PHAR 7633 Chapter 20 Non Compartmental Analysis

Size: px
Start display at page:

Download "PHAR 7633 Chapter 20 Non Compartmental Analysis"

Transcription

1 Student Objectives for this Chapter PHAR 7633 Chapter 20 Non Compartmental Analysis To understand and use the non compartmental approach to parameter estimation be able to define, use, and calculate the parameters: AUMC (area under the first moment curve) MRT (mean residence time) MAT (mean absorption time) MDT (mean dissolution time) Non Compartmental Analysis Non compartmental methods can be used to determine certain pharmacokinetic parameters without deciding on a particular compartmental model. The basic calculations are based on the area under the plasma concentration versus times curve (zero moment) and the first moment curve (AUMC). The AUC can be calculated as before using the trapezoidal rule. The first moment is calculated as concentration times time (Cp t). The AUMC is the area under the concentration times time versus time curve. Maybe best covered with an example. Consider a drug given both by IV and oral administration. Both the AUC and AUMC were calculated using the trapezoidal rule without making any assumption concerning the number of compartments. The final segment of the AUC curve is calculated as Cp(last)/k', where k' is the last exponential term (the slowest) calculated from the Cp versus time graph. The last segment for the AUMC curve is: Equation Equation of the last segment AUMC Page 1 of 8

2 Time (hr) Cp (mg/l) Cp t (mg.hr/l) AUC (mg.hr/l) AUMC (mg.hr 2 /L) Table Typical Cp versus Time Data after 100 mg IV Bolus Administration These data, Cp versus time and Cp x time versus time, can be plotted on linear graph. Page 2 of 8

3 Figure Plot of Cp versus Time (IV) and various parameters can be calculated as: Figure Plot of Cp x Time versus Time (IV) Equation Equation for Mean Residence Time (MRT) Equation Equation for Apparent Elimination Rate constant (kel') Page 3 of 8

4 Equation Equation for Total Body Clearance (TBC) Equation Equation for Apparent Volume of Distribution, Steady State (V ss ) From the AUC and AUMC values we can calculate the mean residence time, MRT. This is the average time that the drug stays in the body (or plasma as measured here). It can be related to the average elimination rate constant as 1/MRT. The values from the above data are MRT = /67.27 = 8.17 hr and kel' = 1/8.17 = 0.12 hr -1 Remember we can also calculate the clearance, CL = Dose/AUC = 100/67.27 = 1.49 L.hr -1 Finally a steady state volume can be calculated as V ss = CL MRT = 1.49 x 8.17 = L Page 4 of 8

5 Oral data can be analyzed by these methods as well. Time (hr) Cp (mg/l) Cp t (mg.hr/l) AUC (mg.hr/l) AUMC (mg.hr 2 /L) Table Typical Cp versus Time Data after 250 mg Oral Administration These data, Cp versus time and Cp x time versus time, can be plotted on linear graph. Figure Plot of Cp versus Time (PO) Page 5 of 8

6 Figure Plot of Cp x Time versus Time (PO) and additional parameters can be calculated (NOTE: We don't calculate Clearance or V ss using oral data). Equation Equation for Mean Absorption Time (MAT) Equation Equation for Apparent Absorption Rate Constant (ka') Equation Equation for Oral Bioavailability (F) The data were calculated after a 250 mg oral dose of the same drug. From these data a MRT was calculated as MRT = AUMC/AUC = 1361/149.8 = 9.08 hr We can subtract from this MRT(PO) the MRT(IV) to get an idea of the absorption process, the mean absorption time (MAT). That is MAT = MRT(PO) - MRT(IV) = = 0.92 hr From this we can calculate an average absorption rate constant ka' = 1/MAT = 1/0.92 = 1.09 hr -1 Of course we can calculate the bioavailability of the oral dosage form using the dose adjusted AUC ratio. Thus F = (149.70/67.27) x (100/250) = 0.89 Page 6 of 8

7 Another Example using Data from Bevill et al Pharmacokinetics of Sulfamethazine in Cattle following IV and Three Oral Dosage Forms Dosage Forms IV Bolus 107 mg/kg Oral Solution 107 mg/kg Oral Rapid Release Tablet 105 mg/kg Oral Sustained Release Tablet 249 mg/kg Figure The Average Data from Each Dosage Form AUC AUMC MRT (hr) MAT (hr) MDT (hr) IV Solution Tablet Slow Tablet Table Non Compartmental Analysis Results Rate Constant (hr -1 ) Non Linear Regression Analysis Non Compartmental Analysis kel' ka' kd' (fast) kd' (slow) Table Comparison with Non Linear Regression Analysis (SAAM) Page 7 of 8

8 Non compartmental analysis: kel' = 1/MRT ka' = 1/MAT kd' = 1/MDT where MDT is the mean dissolution time Want more practice with this type of problem! References Bevill, R.F., Dittert, L.W. and Bourne, D.W.A Pharmacokinetics of Sulfamethazine in Cattle following IV and Three Oral Dosage Forms, J. Pharm. Sci., 66, This page ( was last modified: Wednesday 26 May 2010 at 09:00 AM Material on this website should be used for Educational or Self-Study Purposes Only Copyright David W. A. Bourne (david@boomer.org) Page 8 of 8

1. If the MTC is 100 ng/ml and the MEC is 0.12 ng/ml, which of the following dosing regimen(s) are in the therapeutic window?

