10/13/20151Prof. Mazen Qato. OBJECTIVES 10/13/2015Prof. Mazen Qato2.

Slides:



Advertisements
Similar presentations
Clinical Pharmacokinetics
Advertisements

PHARMACOKINETIC.
DISPOSITION OF DRUGS The disposition of chemicals entering the body (from C.D. Klaassen, Casarett and Doull’s Toxicology, 5th ed., New York: McGraw-Hill,
6/10/20151Prof. Mazen Qato. Objectives At the end of this sessions students should be able to: 1. List and discuss common routes of drug administration.
Selected bioavailability and pharmacokinetic calculations Dr. Osama A. A. Ahmed.
IV Flow Rates –BASED ON BODY WEIGHT
Calculating Heparin Bolus Dosage and IV Rate
One-compartment open model: Intravenous bolus administration
Asmah Nasser, M.D. Pharmacokinetics.
Week 3 - Biopharmaceutics and Pharmacokinetics
Laplace transformation
Pharmacokinetics Based on the hypothesis that the action of a drug requires presence of a certain concentration in the fluid bathing the target tissue.
Dose Adjustment in Renal and Hepatic Disease
Toxicokinetic Calculations
Dosing Regimen Design Infusion regimen.
INTRAVENOUS INFUSION.
Pharmacology Department
Excretion of Drugs By the end of this lecture, students should be able to Identify main and minor routes of Excretion including renal elimination and biliary.
VM 8314 Dr. Jeff Wilcke Pharmacokinetic Modeling (describing what happens)
CLEARANCE CONCEPTS Text: Applied Biopharm. & PK
CLEARANCE (CL) describes the efficiency of irreversible elimination of a drug from the body by excretion of unchanged drug. Metabolic conversion of the.
PHARMACOKINETICS 1. Fate of drugs in the body 1.1 absorption
Objective: Explain the variation in dosing intervals for medications 1)Introduce Half-Life (t 1/2 ) 2)Relate Half-Life to Dosing intervals of aspirin and.
Pharmacokinetics Introduction
Lecture 2.  Clearance Ability to eliminate the drug  Volume of distribution (Vd) The measure of the apparent space in the body available to contain.
From A Physiologic Perspective Chemical Clearance from the Body
PLASMA HALF LIFE ( t 1/2 ).  Minimum Effective Concentration (MEC): The plasma drug concentration below which a patient’s response is too small for clinical.
Pharmacology Department
PHARMACOKINETIC MODELS
Drug Administration Pharmacokinetic Phase (Time course of ADME processes) Absorption Distribution Pharmaceutical Phase Disintegration of the Dosage Form.
BASIC PHARMACOLOGY 2 SAMUEL AGUAZIM(MD).
One Compartment Open Model IV bolus
Intravenous Infusion Previous rates of administration were instantaneous IV bolus and first order absorption. As a rate (mg/hr) a first order rate constantly.
The General Concepts of Pharmacokinetics and Pharmacodynamics
Multiple dosing: intravenous bolus administration
1 Single-dose kinetics Plasma [Drug] curve Upon administration [drug] plasma reaches a max Then begins to decline as the Drug is eliminated Cp max = max.
Clinical Pharmacokinetics Fundamental hypothesis: a relationship exists between the pharmacological or toxic response to a drug and the accessible concentration.
1. Fate of drugs in the body 1.1 absorption 1.2 distribution - volume of distribution 1.3 elimination - clearance 2. The half-life and its uses 3. Repeated.
Continuous intravenous infusion (one-compartment model)
PHARMACOKINETICS Definition: quantitative study of drug absorption, distribution, metabolism, and excretion (ADME), and their mathematical relationship.
BIOPHARMACEUTICS.
Principles of pharmacokinetics Prof. Kršiak Department of Pharmacology, Third Faculty of Medicine, Charles University in Prague Cycle II, Subject: General.
DEFINITIONS T1/2 & Tmax Cmax AUC 1st order kinetics
The General Concepts of Pharmacokinetics and Pharmacodynamics
Learning objectives To know what data is available from pharmacokinetic studies in man and how to handle it To know how to calculate the basic pharmacokinetic.
Practice Problems Biopharmaceutics-I.
Source: Frank M. Balis Concentration and Effect vs. Time Conc./ Amount Effect [% of E MAX ] Time Central Compartment Peripheral Compartment Effect Compartment.
Compartmental Models and Volume of Distribution
Allie punke Pharmacokinetics tutoring Fall 2016
Allie punke Pharmacokinetics tutoring Fall 2016
Pharmacokinetics Tutoring
Lecture-8 Biopharmaceutics
Allie punke Pharmacokinetics tutoring Fall 2016
Pharmacokinetic Modeling (describing what happens)
CLINICAL APPLICATION OF UNDERSTANDING MECHANISMS OF ACTION (EXAMPLE)
Lab-3 practical pharmacology
Pharmaceutics 2.
Kinetics, Modeling Oct 19, 2009 Casarett and Doull,
Kinetics, Modeling Oct 15, 2006 Casarett and Doull,
School of Pharmacy, University of Nizwa
Clinical Pharmacokinetics
Hawler Medical University
Selected Bioavailability and Pharmacokinetic Calculations
1 Concentration-time curve
School of Pharmacy, University of Nizwa
Therapeutic Drug Monitoring chapter 1 part 1
1-C: Renal and Hepatic Elimination
Project #1: Drug Kinetics in Genetically Modified Mice
Presentation transcript:

10/13/20151Prof. Mazen Qato

OBJECTIVES 10/13/2015Prof. Mazen Qato2

10/13/20153Prof. Mazen Qato

Basic PK Definitions and Principles  Volume of distribution (Vd)  Elimination constant (Ke) and half-life (t1/2)  “Steady state”  Loading dose

Volume of Distribution A proportional constant that relates the amount of drug in the body to the serum concentration If you know a drug’s Vd, you can determine how much of the drug should be given to achieve a desired plasma concentration.

10/13/20156Prof. Mazen Qato

Vd = Dose/C O Co= CONCETRATION OF DRUG AT ZERO TIME -If you know the dose and the peak plasma concentration, you can calculate the patients Vd. -If you know the Vd and have a goal plasma concentration, you can calculate the dose

FACTORS AFFECTING THE RATE OF DRUG DISTRIBUTION 1. LIPID SOLUBILITY (Kp) 2. IONISATION CONSTANT 3. MOLECULAR WEIGHT 4. BLOOD FLOW 10/13/2015Prof. Mazen Qato8

FACTORS AFFECTING THE EXTENT OF DRUG DISTRIBUTATION 10/13/2015Prof. Mazen Qato9

10/13/201510Prof. Mazen Qato

10/13/201511Prof. Mazen Qato

10/13/201512Prof. Mazen Qato

10/13/201513Prof. Mazen Qato

10/13/201514Prof. Mazen Qato

10/13/201515Prof. Mazen Qato

10/13/201516Prof. Mazen Qato

10/13/201517Prof. Mazen Qato

THANK YOU 10/13/2015Prof. Mazen Qato18