Division of Pharmaceutics, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany.
Merck KGaA, Darmstadt, Germany.
J Pharm Pharmacol. 2018 May;70(5):648-654. doi: 10.1111/jphp.12699. Epub 2017 Jan 20.
Polyethylene glycol (PEG)-induced protein precipitation is often used to extrapolate apparent protein solubility at specific formulation compositions. The procedure was used for several fields of application such as protein crystal growth but also protein formulation development. Nevertheless, most studies focused on applicability in protein crystal growth. In contrast, this study focuses on applicability of PEG-induced precipitation during high-concentration protein formulation development.
In this study, solubility of three different model proteins was investigated over a broad range of pH. Solubility values predicted by PEG-induced precipitation were compared to real solubility behaviour determined by either turbidity or content measurements.
Predicted solubility by PEG-induced precipitation was confirmed for an Fc fusion protein and a monoclonal antibody. In contrast, PEG-induced precipitation failed to predict solubility of a single-domain antibody construct. Applicability of PEG-induced precipitation as indicator of protein solubility during formulation development was found to be not valid for one of three model molecules.
Under certain conditions, PEG-induced protein precipitation is not valid for prediction of real protein solubility behaviour. The procedure should be used carefully as tool for formulation development, and the results obtained should be validated by additional investigations.
聚乙二醇(PEG)诱导的蛋白质沉淀常用于推断特定配方组成下蛋白质的表观溶解度。该方法已应用于多个领域,如蛋白质晶体生长,但也可用于蛋白质配方开发。然而,大多数研究都集中在蛋白质晶体生长的适用性上。相比之下,本研究侧重于 PEG 诱导沉淀在高浓度蛋白质配方开发过程中的适用性。
在本研究中,三种不同模型蛋白的溶解度在较宽的 pH 范围内进行了研究。通过 PEG 诱导沉淀预测的溶解度值与通过浊度或含量测量确定的实际溶解度行为进行了比较。
PEG 诱导沉淀预测的溶解度在 Fc 融合蛋白和单克隆抗体中得到了证实。相比之下,PEG 诱导沉淀未能预测单域抗体构建体的溶解度。PEG 诱导沉淀作为配方开发过程中蛋白质溶解度指示剂的适用性,对于三种模型分子中的一种并不适用。
在某些条件下,PEG 诱导的蛋白质沉淀不能用于预测真实蛋白质的溶解度行为。该方法应谨慎用作配方开发的工具,并且应通过其他研究验证获得的结果。