1. If the MTC is 100 ng/ml and the MEC is 0.12 ng/ml, which of the following dosing regimen(s) are in the therapeutic window? Page 1 PHAR 750: Biopharmaceutics/Pharmacokinetics October 23, 2009 - Form 1 Name: Total 100 points Please choose the BEST answer of those provided. For numerical answers, choose none of the above if your

More information

BASIC PHARMACOKINETICS

BASIC PHARMACOKINETICS BASIC PHARMACOKINETICS MOHSEN A. HEDAYA CRC Press Taylor & Francis Croup Boca Raton London New York CRC Press is an imprint of the Taylor & Francis Group, an informa business Table of Contents Chapter

More information

PHA Final Exam Fall 2006

PHA Final Exam Fall 2006 PHA 5127 Final Exam Fall 2006 On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name Please transfer the answers onto the bubble sheet. The question number refers

More information

Nontraditional PharmD Program PRDO 7700 Pharmacokinetics Review Self-Assessment

Nontraditional PharmD Program PRDO 7700 Pharmacokinetics Review Self-Assessment Nontraditional PharmD Program PRDO 7700 Pharmacokinetics Review Self-Assessment Please consider the following questions. If you do not feel confident about the material being covered, then it is recommended

More information

PHA Final Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment.

PHA Final Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment. PHA 5127 Final Exam Fall 2012 On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name Please transfer the answers onto the bubble sheet. The question number refers

More information

General Principles of Pharmacology and Toxicology

General Principles of Pharmacology and Toxicology General Principles of Pharmacology and Toxicology Parisa Gazerani, Pharm D, PhD Assistant Professor Center for Sensory-Motor Interaction (SMI) Department of Health Science and Technology Aalborg University

More information

PHAR 7632 Chapter 16

PHAR 7632 Chapter 16 PHAR 7632 Chapter 16 Routes of Excretion Routes of Excretion Student Objectives for this Chapter After completing the material in this chapter each student should:- be able to describe the various routes

More information

Basic Pharmacokinetic Principles Stephen P. Roush, Pharm.D. Clinical Coordinator, Department of Pharmacy

Basic Pharmacokinetic Principles Stephen P. Roush, Pharm.D. Clinical Coordinator, Department of Pharmacy Basic Pharmacokinetic Principles Stephen P. Roush, Pharm.D. Clinical Coordinator, Department of Pharmacy I. General principles Applied pharmacokinetics - the process of using drug concentrations, pharmaco-kinetic

More information

We are IntechOpen, the world s leading publisher of Open Access books Built by scientists, for scientists. International authors and editors

We are IntechOpen, the world s leading publisher of Open Access books Built by scientists, for scientists. International authors and editors We are IntechOpen, the world s leading publisher of Open Access books Built by scientists, for scientists 3,900 116,000 120M Open access books available International authors and editors Downloads Our

More information

PHA 5127 FINAL EXAM FALL On my honor, I have neither given nor received unauthorized aid in doing this assignment.

PHA 5127 FINAL EXAM FALL On my honor, I have neither given nor received unauthorized aid in doing this assignment. PHA 5127 FINAL EXAM FALL 1997 On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name Question Points 1. /14 pts 2. /10 pts 3. /8 pts 4 /8 pts 5. /12 pts 6. /8 pts

More information

Multiple IV Bolus Dose Administration

Multiple IV Bolus Dose Administration PHARMACOKINETICS Multiple IV Bolus Dose Administration ١ Multiple IV Bolus Dose Administration Objectives: 1) To understand drug accumulation after repeated dose administration 2) To recognize and use

More information

Osnove farmakokinetike. Aleš Mrhar. Prirejeno po. A First Course in Pharmacokinetics and Biopharmaceutics by David Bourne,

Osnove farmakokinetike. Aleš Mrhar. Prirejeno po. A First Course in Pharmacokinetics and Biopharmaceutics by David Bourne, Osnove farmakokinetike Aleš Mrhar Prirejeno po A First Course in Pharmacokinetics and Biopharmaceutics by David Bourne, College of Pharmacy, University of Oklahoma Pharmacokinetics/Pharmacodynamics Pharmacodynamics

More information

Flecainide pharmacokinetics in healthy volunteers: the influence of urinary ph

Flecainide pharmacokinetics in healthy volunteers: the influence of urinary ph Br. J. clin. Pharmac. (1985), 20, 333-338 Flecainide pharmacokinetics in healthy volunteers: the influence of urinary ph A. JOHNSTON, S. WARRNGTON' & P. TURNER Department of Clinical Pharmacology, St Bartholomew's

More information

BIOPHARMACEUTICS and CLINICAL PHARMACY

BIOPHARMACEUTICS and CLINICAL PHARMACY 11 years papers covered BIOPHARMACEUTICS and CLINICAL PHARMACY IV B.Pharm II Semester, Andhra University Topics: Absorption Distribution Protein binding Metabolism Excretion Bioavailability Drug Interactions

More information

PHA Second Exam Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment.

