JoVE Logo

Oturum Aç

7.2 : Model Approaches for Pharmacokinetic Data: Compartment Models

Compartmental analysis is a widely adopted approach to characterizing drug pharmacokinetics. It uses compartment models that conceptualize the body as a collection of reversibly communicating compartments, each representing a group of tissues exhibiting similar drug distribution characteristics. The movement rate of the drug between these compartments is typically described by first-order kinetics.

Two primary types of compartment models are recognized: mammillary and catenary. The more prevalent of the two, the mammillary model, comprises peripheral compartments characterized by low vascularity and poor perfusion linked to a central compartment such as plasma and highly perfused tissues. In contrast, the catenary model assumes a series of interconnected compartments despite its rarity in practical application, owing to its limited physiological relevance.

The simplicity, flexibility, and widespread applicability of compartment modeling enable the effective monitoring of drug concentration changes even with limited data. Nevertheless, it is important to note that different compartment models are required due to the diverse drug administration routes, reflecting the nuanced nature of drug behavior within the body.

Compartmental analysis stands as a fundamental method for describing the intricacies of drug disposition, providing valuable insights into the dynamics of drug distribution and elimination within the body.

Etiketler

PharmacokineticsCompartment ModelsCompartmental AnalysisMammillary ModelCatenary ModelDrug DistributionFirst order KineticsDrug Administration RoutesDrug Concentration MonitoringDrug DispositionPhysiological RelevanceTissue Characteristics

Bölümden 7:

article

Now Playing

7.2 : Model Approaches for Pharmacokinetic Data: Compartment Models

Pharmacokinetic Models

74 Görüntüleme Sayısı

article

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

Pharmacokinetic Models

86 Görüntüleme Sayısı

article

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

Pharmacokinetic Models

153 Görüntüleme Sayısı

article

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

Pharmacokinetic Models

187 Görüntüleme Sayısı

article

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

Pharmacokinetic Models

58 Görüntüleme Sayısı

article

7.6 : One-Compartment Model: IV Infusion

Pharmacokinetic Models

144 Görüntüleme Sayısı

article

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

Pharmacokinetic Models

59 Görüntüleme Sayısı

article

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

Pharmacokinetic Models

190 Görüntüleme Sayısı

article

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

Pharmacokinetic Models

371 Görüntüleme Sayısı

article

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

Pharmacokinetic Models

128 Görüntüleme Sayısı

article

7.11 : Multicompartment Models: Overview

Pharmacokinetic Models

88 Görüntüleme Sayısı

article

7.12 : Two-Compartment Open Model: Overview

Pharmacokinetic Models

91 Görüntüleme Sayısı

article

7.13 : Two-Compartment Open Model: IV Bolus Administration

Pharmacokinetic Models

384 Görüntüleme Sayısı

article

7.14 : Two-Compartment Open Model: IV Infusion

Pharmacokinetic Models

189 Görüntüleme Sayısı

article

7.15 : Two-Compartment Open Model: Extravascular Administration

Pharmacokinetic Models

137 Görüntüleme Sayısı

See More

JoVE Logo

Gizlilik

Kullanım Şartları

İlkeler

Araştırma

Eğitim

JoVE Hakkında

Telif Hakkı © 2020 MyJove Corporation. Tüm hakları saklıdır