BMLGJan 5

Predicting Early and Complete Drug Release from Long-Acting Injectables Using Explainable Machine Learning

arXiv:2601.02265v11 citationsh-index: 14
Originality Incremental advance
AI Analysis

This provides a quantitative strategy for scientists to optimize drug-release dynamics in long-acting injectables, addressing a domain-specific bottleneck with incremental improvements.

The paper tackled predicting drug release from long-acting injectables using explainable machine learning, achieving a correlation >0.65 for 72-hour release and an F1-score of 0.87 for classifying release profiles.

Polymer-based long-acting injectables (LAIs) have transformed the treatment of chronic diseases by enabling controlled drug delivery, thus reducing dosing frequency and extending therapeutic duration. Achieving controlled drug release from LAIs requires extensive optimization of the complex underlying physicochemical properties. Machine learning (ML) can accelerate LAI development by modeling the complex relationships between LAI properties and drug release. However, recent ML studies have provided limited information on key properties that modulate drug release, due to the lack of custom modeling and analysis tailored to LAI data. This paper presents a novel data transformation and explainable ML approach to synthesize actionable information from 321 LAI formulations by predicting early drug release at 24, 48, and 72 hours, classification of release profile types, and prediction of complete release profiles. These three experiments investigate the contribution and control of LAI material characteristics in early and complete drug release profiles. A strong correlation (>0.65) is observed between the true and predicted drug release in 72 hours, while a 0.87 F1-score is obtained in classifying release profile types. A time-independent ML framework predicts delayed biphasic and triphasic curves with better performance than current time-dependent approaches. Shapley additive explanations reveal the relative influence of material characteristics during early and for complete release which fill several gaps in previous in-vitro and ML-based studies. The novel approach and findings can provide a quantitative strategy and recommendations for scientists to optimize the drug-release dynamics of LAI. The source code for the model implementation is publicly available.

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