modelS01AD05

Diagram of S01AD05

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:Interferon
ATC code:S01AD05
route:ocular
compartments:1
dosage:1mg
volume of distribution:0.2L
clearance:0.01L/kg/h
other parameters in model implementation

Interferons are a group of signaling proteins produced and released by host cells in response to the presence of various pathogens, such as viruses, bacteria, or tumor cells. Interferon alfa is used therapeutically for the treatment of various conditions including viral infections (such as hepatitis B and C), certain cancers, and multiple sclerosis. Formulations with ocular use (ATC S01AD05) are indicated for certain eye diseases, but as of now, they are not widely used or approved for routine ophthalmic practice.

Pharmacokinetics

Estimated pharmacokinetic parameters for interferon in an ophthalmic (ocular) application; limited or no published peer-reviewed clinical PK data available for ATC code S01AD05. Parameters below are generalized estimates or extrapolations from systemic use.

References

  1. Ang, M, et al., & Chee, SP (2012). Interferon-gamma release assay as a diagnostic test for tuberculosis-associated uveitis. Eye (London, England) 26(5) 658–665. DOI:10.1038/eye.2012.1 PUBMED:https://pubmed.ncbi.nlm.nih.gov/22302066

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)