Implementation of machine learning tool for continued process verification of process chromatography unit operation.

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography A Pub Date : 2025-02-08 Epub Date: 2024-12-29 DOI:10.1016/j.chroma.2024.465642
Anupa Anupa, Naveen G Jesubalan, Rishika Trivedi, Nitika Nitika, Venkata Sudheendra Buddhiraju, Venkataramana Runkana, Anurag S Rathore
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Abstract

Recent advancements in technology, such as the emergence of artificial intelligence (AI) and machine learning (ML), have facilitated the progression of the biopharmaceutical industry toward the implementation of Industry 4.0. As per the guidelines set by the USFDA, process validation for biopharmaceutical production consists of three stages: process design, process qualification, and continuous process verification (CPV). This paper proposes a strategy for achieving CPV for a cation exchange chromatography unit operation, emphasizing the urgent need for such strategies in the biopharmaceutical industry. Statistical process control (SPC) charts were generated based on real-time measurement of the various critical process parameters (CPPs) measured via in-built sensors (pH, conductivity, UV, and delta column pressure) as well as of critical quality attributes (CQAs) like charge variant composition (Raman spectroscopy) and concentration (Near infrared spectroscopy). A Python-based program was created to read these SPC charts and respond to any deviation. The developed models for NIR coupled DNN PAT tool and Raman coupled DNN PAT tool exhibited satisfactory R2 values (> 0.90), highlighting the statistical significance of the proposed model. Further, the control strategy designed based on Raman spectroscopy for charge variant composition in CEX eluate has been demonstrated by intentional perturbations in the CEX load. The resulting CEX eluate output showed a consistent charge variant composition as that of control runs (acidic ∼20 ± 2 %, main ∼62 ± 2 % and basic ∼18 ± 2 %). It has been demonstrated how an appropriate selection of analyzers, soft sensors, and advanced data analytics can be used to execute CPV and enable the biopharmaceutical industry to implement Industry 4.0.

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实现用于过程色谱单元操作的持续过程验证的机器学习工具。
最近的技术进步,如人工智能(AI)和机器学习(ML)的出现,促进了生物制药行业向工业4.0的发展。根据USFDA制定的指南,生物制药生产的工艺验证包括三个阶段:工艺设计、工艺确认和持续工艺验证(CPV)。本文提出了实现阳离子交换色谱单元操作CPV的策略,强调了生物制药行业对CPV策略的迫切需求。通过内置传感器(pH、电导率、UV和δ柱压力)实时测量各种关键工艺参数(CPPs),以及电荷变化组成(拉曼光谱)和浓度(近红外光谱)等关键质量属性(cqa),生成统计过程控制(SPC)图表。创建了一个基于python的程序来读取这些SPC图表并响应任何偏差。建立的NIR耦合DNN - PAT工具和Raman耦合DNN - PAT工具模型显示出令人满意的R2值(> 0.90),突出了所提出模型的统计学意义。此外,基于拉曼光谱设计的CEX洗脱液中电荷变化组成的控制策略已经通过CEX负载的故意扰动得到了验证。所得到的CEX洗脱液输出显示出与对照组一致的电荷变化组成(酸性~ 20±2%,主要~ 62±2%和碱性~ 18±2%)。它已经展示了如何使用适当的分析仪,软传感器和高级数据分析来执行CPV,并使生物制药行业实现工业4.0。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Chromatography A
Journal of Chromatography A 化学-分析化学
CiteScore
7.90
自引率
14.60%
发文量
742
审稿时长
45 days
期刊介绍: The Journal of Chromatography A provides a forum for the publication of original research and critical reviews on all aspects of fundamental and applied separation science. The scope of the journal includes chromatography and related techniques, electromigration techniques (e.g. electrophoresis, electrochromatography), hyphenated and other multi-dimensional techniques, sample preparation, and detection methods such as mass spectrometry. Contributions consist mainly of research papers dealing with the theory of separation methods, instrumental developments and analytical and preparative applications of general interest.
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