modelPeginterferonAlfa2a

Diagram of PeginterferonAlfa2a

Extends from Pharmacolibrary.Drugs.ATC.L.L03AB11.

Information

name:PeginterferonAlfa2a
ATC code:L03AB11
route:subcutaneous
compartments:1
dosage:180mg
volume of distribution:8L
clearance:100ml/h
other parameters in model implementation

Peginterferon alfa-2a is a pegylated form of interferon alfa-2a, an immunomodulatory drug used primarily in the treatment of chronic hepatitis B and C infections. By attaching polyethylene glycol (PEG) to interferon alfa-2a, the drug has an extended half-life, allowing for less frequent dosing. Peginterferon alfa-2a is approved and widely used for antiviral therapy, though its use has decreased with the advent of newer direct-acting antivirals for hepatitis C.

Pharmacokinetics

Pharmacokinetic parameters reported for adults with chronic hepatitis C, both male and female, under standard clinical dosing.

References

  1. Jung, YS, et al., & Park, K (2018). Population PK-PD Model of Pegylated Interferon Alfa-2a in Healthy Korean Men. Journal of pharmaceutical sciences 107(12) 3171–3178. DOI:10.1016/j.xphs.2018.08.017 PUBMED:https://pubmed.ncbi.nlm.nih.gov/30179597

  2. Keating, GM, & Curran, MP (2003). Peginterferon-alpha-2a (40kD) plus ribavirin: a review of its use in the management of chronic hepatitis C. Drugs 63(7) 701–730. DOI:10.2165/00003495-200363070-00008 PUBMED:https://pubmed.ncbi.nlm.nih.gov/12656650

  3. Howell, CD, et al., & Hoofnagle, JH (2008). Peginterferon pharmacokinetics in African American and Caucasian American patients with hepatitis C virus genotype 1 infection. Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 6(5) 575–583. DOI:10.1016/j.cgh.2008.02.035 PUBMED:https://pubmed.ncbi.nlm.nih.gov/18407798

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)