modelR06AX28

Extends from Pharmacokinetic.Models.PK_1C_enteral.

Information

name:Rupatadine
ATC code:R06AX28
route:oral
compartments:1
dosage:10mg
volume of distribution:652L
clearance:13.1L/h
other parameters in model implementation

Rupatadine is a second-generation antihistamine and platelet-activating factor (PAF) antagonist used primarily for the symptomatic treatment of allergic rhinitis and urticaria. It is an orally active, non-sedating agent that is approved and available in many countries for these indications.

Pharmacokinetics

Pharmacokinetic parameters reported for healthy adult volunteers, both male and female, after a single oral dose administration.

References

  1. Santamaria, E, et al., & Valle, M (2021). Rupatadine Oral Solution Titration by Body Weight in Paediatric Patients Suffering from Allergic Rhinitis: A Population Pharmacokinetic Study. Clinical pharmacology : advances and applications 13 115–122. DOI:10.2147/CPAA.S312911 PUBMED:https://pubmed.ncbi.nlm.nih.gov/34135645

  2. Xiong, Y, et al., & Liu, M (2016). CYP3A5*3 and MDR1 C3435T are influencing factors of inter-subject variability in rupatadine pharmacokinetics in healthy Chinese volunteers. European journal of drug metabolism and pharmacokinetics 41(2) 117–124. DOI:10.1007/s13318-014-0236-3 PUBMED:https://pubmed.ncbi.nlm.nih.gov/25427746

  3. Peña, J, et al., & Merlos, M (2008). Antihistaminic effects of rupatadine and PKPD modelling. European journal of drug metabolism and pharmacokinetics 33(2) 107–116. DOI:10.1007/BF03191027 PUBMED:https://pubmed.ncbi.nlm.nih.gov/18777946

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.TransferRateka (from PK_1C_enteral)0.016666666666666666first order absorption rate
Modelica.Units.SI.TimeTlag (from PK_1C_enteral)600delay between oral administration and absorption (default 10min)

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)