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离子交换溶剂去污剂处理的高纯度凝血因子VIII浓缩剂的药代动力学研究。苏格兰和北爱尔兰血友病主任组织

A pharmacokinetic study of an ion-exchange solvent-detergent-treated high-purity factor VIII concentrate. Haemophilia Directors for Scotland and Northern Ireland.

作者信息

Ludlam C A, Lowe G D, Mayne E E

机构信息

Department of Haematology, Royal Infirmary, Edinburgh, UK.

出版信息

Transfus Med. 1995 Dec;5(4):289-92. doi: 10.1111/j.1365-3148.1995.tb00217.x.

Abstract

An ion-exchange chromatography purified factor VIII concentrate (Liberate) that had undergone a solvent-detergent viral inactivation treatment was compared with an intermediate-purity concentrate (Z8), which was terminally heated at 80 degrees C for 72 h, in 15 haemophilia A patients in a blinded crossover pharmacokinetic study. Both products achieved a peak level close to that predicted (100 IU/dl for Liberate and 103 IU/dl for Z8) and there were no significant differences in the recoveries achieved nor of any of the other pharmacokinetic parameters. We conclude that the pharmacokinetic properties of factor VIII:C, following solvent-detergent treatment and ion-exchange chromatography, are equivalent to those of the lower purity terminally heat-treated product (Z8), and it is therefore likely to be a clinically efficacious concentrate.

摘要

在一项双盲交叉药代动力学研究中,将经过溶剂-去污剂病毒灭活处理并通过离子交换色谱法纯化的凝血因子VIII浓缩物(Liberate)与在80℃终末加热72小时的中间纯度浓缩物(Z8),在15例甲型血友病患者中进行了比较。两种产品均达到接近预测的峰值水平(Liberate为100 IU/dl,Z8为103 IU/dl),在回收率以及任何其他药代动力学参数方面均无显著差异。我们得出结论,经过溶剂-去污剂处理和离子交换色谱法后,凝血因子VIII:C的药代动力学特性与较低纯度的终末热处理产品(Z8)相当,因此它可能是一种临床有效的浓缩物。

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