Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
Pharmaceutical Research and Development, Pfizer Biotherapeutics Pharmaceutical Sciences, Chesterfield, Missouri 63017.
J Pharm Sci. 2019 Apr;108(4):1631-1635. doi: 10.1016/j.xphs.2018.11.031. Epub 2018 Nov 29.
Polysorbates are frequently used in biotherapeutic formulations. Interest in assessing their stability, in particular the impact of their degradation products on the stability of therapeutic proteins, has been steadily growing in the past decade. The work presented summarizes a case study of a monoclonal antibody formulation that demonstrated a simultaneous loss of polysorbate and an increase in methionine oxidation. Spiking studies were conducted to determine both the cause and a potential mitigation for the monoclonal antibody (mAb) oxidation and polysorbate 80 (PS80) loss. The results indicated that a different source material exhibited different rates of mAb oxidation and PS80 loss and that in all evaluated materials, the addition of edetate disodium to the formulation mitigated both observed issues. The mAb was assessed for the presence of lipases and lipoprotein lipase was detected at low levels. It is proposed that edetate disodium was effective in mitigating the mAb oxidation and PS80 loss by chelating calcium in the formulation and therefore decreasing the activity of the lipases.
聚山梨酯经常用于生物治疗制剂中。在过去十年中,人们对评估其稳定性,特别是其降解产物对治疗蛋白稳定性的影响的兴趣一直在稳步增长。本文总结了一个单克隆抗体制剂的案例研究,该制剂同时表现出聚山梨酯的损失和蛋氨酸氧化的增加。进行了加标研究,以确定单克隆抗体 (mAb) 氧化和聚山梨酯 80 (PS80) 损失的原因和潜在缓解方法。结果表明,不同的原料表现出不同的 mAb 氧化和 PS80 损失速率,并且在所评估的所有材料中,向制剂中添加乙二胺四乙酸二钠都可以缓解这两个观察到的问题。对 mAb 进行了脂酶存在的评估,并在低水平检测到脂蛋白脂酶。据推测,乙二胺四乙酸二钠通过螯合制剂中的钙从而降低脂酶的活性,从而有效缓解了 mAb 氧化和 PS80 损失。