A quantitative size stability metrics for long-acting suspensions and its prediction with machine learning

Defining suspension stability can be extremely complex, but beyond critical during the formulation development of nano- and microsuspensions intended for long-acting injectables. As of now, the current practice is based on the trial-and-error approach to determine suitable stabilizers and corresponding stabilization concentrations to allow size reduction due to proper wetting while minimizing particle agglomeration or crystal growth by Ostwald ripening during storage, making the definition of suspension stability subjective in the existing literature. The present study proposed a quantitative measurement of the suspension stability (i.e., suspension stability index (SSI)) defined by two coefficients of variation from the suspension population median, i.e., D<sub>50</sub>CV, and distribution, i.e., SpanCV, over 28 days of storage under accelerated conditions. Various predictive models for SSI were constructed with a defined threshold for the D<sub>50</sub>CV and SpanCV where the support vector classification (SVC) model was found to hold the best performance based on a 5-fold cross-validated accuracy of 0.82 and F1 score of 0.82 while also having a good transferability. Critical factors that impacted the SSI included the stabilizer type and its corresponding concentration while the drug compound was found to interact with multiple parameters with the exception of the bead size. Overall, the presented quantitative metric of suspension stability based on the SSI could potentially contribute to a more comparable investigation of suspension stability during formulation development by using the classification model from the presented dataset as a screening tool.

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Publication Details

Journal
International Journal of Pharmaceutics
Published
2025-11-25
DOI
https://doi.org/10.1016/j.ijpharm.2025.126432
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
0.00

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article

A quantitative size stability metrics for long-acting suspensions and its prediction with machine learning

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

A quantitative size stability metrics for long-acting suspensions and its prediction with machine learning

Maryam Parhizkar, René Holm, Fanjin Wang, Nadina Zulbeari, Basel Atieh Dasous
article en

Abstract

Defining suspension stability can be extremely complex, but beyond critical during the formulation development of nano- and microsuspensions intended for long-acting injectables. As of now, the current practice is based on the trial-and-error approach to determine suitable stabilizers and corresponding stabilization concentrations to allow size reduction due to proper wetting while minimizing particle agglomeration or crystal growth by Ostwald ripening during storage, making the definition of suspension stability subjective in the existing literature. The present study proposed a quantitative measurement of the suspension stability (i.e., suspension stability index (SSI)) defined by two coefficients of variation from the suspension population median, i.e., D<sub>50</sub>CV, and distribution, i.e., SpanCV, over 28 days of storage under accelerated conditions. Various predictive models for SSI were constructed with a defined threshold for the D<sub>50</sub>CV and SpanCV where the support vector classification (SVC) model was found to hold the best performance based on a 5-fold cross-validated accuracy of 0.82 and F1 score of 0.82 while also having a good transferability. Critical factors that impacted the SSI included the stabilizer type and its corresponding concentration while the drug compound was found to interact with multiple parameters with the exception of the bead size. Overall, the presented quantitative metric of suspension stability based on the SSI could potentially contribute to a more comparable investigation of suspension stability during formulation development by using the classification model from the presented dataset as a screening tool.

International Journal of PharmaceuticsVol. 687
Medway School of Pharmacy (GB), University of Southern Denmark (DK), University College London (GB)
Bill and Melinda Gates Foundation
Openalex Percentile: Top 70%
Drug Solubulity and Delivery Systems
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