DemoTox-PK

DemoTox-PK visualizes pharmacokinetic and toxicodynamic alterations to elucidate mechanisms underlying idiosyncratic drug-induced liver injury (IDILI).


Key Features:

  • Visualization of pharmacokinetic and toxicodynamic alterations: Visualizes how changes in pharmacokinetics (drug metabolism alterations, transporter polymorphisms) and toxicodynamics (mitochondrial injury, accumulation of toxic endogenous factors, harmful immune responses) can contribute to IDILI.
  • Graphical illustration of pathogenesis hypotheses: Represents mechanistic hypotheses linking specific PK and TD alterations to IDILI to facilitate mechanistic interpretation.
  • Mechanism-based biomarker and target support: Highlights mechanistic links between PK/TD alterations and liver injury to support identification and prioritization of potential biomarkers and therapeutic targets.

Scientific Applications:

  • IDILI pathogenesis research: Examines how alterations in drug metabolism, transporter polymorphisms, mitochondrial injury, endogenous toxic factor accumulation, or immune responses contribute to liver injury.
  • Biomarker and therapeutic target identification: Aids prioritization of mechanistic biomarkers and therapeutic targets based on illustrated PK/TD mechanisms.
  • Education and training: Provides graphical representations of pharmacokinetic and toxicodynamic concepts to support instruction on drug-induced liver toxicities.

Methodology:

Graphical illustration of pharmacokinetic and toxicodynamic concepts related to IDILI.

Topics

Details

License:
Freeware
Cost:
Free of charge
Tool Type:
web application
Operating Systems:
Mac, Linux, Windows
Added:
11/17/2022
Last Updated:
11/24/2024

Operations

Publications

Roth RA, Kana O, Filipovic D, Ganey PE. Pharmacokinetic and toxicodynamic concepts in idiosyncratic, drug-induced liver injury. Expert Opinion on Drug Metabolism & Toxicology. 2022;18(7-8):469-481. doi:10.1080/17425255.2022.2113379. PMID:36003040. PMCID:PMC9484408.

PMID: 36003040
PMCID: PMC9484408
Funding: - NIH: ES031937

Documentation