modelJ07AH07

Diagram of J07AH07

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:MeningococcusCPurifiedPolysaccharidesAntigenConjugated
ATC code:J07AH07
route:intramuscular
compartments:1
dosage:10mg
volume of distribution:1L
clearance:0
other parameters in model implementation

Meningococcus C conjugate vaccine is composed of purified polysaccharide antigens from Neisseria meningitidis group C, conjugated to a carrier protein (often tetanus toxoid, CRM197 or diphtheria toxoid) to enhance immunogenicity. It is used for the prevention of invasive meningococcal disease caused by Neisseria meningitidis serogroup C in infants, children, adolescents, and adults. The vaccine is approved and widely used for routine immunization in many countries.

Pharmacokinetics

Pharmacokinetic parameters for meningococcus C polysaccharide conjugate vaccines are not conventionally reported, as the vaccine consists of high molecular weight antigens and is administered intramuscularly, where the PK is characterized by antigen presentation and immune response rather than standard PK parameters such as those for small molecule drugs. No published PK data are available in the scientific literature for this vaccine in any population.

References

    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)