modelDisulfiram

Extends from Pharmacolibrary.Drugs.ATC.P.P03AA04.

Information

name:Disulfiram
ATC code:P03AA04
route:oral
compartments:1
dosage:500mg
volume of distribution:1.5L
clearance:0.05L/kg/h
other parameters in model implementation

Disulfiram is an aldehyde dehydrogenase inhibitor historically used in the treatment of chronic alcoholism as a deterrent due to the unpleasant effects caused when alcohol is consumed. It is approved for human use in several countries but its clinical use has declined.

Pharmacokinetics

Pharmacokinetic parameters estimated based on available pharmacology literature for healthy adult subjects; precise published PK modeling parameters are lacking.

References

  1. Foster, PM, et al., & Gray, TJ (1984). Testicular toxicity produced by ethylene glycol monomethyl and monoethyl ethers in the rat. Environmental health perspectives 57 207–217. DOI:10.1289/ehp.8457207 PUBMED:https://pubmed.ncbi.nlm.nih.gov/6499806

  2. Krall, LP (1984). Glyburide (DiaBeta): a new second-generation hypoglycemic agent. Clinical therapeutics 6(6) 746–762. PUBMED:https://pubmed.ncbi.nlm.nih.gov/6439409

  3. Johnson, DJ, et al., & Valentine, WM (1996). The measurement of 2-thiothiazolidine-4-carboxylic acid as an index of the in vivo release of CS2 by dithiocarbamates. Chemical research in toxicology 9(5) 910–916. DOI:10.1021/tx960006v PUBMED:https://pubmed.ncbi.nlm.nih.gov/8828929

Parameters

TypeNameDefaultDescription
Modelica.Units.SI.Massweight (from PK_1C)75patient weight (kg)
Modelica.Units.SI.SpecificVolumeVdPerKg (from PK_1C)0.9Volume of distribution (L/kg)
Modelica.Units.SI.MassFractionF (from PK_1C)0.8bioavailiability (0-1)
Pharmacolibrary.Types.ClearanceCl (from PK_1C)20clearance
Modelica.Units.SI.TimeadminTime (from PK_1C)60first administration time (s)
Modelica.Units.SI.TimeadminDuration (from PK_1C)600administration duration (s)
Modelica.Units.SI.TimeadminPeriod (from PK_1C)8*60*60period of administration (default 8 hours)(s)
Pharmacolibrary.Types.MassadminMass (from PK_1C)1000administration mass (mg)
IntegeradminCount (from PK_1C)8number of dose administered (1)
Pharmacolibrary.Types.VolumeVd (from PK_1C)VdPerKg*weightVolume of distribution (m3)
Pharmacolibrary.Types.MassConcentrationCmin (from PK_1C)0.004minimal therapeutic range
Pharmacolibrary.Types.MassConcentrationCmax (from PK_1C)0.008minimal therapeutic range
Pharmacolibrary.Types.MassConcentrationCtox_peak (from PK_1C)0.012toxicity peak level
Pharmacolibrary.Types.MassConcentrationCtox_trough (from PK_1C)0.006toxicity trough level
Pharmacolibrary.Types.TransferRateka (from PK_1C_enteral)0.016666666666666666first order absorption rate
Modelica.Units.SI.TimeTlag (from PK_1C_enteral)600delay between oral administration and absorption (default 10min)

Connectors

TypeNameDefaultDescription
Types.ConcentrationOutputC_central (from PK_1C)
Interfaces.ConcentrationPort_bcentralCPort (from PK_1C)

Components

TypeNameDefaultDescription
Pharmacokinetic.NoPerfusedTissueCompartmentcentral (from PK_1C)
Pharmacokinetic.ClearanceDrivenEliminationelim (from PK_1C)
Sources.PeriodicDoseperiodicDose (from PK_1C)
Modelica.Units.SI.Timet1_2 (from PK_1C)elimination half-life

Revisions

  • 06/2025 Tomas Kulhanek, generated model from data extracted from PUBMED, DrugBank and LLM(GPT4.1)