Chapter 7 COMPARTMENT MODELS

Slides:



Advertisements
Similar presentations
Karunya Kandimalla, Ph.D
Advertisements

PHARMACOKINETIC MODELS
PHARMACOKINETIC.
SEMINAR ON NONCOMPARTMENTAL PHARMACOKINETICS
Selected bioavailability and pharmacokinetic calculations Dr. Osama A. A. Ahmed.
Pharmacokinetics of Drug Absorption
Nonlinear pharmacokinetics
Two-compartment model
Pharmacokinetics & Pharmacodynamics of Controlled Release Systems Presented By: Govardhan.P Dept. of pharmaceutics, University College of Pharmaceutical.
Determining Elimination Rate (K)
One-compartment open model: Intravenous bolus administration
Week 5- Pharmacokinetics of oral absorption
Week 3 - Biopharmaceutics and Pharmacokinetics
Index of Simulations 1-Compartment, IV bolus 1-Compartment, IV infusion: Steady- State1-Compartment, IV infusion: Steady- State 1-Compartment, IV infusion:
Laplace transformation
Practical Pharmacokinetics
Practical Pharmacokinetics September 11, 2007 Frank F. Vincenzi.
Week 4 - Biopharmaceutics and Pharmacokinetics
Toxicokinetic Calculations
Gokaraju Rangaraju College of Pharmacy
INTRAVENOUS INFUSION.
VM 8314 Dr. Jeff Wilcke Pharmacokinetic Modeling (describing what happens)
CLEARANCE CONCEPTS Text: Applied Biopharm. & PK
The General Concepts of Pharmacokinetics and Pharmacodynamics Hartmut Derendorf, PhD University of Florida.
Pharmacokinetics Introduction
PHARMACOKINETIC MODELS
Touqeer Ahmed Ph.D. Atta-ur-Rahman School of Applied Bioscience, National University of Sciences and Technology 21 st October, 2013.
1-Compartment Oral Dosing 400 mg of moxifloxacin is administered orally to Mr BB, a 68 yr old male who weighs 75 kg. Blood samples were drawn following.
Area under the plasma concentration time curve. IMPORTANCE OF AUC Pharmacokinetics - measurement of bioavaibility absolute, relative Biopharmaceutics.
One Compartment Open Model IV bolus
The General Concepts of Pharmacokinetics and Pharmacodynamics
Noncompartmental Models. Introduction The noncompartmental approach for data analysis does not require any specific compartmental model for the system.
Clinical Pharmacokinetics Fundamental hypothesis: a relationship exists between the pharmacological or toxic response to a drug and the accessible concentration.
Continuous intravenous infusion (one-compartment model)
Pharmacokinetics of Drug Absorption Dr. Basavaraj K. Nanjwade M. Pharm., Ph. D Department of Pharmaceutics Faculty of Pharmacy Omer Al-Mukhtar University.
Multicompartment Models
ــــــــــــــ February 17 th, PHT - LECTURE Mathematical Fundamental in Pharmacokinetics Dr. Ahmed Alalaiwe.
The General Concepts of Pharmacokinetics and Pharmacodynamics
Time Plasma Conc (hr) (mg/L) Below limit of detection 1 Compartment IV Analysis & Renal Elimination 500 mg of tobramycin.
415 PHT Plasma Level – Time Curve
Pharmacokinetics 3rd Lecture

Compartmental Models and Volume of Distribution
Allie punke Pharmacokinetics tutoring Fall 2016
Physiology for Engineers
Pharmacology Phone Number: (203)
Allie punke Pharmacokinetics tutoring Fall 2016
Chapter 8 BIOAVAILABILITY & BIOEQUIVALENCE
Lecture-8 Biopharmaceutics
Pharmacokinetic Modeling (describing what happens)
CONCEPT OF PHARMACOKINETICS- ONE COMPARTMENT MODEL
Applications of Pharmacokinetics
Chapter 1 Introduction to Biopharmaceutics & Pharmacokinetics
BTP3822 BIOPHARMACEUTICS by
Lab-3 practical pharmacology
Quantitative Pharmacokinetics
Pharmaceutics 2.
Kinetics, Modeling Oct 19, 2009 Casarett and Doull,
به نام خدا فارماکوکینتیک نیمسال دوم دکتر ساسان زائری
Dosimetry and Kinetics
Kinetics, Modeling Oct 15, 2006 Casarett and Doull,
School of Pharmacy, University of Nizwa
Hawler Medical University
Selected Bioavailability and Pharmacokinetic Calculations
Biopharmaceutics Chapter-6
Hawler Medical University
School of Pharmacy, University of Nizwa
Therapeutic Drug Monitoring chapter 1 part 1
Clinical Pharmacokinetics
Presentation transcript:

