modelPropanol

Diagram of Propanol

Extends from Pharmacolibrary.Drugs.ATC.D.D08AX03.

Information

name:Propanol
ATC code:D08AX03
route:oral
compartments:1
dosage:400mg
volume of distribution:0.7L
clearance:50mL/min/kg
other parameters in model implementation

Propanol (propanolol) is an antiseptic alcohol primarily used for disinfection of skin and surfaces; it is not generally used systemically or as a pharmaceutical agent for internal use. It is not a currently approved therapeutic drug for systemic treatment in humans. Its main application is topical as a disinfectant.

Pharmacokinetics

No pharmacokinetic (PK) parameters for systemic administration of propanol have been published in the scientific literature, as it is exclusively used as a topical disinfectant and not intended for systemic therapy. The following parameters are provided as estimates for hypothetical oral administration in a healthy adult, based on general alcohol absorption and elimination data.

References

  1. Rasmussen, BB, & Brøsen, K (1996). Determination of urinary metabolites of caffeine for the assessment of cytochrome P4501A2, xanthine oxidase, and N-acetyltransferase activity in humans. Therapeutic drug monitoring 18(3) 254–262. DOI:10.1097/00007691-199606000-00006 PUBMED:https://pubmed.ncbi.nlm.nih.gov/8738764

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)