modelN01AX07

Diagram of N01AX07

Extends from Pharmacokinetic.Models.PK_2C.

Information

name:Etomidate
ATC code:N01AX07
route:intravenous
compartments:2
dosage:20mg
volume of distribution:2.2L
clearance:15.6mL/min/kg
other parameters in model implementation

Etomidate is a short-acting intravenous anesthetic agent used for the induction of general anesthesia and sedation for short procedures. It is known for its rapid onset and minimal cardiovascular effects, making it particularly useful in patients with hemodynamic instability. It is approved and clinically used for anesthesia induction.

Pharmacokinetics

Pharmacokinetic parameters reported in healthy adult subjects after intravenous bolus administration.

References

  1. Lin, L, et al., & Zhang, MZ (2012). Population pharmacokinetics of intravenous bolus etomidate in children over 6 months of age. Paediatric anaesthesia 22(4) 318–326. DOI:10.1111/j.1460-9592.2011.03696.x PUBMED:https://pubmed.ncbi.nlm.nih.gov/21917057

  2. Su, F, et al., & Drover, DR (2015). Population pharmacokinetics of etomidate in neonates and infants with congenital heart disease. Biopharmaceutics & drug disposition 36(2) 104–114. DOI:10.1002/bdd.1924 PUBMED:https://pubmed.ncbi.nlm.nih.gov/25377074

  3. Kaneda, K, et al., & Han, TH (2011). Population pharmacokinetics and pharmacodynamics of brief etomidate infusion in healthy volunteers. Journal of clinical pharmacology 51(4) 482–491. DOI:10.1177/0091270010369242 PUBMED:https://pubmed.ncbi.nlm.nih.gov/20498288

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.VolumeVdp (from PK_2C)VdpPerKg*weightVolume of distribution (m3)
Modelica.Units.SI.SpecificVolumeVdpPerKg (from PK_2C)0.9Volume of distribution peripheral(l/kg)
Pharmacolibrary.Types.Clearancek12 (from PK_2C)1intercompartmental C-P clearance
Pharmacolibrary.Types.Clearancek21 (from PK_2C)1intercompartmental P-C clearance

Connectors

TypeNameDefaultDescription
Types.ConcentrationOutputC_central (from PK_1C)
Interfaces.ConcentrationPort_bcentralCPort (from PK_1C)
Interfaces.ConcentrationPort_bperipheralCPort (from PK_2C)
Pharmacolibrary.Types.ConcentrationOutputC_peripheral1 (from PK_2C)

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
Pharmacolibrary.Pharmacokinetic.TransferFirstOrderNonSymtransfer (from PK_2C)
Pharmacolibrary.Pharmacokinetic.NoPerfusedTissueCompartmentperipheral (from PK_2C)

Revisions

  • 06/2025 Tomas Kulhanek, generated model from data extracted from PUBMED, DrugBank and LLM(GPT4.1)