modelDeferasirox

Extends from Pharmacolibrary.Drugs.ATC.V.V03AC03.

Information

name:Deferasirox
ATC code:V03AC03
route:oral
compartments:2
dosage:20mg
volume of distribution:14.4L
clearance:0.6L/h
other parameters in model implementation

Deferasirox is an oral iron chelator used for the treatment of chronic iron overload due to blood transfusions in patients with conditions such as thalassemia, sickle cell disease, and other chronic anemias. It is approved for clinical use and is currently available in many countries.

Pharmacokinetics

Pharmacokinetic parameters following oral administration in adult patients with transfusional iron overload. Values reflect a typical population (mean age ~27 years, both sexes) receiving once-daily dosing.

References

  1. Tanaka, C (2014). Clinical pharmacology of deferasirox. Clinical pharmacokinetics 53(8) 679–694. DOI:10.1007/s40262-014-0151-4 PUBMED:https://pubmed.ncbi.nlm.nih.gov/24996374

  2. Chen, J, et al., & Ruan, Z (2020). Effect of Genetic Polymorphisms on the Pharmacokinetics of Deferasirox in Healthy Chinese Subjects and an Artificial Neural Networks Model for Pharmacokinetic Prediction. European journal of drug metabolism and pharmacokinetics 45(6) 761–770. DOI:10.1007/s13318-020-00647-z PUBMED:https://pubmed.ncbi.nlm.nih.gov/32930952

  3. Lindsey, WT, & Olin, BR (2007). Deferasirox for transfusion-related iron overload: a clinical review. Clinical therapeutics 29(10) 2154–2166. DOI:10.1016/j.clinthera.2007.10.015 PUBMED:https://pubmed.ncbi.nlm.nih.gov/18042472

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.VolumeVdp (from PK_2C)VdpPerKg*weightVolume of distribution (m3)
Modelica.Units.SI.SpecificVolumeVdpPerKg (from PK_2C)0.9Volume of distribution peripheral(l/kg)
Pharmacolibrary.Types.Clearancek12 (from PK_2C)1intercompartmental C-P clearance
Pharmacolibrary.Types.Clearancek21 (from PK_2C)1intercompartmental P-C clearance
Pharmacolibrary.Types.TransferRateka (from PK_2C_enteral)0.016666666666666666first order absorption rate
Modelica.Units.SI.TimeTlag (from PK_2C_enteral)600delay between oral administration and absorption (default 10min)

Connectors

TypeNameDefaultDescription
Types.ConcentrationOutputC_central (from PK_1C)
Interfaces.ConcentrationPort_bcentralCPort (from PK_1C)
Interfaces.ConcentrationPort_bperipheralCPort (from PK_2C)
Pharmacolibrary.Types.ConcentrationOutputC_peripheral1 (from PK_2C)

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
Pharmacolibrary.Pharmacokinetic.TransferFirstOrderNonSymtransfer (from PK_2C)
Pharmacolibrary.Pharmacokinetic.NoPerfusedTissueCompartmentperipheral (from PK_2C)

Revisions

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