modelVitaminAConcentrates

Extends from Pharmacolibrary.Drugs.ATC.V.V04CB01.

Information

name:VitaminAConcentrates
ATC code:V04CB01
route:oral
compartments:1
dosage:100000mg
volume of distribution:1.0L
clearance:0.05L/kg/h
other parameters in model implementation

Vitamin A concentrates are formulations of fat-soluble vitamin A (retinol or its esters) used in dietary supplementation or treatment of deficiency. They are administered to prevent or treat vitamin A deficiency, particularly in populations at risk (children, pregnant women) or in cases of malnutrition. Vitamin A is essential for vision, immune function, and cellular growth. These concentrates are approved and used today in clinical practice, mostly as oral or injectable preparations.

Pharmacokinetics

No published population pharmacokinetic model exists for 'vitamin A concentrates' as a formulated medicine. The following are estimated typical parameters for adult healthy subjects receiving oral administration of retinyl palmitate, a representative vitamin A ester. These are based on known pharmacokinetic principles and analogous values from retinol studies.

References

  1. Haskell, MJ, et al., & Brown, KH (2003). Population-based plasma kinetics of an oral dose of [2H4]retinyl acetate among preschool-aged, Peruvian children. The American journal of clinical nutrition 77(3) 681–686. DOI:10.1093/ajcn/77.3.681 PUBMED:https://pubmed.ncbi.nlm.nih.gov/12600861

  2. Zachman, RD, & Chen, XM (1991). Intramuscular relative dose response (RDR) determination of liver vitamin A stores in rats. The Journal of nutrition 121(2) 187–191. DOI:10.1093/jn/121.2.187 PUBMED:https://pubmed.ncbi.nlm.nih.gov/1825326

  3. Rigas, JR, et al., & Warrell, RP (1993). Constitutive variability in the pharmacokinetics of the natural retinoid, all-trans-retinoic acid, and its modulation by ketoconazole. Journal of the National Cancer Institute 85(23) 1921–1926. DOI:10.1093/jnci/85.23.1921 PUBMED:https://pubmed.ncbi.nlm.nih.gov/8230282

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
Pharmacolibrary.Types.TransferRateka (from PK_1C_enteral)0.016666666666666666first order absorption rate
Modelica.Units.SI.TimeTlag (from PK_1C_enteral)600delay between oral administration and absorption (default 10min)

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)