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7.24 : Model Approaches for Pharmacokinetic Data: Distributed Parameter Models

Pharmacokinetic models are mathematical constructs that represent and predict the time course of drug concentrations in the body, providing meaningful pharmacokinetic parameters. These models are categorized into compartment, physiological, and distributed parameter models.

The distributed parameter models are specifically designed to account for variations and differences in some drug classes. This model is particularly useful for assessing regional concentrations of anticancer or cardiovascular medications that target specific tumors and specific areas of the heart, respectively. However, the exhaustive data collection is challenging, and the mathematical equations are quite complex.

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Pharmacokinetic ModelsDistributed Parameter ModelsCompartment ModelsPhysiological ModelsDrug ConcentrationsPharmacokinetic ParametersRegional ConcentrationsAnticancer MedicationsCardiovascular MedicationsMathematical EquationsData Collection Challenges

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7.24 : Model Approaches for Pharmacokinetic Data: Distributed Parameter Models

Pharmacokinetic Models

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

Pharmacokinetic Models

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7.2 : Model Approaches for Pharmacokinetic Data: Compartment Models

Pharmacokinetic Models

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

Pharmacokinetic Models

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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

Pharmacokinetic Models

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7.6 : One-Compartment Model: IV Infusion

Pharmacokinetic Models

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

Pharmacokinetic Models

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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

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

Pharmacokinetic Models

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7.11 : Multicompartment Models: Overview

Pharmacokinetic Models

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7.12 : Two-Compartment Open Model: Overview

Pharmacokinetic Models

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7.13 : Two-Compartment Open Model: IV Bolus Administration

Pharmacokinetic Models

262 Visualizações

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7.14 : Two-Compartment Open Model: IV Infusion

Pharmacokinetic Models

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