一种可扩展的深度学习方法,用于生物制药过程的实时多元监测,没有先前的产品特定历史

IF 3.6 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Nima Sammaknejad, Jessica Lee, Jan Michael Austria, Nadia Duenas, Leila Heiba, Govi Sridharan, Jeff Davis, Cenk Undey
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引用次数: 0

摘要

实时多变量统计过程监测(RT-MSPM)对于监测生物制药过程的健康状况和早期发现过程中的异常和故障至关重要。RT-MSPM方法通常用于监测生物制剂原料药生产中的细胞培养过程操作。批演化模型是常用的RT-MSPM方法之一。作为bem的替代方案,可以开发多个模型来监视批处理过程的不同阶段。如果满足某些统计特性,则可以利用多阶段算法来检测批处理的稳态操作,并处理相应的时间序列,从而利用来自其他产品配方的数据来监视没有先前历史的新产品。这在现代生物制药生产设施中特别有用,这些设施经常从生产一种药物切换到另一种药物。在本文中,提出了一种新的实时深度学习框架,用于监测没有特定产品历史的生物制药过程的健康状况。自动编码器(AEs)与多阶段实时数据处理算法相结合,用于检测、预防和识别细胞培养制造过程中潜在异常和故障的根本原因,以生产没有先前历史的单克隆抗体。提出了一种实时异常根本原因识别算法,用于生成ae的实时贡献图。并与传统的故障检测隔离方法进行了性能比较。考虑到ae的非线性结构,与传统的线性方法相比,ae始终使用残差和潜在空间中的信息组合为异常模式提供更鲁棒和更有力的证据。所提出的框架已在可扩展的软件产品中成功测试,用于实时监控制造细胞培养生物反应器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Scalable Deep Learning Approach for Real-Time Multivariate Monitoring of Biopharmaceutical Processes With No Prior Product-Specific History

A Scalable Deep Learning Approach for Real-Time Multivariate Monitoring of Biopharmaceutical Processes With No Prior Product-Specific History

A Scalable Deep Learning Approach for Real-Time Multivariate Monitoring of Biopharmaceutical Processes With No Prior Product-Specific History

A Scalable Deep Learning Approach for Real-Time Multivariate Monitoring of Biopharmaceutical Processes With No Prior Product-Specific History

Real-time multivariate statistical process monitoring (RT-MSPM) is essential to monitor health of bio-pharmaceutical processes and detect anomalies and faults early in the process. RT-MSPM methods are commonly used to monitor cell culture process operations in biologics drug substance manufacturing. Batch evolution models (BEMs) are among common RT-MSPM methods. As an alternative to BEMs, it is possible to develop multiple models to monitor different phases of a batch process. If certain statistical properties are satisfied, a multistage algorithm can be leveraged to detect steady state operation of a batch and process the corresponding time-series in a manner to leverage data from other product recipes to monitor a new product with no prior history. This is specifically useful in modern biopharmaceutical manufacturing facilities, which frequently switch from producing one medicine to another. In this article, a novel real-time deep learning framework to monitor the health of biopharmaceutical processes with no prior product-specific history is proposed. Autoencoders (AEs), in conjunction with a multistage real-time data processing algorithm, are leveraged to detect, prevent and identify the root causes of potential anomalies and faults in cell culture manufacturing processes to produce monoclonal antibodies with no prior history. A novel algorithm for real-time root cause identification of anomalies is developed to generate real-time contribution charts for AEs. The performance of the new fault detection and isolation strategy is compared with conventional methods. Given the nonlinear architecture of AEs in comparison to conventional linear methods, AEs consistently provide more robust and stronger evidence for anomalous patterns using a combination of information in residuals and latent space. The proposed framework is successfully tested within a scalable software product for real-time monitoring of manufacturing cell culture bioreactors.

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来源期刊
Biotechnology and Bioengineering
Biotechnology and Bioengineering 工程技术-生物工程与应用微生物
CiteScore
7.90
自引率
5.30%
发文量
280
审稿时长
2.1 months
期刊介绍: Biotechnology & Bioengineering publishes Perspectives, Articles, Reviews, Mini-Reviews, and Communications to the Editor that embrace all aspects of biotechnology. These include: -Enzyme systems and their applications, including enzyme reactors, purification, and applied aspects of protein engineering -Animal-cell biotechnology, including media development -Applied aspects of cellular physiology, metabolism, and energetics -Biocatalysis and applied enzymology, including enzyme reactors, protein engineering, and nanobiotechnology -Biothermodynamics -Biofuels, including biomass and renewable resource engineering -Biomaterials, including delivery systems and materials for tissue engineering -Bioprocess engineering, including kinetics and modeling of biological systems, transport phenomena in bioreactors, bioreactor design, monitoring, and control -Biosensors and instrumentation -Computational and systems biology, including bioinformatics and genomic/proteomic studies -Environmental biotechnology, including biofilms, algal systems, and bioremediation -Metabolic and cellular engineering -Plant-cell biotechnology -Spectroscopic and other analytical techniques for biotechnological applications -Synthetic biology -Tissue engineering, stem-cell bioengineering, regenerative medicine, gene therapy and delivery systems The editors will consider papers for publication based on novelty, their immediate or future impact on biotechnological processes, and their contribution to the advancement of biochemical engineering science. Submission of papers dealing with routine aspects of bioprocessing, description of established equipment, and routine applications of established methodologies (e.g., control strategies, modeling, experimental methods) is discouraged. Theoretical papers will be judged based on the novelty of the approach and their potential impact, or on their novel capability to predict and elucidate experimental observations.
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