Pfizer Inc., Biotherapeutics Pharmaceutical Sciences, Andover, Massachusetts 01810, USA.
J Pharm Sci. 2011 Nov;100(11):4617-30. doi: 10.1002/jps.22670. Epub 2011 Jun 21.
Aqueous extractables/leachables from three sterilizing-grade filter membranes [polyvinylidene fluoride (PVDF), polyethersulfone (PES), and mixed cellulose ester (MCE)] were found to significantly reduce the surface tension of aqueous solutions. To evaluate the effect of these extractables/leachables from filter membranes on stability of protein formulations, model IgG2 formulations (with or without added surfactant) were spiked with different levels of filter extractables from stock solutions as a stress study. The stock solutions of extractables were created by processing the filter membranes through autoclaving and soaking steps. The IgG2 formulations were subsequently subject to agitation and temperature stress. Extractables/leachables from the filters were found to have a significant protective (PVDF, PES) and destabilizing (MCE) impact on both visible and subvisible particulates formation under agitation stress for formulations that did not contain any additional surfactant such as polysorbate 80. The impact of filter extractables/leachables on chemical stability of the antibody formulation displayed a more complicated pattern, but was generally destabilizing, causing increases in aggregation, oxidation, and acidic species. In conclusion, extractables/leachables from filter membranes may have impact on protein formulation stability and caution should be exercised during protein filtration, especially when filtering small volumes and in preformulation or high-throughput screening studies.
三种灭菌级别的过滤膜(聚偏二氟乙烯(PVDF)、聚醚砜(PES)和混合纤维素酯(MCE))的水性萃取物/浸出物被发现显著降低了水溶液的表面张力。为了评估过滤膜中的这些萃取物/浸出物对蛋白质制剂稳定性的影响,在模型 IgG2 制剂(有或没有添加表面活性剂)中加入不同水平的过滤萃取物作为应激研究。萃取物的储备溶液是通过对过滤膜进行高压灭菌和浸泡步骤来制备的。随后,将 IgG2 制剂进行搅拌和温度应激处理。发现过滤膜中的萃取物/浸出物对在没有添加任何额外表面活性剂(如聚山梨酯 80)的制剂中,搅拌应激下可见和亚可见颗粒形成有显著的保护(PVDF、PES)和不稳定(MCE)影响。萃取物/浸出物对抗体制剂化学稳定性的影响呈现出更复杂的模式,但通常是不稳定的,导致聚集、氧化和酸性物质增加。总之,过滤膜中的萃取物/浸出物可能会对蛋白质制剂的稳定性产生影响,因此在蛋白质过滤过程中应谨慎操作,特别是在过滤小体积和制剂前筛选或高通量筛选研究中。