2020
DOI: 10.1007/s10928-020-09719-8
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Exact solutions and equi-dosing regimen regions for multi-dose pharmacokinetics models with transit compartments

Abstract: Compartmental models which yield linear ordinary differential equations (ODEs) provide common tools for pharmacokinetics (PK) analysis, with exact solutions for drug levels or concentrations readily obtainable for low-dimensional compartment models. Exact solutions enable valuable insights and further analysis of these systems. Transit compartment models are a popular semi-mechanistic approach for generalising simple PK models to allow for delayed kinetics, but computing exact solutions for multi-dosing inputs… Show more

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Cited by 6 publications
(2 citation statements)
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“…The copyright holder for this preprint this version posted November 18, 2022. ; https://doi.org/10.1101/2022.11.17.517003 doi: bioRxiv preprint in pharmacokinetic modeling and is generally used as a model input to simulate PK profiles of drugs following different dosing regimens or under various pathophysiological conditions (Zhang, Wang et al 2012, Hof andBridge 2021). In this study, a biexponential equation, which adequately describes the concentration-time data of both intact 125 I-insulin and 125 I-Aβ40 peptides, was used as the forcing function (Figure 3A, C).…”
Section: Discussionmentioning
confidence: 99%
“…The copyright holder for this preprint this version posted November 18, 2022. ; https://doi.org/10.1101/2022.11.17.517003 doi: bioRxiv preprint in pharmacokinetic modeling and is generally used as a model input to simulate PK profiles of drugs following different dosing regimens or under various pathophysiological conditions (Zhang, Wang et al 2012, Hof andBridge 2021). In this study, a biexponential equation, which adequately describes the concentration-time data of both intact 125 I-insulin and 125 I-Aβ40 peptides, was used as the forcing function (Figure 3A, C).…”
Section: Discussionmentioning
confidence: 99%
“…En la Figura 6.29 se observan las superficies de respuesta de PTA para los dos indicadores. Las superficies tienen forma de pétalo con un comportamiento similar a las regiones de régimen de equidosificación descritas por Hof F y Bridge LJ [124]. Se hace evidente que al utilizar el objetivo PK/PD de AUC entre 400 − 600 mg • h/L se alcanza un PTA máximo de 0.65, mientras que al utilizar el objetivo PK/PD de C min entre 15 − 20 mg/L se alcanza un PTA máximo de 0.35.…”
Section: Evaluación De Indicadores Pk/pd Alternativosunclassified