折射率作为测量实时蛋白质浓度的过程分析技术,用于商业规模切向流过滤操作的监测和控制

Yik Lam, Devin McCann, Abdullah Loman, John Paul Smelko, Alex Brinkmann
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引用次数: 1

摘要

生物治疗制剂越来越多地被配制成高蛋白质浓度,以减少药物的储存空间,增加给药的灵活性给病人。随着蛋白质浓度目标的提高,下游纯化制造过程也面临着新的挑战。切向流过滤(TFF)操作通常用于达到目标蛋白浓度。给定原料药的TFF操作可能包括超滤和滤过(UFDF)步骤,或UFDF步骤之后是单道切向流过滤(SPTFF)步骤。TFF步骤是否达到目标蛋白浓度是通过在工艺步骤完成时进行的在线蛋白浓度测量来确定的。如果测量的蛋白质浓度超出规定范围,则可能需要重新开始单元操作,可能需要进行再处理,或者可能需要终止批次。超出规格的蛋白质浓度测量可能是TFF操作或样品测量的结果。与高浓度TFF操作相关的粘度增加给TFF过程和样品测量带来了额外的挑战。实施在线过程分析技术(PAT)来监测TFF操作期间的实时蛋白质浓度,有可能提高操作的准确性,以达到目标蛋白质浓度。这将提高过程的一致性和效率,增加操作员的信心,减少批次失败的可能性。本文研究了K-Patents的PR-23折射仪(Vaisala)作为PAT来监测和控制商业规模单克隆抗体纯化过程中UFDF和SPTFF单元操作的性能。
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Refractive index as a process analytical technology to measure real time protein concentration for monitoring and control of commercial scale tangential flow filtration operations

Biological therapeutics are increasingly being formulated to high protein concentrations to decrease drug substance storage space and increase the flexibility of administration to patients. With the higher protein concentration targets comes added challenges to the downstream purification manufacturing process. Tangential flow filtration (TFF) operations are typically performed to reach target protein concentration. TFF operations for a given drug substance may include an Ultrafiltration and Diafiltration (UFDF) step, or a UFDF step followed by a single pass tangential flow filtration (SPTFF) step. Whether a TFF step achieves a target protein concentration is determined by at-line protein concentration measurements performed at the completion of a process step. If the measured protein concentration is outside the specified range, the unit operation may need to be restarted, reprocessing may need to be performed, or a batch may need to be terminated. Out of specification protein concentration measurements may be a result of the TFF operation or sample measurement. Increased viscosities associated with high concentration TFF operations pose added challenges to the TFF process and sample measurement. Implementation of an inline process analytical technology (PAT) to monitor real-time protein concentration during TFF operations has the potential to improve the accuracy of the operations in achieving target protein concentrations. This will result in improved process consistency and efficiency, increased operator confidence and decreased likelihood of batch failures. This paper studies the performance of a K-Patents PR-23 refractometer (Vaisala) as a PAT to monitor and control the UFDF and SPTFF unit operations of a commercial scale monoclonal antibody purification process.

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