PHA Second Exam Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment. PHA 5127 Second Exam Fall 2013 On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name Question/Points Set I 20 pts Set II 20 pts Set III 20 pts Set IV 20 pts Set

More information

PHA Spring First Exam. 8 Aminoglycosides (5 points)

PHA Spring First Exam. 8 Aminoglycosides (5 points) PHA 5128 Spring 2012 First Exam 1 Aminoglycosides (5 points) 2 Aminoglycosides (10 points) 3 Basic Principles (5 points) 4 Basic Principles (5 points) 5 Bioavailability (5 points) 6 Vancomycin (5 points)

More information

Biomath M263 Clinical Pharmacology

Biomath M263 Clinical Pharmacology Training Program in Translational Science Biomath M263 Clinical Pharmacology Spring 2013 www.ctsi.ucla.edu/education/training/webcasts Wednesdays 3 PM room 17-187 CHS 4/3/2013 Pharmacokinetics and Pharmacodynamics

More information

Basic Pharmacokinetics and Pharmacodynamics: An Integrated Textbook with Computer Simulations

Basic Pharmacokinetics and Pharmacodynamics: An Integrated Textbook with Computer Simulations Basic Pharmacokinetics and Pharmacodynamics: An Integrated Textbook with Computer Simulations Rosenbaum, Sara E. ISBN-13: 9780470569061 Table of Contents 1 Introduction to Pharmacokinetics and Pharmacodynamics.

More information

PHA Second Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment.

PHA Second Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment. PHA 5127 Second Exam Fall 2011 On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name Put all answers on the bubble sheet TOTAL /200 pts 1 Question Set I (True or

More information

PHARMACOKINETICS SMALL GROUP II:

PHARMACOKINETICS SMALL GROUP II: PHARMACOKINETICS SMALL GROUP II: Question 1 Why are some drug therapies initiated with a loading dose? Emphasize that LD establishes initial therapeutic level quickly. The time to reach the steady-state

More information

PHARMACOKINETICS SMALL GROUP I:

PHARMACOKINETICS SMALL GROUP I: PHARMACOKINETICS SMALL GROUP I: Question 1 Absorption of the anti-fungal agent, itraconazole, is dependent on a low gastric ph. Calculate the relative concentrations of a weak acid (with a pka of 5.4)

More information

PHARMACOKINETICS OF DRUG ABSORPTION

PHARMACOKINETICS OF DRUG ABSORPTION Print Close Window Note: Large images and tables on this page may necessitate printing in landscape mode. Applied Biopharmaceutics & Pharmacokinetics > Chapter 7. Pharmacokinetics of Oral Absorption >

More information

Pharmacokinetics Overview

Pharmacokinetics Overview Pharmacokinetics Overview Disclaimer: This handout and the associated lectures are intended as a very superficial overview of pharmacokinetics. Summary of Important Terms and Concepts - Absorption, peak

More information

Name: UFID: PHA Exam 2. Spring 2013

Name: UFID: PHA Exam 2. Spring 2013 PHA 5128 Exam 2 Spring 2013 1 Carbamazepine (5 points) 2 Theophylline (10 points) 3 Gentamicin (10 points) 4 Drug-drug interaction (5 points) 5 Lidocaine (5 points) 6 Cyclosporine (5 points) 7 Phenobarbital

More information

PHA 4120 Second Exam Key Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment.

PHA 4120 Second Exam Key Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment. PHA 4120 Second Exam Key Fall 1997 On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name Question Points 1. /10 ponts 2. /20 points 3. /10 points 4. /10 points

More information

Biopharmaceutics Lecture-11 & 12. Pharmacokinetics of oral absorption

Biopharmaceutics Lecture-11 & 12. Pharmacokinetics of oral absorption Biopharmaceutics Lecture-11 & 12 Pharmacokinetics of oral absorption The systemic drug absorption from the gastrointestinal (GI) tract or from any other extravascular site is dependent on 1. 2. 3. In the

More information

PHA Final Exam Fall 2001

PHA Final Exam Fall 2001 PHA 5127 Final Exam Fall 2001 On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name Question/Points 1. /12 pts 2. /8 pts 3. /12 pts 4. /20 pts 5. /27 pts 6. /15

More information

Nonlinear Pharmacokinetics

Nonlinear Pharmacokinetics Nonlinear Pharmacokinetics Non linear pharmacokinetics: In some cases, the kinetics of a pharmacokinetic process change from predominantly first order to predominantly zero order with increasing dose or

More information

PHA5128 Dose Optimization II Case Study I Spring 2013

PHA5128 Dose Optimization II Case Study I Spring 2013 Silsamicin is an investigational compound being evaluated for its antimicrobial effect. The route of administration for this drug is via intravenous bolus. Approximately 99.9% of this drug is eliminated

More information

Pharmacokinetics of ibuprofen in man. I. Free and total

Pharmacokinetics of ibuprofen in man. I. Free and total Pharmacokinetics of ibuprofen in man. I. Free and total area/dose relationships Ibuprofen kinetics were studied in 15 subjects after four oral doses. Plasma levels of both total and free ibuprofen were

More information

Clinical Pharmacology. Pharmacodynamics the next step. Nick Holford Dept Pharmacology & Clinical Pharmacology University of Auckland, New Zealand

Clinical Pharmacology. Pharmacodynamics the next step. Nick Holford Dept Pharmacology & Clinical Pharmacology University of Auckland, New Zealand 1 Pharmacodynamic Principles and the Course of Immediate Drug s Nick Holford Dept Pharmacology & Clinical Pharmacology University of Auckland, New Zealand The time course of drug action combines the principles

More information

Thus, we can group the entire loading dose together as though it was given as a single dose, all administered when the first dose was given.

