Protein A Chromatography Purification for a Monoclonal Antibody from Process Development to Scale-up

Dilara Bas, Emre Burak Erkal, Melis Korkmaz, A. Recepoglu, Hazal Elitas, Deniz Baycin Demirhan
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引用次数: 1

Abstract

Monoclonal antibodies have been established as a major product class of biotechnology-based drugs. The increasing demand of monoclonal antibodies has led pharmaceutical companies to adopt efficient production processes. Transferring monoclonal antibody production to the industrial manufacturing requires adequate effort in process development. The strategy to reduce development time and cost comprises high-throughput process development which is especially central for the rapid optimization of the purification process. Chromatography process is the backbone of the purification process that can deliver high purity but it requires significant resources. Combined with high-throughput process development approach, the chromatography process is easy to develop and scale-up from laboratory to manufacturing scale. Design of experiments helps high-throughput process development workflow to provide decision-support techniques. This approach ensures significantly decreased time and material needs while improving the chromatography process. Protein A affinity chromatography is one of the most important chromatographic steps because of its great performance and capabilities. Most of the working parameters can be predefined and are identical for several monoclonal antibodies. However, some parameters like elution pH, loading capacity, resin type need further optimization for each monoclonal antibody. In this study, the loading and elution parameters were screened for Protein A chromatography to identify the best purification conditions using the combination of Design of Experiments and high-throughput process development approach in micro-volume columns. Developed working parameters were used for scale-up and tested under robust process conditions. Specific chromatography conditions were applied in pilot-scale and data comparison was done with micro-volume columns, lab-column scale to validate high-throughput strategy approach
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从工艺开发到规模化生产的单克隆抗体蛋白A层析纯化
单克隆抗体已成为生物技术基础药物的主要产品类别。对单克隆抗体日益增长的需求促使制药公司采用高效的生产工艺。将单克隆抗体生产转移到工业生产需要在工艺开发方面付出足够的努力。减少开发时间和成本的策略包括高通量工艺开发,这对于净化过程的快速优化尤其重要。色谱法是纯化过程的支柱,可以提供高纯度,但需要大量的资源。结合高通量工艺开发方法,色谱法易于开发和扩大从实验室到生产规模。实验设计有助于高通量工艺开发工作流提供决策支持技术。这种方法确保显著减少时间和材料需求,同时改进色谱过程。蛋白A亲和层析是最重要的层析步骤之一,因为它具有很高的性能和能力。大多数工作参数可以预先定义,并且对于几种单克隆抗体是相同的。但各单克隆抗体的洗脱pH、载药量、树脂类型等参数需要进一步优化。本研究采用实验设计与微体积柱高通量工艺开发相结合的方法,对蛋白A层析的上样和洗脱参数进行筛选,确定最佳纯化条件。开发的工作参数用于放大,并在稳健的工艺条件下进行了测试。采用特定的色谱条件进行中试,并与微体积柱和实验室柱进行了数据比较,以验证高通量策略方法
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