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    • 34. 发明授权
    • Method of obtaining urokinase
    • 获得尿激酶的方法
    • US4028187A
    • 1977-06-07
    • US701930
    • 1976-07-01
    • Abe TsutomuHashino YasuoKobayashi Hidehiko
    • Abe TsutomuHashino YasuoKobayashi Hidehiko
    • C12N9/72C07G7/026
    • C12N9/6462C12Y304/21073Y10S435/815
    • A method of obtaining urokinase directly from human urine comprising contacting human urine with an acrylonitrile polymer of a unique porous structure formed at the time of polymerization for formation of the polymer and having a porosity of not less than 10% and a specific surface area of 5 m.sup.2 /g. and subsequently eluting the urokinase adsorbed on the polymer. The acrylonitrile polymer employed in the method of the present invention has an excellent adsorption activity to urokinase and therefore, with use of an extremely small amount of the adsorbent, the satisfactory results can be obtained. Moreover, the porous polymer of the present method can also be utilized for purification of low purity crude urokinase obtained by the prior art methods.
    • 一种从人尿中直接获得尿激酶的方法,包括使人尿与聚合时形成的独特多孔结构的丙烯腈聚合物接触形成聚合物,孔隙率不小于10%,比表面积为5 m2 / g。 随后洗脱吸附在聚合物上的尿激酶。 本发明方法中使用的丙烯腈聚合物对尿激酶具有优异的吸附活性,因此,通过使用极少量的吸附剂,可以获得令人满意的结果。 此外,本方法的多孔聚合物也可用于纯化通过现有技术方法获得的低纯度尿尿激酶。
    • 37. 发明授权
    • Purification of kallikrein
    • 激肽释放酶的纯化
    • US3905870A
    • 1975-09-16
    • US43154673
    • 1973-12-26
    • BAYER AG
    • KUTZBACH CARLSCHMIDT-KASTNER GUNTHER
    • C12N9/64A61K19/00C07G7/026
    • C12N9/6445Y10S435/815Y10S435/816
    • There is disclosed a process for the purification of Kallikrein, comprising components, Kallikrein A and Kallikrein B, otherwise known as the enzyme, Kininogenase, which includes the process steps of: 1. TREATING A CRUDE AQUEOUS SOLUTION CONTAINING Kallikrein with a solution of a lead or zinc salt to produce a precipitate containing Kallikrein; 2. ELUTING Kallikrein from said precipitate to produce a solution of Kallikrein; 3. DESALINATING SAID SOLUTION OF Kallikrein to produce a desalinated solution of Kallikrein; 4. ADSORBING THE Kallikrein from the desalinated solution onto a macroporous anion exchange resin and eluting it therefrom to obtain an eluted solution containing Kallikrein; and thereupon 5. CONTACTING THE ELUTED SOLUTION WITH A MACROPOROUS CATION EXCHANGER; AND SEPARATING SAID CATION EXCHANGER TO PRODUCE A PURE SOLUTION OF Kallikrein. The disclosed process also includes means for the production of purified components, Kallikrein A and Kallikrein B, as well as the crystallization of Kallikrein and its components and to pharmaceuticals and medicaments containing the same.
    • 公开了一种用于纯化激肽释放酶的方法,其包括组分,激肽释放酶A和激肽释放酶B,还称为酶,激肽原酶,其包括以下步骤:
    • 38. 发明授权
    • Enhanced production of plasminogen activator
    • 增强纤溶酶原激活物的产生
    • US3904480A
    • 1975-09-09
    • US48548974
    • 1974-07-03
    • LILLY CO ELI
    • HULL ROBERT NHUSEBY ROLF M
    • C12N9/72C07G7/026
    • C12N9/6456Y10S435/815
    • Enhanced plasminogen activator yields are obtained by culturing plasminogen activator producing mammalian tissue cells in an aqueous nutrient culture medium until cells have attained development to confluency or maximum population density; continuing incubation in the presence of an antimitotic agent, e.g., podophylotoxin, colchicine and derivatives thereof, vincristine, vinblastine and derivatives thereof; recovering the activator from the separated aqueous culture medium by adsorption on hydroxyapatite and elution therefrom; and purifying the activator via salt precipitation followed by DEAE cellulose chromatography and gel filtration chromatography. Plasminogen activator is provided in clinically useful amounts for treatment of thromboembolic conditions.
    • 通过在水性营养培养基中培养产生哺乳动物组织细胞的纤溶酶原激活剂获得增强的纤溶酶原激活物产量,直到细胞达到融合或最大群体密度; 在抗有丝分裂剂,例如足细菌毒素,秋水仙素及其衍生物,长春新碱,长春花碱及其衍生物的存在下继续孵育; 通过在羟基磷灰石上吸附并从其中洗脱从分离的水培养基中回收活化剂; 并通过盐沉淀,然后用DEAE纤维素层析和凝胶过滤层析纯化活化剂。 提供临床有用量的纤溶酶原激活剂用于治疗血栓栓塞症状。