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作为过程开发中质量源于设计/过程分析技术工具的混合建模:一个工业大肠杆菌案例研究。

Hybrid modeling as a QbD/PAT tool in process development: an industrial E. coli case study.

作者信息

von Stosch Moritz, Hamelink Jan-Martijn, Oliveira Rui

机构信息

CEAM, Faculty of Science, Agriculture and Engineering, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.

REQUIMTE/DQ, Faculty of Science and Technology, University Nova de Lisboa, Campus de Caparica, 2829-516, Caparica, Portugal.

出版信息

Bioprocess Biosyst Eng. 2016 May;39(5):773-84. doi: 10.1007/s00449-016-1557-1. Epub 2016 Feb 15.

DOI:10.1007/s00449-016-1557-1
PMID:26879643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4839057/
Abstract

Process understanding is emphasized in the process analytical technology initiative and the quality by design paradigm to be essential for manufacturing of biopharmaceutical products with consistent high quality. A typical approach to developing a process understanding is applying a combination of design of experiments with statistical data analysis. Hybrid semi-parametric modeling is investigated as an alternative method to pure statistical data analysis. The hybrid model framework provides flexibility to select model complexity based on available data and knowledge. Here, a parametric dynamic bioreactor model is integrated with a nonparametric artificial neural network that describes biomass and product formation rates as function of varied fed-batch fermentation conditions for high cell density heterologous protein production with E. coli. Our model can accurately describe biomass growth and product formation across variations in induction temperature, pH and feed rates. The model indicates that while product expression rate is a function of early induction phase conditions, it is negatively impacted as productivity increases. This could correspond with physiological changes due to cytoplasmic product accumulation. Due to the dynamic nature of the model, rational process timing decisions can be made and the impact of temporal variations in process parameters on product formation and process performance can be assessed, which is central for process understanding.

摘要

在过程分析技术倡议和质量源于设计范式中,过程理解被强调为生产具有持续高质量的生物制药产品的关键要素。开发过程理解的一种典型方法是将实验设计与统计数据分析相结合。混合半参数建模作为纯统计数据分析的替代方法进行了研究。混合模型框架提供了根据可用数据和知识选择模型复杂度的灵活性。在此,一个参数化动态生物反应器模型与一个非参数人工神经网络相结合,该神经网络将生物量和产物形成速率描述为不同补料分批发酵条件的函数,用于大肠杆菌的高细胞密度异源蛋白生产。我们的模型能够准确描述在诱导温度、pH值和进料速率变化时的生物量生长和产物形成。该模型表明,虽然产物表达速率是早期诱导阶段条件的函数,但随着生产力的提高,它会受到负面影响。这可能与由于细胞质产物积累导致的生理变化相对应。由于模型的动态性质,可以做出合理的过程时间决策,并评估过程参数的时间变化对产物形成和过程性能的影响,这对于过程理解至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/ea88c63e44bc/449_2016_1557_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/d753a9a87067/449_2016_1557_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/a158e6fb644a/449_2016_1557_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/faad9f96fe8f/449_2016_1557_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/11423f169a1c/449_2016_1557_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/ea88c63e44bc/449_2016_1557_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/d753a9a87067/449_2016_1557_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/a158e6fb644a/449_2016_1557_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/faad9f96fe8f/449_2016_1557_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/11423f169a1c/449_2016_1557_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4854/4839057/ea88c63e44bc/449_2016_1557_Fig5_HTML.jpg

