modelV04CE01

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:Galactose
ATC code:V04CE01
route:intravenous
compartments:1
dosage:400mg
volume of distribution:0.35L
clearance:60ml/min/kg
other parameters in model implementation

Galactose is a monosaccharide sugar, part of the lactose disaccharide found in milk. It is used rarely as a diagnostic agent for liver function and galactose metabolism disorders, but is not an approved medication for therapeutic use in most countries today.

Pharmacokinetics

Estimated pharmacokinetic parameters for adult healthy individuals. No definitive PK profile reported in literature for therapeutic use; estimates derived based on monosaccharide similarities and diagnostic use.

References

  1. Mion, F, et al., & Minaire, Y (1999). [13C]-Galactose breath test: correlation with liver fibrosis in chronic hepatitis C. European journal of clinical investigation 29(7) 624–629. DOI:10.1046/j.1365-2362.1999.00512.x PUBMED:https://pubmed.ncbi.nlm.nih.gov/10411669

  2. Joffe, P, et al., & Sidhu, J (1998). Single-dose pharmacokinetics of citalopram in patients with moderate renal insufficiency or hepatic cirrhosis compared with healthy subjects. European journal of clinical pharmacology 54(3) 237–242. DOI:10.1007/s002280050452 PUBMED:https://pubmed.ncbi.nlm.nih.gov/9681666

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)