Prodrugs: ADMET Fundamentals, Bioactivation Kinetics, and Their Role in Clinical Pharmacokinetics and Toxicology

A prodrug is a pharmacologically inactive or substantially less active compound that undergoes enzymatic or chemical conversion in the body to release its active therapeutic moiety, a design strategy used to improve oral absorption, solubility, target-site delivery, or duration of action relative to the active moiety administered directly (Rautio et al., 2008). This article examines the ADMET fundamentals specific to this drug category, the assays used to characterize bioactivation kinetics and converting-enzyme identity, the toxicology considerations relevant to a molecule that exists in two pharmacologically distinct forms, and the clinical pharmacokinetic study design implications of characterizing both prodrug and active moiety simultaneously. The article closes with recommendations for regulatory affairs and clinical pharmacology professionals developing a prodrug program.Keywords: prodrug; bioactivation; esterase; converting enzyme; active metabolite; interconversion kinetics; regulatory artificial intelligence

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-11-02
DOI
https://doi.org/10.5281/zenodo.23890195
Primary Topic
Pharmacogenetics and Drug Metabolism
Type
article
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article

Prodrugs: ADMET Fundamentals, Bioactivation Kinetics, and Their Role in Clinical Pharmacokinetics and Toxicology

Peivand Pirouzi
Zenodo (CERN European Organization for Nuclear Research)
Pharmacogenetics and Drug Metabolism
article

Prodrugs: ADMET Fundamentals, Bioactivation Kinetics, and Their Role in Clinical Pharmacokinetics and Toxicology

Peivand Pirouzi
article en

Abstract

A prodrug is a pharmacologically inactive or substantially less active compound that undergoes enzymatic or chemical conversion in the body to release its active therapeutic moiety, a design strategy used to improve oral absorption, solubility, target-site delivery, or duration of action relative to the active moiety administered directly (Rautio et al., 2008). This article examines the ADMET fundamentals specific to this drug category, the assays used to characterize bioactivation kinetics and converting-enzyme identity, the toxicology considerations relevant to a molecule that exists in two pharmacologically distinct forms, and the clinical pharmacokinetic study design implications of characterizing both prodrug and active moiety simultaneously. The article closes with recommendations for regulatory affairs and clinical pharmacology professionals developing a prodrug program.Keywords: prodrug; bioactivation; esterase; converting enzyme; active metabolite; interconversion kinetics; regulatory artificial intelligence

Zenodo (CERN European Organization for Nuclear Research)
Seneca Polytechnic (CA)
Good health and well-being
Openalex Percentile: Top 12%
Pharmacogenetics and Drug Metabolism
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Prodrugs: ADMET Fundamentals, Bioactivation Kinetics, and Their Role in Clinical Pharmacokinetics and Toxicology — Peivand Pirouzi · Zenodo (CERN European Organization for Nuclear Research) (2026) | TGRS Research Map | TGRS