Saggu Miguel, Liu Jun, Patel Ankit
Late Stage Pharmaceutical Development, Genentech Inc., South San Francisco, California, 94080, USA,
Pharm Res. 2015 Sep;32(9):2877-88. doi: 10.1007/s11095-015-1670-x. Epub 2015 Mar 14.
To study composition and heterogeneity of insoluble subvisible particles in Mab formulations resulting from degradation of polysorbate 20 and to develop a better understanding of the mechanisms of polysorbate degradation leading to particle formation.
In this study, we exploit the potential of Raman microscopy for chemical identification of particles in monoclonal antibody formulations. Through a combination of experiments and density functional theory (DFT) calculations, we identified unique spectral marker bands for insoluble degradation products of polysorbate 20. We first applied our methodology to identify particles in model systems containing complex mixtures of fatty acids and then to subvisible particles in antibody formulations stored at 5°C for several years.
Most of the subvisible particles identified were comprised of mixtures of fatty acids with no observable signal from fatty acid esters consistent with hydrolysis being the predominant degradation mechanism leading to particulate formation under these storage conditions.
Our methodology is generally applicable for identification of particles in antibody formulations and, in particular, has the potential to give detailed information about particle heterogeneity and insight into mechanistic aspects of particle formation.
研究因聚山梨酯20降解导致的单克隆抗体制剂中不溶性亚可见颗粒的组成和异质性,并更好地理解聚山梨酯降解导致颗粒形成的机制。
在本研究中,我们利用拉曼显微镜对单克隆抗体制剂中的颗粒进行化学鉴定。通过实验和密度泛函理论(DFT)计算相结合的方法,我们确定了聚山梨酯20不溶性降解产物的独特光谱标记带。我们首先将我们的方法应用于鉴定含有脂肪酸复杂混合物的模型系统中的颗粒,然后应用于在5°C下储存数年的抗体制剂中的亚可见颗粒。
鉴定出的大多数亚可见颗粒由脂肪酸混合物组成,未观察到脂肪酸酯的信号,这与水解是在这些储存条件下导致颗粒形成的主要降解机制一致。
我们的方法一般适用于鉴定抗体制剂中的颗粒,特别是有潜力提供有关颗粒异质性的详细信息,并深入了解颗粒形成的机制方面。