modelR03BB03

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:StramoniPreparations
ATC code:R03BB03
route:inhalation
compartments:1
dosage:2mg
volume of distribution:2.6L
clearance:1.0L/h/kg
other parameters in model implementation

Stramoni preparations are derived from the plant Datura stramonium, containing tropane alkaloids such as atropine, hyoscyamine, and scopolamine. Historically, they were used as bronchodilators in the treatment of asthma and other respiratory disorders, primarily in the form of inhaled powders or cigarettes. Due to significant toxicity and safer alternatives, such preparations are no longer in common or approved therapeutic use.

Pharmacokinetics

No clinical pharmacokinetic studies or precise population data for stramoni preparations as a mixture exist; parameter estimates are extrapolated from known pharmacokinetics of the major tropane alkaloid component (atropine) in healthy adult subjects following inhaled administration.

References

  1. Zandvliet, AS, et al., & Beijnen, JH (2005). Population pharmacokinetics of caffeine and its metabolites theobromine, paraxanthine and theophylline after inhalation in combination with diacetylmorphine. Basic & clinical pharmacology & toxicology 96(1) 71–79. DOI:10.1111/j.1742-7843.2005.pto960111.x PUBMED:https://pubmed.ncbi.nlm.nih.gov/15667599

  2. Corcoran, TE (2009). Aerosol drug delivery in lung transplant recipients. Expert opinion on drug delivery 6(2) 139–148. DOI:10.1517/17425250802685332 PUBMED:https://pubmed.ncbi.nlm.nih.gov/19239386

  3. Walenga, RL, et al., & Roy, P (2024). Use of the Same Model or Modeling Strategy Across Multiple Submissions: Focus on Complex Drug Products. The AAPS journal 26(1) 12–None. DOI:10.1208/s12248-023-00879-2 PUBMED:https://pubmed.ncbi.nlm.nih.gov/38177638

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)