{"title":"Machine Learning-Based PAT Tool for Real-Time Residual Moisture Monitoring in Lyophilized Biopharmaceuticals Using NIR Spectroscopy","authors":"Samuele Fiorenza, Mariapia D'Urso, Ambra Massei, Nunzia Falco, Davide Fissore, Enza Torino","doi":"10.1002/bit.70302","DOIUrl":null,"url":null,"abstract":"<p>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.</p>","PeriodicalId":9168,"journal":{"name":"Biotechnology and Bioengineering","volume":"123 11","pages":"3030-3046"},"PeriodicalIF":3.9000,"publicationDate":"2026-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bit.70302","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology and Bioengineering","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bit.70302","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/12 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
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.
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.