Thus, we can group the entire loading dose together as though it was given as a single dose, all administered when the first dose was given. PHA 5128 Dose Optimization II, Spring 2012, Case Study V Solution If you have any questions regarding this case study, do not hesitate to contact Benjamin Weber (benjaminweber@ufl.edu). Please remember

More information

Pharmacokinetic Calculations

Pharmacokinetic Calculations Pharmacokinetic Calculations Introduction. Pharmacokinetics involves the relationship between concentration of drug (and its metabolites), measured most often in plasma, drug dosage, and time. A vast majority

More information

Carbamazepine has a clearance of L/h/kg for monotherapy. For immediate release carbamazepine, the oral bioavailbility is 0.8

Carbamazepine has a clearance of L/h/kg for monotherapy. For immediate release carbamazepine, the oral bioavailbility is 0.8 PHA 5128 Dose Optimization II, Spring 2013, Case Study IV Solution If you have any questions regarding this case study, do not hesitate to contact Benjamin Weber (benjaminweber@ufl.edu). Please remember

More information

Pharmacokinetics Applied to the Treatment of Asthma

Pharmacokinetics Applied to the Treatment of Asthma Pharmacokinetics Applied to the Treatment of Asthma 2016 edition by David C. McMillan, PhD Department of Pharmacology and Experimental Neuroscience College of Medicine University of Nebraska Medical Center

More information

Basic Concepts of TDM

Basic Concepts of TDM TDM Lecture 1 5 th stage What is TDM? Basic Concepts of TDM Therapeutic drug monitoring (TDM) is a branch of clinical pharmacology that specializes in the measurement of medication concentrations in blood.

More information

One-Compartment Open Model: Intravenous Bolus Administration:

One-Compartment Open Model: Intravenous Bolus Administration: One-Compartment Open Model: Intravenous Bolus Administration: Introduction The most common and most desirable route of drug administration is orally by mouth using tablets, capsules, or oral solutions.

More information

Lippincott Questions Pharmacology

Lippincott Questions Pharmacology Lippincott Questions Pharmacology Edition Two: Chapter One: 1.Which one of the following statements is CORRECT? A. Weak bases are absorbed efficiently across the epithelial cells of the stomach. B. Coadministration

More information

In vitro and in vivo deconvolution assessment of drug release kinetics from oxprenolol Oros preparations

In vitro and in vivo deconvolution assessment of drug release kinetics from oxprenolol Oros preparations Br. J. clin. Pharmac. (1985), 19, 151S-162S In vitro and in vivo deconvolution assessment of drug release kinetics from oxprenolol Oros preparations F. LANGENBUCHER & J. MYSICKA Pharmaceutical Development,

More information

Determination of bioavailability

Determination of bioavailability Pharmaceutics 2 Bioavailability Bioavailability is the rate and extent to which an administered drug reaches the systemic circulation. For example, if 100 mg of a drug is administered orally and 70 mg

More information

PHA Final Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment.

PHA Final Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment. PHA 5127 Final Exam Fall 2010 On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name Please transfer the answers onto the bubble sheet. The question number refers

More information

LD = (Vd x Cp)/F (Vd x Cp)/F MD = (Css x CL x T)/F DR = (Css x (Vm-DR))/Km Css = (F x D)/(CL x T) (Km x DR)/(Vm DR)

LD = (Vd x Cp)/F (Vd x Cp)/F MD = (Css x CL x T)/F DR = (Css x (Vm-DR))/Km Css = (F x D)/(CL x T) (Km x DR)/(Vm DR) PHARMKIN WORKSHOP A PHARMACOKINETICS TEACHING SIMULATION Joseph K. Ritter, Ph.D. Associate Professor, Pharmacology and Toxicology MSB 536, 828-1022, jritter@mail2.vcu.edu Tompkins-McCaw Libray Room 2-006

More information

Pharmacodynamic principles and the time course of immediate drug effects

Pharmacodynamic principles and the time course of immediate drug effects TCP 2017;25(4):157-161 http://dx.doi.org/10.12793/tcp.2017.25.4.157 Pharmacodynamic principles and the time course of immediate drug effects TUTORIAL Department of Pharmacology & Clinical Pharmacology,

More information

CLINICAL PHARMACOKINETICS INDEPENDENT LEARNING MODULE

CLINICAL PHARMACOKINETICS INDEPENDENT LEARNING MODULE CLINICAL PHARMACOKINETICS INDEPENDENT LEARNING MODULE Joseph K. Ritter, Ph.D. Assoc. Professor, Pharmacology and Toxicology MSB 536, 828-1022, jritter@vcu.edu This self study module will reinforce the

More information

TDM. Measurement techniques used to determine cyclosporine level include:

TDM. Measurement techniques used to determine cyclosporine level include: TDM Lecture 15: Cyclosporine. Cyclosporine is a cyclic polypeptide medication with immunosuppressant effect. It has the ability to block the production of interleukin-2 and other cytokines by T-lymphocytes.

