modelHydrocortisoneAndAntiinf

Diagram of HydrocortisoneAndAntiinf

Extends from Pharmacolibrary.Drugs.ATC.S.S01CA03.

Information

name:HydrocortisoneAndAntiinfectives
ATC code:S01CA03
route:ophthalmic
compartments:1
dosage:1mg
volume of distribution:40L
clearance:15liter/hour
other parameters in model implementation

This combination drug includes hydrocortisone, a corticosteroid used for its anti-inflammatory and immunosuppressive activity, and various antiinfective agents (typically antibiotics) for the treatment of eye infections and associated inflammatory conditions such as conjunctivitis or blepharitis. It is usually formulated as an ophthalmic (eye) preparation and is approved in several countries for short-term relief of inflammation and infection of the eye.

Pharmacokinetics

No published population or compartmental pharmacokinetic models are available for fixed-dose ophthalmic hydrocortisone and antiinfective combinations in humans. Systemic absorption following ophthalmic administration is known to be low and variable; pharmacokinetic parameters for systemic exposure can be extrapolated from studies on ocular hydrocortisone in healthy adults.

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)