modelAminohippuricAcid

Extends from Pharmacolibrary.Drugs.ATC.V.V04CH30.

Information

name:AminohippuricAcid
ATC code:V04CH30
route:intravenous
compartments:1
dosage:500mg
volume of distribution:0.21L
clearance:600ml/min
other parameters in model implementation

Aminohippuric acid (also known as para-aminohippuric acid, PAH) is an organic acid historically used as a diagnostic agent to measure renal plasma flow and renal function. It is not approved or used today as a therapeutic drug.

Pharmacokinetics

Adults, healthy volunteers. Classic renal clearance and renal plasma flow tests, intravenous bolus administration.

References

  1. Dhondt, L, et al., & Devreese, M (2020). Unraveling the Contribution of Fluid Therapy to the Development of Augmented Renal Clearance in a Piglet Model. Frontiers in pharmacology 11 607101–None. DOI:10.3389/fphar.2020.607101 PUBMED:https://pubmed.ncbi.nlm.nih.gov/33574754

  2. Dubinsky, S, et al., & Edginton, A (2022). Determining the Effects of Chronic Kidney Disease on Organic Anion Transporter1/3 Activity Through Physiologically Based Pharmacokinetic Modeling. Clinical pharmacokinetics 61(7) 997–1012. DOI:10.1007/s40262-022-01121-6 PUBMED:https://pubmed.ncbi.nlm.nih.gov/35508593

  3. Dhondt, L, et al., & Devreese, M (2021). The Development of a Juvenile Porcine Augmented Renal Clearance Model Through Continuous Infusion of Lipopolysaccharides: An Exploratory Study. Frontiers in veterinary science 8 639771–None. DOI:10.3389/fvets.2021.639771 PUBMED:https://pubmed.ncbi.nlm.nih.gov/33996970

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)