Binabaji Elaheh, Ma Junfen, Rao Suma, Zydney Andrew L
Dept. of Chemical Engineering, the Pennsylvania State University, University Park, PA, 16802.
Amgen, Inc., Thousand Oaks, CA, 91320.
Biotechnol Prog. 2016 May;32(3):692-701. doi: 10.1002/btpr.2252. Epub 2016 May 17.
Although ultrafiltration is currently used for the concentration and formulation of nearly all biotherapeutics, obtaining the very high target concentrations for monoclonal antibody products is challenging. The objective of this work was to examine the effects of the membrane module design and buffer conditions on both the filtrate flux and maximum achievable protein concentration during the ultrafiltration of highly concentrated monoclonal antibody solutions. Experimental data were obtained using both hollow fiber and screened cassettes and in the presence of specific excipients that are known to alter the solution viscosity. Data were compared with predictions of a recently developed model that accounts for the complex thermodynamic and hydrodynamic behavior in these systems, including the effects of back-filtration arising from the large pressure drop through the module due to the high viscosity of the concentrated antibody solutions. Model calculations were in good agreement with experimental data in hollow fiber modules with very different fiber length and in screened cassettes having different screen geometries. These results provide important insights into the key factors controlling the filtrate flux and maximum achievable protein concentration during ultrafiltration of highly concentrated antibody solutions as well as a framework for the development of enhanced ultrafiltration processes for this application. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:692-701, 2016.
尽管目前超滤被用于几乎所有生物治疗药物的浓缩和制剂过程,但要获得单克隆抗体产品所需的极高目标浓度仍具有挑战性。本研究的目的是考察膜组件设计和缓冲条件对高浓度单克隆抗体溶液超滤过程中滤液通量和可达到的最大蛋白质浓度的影响。使用中空纤维和筛网盒在特定赋形剂存在的情况下获取实验数据,已知这些赋形剂会改变溶液粘度。将数据与最近开发的一个模型的预测结果进行比较,该模型考虑了这些系统中复杂的热力学和流体动力学行为,包括由于浓缩抗体溶液的高粘度导致通过膜组件的大压降引起的反向过滤的影响。模型计算结果与具有非常不同纤维长度的中空纤维膜组件以及具有不同筛网几何形状的筛网盒中的实验数据吻合良好。这些结果为控制高浓度抗体溶液超滤过程中滤液通量和可达到的最大蛋白质浓度的关键因素提供了重要见解,同时也为开发针对该应用的强化超滤工艺提供了一个框架。© 2016美国化学工程师学会生物技术进展,32:692 - 701, 2016。