modelB01AB05

Diagram of B01AB05

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:Enoxaparin
ATC code:B01AB05
route:subcutaneous
compartments:1
dosage:40mg
volume of distribution:4.3L
clearance:0.21L/h
other parameters in model implementation

Enoxaparin is a low molecular weight heparin (LMWH) used primarily for the prevention and treatment of deep vein thrombosis (DVT), pulmonary embolism (PE), and acute coronary syndromes. It works by inhibiting factor Xa and is widely approved and used in clinical practice for anticoagulation.

Pharmacokinetics

Pharmacokinetics in healthy adult subjects following subcutaneous injection.

References

  1. Moffett, BS, et al., & Yee, D (2018). Population Pharmacokinetics of Enoxaparin in Pediatric Patients. The Annals of pharmacotherapy 52(2) 140–146. DOI:10.1177/1060028017734234 PUBMED:https://pubmed.ncbi.nlm.nih.gov/28962537

  2. Carreño, FO, et al., & Gonzalez, D (2024). Characterizing Enoxaparin's Population Pharmacokinetics to Guide Dose Individualization in the Pediatric Population. Clinical pharmacokinetics 63(7) 999–1014. DOI:10.1007/s40262-024-01388-x PUBMED:https://pubmed.ncbi.nlm.nih.gov/38955947

  3. Frum, J, et al., & Thomason, J (2022). Anticoagulant profile of subcutaneous enoxaparin in healthy dogs. Journal of veterinary pharmacology and therapeutics 45(1) 34–45. DOI:10.1111/jvp.13015 PUBMED:https://pubmed.ncbi.nlm.nih.gov/34622463

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)