modelD10AE01

Diagram of D10AE01

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:BenzoylPeroxide
ATC code:D10AE01
route:topical
compartments:1
dosage:50mg
volume of distribution:0.15L
clearance:6.3L/h
other parameters in model implementation

Benzoyl peroxide is a topical medication with antimicrobial and keratolytic properties, primarily used for the treatment of acne vulgaris. It is available over-the-counter and by prescription and is approved in many countries for current medical use in dermatology.

Pharmacokinetics

No direct pharmacokinetic studies in humans are available. Systemic absorption after topical administration is minimal, as the compound is largely converted to benzoic acid in the skin and rapidly excreted in the urine.

References

  1. Ino, H, et al., & Hasegawa, S (2015). Systemic exposure to benzoic acid and hippuric acid following topical application of clindamycin 1%/benzoyl peroxide 3% fixed-dose combination gel in Japanese patients with acne vulgaris. Clinical pharmacology in drug development 4(1) 18–24. DOI:10.1002/cpdd.125 PUBMED:https://pubmed.ncbi.nlm.nih.gov/27128000

  2. Meredith, FM, & Ormerod, AD (2013). The management of acne vulgaris in pregnancy. American journal of clinical dermatology 14(5) 351–358. DOI:10.1007/s40257-013-0041-9 PUBMED:https://pubmed.ncbi.nlm.nih.gov/23996075

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)