Oct 2026· Gut microbes· Vol 18· 0 citations· 35 references
Medicine
TL;DR
BiotaPredictor enables early triage of compounds susceptible to microbiota-mediated loss and can inform lead optimization, formulation strategy, and pharmacokinetic prediction, and contribute to safer, more efficacious drug products and support precision delivery of orally administered therapeutics.
Abstract
ABSTRACT The gut microbiota can profoundly influence the performance of oral medicines by metabolizing or bioaccumulating drugs, thereby reducing systemic exposure and contributing to variable patient responses. Despite growing recognition of these interactions, microbiota-driven drug depletion remains insufficiently addressed during early development. Here, we present BiotaPredictor, a freely accessible web-based machine learning platform that predicts the likelihood of drug depletion by human intestinal microbiota from molecular structure. We compiled two curated datasets containing microbial depletion outcomes: (i) a consistently annotated AstraZeneca dataset (158 compounds) and (ii) an expanded integrated dataset incorporating published evidence (522 compounds). Multiple molecular descriptors—including physicochemical properties, 3D conformational features, and fingerprint-based encodings—were evaluated across a suite of classification algorithms. A logistic regression model trained on the AstraZeneca dataset using physicochemical parameters achieved the highest performance, correctly classifying all compounds in an external validation study (3 depleted, 9 stable). BiotaPredictor enables early triage of compounds susceptible to microbiota-mediated loss and can inform lead optimization, formulation strategy, and pharmacokinetic prediction. Integrating microbiota liability assessment into development pipelines will contribute to safer, more efficacious drug products and support precision delivery of orally administered therapeutics.
INTRODUCTION
The human gut microbiota significantly influences drug pharmacokinetics and pharmacodynamics, driving interindividual variability in efficacy and toxicity. As experimental characterization of microbiome-mediated metabolism remains resource-intensive, computational prediction has emerged as an auxiliary str...
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Motivation
Drug metabolism plays a key role in determining a compound's pharmacokinetics and overall success in development. While cytochrome P450 enzymes have been widely studied, non-cytochrome P450 enzymes, such as aldehyde oxidase, xanthine oxidase, and carboxylesterases, are increasingly recognized as important co...
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