Pharmaceutical and Molecular Biotechnology Research Centre (PMBRC), South East Technological University (SETU), Main Campus, Cork Road, Waterford, X91 K0EK, Ireland.
Manufacturing Science, Analytics and Technology (MSAT), Sanofi, IDA Industrial Park, Waterford, X91 TP27, Ireland.
AAPS PharmSciTech. 2023 Mar 22;24(4):84. doi: 10.1208/s12249-023-02529-4.
Biopharmaceuticals are large, complex and labile therapeutic molecules prone to instability due to various factors during manufacturing. To ensure their safety, quality and efficacy, a wide range of critical quality attributes (CQAs) such as product concentration, aggregation, particle size, purity and turbidity have to be met. Size exclusion chromatography (SEC) is the gold standard to measure protein aggregation and degradation. However, other techniques such as dynamic light scattering (DLS) are employed in tandem to measure the particle size distribution (PSD) and polydispersity of biopharmaceutical formulations. In this study, the application of multi-angle dynamic light scattering (MADLS) was evaluated for the determination of particle size, particle concentration and aggregation in 3 different protein modalities, namely bovine serum albumin (BSA) and two biopharmaceuticals including a monoclonal antibody (mAb) and an enzyme. The obtained calibration curve (R > 0.95) for the particle number concentration of the 3 proteins and the observed correlation between MADLS and SEC (R = 0.9938) for the analysis of aggregation in the enzyme can be employed as a 3-in-1 approach to assessing particle size, concentration and aggregation for the screening and development of products while also reducing the number of samples and experiments required for analysis prior to other orthogonal tests.
生物制药是一种大型、复杂且不稳定的治疗分子,由于制造过程中的各种因素,容易变得不稳定。为了确保其安全性、质量和疗效,必须满足广泛的关键质量属性(CQA),如产品浓度、聚集、粒径、纯度和浊度。尺寸排阻色谱(SEC)是测量蛋白质聚集和降解的金标准。然而,还采用其他技术,如动态光散射(DLS),来串联测量生物制药制剂的粒径分布(PSD)和多分散性。在这项研究中,评估了多角度动态光散射(MADLS)在测定 3 种不同蛋白质模式(牛血清白蛋白(BSA)和 2 种生物制药,包括单克隆抗体(mAb)和一种酶)中的粒径、颗粒浓度和聚集的应用。对于 3 种蛋白质的颗粒数浓度的获得的校准曲线(R>0.95),以及 MADLS 和 SEC 之间的观察到的相关性(R=0.9938),用于分析酶中的聚集,可作为一种 3-in-1 方法,用于筛选和开发产品,同时还减少了在进行其他正交测试之前分析所需的样品和实验数量。