A hybrid system of mixture models for the prediction of particle size and shape, density, and flowability of pharmaceutical powder blends

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Abstract

This paper presents a system of hybrid models that combine both mechanistic and data-driven approaches to predict physical powder blend properties from their raw component properties. Mechanistic, probabilistic models were developed to predict the particle size and shape, represented by aspect ratio, distributions of pharmaceutical blends using those of the raw components. Additionally, the accuracy of existing mixture rules for predicting the blend's true density and bulk density was assessed. Two data-driven models were developed to estimate the mixture's tapped density and flowability (represented by the flow function coefficient, FFC) using data from 86 mixtures, which utilized the principal components of predicted particle size and shape distributions in combination with the true density, and bulk density as input data, saving time and material by removing the need for resource-intensive shear testing for raw components. A model-based uncertainty quantification technique was designed to analyse the precision of model-predicted FFCs. The proposed particle size and shape mixture models outperformed the existing approach (weighted average of distribution percentiles) in terms of prediction accuracy while providing insights into the full distribution of the mixture. The presented hybrid system of models accurately predicts the mixture properties of different formulations and components with often R2 > 0.8, utilising raw material properties to reduce time and material resources on preparing and characterising blends.
Original languageEnglish
Article number100298
Number of pages15
JournalInternational Journal of Pharmaceutics: X
Volume8
Early online date28 Oct 2024
DOIs
Publication statusPublished - 1 Dec 2024

Funding

The authors would like to thank the Digital Medicines Manufacturing (DM2 594 ) Research Centre (Grant Ref: EP/V062077/1) for funding this work. DM2 595 is co-funded by the Made Smarter Innovation challenge at UK Research and Innovation, and partner organisations from the medicines manufacturing sector (for more information, visit www.cmac.ac.uk/dm2-home). The authors also thank EPSRC ARTICULAR project, (Grant ref: EP/R032858/1) and EPSRC Future Continuous Manufacturing and Advanced Crystallisation Research Hub (Grant Ref: EP/P006965/1) for the data generated and exploited in this work. Kendal G. Pitt (GSK), Gavin K. Reynolds (AstraZeneca), James Mann (AstraZeneca), Andrew G. P. Maloney (CCDC), Alexandru Moldovan (CCDC), and Robert Taylor (Malvern Panalytical) are appreciated for their feedback throughout the research.

Keywords

  • bulk density
  • computational model
  • flowability
  • particle shape
  • particle size
  • pharmaceutical mixtures
  • tapped density
  • true density

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