More information

Guideline for Bioequivalence Studies of Generic Products

Guideline for Bioequivalence Studies of Generic Products English translation of Attachment 1 of Division-tification 0229. 10 of the Pharmaceutical and Food Safety Bureau, dated February 29, 2012 Guideline for Bioequivalence Studies of Generic Products Index

More information

DEVELOPMENT OF IN VITRO-IN VIVO CORRELATION FOR ENCAPSULATED METOPROLOL TARTRATE

DEVELOPMENT OF IN VITRO-IN VIVO CORRELATION FOR ENCAPSULATED METOPROLOL TARTRATE Acta Poloniae Pharmaceutica ñ Drug Research, Vol. 70 No. 4 pp. 743ñ747, 2013 ISSN 0001-6837 Polish Pharmaceutical Society DEVELOPMENT OF IN VITRO-IN VIVO CORRELATION FOR ENCAPSULATED METOPROLOL TARTRATE

More information

Principles of Toxicokinetics/Toxicodynanics

Principles of Toxicokinetics/Toxicodynanics Biochemical and Molecular Toxicology ENVR 442; TOXC 442; BIOC 442 Principles of Toxicokinetics/Toxicodynanics Kim L.R. Brouwer, PharmD, PhD kbrouwer@unc.edu; 919-962-7030 Pharmacokinetics/ Toxicokinetics:

More information

. Although there is a little

. Although there is a little PHA 58 Spring 007 Case study 4. Baby girl A, 3kg, 5 days, is receiving phenobarbital because of neonatal seizures. An IV loading dose of phenobarbital sodium of 0mg/kg was given followed by maintenance

More information

C OBJECTIVES. Basic Pharmacokinetics LESSON. After completing Lesson 2, you should be able to:

C OBJECTIVES. Basic Pharmacokinetics LESSON. After completing Lesson 2, you should be able to: LESSON 2 Basic Pharmacokinetics C OBJECTIVES After completing Lesson 2, you should be able to: 1. Define the concept of apparent volume of distribution and use an appropriate mathematical equation to calculate

More information

Pharmacokinetics of drug infusions

Pharmacokinetics of drug infusions SA Hill MA PhD FRCA Key points The i.v. route provides the most predictable plasma concentrations. Pharmacodynamic effects of a drug are related to plasma concentration. Both plasma and effect compartments

More information

NONLINEAR PHARMACOKINETICS: INTRODUCTION

NONLINEAR PHARMACOKINETICS: INTRODUCTION Print Close Window Note: Large images and tables on this page may necessitate printing in landscape mode. Applied Biopharmaceutics & Pharmacokinetics > Chapter 9. Nonlinear Pharmacokinetics > NONLINEAR

More information

Case Study 2 Answers Spring 2006

Case Study 2 Answers Spring 2006 Case Study 2 Answers Spring 2006 1. The volume of distribution of diazepam in a group of normal subjects (60 kg, ideal body weight) was found to be 105 L. In another group of patients (110 kg), the volume

More information

Understand the physiological determinants of extent and rate of absorption

Understand the physiological determinants of extent and rate of absorption Absorption and Half-Life Nick Holford Dept Pharmacology & Clinical Pharmacology University of Auckland, New Zealand Objectives Understand the physiological determinants of extent and rate of absorption

More information

Clinical Trials A Practical Guide to Design, Analysis, and Reporting

Clinical Trials A Practical Guide to Design, Analysis, and Reporting Clinical Trials A Practical Guide to Design, Analysis, and Reporting Duolao Wang, PhD Ameet Bakhai, MBBS, MRCP Statistician Cardiologist Clinical Trials A Practical Guide to Design, Analysis, and Reporting

More information

Chapter 5 Herb-Drug Interactions: Glibenclamide

Chapter 5 Herb-Drug Interactions: Glibenclamide 5. 5.1. Background Glibenclamide (GLI) is an oral hypoglycemic agent, belonging to the class of second generation sulfonylureas. Like all other sulfonylureas, it lowers the blood glucose by stimulating

More information

Take-Home Exam Distributed: October 16, 2013, at 1:30 p.m. Due: October 21, 2013, at 10:00 a.m.

Take-Home Exam Distributed: October 16, 2013, at 1:30 p.m. Due: October 21, 2013, at 10:00 a.m. 20.201 Take-Home Exam Distributed: October 16, 2013, at 1:30 p.m. Due: October 21, 2013, at 10:00 a.m. Directions: This take-home exam is to be completed without help from any other individual except:

More information

Vancomycin Pharmacokinetics in Normal and Morbidly Obese Subjects

Vancomycin Pharmacokinetics in Normal and Morbidly Obese Subjects ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, Apr. 1982, p. 575-58 66484/82/4575-6$2./ Vol. 21, No. 4 Vancomycin Pharmacokinetics in Normal and Morbidly Obese Subjects ROBERT A. BLOUIN,1 LARRY A. BAUER,3* DELWYN

More information

The general Concepts of Pharmacokinetics

The general Concepts of Pharmacokinetics The general Concepts of Pharmacokinetics What is this jargon? Is it useful? C max, clearance, Vd, half-life, AUC, bioavailability, protein binding F. Van Bambeke, E. Ampe, P.M. Tulkens (Université catholique

More information

Tutorial. & In case studies 1 and 2, we explore intravenous iv. & Then, we move on to extravascular dosing in case

Tutorial. & In case studies 1 and 2, we explore intravenous iv. & Then, we move on to extravascular dosing in case The AAPS Journal, Vol. 1, No. 1, January 2016 ( # 2015) DOI: 10.120/s1224-015-917-6 Tutorial Pattern Recognition in Pharmacokinetic Data Analysis Johan Gabrielsson, 1,4 Bernd Meibohm, 2 and Daniel Weiner

More information

Bioequivalence of Inhaled Corticosteroids. -with emphasis on Pharmacokinetic Tools.

