pharmacokinetics
the actions the body takes on a drug
can be defined in terms of volumes and clearances
pharmacodynamics (PD)
the action a drug has on the body
volume of distribution
that volume in which a substance/marker/drug appears to be homogeneously distributed (dissolved)
an apparent volume of distribution
volume of distribution = amount of substance/concentration
more accurately described as plasma equivalent apparent volume of distribution

the hydraulic model
can be used to compare to drug distribution int he body
aqueous channels vary in size
Describe the body’s water distribution.

first law of pharmacokinetics
amount of drug in body = concentration * volume of distribution
clearance
a term used to describe the time-dependent movement of drug
includes intercompartmental clearance and elimination clearance
rate of elimination = clearance * concentration
intercompartmental clearance
describes the movement of drug between compartments
elimination clearance
describes the metabolic alteration or removal of drug from the blood/body
rate constant (k) = clearance (liters/min)/volume(liters)
time constant (minutes) = volume (liters)/clearance(liters/min)

elimination clearance rate constant
the fraction or percentage of the volume that is cleared per unit time (minutes)
T(1/2) = 0.693/k
elimination clearance time constant
the time it takes for about 63% of the volume to be cleared
95% of a substance is cleared in three time constants
extraction ration
extraction ratio = clearance/flow
renal clearance
that part of the volume of distribution from which a substance is irreversibly removed
creatinine clearance = (U x V)/P
U = concentration of creatinine in the urine
V = time measured collection of urine (urine production rate)
P = concentration of creatinine in the plasma
second law of pharmacokinetics
target (steady state) concentration = infusion rate/clearance
clearance vs. elimination rate
clearance is a physiologic process assumed not to change over the course of observation
elimination rate is constantly changing due to the concentration of the parent drug constantly decreasing as a result of drug being continuously eliminiated from the system