Louisiana Tech University Ruston, LA 71272 Slide 1 Compartmental Models Juan M. Lopez BIEN 501 Friday, May 09, 2008.

Slides:



Advertisements
Similar presentations
Karunya Kandimalla, Ph.D
Advertisements

PHARMACOKINETIC MODELS
Louisiana Tech University Ruston, LA Slide 1 Co-Current and Counter-Current Exchange in Dialysis Steven A. Jones BIEN 501 Monday, May 5, 2008.
Louisiana Tech University Ruston, LA Slide 1 Energy Balance Steven A. Jones BIEN 501 Wednesday, April 18, 2008.
Louisiana Tech University Ruston, LA Slide 1 Krogh Cylinder Steven A. Jones BIEN 501 Friday, April 20, 2007.
Louisiana Tech University Ruston, LA Slide 1 Final Exam Topics Steven A. Jones BIEN 501 Monday, May 12, 2008.
Louisiana Tech University Ruston, LA Slide 1 Time Averaging Steven A. Jones BIEN 501 Monday, April 14, 2008.
Ch 3.8: Mechanical & Electrical Vibrations
Human Body Drug Simulation Nathan Liles Benjamin Munda.
Chapter 13 MIMs - Mobile Immobile Models. Consider the Following Case You have two connected domains that can exchange mass
1 Some Deterministic Models in Mathematical Biology: Physiologically Based Pharmacokinetic Models for Toxic Chemicals Cammey E. Cole Meredith College March.
Two-compartment model
Computational Biology, Part 18 Compartmental Analysis Robert F. Murphy Copyright  1996, All rights reserved.
Drug Delivery and Mass Balance BIOE201-B. The concentration of the drug at the site of action, over time. Drug delivery is about the complex mechanisms.
One-compartment open model: Intravenous bolus administration
Louisiana Tech University Ruston, LA Slide 1 Mass Transport Steven A. Jones BIEN 501 Friday, April 13, 2007.
Week 3 - Biopharmaceutics and Pharmacokinetics
Laplace transformation
Practical Pharmacokinetics
Louisiana Tech University Ruston, LA Slide 1 The Rectangular Channel Steven A. Jones BIEN 501 Friday, April 4th, 2008.
Louisiana Tech University Ruston, LA Slide 1 Krogh Cylinder Steven A. Jones BIEN 501 Wednesday, May 7, 2008.
Week 4 - Biopharmaceutics and Pharmacokinetics
ECE 8443 – Pattern Recognition EE 3512 – Signals: Continuous and Discrete Objectives: Stability and the s-Plane Stability of an RC Circuit 1 st and 2 nd.
CHAPTER III LAPLACE TRANSFORM
Modeling Systems and Processes Anthony McGoron, PhD Associate Professor Department of Biomedical Engineering Florida International University.
Gokaraju Rangaraju College of Pharmacy
Ch. 6 Single Variable Control
By Irfan Azhar Time Response. Transient Response After the engineer obtains a mathematical representation of a subsystem, the subsystem is analyzed for.
The General Concepts of Pharmacokinetics and Pharmacodynamics Hartmut Derendorf, PhD University of Florida.
Principles of Clinical Pharmacology Noncompartmental versus Compartmental Approaches to Pharmacokinetic Data Analysis David Foster, Professor Emeritus.
Chapter 3 mathematical Modeling of Dynamic Systems
Louisiana Tech University Ruston, LA Slide 1 Mass Transport & Boundary Layers Steven A. Jones BIEN 501 Friday, May 2, 2008.
Mathematical Models and Block Diagrams of Systems Regulation And Control Engineering.
PHARMACOKINETIC MODELS
Touqeer Ahmed Ph.D. Atta-ur-Rahman School of Applied Bioscience, National University of Sciences and Technology 21 st October, 2013.
Pharmacokinetics of Drug Absorption Prepared by: KAZI RASHIDUL AZAM.
Chapter 4 Transients. 1.Solve first-order RC or RL circuits. 2. Understand the concepts of transient response and steady-state response.
MECHANISTIC PHARMACOKINETICS: COMPARTMENTAL MODELS
Drug Administration Pharmacokinetic Phase (Time course of ADME processes) Absorption Distribution Pharmaceutical Phase Disintegration of the Dosage Form.
One Compartment Open Model IV bolus
The General Concepts of Pharmacokinetics and Pharmacodynamics
Louisiana Tech University Ruston, LA Slide 1 Review Steven A. Jones BIEN 501 Friday, May 14, 2007.
Imaginary and Complex Numbers Negative numbers do not have square roots in the real-number system. However, a larger number system that contains the real-number.
1 Some Deterministic Models in Mathematical Biology: Physiologically Based Pharmacokinetic Models for Toxic Chemicals Cammey E. Cole Meredith College January.
BIOPHARMACEUTICS.
The Laplace Transform.
The General Concepts of Pharmacokinetics and Pharmacodynamics
Clearance: basic concept (in vitro) Update OCT 2010.
3.4 Chapter 3 Quadratic Equations. x 2 = 49 Solve the following Quadratic equations: 2x 2 – 8 = 40.
Pharmacokinetics 3rd Lecture
Initial Conditions & Passive Network Synthesis. Sarvajanik College of Engineering & Technology Made by: Dhruvita Shah Khushbu Shah
Source: Frank M. Balis Concentration and Effect vs. Time Conc./ Amount Effect [% of E MAX ] Time Central Compartment Peripheral Compartment Effect Compartment.
Compartmental Modelling
Compartmental Models and Volume of Distribution
Mathematical Models of Control Systems
Physiology for Engineers
Chapter 8 BIOAVAILABILITY & BIOEQUIVALENCE
CHAPTER III LAPLACE TRANSFORM
Chapter 7 COMPARTMENT MODELS
Lecture-8 Biopharmaceutics
Quantitative Pharmacokinetics
Kinetics, Modeling Oct 19, 2009 Casarett and Doull,
Dosimetry and Kinetics
Kinetics, Modeling Oct 15, 2006 Casarett and Doull,
Model Part – Yiming Weng
Hawler Medical University
Clinical Pharmacokinetics
Unsteady Diffusion into a Sphere
LAPLACE TRANSFORMATION
Presentation transcript:

