活化凝血酶原复合物制剂治疗抗凝血友病。准备-操作方法-供应可能性]。

K Wilms, W Sander
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引用次数: 0

摘要

凝血酶原复合物制剂在循环抗凝治疗血友病中的旁路活性机制至今仍不清楚。以不同方式制备的制剂(DEAE-Sephadex a50, Molselekt a50,磷酸三钙或氢氧化铝吸收)测试了以下参数:凝血因子II, VII, IX, X和XII,活化因子VIIa和Xa以及FEIB活性。然而,旁路活性与制剂的因子VIIa含量密切相关。这些结果与HEDNER和KISIEL的陈述一致,他们使用因子VII a浓缩物治疗血友病并发循环抗凝剂取得了成功。根据进一步的研究,因子VII与起始血浆的脂质含量有关。这一知识对于优化具有旁路活性的凝血酶原复合物制剂的生产过程是重要的。
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[Activated prothrombin complex preparations for the treatment of anticoagulant hemophilia. Preparation--method of operation--supply possibility].

The mechanism of the bypass activity of prothrombin complex preparatives for treatment of haemophiliacs with circulating anticoagulants remains unclear up to now. The following parameters had been tested with preparatives produced in a different manner (absorption by DEAE-Sephadex A 50, Molselekt A 50, tricalcium phosphate or aluminium hydroxide): Coagulation factors II, VII, IX, X and XII, activated factors VIIa and Xa as well as the FEIB activity. The bypass activity is strongly correlated to the factor VIIa content of the preparatives, however. These results agree with the statements by HEDNER and KISIEL, which had used a factor VII a concentrate for treatment of haemophilia complicated by circulating anticoagulants with success. According to farther investigations factor VII is correlated with the lipid content of the starting plasma. This knowledge is important for optimizing the production procedure of prothrombin complex preparatives with bypassing activity.

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