Effects and Detection of Raw Material Variability on the Performance of Near-Infrared Calibration Models for Pharmaceutical Products |
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Affiliation: | 1. Duquesne University Center for Pharmaceutical Technology, School of Pharmacy, Pittsburgh, Pennsylvania 15282;2. Graduate School of Pharmaceutical Sciences, Duquesne University, Pittsburgh, Pennsylvania 15282;1. Research Center Pharmaceutical Engineering GmbH, Graz, Austria;2. Research Center for Non-Destructive Testing GmbH, Linz, Austria;3. ProCept nv, Zelzate, Belgium;4. Institute for Process and Particle Engineering, Graz University of Technology, Graz, Austria;1. Department of Pharmacokinetics and Biopharmaceutics, Subdivision of Biopharmaceutical Sciences, Institute of Health Biosciences,The University of Tokushima, Tokushima 770-8505, Japan;2. Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Zagazig University, Zagazig, Egypt;1. Laboratory of Plant and Process Design, Faculty of Biochemical and Chemical Engineering, TU Dortmund University, Emil-Figge-Straße 70, D-44227 Dortmund, Germany;2. Invite GmbH, Otto-Bayer-Straße 32, D-51061 Cologne, Germany |
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Abstract: | The impact of raw material variability on the prediction ability of a near-infrared calibration model was studied. Calibrations, developed from a quaternary mixture design comprising theophylline anhydrous, lactose monohydrate, microcrystalline cellulose, and soluble starch, were challenged by intentional variation of raw material properties. A design with two theophylline physical forms, three lactose particle sizes, and two starch manufacturers was created to test model robustness. Further challenges to the models were accomplished through environmental conditions. Along with full-spectrum partial least squares (PLS) modeling, variable selection by dynamic backward PLS and genetic algorithms was utilized in an effort to mitigate the effects of raw material variability. In addition to evaluating models based on their prediction statistics, prediction residuals were analyzed by analyses of variance and model diagnostics (Hotelling's T2 and Q residuals). Full-spectrum models were significantly affected by lactose particle size. Models developed by selecting variables gave lower prediction errors and proved to be a good approach to limit the effect of changing raw material characteristics. Hotelling's T2 and Q residuals provided valuable information that was not detectable when studying only prediction trends. Diagnostic statistics were demonstrated to be critical in the appropriate interpretation of the prediction of quality parameters. |
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Keywords: | near-infrared spectroscopy raw material variability variable selection iterative PLS dynamic backward iterative PLS partial least squares polymorph particle size excipients |
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