modelP02DA01

Extends from Pharmacokinetic.Models.PK_1C_enteral.

Information

name:Niclosamide
ATC code:P02DA01
route:oral
compartments:1
dosage:2000mg
volume of distribution:0.16L
clearance:2.12L/h
other parameters in model implementation

Niclosamide is an anthelmintic drug primarily used to treat tapeworm infections in humans, approved for use in many countries since the 1960s. It is listed on the WHO Model List of Essential Medicines. Recently, it has gained renewed interest for repurposing against other conditions, including viral infections and cancer.

Pharmacokinetics

Single oral administration in healthy adult volunteers; pharmacokinetics reported after 2 g oral dose.

References

  1. Schweizer, MT, et al., & Yu, EY (2018). A phase I study of niclosamide in combination with enzalutamide in men with castration-resistant prostate cancer. PloS one 13(6) e0198389–None. DOI:10.1371/journal.pone.0198389 PUBMED:https://pubmed.ncbi.nlm.nih.gov/29856824

  2. Marcelín-Jiménez, G, et al., & García-González, A (2012). Development of a method by UPLC-MS/MS for the quantification of tizoxanide in human plasma and its pharmacokinetic application. Bioanalysis 4(8) 909–917. DOI:10.4155/bio.12.41 PUBMED:https://pubmed.ncbi.nlm.nih.gov/22533565

  3. Senkowski, W, et al., & Fryknäs, M (2015). Three-Dimensional Cell Culture-Based Screening Identifies the Anthelmintic Drug Nitazoxanide as a Candidate for Treatment of Colorectal Cancer. Molecular cancer therapeutics 14(6) 1504–1516. DOI:10.1158/1535-7163.MCT-14-0792 PUBMED:https://pubmed.ncbi.nlm.nih.gov/25911689

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)