Manufacturing of a prothrombin complex concentrate aiming at low thrombogenicity

被引:36
作者
Josic, D
Hoffer, L
Buchacher, A
Schwinn, H
Frenzel, W
Biesert, L
Klöcking, HP
Hellstern, R
Rokicka-Milewska, R
Klukowska, A
机构
[1] Octapharma Pharmazeut Prod Ges MBH, A-1100 Vienna, Austria
[2] Georg Speyer Haus, Octapharma Virol Res Grp, D-60596 Frankfurt, Germany
[3] Klinikum Friedrich Schiller Univ Jena, Inst Pharmakol & Toxikol, Bereich Erfurt, D-99089 Erfurt, Germany
[4] Klinikum Stadt Ludwigshafen, Inst Hamostaseol & Transfus Med, D-67063 Ludwigshafen, Germany
[5] Med Acad Warsaw, PL-00579 Warsaw, Poland
关键词
prothrombin complex concentrate; vitamin K-dependent proteins; thrombogenicity; clotting factors II; VII; VIIa; IX and X; Protein C; Protein S; Protein Z;
D O I
10.1016/S0049-3848(00)00339-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The paper describes the production of a prothrombin complex concentrate (PCC) with high virus safety and a well-balanced content of vitamin K-dependent clotting factors and inhibitors. Solid-phase extraction is followed in a second step by optimized anion exchange chromatography using a radial column. A step for virus removal by nanofiltration is introduced in addition to the solvent/detergent step. By speeding up the chromatographic step, the period of time required for production is reduced considerably. The activities of the four vitamin K-dependent clotting factors II, VII, IX and X are in ratios of about 1:1:1:1. Protein C, Protein S, and Protein Z are also present in therapeutically effective concentrations. The product shows no thrombogenicity, in neither in vivo nor in vitro models. Clinical investigations show that the PCC is a safe and efficient preparation for the substitutive treatment of FIX or FVII in patients suffering from the respective deficiencies. All bleeding episodes ha ire been efficiently controlled with relatively low doses of the concentrate. The surgical procedures have been conducted without any problems in severely FIX and FVIII deficient patients. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:433 / 441
页数:9
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