modelFusidicAcid

Diagram of FusidicAcid

Extends from Pharmacolibrary.Drugs.ATC.S.S01AA13.

Information

name:FusidicAcid
ATC code:S01AA13
route:topical
compartments:1
dosage:10mg
volume of distribution:1L
clearance:0.01L/h
other parameters in model implementation

Fusidic acid is an antibiotic of the steroid class used to treat bacterial infections, particularly those caused by staphylococci, including methicillin-resistant Staphylococcus aureus (MRSA). It is mainly used for skin and eye infections and is formulated topically and systemically. For ocular use (ATC S01AA13), it is available as an ophthalmic gel or drops. Fusidic acid is approved and used in many countries today.

Pharmacokinetics

Estimated pharmacokinetic parameters for topical (ocular) administration in adults. No published compartmental pharmacokinetics models specific to ocular (ATC S01AA13) administration of fusidic acid were found. Most published PK data are from oral or intravenous use or systemic exposure studies.

References

  1. Wadhwa, S, et al., & Katare, OP (2016). Liposomal fusidic acid as a potential delivery system: a new paradigm in the treatment of chronic plaque psoriasis. Drug delivery 23(4) 1204–1213. DOI:10.3109/10717544.2015.1110845 PUBMED:https://pubmed.ncbi.nlm.nih.gov/26592918

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)