modelEthylEstersOfIodisedFatt

Extends from Pharmacolibrary.Drugs.ATC.V.V08AD01.

Information

name:EthylEstersOfIodisedFattyAcids
ATC code:V08AD01
route:intraarterial
compartments:1
dosage:10000mg
volume of distribution:3L
clearance:0.01L/h
other parameters in model implementation

Ethyl esters of iodised fatty acids (e.g. iofetamine, ethiodized oil) are radiopaque contrast media primarily used in diagnostic radiology, particularly for lymphography and hysterosalpingography. They are not used systemically as pharmacological agents and are generally administered to enhance contrast in imaging rather than for therapeutic effects. The use of iodized fatty acid esters has diminished in favor of newer agents but may still be encountered for specific indications.

Pharmacokinetics

No published pharmacokinetic models describing classic parameter values for ethyl esters of iodised fatty acids in humans could be identified. The physicochemical properties of the drug (oil-based, retained for long periods in target tissues) and its typical administration route (intra-arterial or intralymphatic for radiological purposes) suggest very slow systemic clearance and limited systemic absorption.

References

    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

    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)