modelCiprofloxacin_1

Diagram of Ciprofloxacin_1

Extends from Pharmacolibrary.Drugs.ATC.S.S01AE03_1.

Information

name:Ciprofloxacin_1
ATC code:S01AE03_1
route:ophthalmic
compartments:1
dosage:0.3mg
volume of distribution:0.46L
clearance:0.029L/h
other parameters in model implementation

Ciprofloxacin is a broad-spectrum fluoroquinolone antibiotic used to treat a variety of bacterial infections, including urinary tract infections, respiratory tract infections, and eye infections. It is approved for both systemic and ophthalmic uses in many countries.

Pharmacokinetics

One-compartment model following topical ophthalmic administration (eye drops) in healthy subjects.

References

  1. Morlet, N, et al., & Lam, CM (2000). Pharmacokinetics of ciprofloxacin in the human eye: a clinical study and population pharmacokinetic analysis. Antimicrobial agents and chemotherapy 44(6) 1674–1679. DOI:10.1128/AAC.44.6.1674-1679.2000 PUBMED:https://pubmed.ncbi.nlm.nih.gov/10817727

  2. Hendrix, DV, et al., & Cox, SK (2007). Pharmacokinetics of topically applied ciprofloxacin in equine tears. Veterinary ophthalmology 10(6) 344–347. DOI:10.1111/j.1463-5224.2007.00566.x PUBMED:https://pubmed.ncbi.nlm.nih.gov/17970994

  3. Di Marco, MP, et al., & Ducharme, MP (2004). A population pharmacokinetic-metabolism model for individualizing ciprofloxacin therapy in ophthalmology. Therapeutic drug monitoring 26(4) 401–407. DOI:10.1097/00007691-200408000-00010 PUBMED:https://pubmed.ncbi.nlm.nih.gov/15257070

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)