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本文引用的文献

1
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Res Pharm Sci. 2015 Jan-Feb;10(1):75-83.
2
The Future of Pharmaceutical Manufacturing Sciences.制药制造科学的未来。
J Pharm Sci. 2015 Nov;104(11):3612-3638. doi: 10.1002/jps.24594. Epub 2015 Aug 17.
3
Metabolic Regulation of a Bacterial Cell System with Emphasis on Escherichia coli Metabolism.细菌细胞系统的代谢调控,重点是大肠杆菌的代谢
模型辅助实验设计软件:酿酒酵母生物工艺中生长和生物催化的优化。
Bioprocess Biosyst Eng. 2021 Apr;44(4):683-700. doi: 10.1007/s00449-020-02478-3. Epub 2021 Jan 20.
4
From Physics to Bioengineering: Microbial Cultivation Process Design and Feeding Rate Control Based on Relative Entropy Using Nuisance Time.从物理学到生物工程:基于相对熵并利用干扰时间的微生物培养过程设计与进料速率控制
Entropy (Basel). 2018 Oct 11;20(10):779. doi: 10.3390/e20100779.
5
Intensified design of experiments for upstream bioreactors.上游生物反应器实验的强化设计
Eng Life Sci. 2016 Oct 14;17(11):1173-1184. doi: 10.1002/elsc.201600037. eCollection 2017 Nov.
6
Editorial: Bioprocess Development in the era of digitalization.社论:数字化时代的生物工艺开发
Eng Life Sci. 2017 Nov 3;17(11):1140-1141. doi: 10.1002/elsc.201770113. eCollection 2017 Nov.
7
Working within the Design Space: Do Our Static Process Characterization Methods Suffice?在设计空间内工作:我们的静态工艺表征方法是否足够?
Pharmaceutics. 2020 Jun 17;12(6):562. doi: 10.3390/pharmaceutics12060562.
8
Real-time monitoring and model-based prediction of purity and quantity during a chromatographic capture of fibroblast growth factor 2.在纤维细胞生长因子 2 的色谱捕获过程中进行实时监测和基于模型的纯度和数量预测。
Biotechnol Bioeng. 2019 Aug;116(8):1999-2009. doi: 10.1002/bit.26984. Epub 2019 Apr 17.
9
Accelerated Bioprocess Development of Endopolygalacturonase-Production with Using Multivariate Prediction in a 48 Mini-Bioreactor Automated Platform.在48微型生物反应器自动化平台上利用多变量预测加速产内切多聚半乳糖醛酸酶的生物过程开发。
Bioengineering (Basel). 2018 Nov 21;5(4):101. doi: 10.3390/bioengineering5040101.
10
Raman spectroscopy as a process analytical technology for pharmaceutical manufacturing and bioprocessing.拉曼光谱法作为制药制造和生物加工的过程分析技术。
Anal Bioanal Chem. 2017 Jan;409(3):637-649. doi: 10.1007/s00216-016-9824-1. Epub 2016 Aug 4.
ISRN Biochem. 2013 Feb 18;2013:645983. doi: 10.1155/2013/645983. eCollection 2013.
4
Understanding pharmaceutical quality by design.理解药物质量源于设计。
AAPS J. 2014 Jul;16(4):771-83. doi: 10.1208/s12248-014-9598-3. Epub 2014 May 23.
5
Hybrid modeling for quality by design and PAT-benefits and challenges of applications in biopharmaceutical industry.用于质量源于设计和过程分析技术的混合建模——生物制药行业应用的益处与挑战
Biotechnol J. 2014 Jun;9(6):719-26. doi: 10.1002/biot.201300385. Epub 2014 May 8.
6
Multivariate PAT solutions for biopharmaceutical cultivation: current progress and limitations.多变量 PAT 解决方案在生物制药培养中的应用:当前进展和局限性。
Trends Biotechnol. 2014 Jun;32(6):329-36. doi: 10.1016/j.tibtech.2014.03.008. Epub 2014 Apr 12.
7
Statistical approaches to maximize recombinant protein expression in Escherichia coli: a general review.最大化大肠杆菌中重组蛋白表达的统计方法:综述
Protein Expr Purif. 2014 Feb;94:22-32. doi: 10.1016/j.pep.2013.10.016. Epub 2013 Nov 5.
8
Design of experiments applications in bioprocessing: concepts and approach.实验设计在生物工艺学中的应用:概念与方法。
Biotechnol Prog. 2014 Jan-Feb;30(1):86-99. doi: 10.1002/btpr.1821. Epub 2013 Oct 24.
9
Application of adaptive DO-stat feeding control to Pichia pastoris X33 cultures expressing a single chain antibody fragment (scFv).应用自适应 DO 统计量馈送控制技术于表达单链抗体片段 (scFv) 的毕赤酵母 X33 培养。
Bioprocess Biosyst Eng. 2012 Nov;35(9):1603-14. doi: 10.1007/s00449-012-0751-z. Epub 2012 May 19.
10
Experimental designs and their recent advances in set-up, data interpretation, and analytical applications.实验设计及其在设置、数据解释和分析应用方面的最新进展。
J Pharm Biomed Anal. 2011 Sep 10;56(2):141-58. doi: 10.1016/j.jpba.2011.04.023. Epub 2011 May 6.