Abstract

The use of design space (DS) is a key milestone in the quality by design (QbD) of pharmaceutical processes. It should be considered from early laboratory development to industrial production, in order to support scientists with making decisions at each step of the product’s development life. Presently, there are no available data or methodologies for developing models for the implementation of design space (DS) on laboratory-scale spray dryers. Therefore, in this work, a comparison between two different modeling approaches, thermodynamics and computational fluid dynamics (CFD), to a laboratory spray dryer model have been evaluated. The models computed the outlet temperature () of the process with a new modeling strategy that includes machine learning to improve the model prediction. The model metrics calculated indicate how the thermodynamic model fits data better than CFD; indeed, the error of the CFD model increases towards higher values of and feed rate (), with a final mean absolute error of 10.43 K, compared to the 1.74 K error of the thermodynamic model. Successively, a DS of the studied spray dryer equipment has been implemented, showing how is strongly affected by variation, which accounts for about 40 times more than the gas flow rate () in the DS. The thermodynamic model, combined with the machine learning approach here proposed, could be used as a valid tool in the QbD development of spray-dried pharmaceutical products, starting from their early laboratory stages, replacing traditional trial-and-error methodologies, preventing process errors, and helping scientists with the following scale-up.

Highlights

  • Spray drying is a single-step powder-manufacturing process dominated by the evaporation of liquid systems, and it is widely applied in the pharmaceutical, biomedical, food, and cosmetic industries [1,2,3,4,5]

  • A complete computational fluid dynamics (CFD) model approach was compared with a developed thermodynamic model and was experimentally validated

  • The CFD model is a good tool for optimizing and developing machine processes, as it allows for the study of the gas flow pattern that is useful during scale-ups to small- or large-scale production, it shows limitations for the lab-scale spray dryer

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Summary

Introduction

Spray drying is a single-step powder-manufacturing process dominated by the evaporation of liquid systems, and it is widely applied in the pharmaceutical, biomedical, food, and cosmetic industries [1,2,3,4,5]. Over the past 15 years, spray drying has been successfully applied in the manufacturing of pharmaceutical proteins, and its use has been firmly established as a producer of amorphous solid dispersions, enhancing the bioavailability of poorly soluble drugs [6,7]. It is useful for drugs for controlling taste-masking or producing dosage forms that can be administered by inhalation [7]. The liquid is sprayed by the atomizer, and it is mixed with a hot airflow, resulting in the drying of the droplets [8].

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