Bioequivalence of Inhaled Corticosteroids. -with emphasis on Pharmacokinetic Tools. Bioequivalence of Inhaled Corticosteroids -with emphasis on Pharmacokinetic Tools? hochhaus@ufl.edu Topics related to Bioequivalence 10-60 % Deposited in lung Complete absorption from the lung Cl muc Mouth

More information

Introduction to. Pharmacokinetics. University of Hawai i Hilo Pre-Nursing Program NURS 203 General Pharmacology Danita Narciso Pharm D

Introduction to. Pharmacokinetics. University of Hawai i Hilo Pre-Nursing Program NURS 203 General Pharmacology Danita Narciso Pharm D Introduction to 1 Pharmacokinetics University of Hawai i Hilo Pre-Nursing Program NURS 203 General Pharmacology Danita Narciso Pharm D 2 Learning objectives Understand compartment models and how they effects

More information

Public Assessment Report. EU worksharing project paediatric data. Valcyte. Valganciclovir

Public Assessment Report. EU worksharing project paediatric data. Valcyte. Valganciclovir Public Assessment Report EU worksharing project paediatric data Valcyte Valganciclovir Currently approved indication(s): Pharmaceutical form(s) affected by this project: Strength(s) affected by this variation:

More information

Noncompartmental Analysis (NCA) in PK, PK-based Design

Noncompartmental Analysis (NCA) in PK, PK-based Design Noncompartmental Analysis (NCA) in PK, PK-based Design Helmut Schütz BEBAC Consultancy Services for Bioequivalence and Bioavailability Studies 17 Vienna, Austria helmut.schuetz@bebac.at Bioequivalence

More information

Pharmacokinetics One- compartment Open Model Lec:2

Pharmacokinetics One- compartment Open Model Lec:2 22 Pharmacokinetics One- compartment Open Model Lec:2 Ali Y Ali BSc Pharmacy MSc Industrial Pharmaceutical Sciences Dept. of Pharmaceutics School of Pharmacy University of Sulaimani 1 Outline Introduction

More information

PHA 5128 Spring 2009 First Exam (Version B)

PHA 5128 Spring 2009 First Exam (Version B) Name: UFID: PHA 5128 Spring 2009 First Exam (Version B) On my honor, I have neither given nor received unauthorized aid in doing this assignment. Print: Sign: Version B Q1: Phenytoin (10) Q2: procainamide

More information

Intrasubject Variation in Elimination Half-Lives of Drugs Which Are Appreciably Metabolized

Intrasubject Variation in Elimination Half-Lives of Drugs Which Are Appreciably Metabolized Journal of Pharmacokinetics and Biopharrnaceutics, Vol. 1, No. 2, 1973 SCIENTIFIC COMMENTARY Intrasubject Variation in Elimination Half-Lives of Drugs Which Are Appreciably Metabolized John G. Wagner 1

More information

PHA 5128 Final Exam Spring 2004 Version A. On my honor, I have neither given nor received unauthorized aid in doing this assignment.

PHA 5128 Final Exam Spring 2004 Version A. On my honor, I have neither given nor received unauthorized aid in doing this assignment. PHA 5128 Final Exam Spring 2004 Version A On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name There are 18 questions. Total /120 pts Final 2004 1 1. T.P., a 66-year-old,

More information

A Bioequivalence Study of an Albendazole Oral Suspension Produced in Iran and a Reference Product in Sheep

A Bioequivalence Study of an Albendazole Oral Suspension Produced in Iran and a Reference Product in Sheep A Bioequivalence Study of an Albendazole Oral Suspension Produced in Iran and a Reference Product in Sheep Ali Eslami, DVM, PhD 1 Ali Rassouli, DVM, PhD 2 Behnam Meshki, DVM, PhD 1 Gholam Reza Shams, BSc

More information

Comparing Methods for Once Daily Tobramycin Exposure Predictions in Children with Cystic Fibrosis

Comparing Methods for Once Daily Tobramycin Exposure Predictions in Children with Cystic Fibrosis Comparing Methods for Once Daily Tobramycin Exposure Predictions in Children with Cystic Fibrosis Stefanie HENNIG, Franziska STILLER, Beverly TEO, Christine STAATZ, Brisbane Cystic fibrosis (CF) & Once

More information

Determination of free interstitial concentrations of piperacillin tazobactam combinations by microdialysis

Determination of free interstitial concentrations of piperacillin tazobactam combinations by microdialysis Journal of Antimicrobial Chemotherapy (1998) 42, 769 778 Determination of free interstitial concentrations of piperacillin tazobactam combinations by microdialysis JAC Teresa Dalla Costa, Arno Nolting,

More information

ADAM, a hands-on patient simulator for teaching principles of drug disposition and compartmental pharmacokinetics

ADAM, a hands-on patient simulator for teaching principles of drug disposition and compartmental pharmacokinetics British Journal of Clinical Pharmacology PHARMACOKINETICS Br J Clin Pharmacol (2017) 83 2426 2449 2426 ADAM, a hands-on patient simulator for teaching principles of drug disposition and compartmental pharmacokinetics

More information

Pharmacokinetic Study of [Di (4-amino N-acetyl) phenoxy]methyl ketone as Compared to Paracetamol