Louisiana Tech University Ruston, LA Slide 1 Compartmental Models Juan M. Lopez BIEN 501 Friday, May 09, 2008

Louisiana Tech University Ruston, LA Slide 2 Compartment Models Conservation of Mass Initial Conditions: D is the mass injected, and and D  (t) is rate of injection. Well Mixed

Louisiana Tech University Ruston, LA Slide 3 Compare to Distributed Model Concentration varies spatially within the compartment, according to Fick’s Law. Concentration is the same at all locations in the compartment. Distributed Compartmental (lumped)

Louisiana Tech University Ruston, LA Slide 4 Alternative Mathematical Description Conservation of Mass Solution: Delta function: Injection is not instantaneous, but with respect to the larger time scale it can be treated that way. Time for dosage to reduce to half it’s initial value.

Louisiana Tech University Ruston, LA Slide 5 Review Assumptions Rate of clearance is proportional to concentration Well-mixed system Note the relationship to a lumped- parameter analysis.

Louisiana Tech University Ruston, LA Slide 6 Other Physiological Definitions Body Clearance: Rate of drug elimination relative to the drug’s plasma concentration. “Area Under the Curve” For a constant dose:

Louisiana Tech University Ruston, LA Slide 7 Two Compartment Model Conservation of Mass C1C1 C2C2 Clearance Central Compartment Peripheral Compartment

Louisiana Tech University Ruston, LA Slide 8 Two Compartment Model Conservation of Mass In terms of the volume ratio Initial Conditions Solve the two ODEs for C 1

Louisiana Tech University Ruston, LA Slide 9 ICs in terms of C 1

Louisiana Tech University Ruston, LA Slide 10 Solution The solution to: With Is Where:

Louisiana Tech University Ruston, LA Slide 11 Two Compartment Model Rapid Release Slow Release One Compartment

Louisiana Tech University Ruston, LA Slide 12 Two Compartment Model The two-compartment model obeys the same differential equations as the simple RLC circuit. It is useful to compare the individual components to the RLC circuit: Damping Transfer from L to C

Louisiana Tech University Ruston, LA Slide 13 Two Compartment Model One might expect that overshoot (ringing) could happen. However, ringing will only happen for imaginary values of. In our case: And for the RLC Circuit: Can make the square root imaginary with small R or large C. As you increase k 2 or k e, you must also increase (k 1 +k 2 +k 3 ).

Louisiana Tech University Ruston, LA Slide 14 Two Compartment Model To see if the square root can become imaginary, minimize it’s argument w.r.t. k e and see if it can be less than 0.

Louisiana Tech University Ruston, LA Slide 15 Two Compartment Model What value does the argument of the square root take on at the minimum? Since k 2 and k 1 cannot be negative, the argument of the square root can never be negative. I.e. no ringing.

Louisiana Tech University Ruston, LA Slide 16 Pharmacokinetic Models Vascular Interstitial Cellular PBPK: Physiologically-Based Pharmocokinetic Model Q : Plasma Flow L : Lymph Flow J s, q: Exchange rates

Louisiana Tech University Ruston, LA Slide 17 Pharmacokinetic Models Z : Equilibrium concentration ratio between interstitium and lymph.

Louisiana Tech University Ruston, LA Slide 18 More Complicated Models Plasma Liver Kidney Muscle G.I. Track

Louisiana Tech University Ruston, LA Slide 19 Note on Complexity While the equations become more complicated as more components are added, the basic concepts remain the same, and the systems can be analyzed with the same tools you would use to analyze a linear system in electrical engineering (e.g. transfer functions, Laplace transforms, Mason’s rule).

Louisiana Tech University Ruston, LA Slide 20