Department Chemical and Biological Engineering, Center for Pharmaceutical Biotechnology, University of Colorado, Boulder, Colorado 80309.
Exsera Biolabs, Anschutz Medical Campus, Aurora, Colorado 80045.
J Pharm Sci. 2020 Jan;109(1):558-565. doi: 10.1016/j.xphs.2019.10.041. Epub 2019 Oct 28.
When administered intravenously, various particles and nanomedicines activate complement, potentially leading to infusion reactions and other adverse drug reactions. Particles form within formulations of therapeutic proteins due to stresses incurred during shipping, handling, and administration to patients. In this study, IVIg solutions were stored in multiple types of vials and prefilled syringes and exposed to agitation and freeze-thaw stresses to generate particles. The stressed samples were added to human serum to determine whether these particles activated complement. Subvisible IVIg particles ranging in size between 2 and 10 microns activated complement in a fashion that was linearly dependent on the number of particles dosed, whereas little correlation was found between doses of larger particles (>10 microns) and complement activation. Activation of complement by subvisible particles of IVIg followed the alternative pathway, as shown by the release of complement cascade factor Bb and the production of the anaphylatoxins C3a and C5a without generation of C4a. The number and the morphology of subvisible particles formed depended on the applied stress, formulation, and on the container material. But the capacity of the 2- to 10-micron-sized particles to activate complement in human serum appeared to depend only on particle concentration.
当静脉内给药时,各种颗粒和纳米药物会激活补体,可能导致输注反应和其他药物不良反应。由于在运输、处理和给患者给药过程中产生的应激,颗粒会在治疗性蛋白质的制剂中形成。在这项研究中,将 IVIg 溶液储存在多种类型的小瓶和预装注射器中,并暴露于搅拌和冻融应激下以产生颗粒。将受应激的样品添加到人血清中,以确定这些颗粒是否激活了补体。大小在 2 至 10 微米之间的亚可见 IVIg 颗粒以剂量依赖性的方式激活补体,而较大颗粒(>10 微米)的剂量与补体激活之间几乎没有相关性。IVIg 亚可见颗粒通过替代途径激活补体,如补体级联因子 Bb 的释放以及过敏毒素 C3a 和 C5a 的产生而无 C4a 的产生所表明的那样。形成的亚可见颗粒的数量和形态取决于所施加的应激、制剂和容器材料。但是,2 至 10 微米大小的颗粒在人血清中激活补体的能力似乎仅取决于颗粒浓度。