modelD03AX05

Diagram of D03AX05

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:HyaluronicAcid
ATC code:D03AX05
route:intravenous
compartments:1
dosage:80mg
volume of distribution:0.23L
clearance:0.03L/kg/min
other parameters in model implementation

Hyaluronic acid is a naturally occurring glycosaminoglycan distributed in connective, epithelial, and neural tissues. It is used medically as a topical wound healer, intra-articularly for osteoarthritis, and dermally as a cosmetic filler. It is considered safe and is widely used for wound healing and lubrication.

Pharmacokinetics

No peer-reviewed pharmacokinetic studies reporting classic PK parameters in humans for systemic administration. Hyaluronic acid pharmacokinetics is influenced by its molecular weight, formulation, and administration route. For topical and intra-articular use, systemic absorption is minimal; for intravenous administration (studied mostly experimentally), some parameters have been estimated.

References

  1. Hahn, RG, et al., & Björne, H (2019). Fluid volume kinetics of 20% albumin. British journal of clinical pharmacology 85(6) 1303–1311. DOI:10.1111/bcp.13897 PUBMED:https://pubmed.ncbi.nlm.nih.gov/30756411

  2. Levitskaia, TG, et al., & Thrall, KD (2010). Biomaterials for the decorporation of (85)Sr in the rat. Health physics 99(3) 394–400. DOI:10.1097/HP.0b013e3181c4717d PUBMED:https://pubmed.ncbi.nlm.nih.gov/20699703

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)