modelGemcitabine

Diagram of Gemcitabine

Extends from Pharmacolibrary.Drugs.ATC.L.L01BC05.

Information

name:Gemcitabine
ATC code:L01BC05
route:intravenous
compartments:2
dosage:1000mg
volume of distribution:50.2L
clearance:85.6L/h
other parameters in model implementation

Gemcitabine is a nucleoside analog used as an antineoplastic (anticancer) agent. It is approved and widely used for treatment of various carcinomas, including pancreatic cancer, non-small cell lung cancer, bladder cancer, and breast cancer. It works primarily by inhibiting DNA synthesis, leading to cell death.

Pharmacokinetics

Pharmacokinetic parameters reported for adult cancer patients (both sexes), typically aged 18-80 years, receiving intravenous infusion of gemcitabine. No major differences were observed based on sex or cancer type.

References

  1. Sugiyama, E, et al., & Sawada, J (2010). Population pharmacokinetics of gemcitabine and its metabolite in Japanese cancer patients: impact of genetic polymorphisms. Clinical pharmacokinetics 49(8) 549–558. DOI:10.2165/11532970-000000000-00000 PUBMED:https://pubmed.ncbi.nlm.nih.gov/20608756

  2. Boosman, RJ, et al., & Huitema, ADR (2022). Is age just a number? A population pharmacokinetic study of gemcitabine. Cancer chemotherapy and pharmacology 89(5) 697–705. DOI:10.1007/s00280-022-04431-5 PUBMED:https://pubmed.ncbi.nlm.nih.gov/35426526

  3. Jiang, X, et al., & McLachlan, AJ (2008). Population pharmacokinetics of gemcitabine and its metabolite in patients with cancer: effect of oxaliplatin and infusion rate. British journal of clinical pharmacology 65(3) 326–333. DOI:10.1111/j.1365-2125.2007.03040.x PUBMED:https://pubmed.ncbi.nlm.nih.gov/17961191

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)