Nitika Nitika, Thakur Garima, Rathore Anurag S
Department of Chemical Engineering, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
Department of Chemical Engineering, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
J Chromatogr A. 2023 Feb 8;1690:463784. doi: 10.1016/j.chroma.2023.463784. Epub 2023 Jan 7.
We propose a strategy for automation and control of multi-step polishing chromatography in integrated continuous manufacturing of monoclonal antibodies. The strategy is demonstrated for a multi-step polishing process consisting of cation exchange chromatography in bind-and-elute mode followed by mixed-mode chromatography in flowthrough mode. A BioSMB system with a customized Python control layer is used for automation and scheduling of both the chromatography steps. Further, the BioSMB valve manifold is leveraged for in-line conditioning between the two steps, as tight control of pH and conductivity is essential when operating with multimodal resins because even slight fluctuations in load conditions adversely affect the chromatography performance. The pH and conductivity of the load to the multimodal chromatography columns is consistent, despite the elution gradient of the preceding cation exchange chromatography step. Inputs from the BioSMB pH and conductivity sensors are used for real-time control of the 7 pumps and 240 valves to achieve in-line conditioning inside the BioSMB manifold in a fully automated manner. This is confirmed by showcasing different elution strategies in cation exchange chromatography, including linear gradient, step gradient and process deviations like tubing leakage. In all the above cases, the model was able to maintain the pH and conductivity of multimodal chromatography load within the range of 6 ± 0.1 pH and 7 ± 0.3 mS/cm conductivity. The strategy eliminates the need for using multiple BioSMB units or integrating external pumps, valves, mixers, surge tanks, or sensors between the two steps as is currently the standard approach, thus offering a simple and robust structure for integrating multiple polishing chromatography steps in continuous downstream monoclonal antibody purification trains.
我们提出了一种在单克隆抗体集成连续制造中实现多步抛光色谱自动化和控制的策略。该策略在一个多步抛光过程中得到了验证,该过程包括以结合 - 洗脱模式进行的阳离子交换色谱,随后是以流通模式进行的混合模式色谱。一个带有定制Python控制层的BioSMB系统用于这两个色谱步骤的自动化和调度。此外,BioSMB阀组被用于两步之间的在线调节,因为在使用多模式树脂时,严格控制pH值和电导率至关重要,因为即使负载条件的轻微波动也会对色谱性能产生不利影响。尽管前一步阳离子交换色谱有洗脱梯度,但多模式色谱柱负载的pH值和电导率是一致的。来自BioSMB pH值和电导率传感器的输入用于实时控制7个泵和240个阀门,以完全自动化的方式在BioSMB阀组内实现在线调节。通过展示阳离子交换色谱中的不同洗脱策略,包括线性梯度、阶跃梯度和诸如管路泄漏等过程偏差,证实了这一点。在上述所有情况下,该模型都能够将多模式色谱负载的pH值保持在6 ± 0.1 pH范围内,电导率保持在7 ± 0.3 mS/cm范围内。该策略消除了目前标准方法中在两步之间使用多个BioSMB单元或集成外部泵、阀门、混合器、缓冲罐或传感器的需求,从而为在连续下游单克隆抗体纯化流程中集成多个抛光色谱步骤提供了一种简单而稳健的结构。