Liu Yang, Zhang Chi, Chen Jiangchao, Fernandez Janice, Vellala Pragna, Kulkarni Tanmay A, Aguilar Isaiah, Ritz Diana, Lan Kevin, Patel Pramthesh, Liu Aston
Biopharm Product Development & Supply, GlaxoSmithKline, PA 19406, United States.
CMC Analytical, Product Development & Supply, GlaxoSmithKline, PA 19406, United States.
J Pharm Sci. 2022 Feb;111(2):358-367. doi: 10.1016/j.xphs.2021.09.011. Epub 2021 Sep 14.
In response to FDA's call for Quality by Design (QbD) in biopharmaceutical product development, the biopharmaceutical industry has been developing highly sensitive and specific technologies in the monitoring and controlling of product quality attributes for bioprocesses. We previously published the successful application of an off-line multi-attribute method (MAM) to monitor more than 20 critical quality attributes (CQA) with superior sensitivity for the upstream process. To further remove the hurdles of laborious process sampling and sample preparation associated with the offline method, we present here a fully integrated MAM based online platform for automated real time online process monitoring. This integrated system includes Modular Automated Sampling Technology (MAST) based aseptic sampling, multi-function Sequential Injection Analysis (SIA) sample preparation, UHPLC separation and high-resolution mass spectrometry (HRMS) analysis. Continuous automated daily monitoring of a 17-day cell culture process was successfully demonstrated for a model monoclonal antibody (mAb) molecule with similar specificity and sensitivity as we reported earlier. To the best of our knowledge, this is the first report of an end-to-end automated online MAM system, which would allow the MAM to be applied to routine bioprocess monitoring, potentially replacing multiple conventional low resolution and low sensitivity off-line methods. The online HPLC or HPLC/MS platform could be easily adapted to support other processing steps such as downstream purification with minimal software re-configuration.
为响应美国食品药品监督管理局(FDA)对生物制药产品开发中质量源于设计(QbD)的要求,生物制药行业一直在开发高度灵敏且特异的技术,用于监测和控制生物过程的产品质量属性。我们之前发表过离线多属性方法(MAM)的成功应用,该方法能以卓越的灵敏度监测上游过程中的20多个关键质量属性(CQA)。为进一步消除与离线方法相关的繁琐过程取样和样品制备障碍,我们在此展示一个基于MAM的完全集成在线平台,用于自动化实时在线过程监测。这个集成系统包括基于模块化自动取样技术(MAST)的无菌取样、多功能顺序注射分析(SIA)样品制备、超高效液相色谱(UHPLC)分离和高分辨率质谱(HRMS)分析。对于一种模型单克隆抗体(mAb)分子,成功展示了对17天细胞培养过程的连续自动化每日监测,其特异性和灵敏度与我们之前报道的类似。据我们所知,这是关于端到端自动化在线MAM系统的首次报道,该系统将使MAM能够应用于常规生物过程监测,有可能取代多种传统的低分辨率和低灵敏度离线方法。在线HPLC或HPLC/MS平台可以很容易地进行调整,以支持其他处理步骤,如下游纯化,只需进行最少的软件重新配置。