modelR01AD11

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:Triamcinolone
ATC code:R01AD11
route:intranasal
compartments:1
dosage:220mg
volume of distribution:1.5L
clearance:28L/h
other parameters in model implementation

Triamcinolone is a synthetic corticosteroid used primarily for its anti-inflammatory and immunosuppressive properties. It is used in various forms (oral, injectable, topical, and intranasal) to treat conditions such as allergic rhinitis, asthma, arthritis, and dermatological disorders. The intranasal formulation (ATC code R01AD11) is commonly approved and used today for the symptomatic relief of nasal allergy, such as hay fever.

Pharmacokinetics

Pharmacokinetic parameters are estimated for intranasal administration in healthy adults, as no direct human PK data for intranasal triamcinolone is reported. Parameters are based on literature for similar corticosteroids and general knowledge of triamcinolone's pharmacology.

References

  1. Khadka, P, et al., & Golshahi, L (2024). Anatomically-detailed segmented representative adult and pediatric nasal models for assessing regional drug delivery and bioequivalence with suspension nasal sprays. International journal of pharmaceutics 666 124743–None. DOI:10.1016/j.ijpharm.2024.124743 PUBMED:https://pubmed.ncbi.nlm.nih.gov/39343330

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)