Merck Serono, CMC Development, Darmstadt, Germany.
Eur J Pharm Biopharm. 2010 Feb;74(2):139-47. doi: 10.1016/j.ejpb.2009.11.005. Epub 2009 Nov 14.
In protein formulation development, shaking stress is often employed to assess the physical stability of antibody formulations against aggregation. Since there are currently no guidelines describing suitable test conditions, very different shaking stress designs are used. These different designs may influence the resulting stability data. The aim of this study was to establish a shaking stress design within the protein range of 2-5mg/ml which can rapidly distinguish between antibody formulations of poor stability and those with potential for further development. Small scale shaking stress experiments were performed with different monoclonal IgG antibodies (as buffered solutions or marketed formulations). Variables were the filling degree of the sample containers, the container type and size and the shaking intensity. The stability of the samples was assessed by visual inspection, UV-VIS spectrophotometric turbidity measurements and size exclusion chromatography. All tested parameters had a strong influence on the stability results. The most discriminating conditions were obtained when shaking of the formulations was performed at 200rpm in a 2ml injection vial filled with 1ml protein solution. This experimental setup led to clearly different stability results for buffered solutions and marketed products. Moreover, this setup required only relatively small amounts of protein solution which is advantageous in prefomulation studies.
在蛋白质制剂的开发中,常采用摇动应激来评估抗体制剂对聚集的物理稳定性。由于目前尚无描述合适测试条件的指南,因此使用了非常不同的摇动应激设计。这些不同的设计可能会影响到所得的稳定性数据。本研究的目的是建立一个在蛋白质浓度为 2-5mg/ml 范围内的摇动应激设计,该设计可以快速区分稳定性较差的抗体制剂和具有进一步开发潜力的抗体制剂。用不同的单克隆 IgG 抗体(缓冲溶液或市售制剂)进行了小规模的摇动应激实验。变量包括样品容器的填充程度、容器类型和大小以及摇动强度。通过目测、紫外可见分光光度法浊度测量和尺寸排阻色谱法评估样品的稳定性。所有测试的参数对稳定性结果都有很大的影响。当在 2ml 注射器瓶中以 200rpm 的速度摇动填充有 1ml 蛋白质溶液的制剂时,获得了最具区分性的条件。该实验设置导致缓冲溶液和市售产品的稳定性结果明显不同。此外,该设置仅需要相对较少量的蛋白质溶液,这在预配方研究中是有利的。