modelN01AF03

Diagram of N01AF03

Extends from Pharmacokinetic.Models.PK_2C.

Information

name:Thiopental
ATC code:N01AF03
route:intravenous
compartments:2
dosage:250mg
volume of distribution:2.7L
clearance:190ml/min
other parameters in model implementation

Thiopental (formerly marketed as sodium thiopental, known as Pentothal) is a rapid-onset short-acting barbiturate anesthetic. It was widely used for induction of anesthesia and for short surgical or diagnostic procedures. It is no longer widely available or used in many countries today, but remains of historical and pharmacological significance.

Pharmacokinetics

Parameters reported for healthy adult subjects after single intravenous bolus administration.

References

  1. Stanski, DR, & Maitre, PO (1990). Population pharmacokinetics and pharmacodynamics of thiopental: the effect of age revisited. Anesthesiology 72(3) 412–422. DOI:10.1097/00000542-199003000-00003 PUBMED:https://pubmed.ncbi.nlm.nih.gov/2310020

  2. Huynh, F, et al., & Ensom, MH (2009). A critical review: does thiopental continuous infusion warrant therapeutic drug monitoring in the critical care population?. Therapeutic drug monitoring 31(2) 153–169. DOI:10.1097/FTD.0b013e318196fb9f PUBMED:https://pubmed.ncbi.nlm.nih.gov/19177032

  3. Eilers, H, & Niemann, C (2003). Clinically important drug interactions with intravenous anaesthetics in older patients. Drugs & aging 20(13) 969–980. DOI:10.2165/00002512-200320130-00002 PUBMED:https://pubmed.ncbi.nlm.nih.gov/14561101

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)