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Mechanistic models are utilized in individual analysis using single-source data, but imperfections arise due to data collection errors, preventing perfect prediction of observed data. The mathematical equation involves known values (Xi), observed concentrations (Ci), measurement errors (εi), model parameters (ϕj), and the related function (ƒi) for i number of values. Different least-squares metrics quantify differences between predicted and observed values. The ordinary least squares (OLS) method favors better predictions for larger observations. In contrast, weighted least squares (WLS) and maximum likelihood/expected least squares (ML/ELS) methods improve OLS by incorporating a weighting factor.

Population analysis models predict concentration data for multiple individuals, accounting for interindividual variability and providing individual and population predictions. The same structural model fits all individuals' data for a specific drug under study. Different types of population compartmental analysis include naïve-average data, naïve pooled data, and the two-stage approach, which includes standard, global, and iterative types. In the two-stage approach, population parameter estimates are obtained through iterative processes, such as standard two-stage (STS) and global two-stage (GTS).

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Mechanistic ModelsCompartment ModelsIndividual AnalysisPopulation AnalysisSingle source DataMathematical EquationsObserved ConcentrationsMeasurement ErrorsModel ParametersLeast squares MetricsOrdinary Least Squares OLSWeighted Least Squares WLSMaximum Likelihood expected Least Squares ML ELSInterindividual VariabilityPopulation Compartmental AnalysisTwo stage ApproachStandard Two stage STSGlobal Two stage GTS

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7.18 : Mechanistic Models: Compartment Models in Individual and Population Analysis

Pharmacokinetic Models

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7.1 : Analysis Methods of Pharmacokinetic Data: Model and Model-Independent Approaches

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7.2 : Model Approaches for Pharmacokinetic Data: Compartment Models

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7.3 : One-Compartment Open Model for IV Bolus Administration: General Considerations

Pharmacokinetic Models

104 Ansichten

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7.4 : One-Compartment Open Model for IV Bolus Administration: Estimation of Elimination Rate Constant, Half-Life and Volume of Distribution

Pharmacokinetic Models

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7.5 : One-Compartment Open Model for IV Bolus Administration: Estimation of Clearance

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7.6 : One-Compartment Model: IV Infusion

Pharmacokinetic Models

107 Ansichten

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7.7 : One-Compartment Open Model for Extravascular Administration: Zero-Order Absorption Model

Pharmacokinetic Models

37 Ansichten

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7.8 : One-Compartment Open Model for Extravascular Administration: First-Order Absorption Model

Pharmacokinetic Models

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7.9 : One-Compartment Open Model: Wagner-Nelson and Loo Riegelman Method for ka Estimation

Pharmacokinetic Models

197 Ansichten

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7.10 : One-Compartment Open Model: Urinary Excretion Data and Determination of k

Pharmacokinetic Models

58 Ansichten

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7.11 : Multicompartment Models: Overview

Pharmacokinetic Models

50 Ansichten

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7.12 : Two-Compartment Open Model: Overview

Pharmacokinetic Models

73 Ansichten

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7.13 : Two-Compartment Open Model: IV Bolus Administration

Pharmacokinetic Models

164 Ansichten

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7.14 : Two-Compartment Open Model: IV Infusion

Pharmacokinetic Models

137 Ansichten

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