Machine Learning-Based PAT Tool for Real-Time Residual Moisture Monitoring in Lyophilized Biopharmaceuticals Using NIR Spectroscopy

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Biotechnology and Bioengineering Pub Date : 2026-10-14 Epub Date: 2026-07-12 DOI:10.1002/bit.70302
Samuele Fiorenza, Mariapia D'Urso, Ambra Massei, Nunzia Falco, Davide Fissore, Enza Torino
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引用次数: 0

Abstract

There is a growing demand in the pharmaceutical industry to optimize analytical methodologies, reducing time and resource consumption while ensuring rapid process development and cost-efficient manufacturing. Indeed, Food and Drug Administration (FDA) introduced the Process Analytical Technology (PAT) as an initiative enabling manufacturers to measure and control in real-time processes based on the Critical Quality Attributes (CQAs) of the product. This study explores the implementation of PAT as a strategic approach in the lyophilization process design and optimization. In this sense, Residual Moisture (RM) was selected as a CQA to evaluate lyophilized biopharmaceutical products, due to its impact on stability. Traditionally, RM quantification is obtained by Karl-Fischer (KF) titration, a destructive technique. Recently, Near-Infrared Spectroscopy (NIRS) was proposed as a non-destructive alternative; however, its effectiveness is hindered by spectral complexity and non-linear moisture-spectra relationships. Here, PAT tool integrating NIRS with Machine Learning (ML) is developed to enable rapid, at-line RM assessment, handling the complexity of non-linear relationships between RM values and spectral features. Different ML models – Partial Least Squares (PLS), Support Vector Regression (SVR), XGBoost, and an ensemble PLS-SVR approach – were trained on placebo samples and validated on drug products. SVR outperformed PLS at lower moisture levels, while PLS was more accurate at higher RM ranges. The ensemble model combining both approaches improved predictive accuracy across the full RM range tested. External validation using literature-sourced datasets, including placebo and simulated drug products with different excipients, confirmed the model's robustness and adaptability. Furthermore, a minimal dataset augmentation strategy enhanced model specialization for specific formulations. The proposed NIRS-ML ensemble model offers a scalable, non-destructive solution for real-time RM monitoring, supporting pharmaceutical manufacturing within the PAT framework. Its adaptability across formulations highlights its potential as a versatile tool for lyophilized biopharmaceutical manufacturing pipelines.

Abstract Image

基于机器学习的近红外光谱实时监测冻干生物药品残留水分的PAT工具。
制药行业不断增长的需求是优化分析方法,减少时间和资源消耗,同时确保快速的工艺开发和成本效益的制造。事实上,美国食品和药物管理局(FDA)引入了过程分析技术(PAT)作为一项倡议,使制造商能够基于产品的关键质量属性(cqa)实时测量和控制过程。本研究探讨了PAT作为冻干工艺设计和优化的战略方法的实施。从这个意义上说,选择残留水分(RM)作为评价冻干生物制药产品的CQA,因为它对稳定性有影响。传统上,RM的定量是通过卡尔-费舍尔(KF)滴定法获得的,这是一种破坏性的技术。最近,近红外光谱(NIRS)被提出作为一种非破坏性的替代方法;然而,光谱复杂性和非线性水分-光谱关系阻碍了其有效性。在这里,PAT工具集成了近红外光谱与机器学习(ML),以实现快速,在线RM评估,处理RM值和光谱特征之间非线性关系的复杂性。不同的ML模型——偏最小二乘(PLS)、支持向量回归(SVR)、XGBoost和集成PLS-SVR方法——在安慰剂样本上进行了训练,并在药品上进行了验证。SVR优于PLS在较低的湿度水平,而PLS在较高的RM范围更准确。集成模型结合了这两种方法,提高了整个RM测试范围内的预测精度。外部验证使用文献来源的数据集,包括安慰剂和不同赋形剂的模拟药物,证实了模型的鲁棒性和适应性。此外,最小数据集增强策略增强了特定公式的模型专门化。提出的NIRS-ML集成模型为实时RM监控提供了可扩展的非破坏性解决方案,支持PAT框架内的制药制造。其跨配方的适应性突出了其作为冻干生物制药制造管道的多功能工具的潜力。
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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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