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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Increased volume of distribution for recombinant activated factor VII and longer plasma-derived factor VII half-life may explain their long lasting prophylactic effect
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Increased volume of distribution for recombinant activated factor VII and longer plasma-derived factor VII half-life may explain their long lasting prophylactic effect

机译:重组激活因子VII的分配量增加和血浆衍生的因子VII的半衰期延长可能解释了它们的长期预防作用

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摘要

Introduction Prophylaxis with plasma-derived or recombinant activated factor VII is beneficial in severe factor VII deficiency. To understand why prophylactic treatment with both products is efficacious, we conducted a pharmacokinetic study. Materials and Methods Ten factor VII deficient patients were treated with either recombinant activated (20 μg/kg) or plasma-derived (25 IU/kg) factor VII in a cross-over design. Pharmacokinetic parameters were analyzed through activated factor VII activity, factor VII clotting activity, and factor VII antigen levels on depicted time points. Results Factor VII activity half-lifes, determined by non-compartmental and one-compartmental analysis (results in brackets), were shorter for recombinant activated (1.4 h; 0.7 h) than for plasma-derived factor VII (6.8 h; 3.2 h); both recombinant activated (5.1 h; 2.1 h and plasma-derived factor VII (5.8 h; 3.2 h) resulted in longer half-lives of factor VII antigen. Activated factor VII half-lives (based on activated factor VII activity levels) were significantly higher compared to factor VII clotting activity (1.6 h; 0.9 h). Volumes of distribution were significantly higher for activated factor VII (236 ml/kg; 175 ml/kg, measured by activated factor VII) as compared to plasma-derived factor VII (206 ml/kg; 64 ml/kg, measured by factor FVII activity), suggesting a plasma- and extracellular fluid distribution for recombinant activated factor VII. Conclusions Recombinant activated factor VII showed significantly shorter half-lifes than plasma-derived factor VII. Volumes of distribution were significantly higher for treatment with recombinant activated factor VII. The longer half-life for plasma-derived factor VII, compared to recombinant activated factor VII, and the increased volume of distribution for recombinant activated factor VII, compared to plasma-derived factor VII may further elucidate the beneficial effect of prophylactic treatment of both products.
机译:简介血浆衍生或重组活化的因子VII的预防对严重的因子VII缺乏症有益。为了了解两种产品的预防性治疗为何有效,我们进行了药代动力学研究。材料和方法以交叉设计的方式,用重组激活的(20μg/ kg)或血浆来源的(25 IU / kg)因子VII治疗十名VII因子缺乏的患者。通过活化的VII因子活性,VII因子凝结活性和VII因子抗原水平在所示时间点分析药代动力学参数。结果通过非隔室和单隔室分析确定的因子VII活性半衰期(括号中的结果),重组激活的(1.4 h; 0.7 h)比血浆衍生的因子VII(6.8 h; 3.2 h)短。 ;重组激活(5.1 h; 2.1 h和血浆来源的VII因子(5.8 h; 3.2 h))均导致更长的VII因子半衰期,活化的VII半衰期(基于激活的VII活性水平)显着与血浆VII因子相比,活化因子VII的凝血活性更高(1.6 h; 0.9 h);活化VII因子的分布体积(236 ml / kg; 175 ml / kg,由活化VII因子测定)明显更高(206 ml / kg; 64 ml / kg,通过因子FVII活性测量),表明重组激活因子VII在血浆和细胞外液中的分布结论结论重组激活因子VII的半衰期比血浆来源的因子VII明显短。用重组活化因子VII治疗的分布体积明显更高;与重组活化因子VII相比,血浆来源的因子VII的半衰期更长,重组的分布体积增加与血浆来源的因子VII相比,nt活化的因子VII可以进一步阐明两种产品的预防性治疗的有益作用。

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