Pharmacokinetic Study of [Di (4-amino N-acetyl) phenoxy]methyl ketone as Compared to Paracetamol Research Article Pharmacokinetic Study of [Di (4-amino N-acetyl) phenoxy]methyl ketone as Compared to Paracetamol *Bhavna Shah 1, Pravin Patil 1, Hirva Shah 2 1. Department of Chemistry, Veer Narmad South

More information

Use of PBPK in simulating drug concentrations in pediatric populations: Case studies of Midazolam and Gabapentin

Use of PBPK in simulating drug concentrations in pediatric populations: Case studies of Midazolam and Gabapentin Use of PBPK in simulating drug concentrations in pediatric populations: Case studies of Midazolam and Gabapentin WORKSHOP ON MODELLING IN PAEDIATRIC MEDICINES April 2008 Viera Lukacova, Ph.D. Walter Woltosz,

More information

General Principles of Pharmacology and Toxicology

General Principles of Pharmacology and Toxicology General Principles of Pharmacology and Toxicology Parisa Gazerani, Pharm D, PhD Assistant Professor Center for Sensory-Motor Interaction (SMI) Department of Health Science and Technology Aalborg University

More information

Gastrointestinal Transit and Drug Absorption

Gastrointestinal Transit and Drug Absorption February 2002 Biol. Pharm. Bull. 25(2) 149 164 (2002) 149 Review Gastrointestinal Transit and Drug Absorption Toshikiro KIMURA* and Kazutaka HIGAKI Faculty of Pharmaceutical Sciences, Okayama University,

More information

Bioavailability and Related Pharmacokinetics in Man of Orally Administered L-5-Hydroxytryptophan in Steady State

Bioavailability and Related Pharmacokinetics in Man of Orally Administered L-5-Hydroxytryptophan in Steady State Acra pharmacol. et roxicol. 1980, 46, 257-262. From the University Department of Neurology, the Research Laboratory for etabolic Disorders of the University Department of Clinical Chemistry, Aarhus Kornrnunehospital,

More information

PHA Second Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment.

PHA Second Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment. PHA 5127 Second Exam Fall 2010 On my honor, I have neither given nor received unauthorized aid in doing this assignment. Name Put all answers on the bubble sheet TOTAL /200 pts 1 Question Set I (True or

More information

Volume 1(3) May-June 2013 Page 351

Volume 1(3) May-June 2013 Page 351 ISSN: 2321-5674(Print) BIOAVAILABILITY: CRITERIA FOR APPROVING A DRUG PRODUCT FOR MARKETING Sandhya Singh 1, Faheem Ajmal Ansari 1, Shravan Paswan 2*, Rnjan Kumar Sharma 2, Alok Ranjan Gaur 3 1 Azad Institute

More information

PHARMACOKINETICS OF SULFAMETHAZINE IN BUFFALOES

PHARMACOKINETICS OF SULFAMETHAZINE IN BUFFALOES PHARMACOKINETICS OF SULFAMETHAZINE IN BUFFALOES F.H. Khan, M. Nawaz, S. Anwar-Ul-Hassan To cite this version: F.H. Khan, M. Nawaz, S. Anwar-Ul-Hassan. PHARMACOKINETICS OF SULFAMETHAZINE IN BUFFALOES. Annales

More information

These results are supplied for informational purposes only.

These results are supplied for informational purposes only. These results are supplied for informational purposes only. Prescribing decisions should be made based on the approved package insert in the country of prescription Sponsor/company: sanofi-aventis ClinialTrials.gov

More information

PHA5128 Dose Optimization II Case Study 3 Spring 2013

PHA5128 Dose Optimization II Case Study 3 Spring 2013 Use the vancomycin dosing nomogram table below: A female patient, 57 years of age, 5 6 in height and 100 in weight had an infection requiring vancomycin treatment. Her serum creatinine was 0.8 mg/d. What

More information

Noncompartmental Analysis (NCA) in PK, PK-based Design

Noncompartmental Analysis (NCA) in PK, PK-based Design Noncompartmental Analysis (NCA) in PK, PK-based Design Helmut Schütz BEBAC Bioequivalence and Bioavailability, Pre-Conference Workshop Ljubljana, 17 May 21 1 54 Bioequivalence History Surrogate of clinical

More information

TDM of Digoxin. Use of Digoxin Serum Concentrations to Alter Dosages

TDM of Digoxin. Use of Digoxin Serum Concentrations to Alter Dosages TDM Lecture 8 5 th Stage TDM of Digoxin Use of Digoxin Serum Concentrations to Alter Dosages Linear Pharmacokinetics Method This method is used in steady-state condition. We compute the new dose of digoxin

More information

Modeling and Simulation to Support Development and Approval of Complex Products

Modeling and Simulation to Support Development and Approval of Complex Products Modeling and Simulation to Support Development and Approval of Complex Products Mathangi Gopalakrishnan, MS, PhD Research Assistant Professor Center for Translational Medicine, School of Pharmacy, UMB

More information

Pharmacokinetics PCTH 325. Dr. Shabbits September 12, C t = C 0 e -kt. Learning Objectives

Pharmacokinetics PCTH 325. Dr. Shabbits September 12, C t = C 0 e -kt. Learning Objectives PCTH 325 Pharmacokinetics Dr. Shabbits jennifer.shabbits@ubc.ca September 12, 2013 Learning Objectives 1. Interpret Concentration vs graphs and use them to calculate half life and predict drug concentration

