modelIndium111inOxinateLabell

Extends from Pharmacolibrary.Drugs.ATC.V.V09HB01.

Information

name:Indium111inOxinateLabelledCells
ATC code:V09HB01
route:intravenous
compartments:1
dosage:10mg
volume of distribution:4.5L
clearance:0.18L/h
other parameters in model implementation

Indium (111In) oxinate labelled cells are used primarily for radiolabeling autologous leukocytes for diagnostic imaging, especially in infection or inflammation localization (e.g., detection of abscesses and osteomyelitis). The radiopharmaceutical is approved and widely used in nuclear medicine for such imaging applications.

Pharmacokinetics

Pharmacokinetic parameters relate to healthy adult volunteers and patients undergoing nuclear medicine imaging for infection/inflammation. Pharmacokinetics reflect labeled cell distribution rather than a classical drug.

References

  1. Maghazachi, AA, & Fitzgibbon, L (1990). Fate of intravenously administered rat lymphokine-activated killer cells labeled with different markers. Cancer immunology, immunotherapy : CII 31(3) 139–145. DOI:10.1007/BF01744727 PUBMED:https://pubmed.ncbi.nlm.nih.gov/2337903

  2. Melder, RJ, et al., & Jain, RK (2002). Systemic distribution and tumor localization of adoptively transferred lymphocytes in mice: comparison with physiologically based pharmacokinetic model. Neoplasia (New York, N.Y.) 4(1) 3–8. DOI:10.1038/sj.neo.7900209 PUBMED:https://pubmed.ncbi.nlm.nih.gov/11922388

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)