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血友病 A 小鼠体内因子 VIII 及其磷脂酰肌醇脂质复合物的非线性药代动力学。

Nonlinear pharmacokinetics of factor VIII and its phosphatidylinositol lipidic complex in hemophilia A mice.

机构信息

Department of Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, NY, 14214, USA.

出版信息

Biopharm Drug Dispos. 2014 Apr;35(3):154-63. doi: 10.1002/bdd.1880. Epub 2014 Jan 2.

Abstract

Factor VIII (FVIII) is an important cofactor in the blood coagulation cascade and its deficiency or dysfunction causes hemophilia A (HA), a bleeding disorder. Replacement with recombinant FVIII is limited by a short half-life and the development of inhibitory antibodies. A phosphatidylinositol (PI) containing lipid nanoparticle was developed that, when associated with FVIII, reduces immunogenicity and prolongs circulation of the therapeutic protein in HA mice. A multiple dose level pharmacokinetic (PK) study of human free FVIII and its FVIII-PI complex over a clinically relevant range of doses (20, 40 and 200 IU/kg) was conducted in HA mice to investigate linearity of the PK and to determine if the reduced catabolism of FVIII following association with PI particles, previously only observed in the terminal phase following 400 IU/kg, could be extendable over a range of doses. The findings suggest that the disposition of FVIII is best characterized by a two-compartment model with saturable Michaelis-Menten elimination. Spontaneous complexation of FVIII with PI particles significantly increases plasma survival of the protein at 20 and 40 IU/kg doses. Human simulations at 40 IU/kg project an increase in the terminal half-life and the time to reach a minimum therapeutic threshold of 0.01 IU/ml of 5.4 h and 40 h, respectively, compared with free FVIII. Formulation with PI containing lipid particles may represent a viable delivery strategy for improving FVIII therapy.

摘要

凝血因子 VIII(FVIII)是血液凝血级联反应中的一个重要辅助因子,其缺乏或功能障碍会导致血友病 A(HA),这是一种出血性疾病。用重组 FVIII 替代受限于半衰期短和抑制性抗体的产生。开发了一种含有磷脂酰肌醇(PI)的脂质纳米颗粒,当与 FVIII 结合时,可降低免疫原性并延长治疗性蛋白质在 HA 小鼠中的循环时间。在 HA 小鼠中进行了人游离 FVIII 及其 FVIII-PI 复合物的多剂量水平药代动力学(PK)研究,涵盖了临床相关剂量范围(20、40 和 200 IU/kg),以研究 PK 的线性,并确定与 PI 颗粒结合后 FVIII 代谢减少的情况是否可以扩展到一系列剂量。研究结果表明,FVIII 的处置最好用具有饱和米氏消除的两室模型来描述。FVIII 与 PI 颗粒的自发结合可显著提高蛋白在 20 和 40 IU/kg 剂量下的血浆半衰期。与游离 FVIII 相比,在 40 IU/kg 时,人模拟预测半衰期和达到 0.01 IU/ml 的最小治疗阈值的时间分别增加了 5.4 小时和 40 小时。用含有 PI 的脂质颗粒进行制剂可能是改善 FVIII 治疗的一种可行的给药策略。

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本文引用的文献

1
Allometry of factor VIII and informed scaling of next-generation therapeutic proteins.
J Pharm Sci. 2013 Jul;102(7):2380-94. doi: 10.1002/jps.23566. Epub 2013 Apr 25.
2
Prolonged activity of a recombinant factor VIII-Fc fusion protein in hemophilia A mice and dogs.
Blood. 2012 Mar 29;119(13):3024-30. doi: 10.1182/blood-2011-08-367813. Epub 2012 Jan 13.
3
Population pharmacokinetics of recombinant factor VIII: the relationships of pharmacokinetics to age and body weight.
Blood. 2012 Jan 12;119(2):612-8. doi: 10.1182/blood-2011-07-360594. Epub 2011 Oct 31.
5
Pharmacokinetics and pharmacodynamics of a new recombinant FVIII (N8) in haemophilia A mice.
Haemophilia. 2012 Jan;18(1):139-45. doi: 10.1111/j.1365-2516.2011.02608.x. Epub 2011 Jul 19.
7
Phospholipid binding improves plasma survival of factor VIII.
Thromb Haemost. 2010 Nov;104(5):1073-5. doi: 10.1160/TH10-06-0422. Epub 2010 Sep 13.
9
Rational design of a fully active, long-acting PEGylated factor VIII for hemophilia A treatment.
Blood. 2010 Jul 15;116(2):270-9. doi: 10.1182/blood-2009-11-254755. Epub 2010 Mar 1.
10
Enhanced efficacy of recombinant FVIII in noncovalent complex with PEGylated liposome in hemophilia A mice.
Blood. 2009 Sep 24;114(13):2802-11. doi: 10.1182/blood-2009-03-212423. Epub 2009 Aug 4.

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