modelCyfluthrin

Extends from Pharmacolibrary.Drugs.ATC.P.P03BA01.

Information

name:Cyfluthrin
ATC code:P03BA01
route:oral
compartments:1
dosage:1mg
volume of distribution:1.5L
clearance:0.05L/kg/h
other parameters in model implementation

Cyfluthrin is a synthetic pyrethroid insecticide used primarily for control of pests in agriculture, public health, and domestic settings. It is not approved for human therapeutic use but is widely used as a pesticide on crops, livestock, and in households.

Pharmacokinetics

No published pharmacokinetic parameters for human administration found; estimations based on pyrethroid class data and animal studies.

References

  1. Wang, Z, et al., & Diao, J (2020). Thermal effects on tissue distribution, liver biotransformation, metabolism and toxic responses in Mongolia racerunner (Eremias argus) after oral administration of beta-cyfluthrin. Environmental research 185 109393–None. DOI:10.1016/j.envres.2020.109393 PUBMED:https://pubmed.ncbi.nlm.nih.gov/32203733

  2. Hays, SM, et al., & Krishnan, K (2009). Derivation of Biomonitoring Equivalents for cyfluthrin. Regulatory toxicology and pharmacology : RTP 55(3) 268–275. DOI:10.1016/j.yrtph.2009.09.002 PUBMED:https://pubmed.ncbi.nlm.nih.gov/19751788

  3. Vanacker, M, et al., & Crépet, A (2020). Aggregate and cumulative chronic risk assessment for pyrethroids in the French adult population. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 143 111519–None. DOI:10.1016/j.fct.2020.111519 PUBMED:https://pubmed.ncbi.nlm.nih.gov/32619558

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)