Method for preparing sample for use in endotoxin test
    92.
    发明授权
    Method for preparing sample for use in endotoxin test 失效
    制备用于内毒素试验的样品的方法

    公开(公告)号:US4414336A

    公开(公告)日:1983-11-08

    申请号:US306647

    申请日:1981-09-29

    摘要: (1) A method for preparing a sample for use in the endotoxin test which comprises subjecting a sample of plasma or blood preparation to a contact with water-insoluble anti-human .alpha..sub.2 -macroglobulin antibody and to a gel filtration by means of a gel of allyl dextran crosslinked with N,N'-methylenebis acrylamide or a gel of polyvinyl alcohol having many hydrophilic hydroxyl groups, and recovering the maximum molecular weight fraction.(2) A kit for preparing a sample for use in the endotoxin test consisting of a set of a sample-developing column prepared by packing a water-insoluble anti-human .alpha..sub.2 -macroglobulin antibody and a gel of allyl dextran crosslinked with N,N'-methylenebis acrylamide or a gel of polyvinyl alcohol having many hydrophilic hydroxyl groups, both equilibrated with a buffer solution of pH 7.0-7.4, into a column and tightly sealing the column, an aqueous solution of a high molecular colored substance to be added to the sample and a buffer solution for use in developing the sample.

    摘要翻译: (1)一种制备用于内毒素试验的样品的方法,其包括使血浆或血液制剂的样品与不溶于水的抗人α2-巨球蛋白抗体接触并通过凝胶进行凝胶过滤 的与N,N'-亚甲基双丙烯酰胺交联的烯丙基葡聚糖或具有许多亲水性羟基的聚乙烯醇凝胶,并回收最大分子量分数。 (2)一种用于制备用于内毒素测试的样品的试剂盒,其由一组通过包装不溶于水的抗人α2-巨球蛋白抗体和与N交联的烯丙基葡聚糖凝胶制备的样品显影柱组成, N'-亚甲基双丙烯酰胺或具有许多亲水性羟基的聚乙烯醇凝胶,两者都用pH 7.0-7.4的缓冲溶液平衡,并将柱紧密密封,加入高分子色素物质的水溶液 到样品和用于开发样品的缓冲溶液。

    Fat emulsion containing steroid
    93.
    发明授权
    Fat emulsion containing steroid 失效
    包含类固醇的脂肪乳液

    公开(公告)号:US4340594A

    公开(公告)日:1982-07-20

    申请号:US260607

    申请日:1981-05-06

    CPC分类号: A61K9/1075 A61K31/57

    摘要: A fat emulsion containing a steroid having an anti-inflammatory activity, comprising an effective quantity of a steroid having an anti-inflammatory activity, 5 to 50% (W/V) of soybean oil, a phospholipid in a weight ratio of 1-50 to 100 of said soybean oil, and a proper quantity of water. This fat emulsion exhibits a long-lasting activity in the region of inflammation and is especially useful in the therapeutic or prophylactic treatment of rheumatism, immunological hemolytic anemia, idiopathic thrombocytopenic purpura, and Paget disease, or in conjunction with kidney transplantation.

    摘要翻译: 含有具有抗炎活性的类固醇的脂肪乳剂,其包含有效量的具有抗炎活性的类固醇,大豆油为5〜50%(W / V),重量比为1〜50的磷脂 至100份所述大豆油,并加入适量的水。 这种脂肪乳剂在炎症区域表现出持久的活性,特别可用于治疗或预防性治疗风湿病,免疫性溶血性贫血,特发性血小板减少性紫癜和佩吉特病,或与肾移植有关。

    Method for recovering myeloperoxidase and pharmaceutical composition
containing myeloperoxidase as major constituent
    95.
    发明授权
    Method for recovering myeloperoxidase and pharmaceutical composition containing myeloperoxidase as major constituent 失效
    回收髓过氧化物酶和含有髓过氧化物酶作为主要成分的药物组合物的方法

    公开(公告)号:US4306025A

    公开(公告)日:1981-12-15

    申请号:US179783

    申请日:1980-08-20

    IPC分类号: B65B5/02 C12N9/08

    CPC分类号: B65B5/02 Y10S435/816

    摘要: Myeloperoxidase can be separated and recovered from a supernatant liquid of an aqueous dispersion of a disintegration product of human myelogenous leukocytes, which dispersion has been admixed with at least one member selected from the group consisting of manganese salts and protamine sulfate. The recovered myeloperoxidase in combination with an alkali metal halide can be used as a pharmaceutical composition effective against microorganisms deficient or diminished in catalase synthesizing activity.

    摘要翻译: 髓过氧化物酶可以从人骨髓白质细胞的崩解产物的水性分散体的上清液中分离回收,该分散体已经与选自锰盐和鱼精蛋白硫酸盐的至少一种混合。 回收的髓过氧化物酶与碱金属卤化物的组合可以用作对过氧化氢酶合成活性缺乏或减少的微生物有效的药物组合物。

    Method for producing thrombolytic preparation
    96.
    发明授权
    Method for producing thrombolytic preparation 失效
    溶栓制剂的制备方法

    公开(公告)号:US4286063A

    公开(公告)日:1981-08-25

    申请号:US105116

    申请日:1979-12-19

    申请人: Tadakazu Suyama

    发明人: Tadakazu Suyama

    IPC分类号: A61K38/00 C12N9/72

    摘要: A method for producing a thrombolytic preparation characterized in that among treatment conditions in the urokinase production pH is maintained within the neutral or weakly alkaline range throughout each treatment step to produce a thrombolytic preparation containing urokinase having a molecular weight of 54,000.+-.10,000 as major ingredient.

    摘要翻译: 一种血栓溶解制剂的制造方法,其特征在于,在每个处理步骤中,在尿激酶产生pH的处理条件下,保持在中性或弱碱性范围内,以产生含有分子量为54,000 +/- 10,000的尿激酶的血栓溶解制剂作为主要 成分。

    Process for concentrating blood coagulation Factor XIII derived from
human placentae
    97.
    发明授权
    Process for concentrating blood coagulation Factor XIII derived from human placentae 失效
    浓缩凝血因子ⅩⅢ衍生自人胎盘的方法

    公开(公告)号:US4285933A

    公开(公告)日:1981-08-25

    申请号:US091245

    申请日:1979-11-02

    摘要: The invention relates to a process for concentrating blood coagulation Factor XIII (Fibrin stabilizing factor) which comprises removing a fraction precipitated at a pH of 6 to 9 in a concentration of 4 to 9% (W/V) of an alkylenoxide polymer or copolymer having a molecular weight of 2,000 to 20,000 from a crude globulin fraction obtained from human placentae by separating in albumin fraction therefrom, and then collecting the fraction precipitated in the concentration of 20 to 30% (W/V) of said polymer or copolymer, thereby obtaining easily said blood coagulation Factor XIII free from pyrogen in good yield.

    摘要翻译: 本发明涉及一种浓缩凝血因子XIII(纤维蛋白稳定因子)的方法,其包括以4至9%(W / V)的浓度在6至9的pH下除去沉淀的级分的亚烷基氧化物聚合物或共聚物 通过从白蛋白馏分中分离从人胎盘获得的粗球蛋白部分分子量为2,000〜20,000,然后收集以所述聚合物或共聚物的20〜30%(W / V)的浓度沉淀的级分,从而得到 容易地说凝血因子XIII不含热原,产率良好。