。治疗药物续还要求保护一种γ-球蛋白和人尿素蛋白酶或尿素蛋白酶原作为稳定剂。首选0.01-5%,特别是使用0.1-1%的酶。通过静脉内注射γ-球蛋白用于细菌和病毒感染的预防和治疗。当通过静脉内给药时,通过已知方法纯化的γ-球蛋白会产生严重的副作用(血压突然降低,发冷,呕吐,发热,发,发shock和休克)。通过已知方法处理纯化的γ-球蛋白(例如用蛋白水解酶(胃蛋白酶)处理)以避免由于补体激活而引起的副作用,从而得到具有非常短半衰期的产物。用中性pH的pepin或uropepsin进行的本处理可提供适合静脉内注射的产品,并具有长的循环半衰期并保留了γ-球蛋白的调理活性。

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