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Thrombolytic compsns. of purified urokinase - esp. contg. urokinase I made by chromatography on CMC

机译:溶栓药。纯化的尿激酶-尤其是续在CMC上通过色谱法制备的尿激酶I

摘要

Urokinase with mol.wt. of 33000 (urokinase I) substantially free of urokinase of mol. wt. about 55000 (urokinase II) having an activity in the fibrin clot test of 50000 uCTA/mg of proteins and activities on AGLME substrate and fibrin plague of 150000 uCTA/mg of protein, its purity being such that dissolution in 0.04 M (NH4)2SO4 soln. at pH 6 and contacting it with a Sepharose (RTM) carboxymethyl gel chromatography column and linear gradient elution to obtain an eluate at pH 6 with an ammonium sulphate content of 0.25 M permits isolation of urokinase with substantially a single peak. Medicinal compsn. for thrombolytic treatment as the first component, a modified plasminogen, and as the second urokinase I having a single peak of activity. Urokinase I or urokinase II, each substantially free of the other, may be injected or perfused for treatment of blood disorders, e.g. deep venous thrombosis. Lower doses may be given of a specific type and the dose may be better tolerated by the patient.
机译:尿激酶与mol.wt. 33000(尿激酶I)基本上不含摩尔的尿激酶。重量大约55000(尿激酶II)在纤维蛋白凝块测试中的活性为50000 uCTA / mg蛋白质,在AGLME底物和纤维蛋白鼠疫中的活性为150000 uCTA / mg蛋白质,其纯度应溶于0.04 M(NH4)2SO4 soln。在pH 6时,将其与Sepharose(RTM)羧甲基凝胶色谱柱接触,然后进行线性梯度洗脱,以在pH 6时获得硫酸铵含量为0.25 M的洗脱液,从而可以分离出具有单个峰的尿激酶。药用成分。作为溶栓治疗的第一组分,修饰的纤溶酶原和具有单个活性峰的第二尿激酶I。彼此基本不含的尿激酶I或尿激酶II可以被注射或灌注以治疗血液疾病,例如糖尿病。深静脉血栓形成。可以给予特定类型的较低剂量,并且患者可以更好地耐受该剂量。

著录项

  • 公开/公告号FR2387241B1

    专利类型

  • 公开/公告日1980-02-08

    原文格式PDF

  • 申请/专利权人 CHOAY SA;

    申请/专利号FR19770011003

  • 发明设计人

    申请日1977-04-12

  • 分类号C07G7/02;A61K37/48;

  • 国家 FR

  • 入库时间 2022-08-22 17:23:59

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