Synthetic Molecule Analytical Chemistry, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, United States.
Synthetic Molecule Analytical Chemistry, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, United States.
J Pharm Biomed Anal. 2024 Jan 20;238:115854. doi: 10.1016/j.jpba.2023.115854. Epub 2023 Nov 7.
Polyethylene glycol (PEG) has found tremendous applications in pharmaceutical products and has played a critical role in PEGylated drug modalities to improve pharmacokinetic properties and biological efficacy. The characterization and quantitation of PEGs are essential to control manufacture process and drug product quality. However, the assay value of PEG could change dramatically depending on the structures of the PEG and the detection techniques used. In this study, we developed a size exclusion chromatographic (SEC) method for quantitative PEG analysis, and we systematically evaluated the performance of three online detectors with different operating principles: a charged aerosol detector (CAD), a differential refractive index (dRI) detector, and a multi-angle light scattering detector (MALS). Fourteen PEG compounds covering a wide range of molecular weight (MW, 1 - 40 kDa) and molecular architectures (linear, branched, Y-shaped and multi-arm geometries) were evaluated by these three detection techniques. Our study revealed that the dRI showed the most universal responses among all the PEGs regardless of their molecular weight or geometries. In the contrast, CAD and MALS detector showed MW-dependent and semi-universal geometry-dependent responses. Another key finding is that the relative response factor for each multi-arm PEG in the CAD and the MALS were inversely correlated, suggesting both can be applied to qualitatively assess polymers of different architectures, including the ones with subtle differences in their core structures. The comparison of the three detectors not only provides the fundamental and comprehensive understanding of PEG quantitation but also enables the process development and control of high-quality PEGs in producing PEGylated therapeutics in the pharmaceutical industry.
聚乙二醇(PEG)在药物产品中有着广泛的应用,在聚乙二醇化药物模式中发挥了关键作用,以改善药代动力学性质和生物功效。PEG 的特性和定量分析对于控制制造过程和药物产品质量至关重要。然而,PEG 的测定值会因 PEG 的结构和所用检测技术的不同而发生显著变化。在本研究中,我们开发了一种用于定量 PEG 分析的尺寸排阻色谱(SEC)方法,并系统地评估了三种具有不同工作原理的在线检测器的性能:带电气溶胶检测器(CAD)、差示折射指数(dRI)检测器和多角度光散射检测器(MALS)。我们用这三种检测技术评估了 14 种涵盖广泛分子量(MW,1-40 kDa)和分子结构(线性、支化、Y 型和多臂几何形状)的 PEG 化合物。我们的研究表明,dRI 对所有 PEG 都表现出最普遍的响应,无论其分子量或几何形状如何。相比之下,CAD 和 MALS 检测器表现出依赖分子量和半普遍依赖几何形状的响应。另一个关键发现是,CAD 和 MALS 中每个多臂 PEG 的相对响应因子呈反比相关,这表明两者都可以用于定性评估不同结构的聚合物,包括其核心结构略有差异的聚合物。三种检测器的比较不仅提供了 PEG 定量分析的基本和全面的理解,而且还能够在制药行业中开发和控制生产聚乙二醇化治疗剂的高质量 PEG。