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Pharmacokinetics
is the quantitative measurement of drug absorption, distribution, and elimination (ex. excretion and metabolism) and includes the rate processes for drug movement into the body, within the body, and out of the body.
rate of reaction
refers to the velocity of reaction occurs.
order of a reaction
refers to the way in which the concentration of a drug or reactant in a chemical reaction affects the rate.
Zero-order kinetics
constant AMOUNT per unit time is metabolized
rate does not increase as drug concentration increases
first-order kinetics
constant FRACTION per unit time is metabolized
rate increases as drug concentration increases
drug metabolism

zero-order kinetics
the rate is independent of the concentration of the reactants.
the drug concentration changes with respect to time at a constant rate.

zero order
Followed by SUSPENSION, ALCOHOL
Graph (conc vs time) straight line downward
Slope = -ko

first-order kinetics
the rate is dependent of the concentration of the reactants
the drug concentration changes with respect to time equal the product of the rate constant and the concentration of drug remaining.

first-order kinetics
Followed by most of the drugs (85%)
•Graph (conc vs time) HYPERBOLA
•Graph ( log conc vs time) STRAIGHT LINE DOWNWARD
•Slope = -k/2.3

half-life
period of time required for the amount or concentration of a drug to decrease by one half
zero-order half-lfe
not constant
t1/2= 0.5 Co/Ko
first-order half-life
constant
t1/2= 0.693/k
common units used in pharmacokinetics
zero-order rate constant
first-order rate constant
clearance
half-life
zero-order rate constant
symbol: k0
unit: concentration/time
mass/time
example: μg/mL hr & mg/hr
first-order rate constant
symbol: k
unit: 1/time or time^-1
example: 1/hr or hr-1
clearance
symbol: Cl
unit: volume/time
example: mL/hr
half-life
symbol: t1/2
unit: time
example: hr