Machine learning strengthened formulation design of pharmaceutical suspensions

Many different formulation strategies have been investigated to oppose suboptimal treatment of long-term or chronic conditions, one of which are the nano- and microsuspensions prepared as long-acting injectables to prolong the release of an active pharmaceutical compound for a defined period of time by regulating the size of particles by milling. Typically, surfactant and/or polymers are added in the dispersion medium of the suspension during processing for stabilization purposes. However, current formulation investigations with milling are heavily based on prior expertise and trial-and-error approaches. Various interacting parameters such as the milling bead size, stabilizer type and concentration have confounded the investigation of milling process. The present study systematically exploited statistical and machine learning (ML) strategies to understand the relationship between suspension characteristics and formulation parameters under full-factorial milling experiments. Stabilizer concentration was identified as a significant factor (p < 0.001) for median suspension diameter (D<sub>50</sub>). A formulation stability classification ML model with high prediction accuracy (0.91) and F1-score (0.91) under 10-fold cross-validation was constructed based on 72 formulation datapoints. Model interpretation through Shapley additive explanations (SHAP) revealed the prominent impact of stabilizer concentration and milling bead size on formulation stability. The present work demonstrated the potential to achieve a deeper understanding of the design and optimization of nano- and microsuspensions through explainable ML modelling on formulation screening data.

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Publication Details

Journal
International Journal of Pharmaceutics
Published
2024-11-19
DOI
https://doi.org/10.1016/j.ijpharm.2024.124967
Citations
10
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
2.08

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article

Machine learning strengthened formulation design of pharmaceutical suspensions

Maryam Parhizkar, René Holm, Fanjin Wang, Nadina Zulbeari et al.
10 citations
International Journal of Pharmaceutics
Drug Solubulity and Delivery Systems
2.08
article

Machine learning strengthened formulation design of pharmaceutical suspensions

Maryam Parhizkar, René Holm, Fanjin Wang, Nadina Zulbeari, Sibel Selyatinova Mustafova
article en
10 citations

Abstract

Many different formulation strategies have been investigated to oppose suboptimal treatment of long-term or chronic conditions, one of which are the nano- and microsuspensions prepared as long-acting injectables to prolong the release of an active pharmaceutical compound for a defined period of time by regulating the size of particles by milling. Typically, surfactant and/or polymers are added in the dispersion medium of the suspension during processing for stabilization purposes. However, current formulation investigations with milling are heavily based on prior expertise and trial-and-error approaches. Various interacting parameters such as the milling bead size, stabilizer type and concentration have confounded the investigation of milling process. The present study systematically exploited statistical and machine learning (ML) strategies to understand the relationship between suspension characteristics and formulation parameters under full-factorial milling experiments. Stabilizer concentration was identified as a significant factor (p < 0.001) for median suspension diameter (D<sub>50</sub>). A formulation stability classification ML model with high prediction accuracy (0.91) and F1-score (0.91) under 10-fold cross-validation was constructed based on 72 formulation datapoints. Model interpretation through Shapley additive explanations (SHAP) revealed the prominent impact of stabilizer concentration and milling bead size on formulation stability. The present work demonstrated the potential to achieve a deeper understanding of the design and optimization of nano- and microsuspensions through explainable ML modelling on formulation screening data.

International Journal of PharmaceuticsVol. 668
Medway School of Pharmacy (GB), University of Southern Denmark (DK), University College London (GB)
Novo Nordisk Fonden
Openalex Percentile: Top 14%
Drug Solubulity and Delivery Systems
2.08
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