Ch 2 - Pharmacokinetics and Pharmacodynamics Flashcards
Movement of drug through the body and how the body affects the drug
Pharmacokinetics
How the drug affects the body; how the drug initiates its therapeutic or toxic effect at the cellular or systemic level
Pharmacodynamics
Drug administration, absorption, distribution, and elimination
Pharmacokinetics
Range of drug concentration in the blood that yields a sufficient therapeutic response without toxic reactions. Varies between individuals.
Therapeutic Window
Following administration by oral, sublingual or rectal routes
Enteral absorption
Following administration by inhalation, IV, IM, Subq, topical or transdermal route
Parenteral absorption
Fraction of drug that reaches systemic circulation.
IV drugs = 100%
Bioavailability
Presence or absence of food in stomach
Blood flow to area or absorption
Dosage form of drug
GI motility
Factors affecting Absorption
Molecules move from one side of a barrier to another without expending energy
Passive diffusion
Membrane proteins act as carrier molecules to transport substances across all membranes
Active transport
Blood flow to an area
Lipid or water solubility
Protein binding
Obesity (lipid soluble drugs)
Factors affecting Distribution
Drug is available to exert its effect
Free/Unbound Drug
Drug is inactive; cannot leave bloodstream
Protein Bound Drug
Theoretical parameter calculated by determining amount of drug in the body (dose administered) divided by the concentration of drug in the plasma
Apparent Volume of Distribution
Metabolism and Excretion
Methods of Elimination
Liver, kidneys, GI tract
Sites of Metabolism
Kidneys, lower GI tract, lungs, skin
Sites of Excretion
Change to water soluble form by enzymes
Biotransformation
Drug may be excreted in bile and then reabsorbed in lower GI tract
Enterohepatic Recirculation
Time required for half of drug to be eliminated
Half-life
Equilibrium between rates of absorption and elimination
Steady state
Removal of drug from plasma or organ
Clearance
Rate of elimination is constant but amount of drug eliminated is proportional to concentration
First-order kinetics
Fixed amount of drug eliminated, independent of concentration
Zero-order kinetics