More information

Pharmacokinetics of Rifampicin in African Children Evaluation of the new WHO dosing guidelines

Pharmacokinetics of Rifampicin in African Children Evaluation of the new WHO dosing guidelines Pharmacokinetics of Rifampicin in African Children Evaluation of the new WHO dosing guidelines Paolo Denti, Carmen Gonzalez-Martinez, Jana Winckler, Adrie Bekker, Heather Zar, Gerry Davies, Annelies van

More information

Package NonCompart. August 16, 2017

Package NonCompart. August 16, 2017 Version 0.3.3 Date 2017-08-16 KST Package NonCompart August 16, 2017 Title Noncompartmental Analysis for Pharmacokinetic Data Conduct a noncompartmental analysis as closely as possible to the most widely

More information

Pharmacokinetics and allometric scaling of levormeloxifene, a selective oestrogen receptor modulator

Pharmacokinetics and allometric scaling of levormeloxifene, a selective oestrogen receptor modulator BIOPHARMACEUTICS & DRUG DISPOSITION Biopharm. Drug Dispos. 24: 121 129 (2003) Published online in Wiley InterScience (www.interscience.wiley.com). DOI: 10.1002/bdd.344 Pharmacokinetics and allometric scaling

More information

Mechanisms of Drug Action

Mechanisms of Drug Action 10/31/05 Page 1 20.201 Mechanisms of Drug Action Lecture #18: Pharmacokinetics October 31, 2005 Review Dose-response Protein binding, drug transport(ers) Metabolism NOW: PHARMACOKINETICS Circulatory System

More information

Redacted for privacy

Redacted for privacy AN ABSTRACT OF THE THESIS OF Chandrahas G. Saha.iwalla for the degree of Doctor of Philosophy in Pharmacy presented on January 15,1987. Title: New Product Formulation and Multiple dose Pharmacokinetics

More information

NIH Public Access Author Manuscript Am J Nephrol. Author manuscript; available in PMC 2015 January 22.

NIH Public Access Author Manuscript Am J Nephrol. Author manuscript; available in PMC 2015 January 22. NIH Public Access Author Manuscript Published in final edited form as: Am J Nephrol. 2012 ; 36(2): 144 150. doi:10.1159/000339937. Gentamicin Pharmacokinetics and Pharmacodynamics during Short-daily Hemodialysis

More information

Pharmacogenetics and Pharmacokinetics

Pharmacogenetics and Pharmacokinetics Chapter 2 Pharmacogenetics and Pharmacokinetics Mauro Saivezzo/ShutterStock, Inc. L earning O bjectives Upon completion of this chapter, the student will be able to: 1. Recognize the influence of genetic

More information

Applied Biopharmaceutics & Pharmacokinetics Sixth Edition

Applied Biopharmaceutics & Pharmacokinetics Sixth Edition Applied Biopharmaceutics & Pharmacokinetics Sixth Edition Hill Leon Shargel, PHD, RPh Applied Biopharmaceutics, LLC Raleigh, North Carolina Affiliate Associate Professor, School of Pharmacy Virginia Commonwealth

More information

PHA 5128 CASE STUDY 5 (Digoxin, Cyclosporine, and Methotrexate) Spring 2007

PHA 5128 CASE STUDY 5 (Digoxin, Cyclosporine, and Methotrexate) Spring 2007 PHA 5128 CASE STUDY 5 (Digoxin, Cyclosporine, and Methotrexate) Spring 2007 1. L.J., a 30 year old male, was diagnosed congestive heart failure (CHF). He is 5'9" tall and weights 80 kg. He was given Furosemide

More information

7. SUMMARY, CONCLUSION AND RECOMMENDATIONS

7. SUMMARY, CONCLUSION AND RECOMMENDATIONS 211 7. SUMMARY, CONCLUSION AND RECOMMENDATIONS Drug absorption from the gastro intestinal tract can be limited by various factors with the most common one being poor aqueous solubility and poor permeability

More information

PART 1. Pharmacology

PART 1. Pharmacology PART 1 Pharmacology WEB_01.indd 1 7/5/2006 10:10:33 AM WEB_01.indd 2 7/5/2006 10:10:33 AM CHAPTER 1 Pharmacokinetic principles Michel M.R.F. Struys, Alain Kalmar and Peter De Paepe Introduction Pharmacokinetics

More information

The comparative effects of verapamil and a new dihydropyridine calcium channel blocker on digoxin pharmacokinetics

The comparative effects of verapamil and a new dihydropyridine calcium channel blocker on digoxin pharmacokinetics The comparative effects of verapamil and a new dihydropyridine calcium channel blocker on digoxin pharmacokinetics Conflicting conclusions have been reported about interaction of calcium channel blockers

More information

Bioavailability and Pharmacokinetics of Isradipine after Oral and Intravenous Administration: Half-Life Shorter than Expected?

Bioavailability and Pharmacokinetics of Isradipine after Oral and Intravenous Administration: Half-Life Shorter than Expected? C Pharmacology & Toxicology 2000, 86, 178 182. Printed in Denmark. All rights reserved Copyright C ISSN 0901-9928 Bioavailability and Pharmacokinetics of Isradipine after Oral and Intravenous Administration:

More information