Fischer Thomas H, Wolberg Alisa S, Bode Arthur P, Nichols Timothy C
Francis Owen Blood Research Laboratory, Department of Pathology and Laboratory Medicine, 125 University Lake Dr., University of North Carolina at Chapel Hill, NC 27516, USA.
Platelets. 2008 May;19(3):182-91. doi: 10.1080/09537100701493794.
The experiments presented here were undertaken to determine if factor VIIa (rFVIIa, the Novo Nordisk product NovoSeven) will directly bind to rehydrated, lyophilized (RL) platelets for the formation of a catalytic surface with an enhanced ability to generate thrombin. The interaction between rFVIIa and the RL platelet surface was examined by measuring equilibrium and non-equilibrium binding of the coagulation factor to the cells and by following the effects of the surface modification on the kinetics of thrombin generation. The association of rFVIIa with RL platelets was rapid with saturation occurring within minutes. Disassociation was slow, with over half of the coagulation factor remaining bound after two hours. Densities of over one million molecules of rFVIIa per RL platelet were obtained when high concentrations of rFVIIa were incubated with RL platelets. Thrombin generation measurements showed that RL platelet-bound rFVIIa was catalytically active. Thus we can expect that RL platelets, which have been shown to effectively bind to sites of vascular injury, will localize rFVIIa to wounds for an increase in therapeutic index. These studies indicate that rFVIIa-RL platelets are worthy of preclinical and clinical development as an infusion agent for severe bleeding.
开展此处所述实验是为了确定凝血因子VIIa(重组凝血因子VIIa,诺和诺德公司产品诺其)是否会直接结合至复水冻干(RL)血小板,以形成具有增强生成凝血酶能力的催化表面。通过测量凝血因子与细胞的平衡和非平衡结合,并跟踪表面修饰对凝血酶生成动力学的影响,来研究重组凝血因子VIIa与RL血小板表面之间的相互作用。重组凝血因子VIIa与RL血小板的结合迅速,数分钟内即可达到饱和。解离缓慢,两小时后仍有超过一半的凝血因子保持结合状态。当高浓度的重组凝血因子VIIa与RL血小板孵育时,每个RL血小板上可获得超过一百万个重组凝血因子VIIa分子的密度。凝血酶生成测量结果表明,结合在RL血小板上的重组凝血因子VIIa具有催化活性。因此我们可以预期,已证明能有效结合至血管损伤部位的RL血小板,将使重组凝血因子VIIa定位于伤口处,从而提高治疗指数。这些研究表明,重组凝血因子VIIa - RL血小板作为一种用于严重出血的输注剂,值得进行临床前和临床开发。