modelA01AA30

Diagram of A01AA30

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:Combinations
ATC code:A01AA30
route:topical
compartments:1
dosage:20mg
volume of distribution:50L
clearance:48L/h
other parameters in model implementation

ATC code A01AA30 covers combinations of tetracycline antibiotics for dental use. These formulations are typically used topically in the oral cavity to manage gingivitis, periodontitis, and other oral infections. Such combinations may be rarely used today, and have largely been replaced by more targeted or systemic therapies in clinical practice.

Pharmacokinetics

No published pharmacokinetic model parameters are available for tetracycline combinations formulated for dental topical use in humans. Estimates here are deduced from single-component topical tetracycline oral gel studies in adults.

References

  1. Petersson, LG (1993). Fluoride mouthrinses and fluoride varnishes. Caries research 27 Suppl 1 35–42. DOI:10.1159/000261600 PUBMED:https://pubmed.ncbi.nlm.nih.gov/8500123

  2. Tran, AN, & Koo, JY (2014). Risk of systemic toxicity with topical lidocaine/prilocaine: a review. Journal of drugs in dermatology : JDD 13(9) 1118–1122. PUBMED:https://pubmed.ncbi.nlm.nih.gov/25226014

  3. Li, L, et al., & Ma, P (2023). Dermal effects and pharmacokinetic evaluation of the lidocaine/prilocaine cream in healthy Chinese volunteers. BMC pharmacology & toxicology 24(1) 51–None. DOI:10.1186/s40360-023-00690-x PUBMED:https://pubmed.ncbi.nlm.nih.gov/37828535

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)