Chapter 7 COMPARTMENT MODELS by Dr. Arshad Ali Khan Faculty of Engineering Technology arshad@ump.edu.my

Topic outcomes Classify to open compartmental models Discuss the non-compartmental models

One compartment

One compartment

More than one compartment

More than one compartment

One compartment open model It is a simple way to explain the drug distribution and elimination in the body. In this model, the body assumes as a single uniform compartment in which drug can enter and exit the body. The intravenous injection (IV bolus) is a easiest route of administration for the modeling prospective. The drug elimination starts from the body (compartment) suddenly after the injection.

One compartment: IV bolus administration (dose = X0) Drug amount in the Body (DB) IV bolus administration (dose = X0) Elimination process Elimination rate constant (K) Based on the assumption of first order elimination process:

Elimination rate constant (K) Elimination rate constant tells about the amount of drug eliminate per unit of time K has a unit of reciprocal of time such as minute-1.

Elimination Rate Constant D B = drug inside the body after time t and D B 0 = drug inside the body at t = 0. When log D B is plotted against t for this equation, a straight line is obtained Rate expression: Semilog graph showing the rate of drug elimination in one compartment model

Apparent Volume of Distribution (Vd) In general, drug equilibrates rapidly in the body. When plasma or any other biologic compartment is sampled and analyzed for drug content, the results are usually reported in units of concentration instead of amount Each individual tissue in the body may contain a different concentration of drug due to differences in drug affinity for that tissue. Therefore, the amount of drug in a given location can be related to its concentration by a proportionality constant that reflects the volume of fluid the drug is dissolved in The volume of distribution represents a volume that must be considered in estimating the amount of drug in the body from the concentration of drug found in the sampling compartment

The real Volume of Distribution has physiological meaning and is related to body water Total body water 42 L Plasma Plasma volume 4 L Interstitial fluid Interstitial fluid volume 10 L Intracellular fluid Intracellular fluid volume 28 L

Apparent Volume of Distribution: Mathematics In order to determine the Vd of a drug, it is necessary to have plasma/serum concentration versus time data where C p = concentration of drug in plasma t = t C p 0 = concentration of drug in plasma at t = 0

Calculation of Volume of Distribution Semilog graph giving the value of C p0 .

The The apparent V D can be estimated from the dose (D0) at time t=0, elimination rate constant (k), and the area under the curve (AUC) from t = 0 to t = ∞.

Elimination half life (t1/2) Elimination half life (t1/2) is a time at which the amount of bioavailable drug become 50% (half) of the initial amount of the bioavailable drug.

Elimination half life (t1/2) estimation Two methods: From the value of K: Directly from Conc vs. time plot Select a concentration on the best fit line (C1) Look for the time that is needed to get to 50% of C1  half-life

Clearance (Cl) Clearance is a the measurement of the depletion of drug from the body The drug half life can be determined by drug Cl and Vd For One compartment pharmacokinetics , clearance is calculated using:

Area Under the Conc. Time Curve (AUC) calculation Two methods: Model dependent: can be used only for one compartment IV bolus Model independent: Can be used for any drug with any route of administration

AUC calculation: Model dependent For intravenous drug administration following first order elimination in one compartment model, the AUC can be estimated using:

AUC calculation: Model independent

AUC calculation: Model independent 1- Divide the area into different parts based on the observed concentration points (parts 1-5) 1 2 3 4 5

AUC calculation: Model independent 2- Calculate the area for each part of the parts 1,2,3 and 4 (until the last observed concentration) using trapezoidal rule 1 2 3 4 5

Trapezoidal rule C1 C2 where C = concentration t = time t1 t2

AUC calculation: Model independent 3- For part 5 (area between the last observed concentration and infinity) use the following equation: C*

AUC calculation: Model independent 4- The total AUC (from zero to infinity) is the sum of the areas of parts: 1,2,3,4, and 5 1 2 3 4 5

Thank you