1. VM 8314 Dr. Jeff Wilcke Pharmacokinetic Modeling (describing what happens)

2. VM 8314 Dr. Jeff Wilcke  AKA “Apparent volume of distribution”  The volume of fluid that appears to contain the amount of drug in the body  May not be actual physiologic space(s)  Relates amount to plasma concentration  The volume that must be processed by organs of elimination Volume of distribution

3. VM 8314 Dr. Jeff Wilcke Volume of distribution  Equations  Experimentally:  Vz = Dose / Cp0  Intellectually:  Vz = Amount in the body / Cpt  Units  Liters or milliliters (whole animal or human beings)  Liters/kg or milliliters/kg (typical vet med)

4. VM 8314 Dr. Jeff Wilcke Volume of distribution 1)Give IV Bolus 2)Take samples over time 3)Cp0 is Y axis interecept 4)You know the dose Vz = Dose / Cp0

5. VM 8314 Dr. Jeff Wilcke Volume of Distribution ScenarioPhysiologic SpaceVz Drug distributed only to plasma water Blood volume = 7% of body weight Plasma water = 55% of blood volume 0.0385 liters/kg Drug distributed evenly in ECF only Extracellular fluid volume = 25% of body weight 0.25 liters/kg Drug distributed evenly ECF and ICF only. Intracellular fluid volume = 40% of body weight0.65 liters/kg ICF concentration = 3 x’s ECFExtracellular fluid volume + 3x intracellular fluid volume 1.45 liters/kg

6. VM 8314 Dr. Jeff Wilcke Volume of distribution Much like row 2 or 3 of table Much like row 4 of table

7. VM 8314 Dr. Jeff Wilcke Clearance  The volume of plasma water cleared of drug during a specified period of time

8. VM 8314 Dr. Jeff Wilcke Clearance  Organ clearance is:  Efficiency X Flow (fraction of drug removed X organ flow)  Clearance = Q x E  Total clearance is:  The sum of all organ clearances  Cl total =Cl hepatic + Cl renal + Cl pulmonary  Experimentally:  Clearance = V z x λ z

9. VM 8314 Dr. Jeff Wilcke Clearance  I know it’s weird but:  At a particular concentration, extracting ½ the drug from ALL the flow is the same thing as extracting ALL the drug from ½ the flow  (We “clearance” not “amount removed” because it works int with the samples we take and the math we can do).

10. VM 8314 Dr. Jeff Wilcke So in one minute… 200 µg/ml (1 ml) 100 µg/ml (1 ml) 0% cleared from 0.5 ml. 100 % cleared from 0.5 ml. Clearance is 0.5 ml/min Passes through liver in 1 minute

11. VM 8314 Dr. Jeff Wilcke Clearance  Units  Volume / unit time (l/hr, l/min, ml/min, etc.)  Whole animals or human beings  Volume / kilogram / unit time  Animals

12. VM 8314 Dr. Jeff Wilcke Rate constant of elimination (λz)  The fraction of the volume of distribution cleared per unit time.  The slope of the natural log plot of drug concentration verus time profile.

13. VM 8314 Dr. Jeff Wilcke Clearing the tank…

14. VM 8314 Dr. Jeff Wilcke Clearing the tank Concentration vs time points represent concentrations determined for samples taken from the tank.

15. VM 8314 Dr. Jeff Wilcke Elimination half-life  The time for elimination of one half of the total amount in the body  Equation:  T 1/2 = 0.693/λz (elimination rate constant)  Units:  Time (hours, minutes, seconds…)

16. VM 8314 Dr. Jeff Wilcke Elimination half life  Utility  Tissue Residues  At 5 x T 1/2 (after you stop dosing) 97% has been eliminated.  Make sure you use the longest half-life  Metabolites MAY be more important than the drug  Absorption may have the longest half-life.

17. VM 8314 Dr. Jeff Wilcke Elimination half-life  Utility  Approach to “Steady state”  Drugs with long half-lifes “accumulate” during repeated administration  A 5 x T 1/2 concentrations reach 97% of steady state  Digoxin – maximum effects 8 days after therapy starts  Need for loading dose  A loading dose is an initial dose given to shorten the time it takes to reach steady state (“load” the body to steady state amounts and concentrations).

18. VM 8314 Dr. Jeff Wilcke Steady state

19. VM 8314 Dr. Jeff Wilcke Absorption rate constant (ka)  Fractional rate at which drug moves from the place the dose was put INTO the circulatory system.  Units  Time (hours, minutes, seconds…)  Application  Combined with elimination rate, determines time to reach peak concentration (C max )

20. VM 8314 Dr. Jeff Wilcke Fraction of dose absorbed  Other than IV, it is rare that the ENTIRE dose is actually absorbed  Oral  Destroyed, eliminated unchanged  IM  Hydrolyzed in tissue, bound to tissues, stuck in abscess  Units  Percentage or decimal (80% = 0.8)

21. VM 8314 Dr. Jeff Wilcke Fraction of dose absorbed  Bioavailability Two oral dose forms of the same drug. F of the “open triangle” dose form is ½ the “filled triangle” dose form.

22. VM 8314 Dr. Jeff Wilcke Fraction of dose aborbed  Bioavailability and Bioequivalence Equal bioavailability (same F) and Bioequivalent Equal bioavailability (same F) and not Bioequivalent