Class 3 - Principles of Pharmacology Flashcards
pharmacokinetics
the process of a drug movement through the body. all drugs go through the 4 stages
pharmacodynamics
the study of the effect of a drug on cells, and the drugs mechanism of action
what are the 4 stages of pharmacokinetics
absorption, distribution, metabolism, excretion
absorption
process of moving a substance from its site of administration, across the body membranes to the bloodstream.
depends on size, lipid solubility, degree of ionization, and interaction with food and other drugs
the more rapid the absorption, the faster the onset of drug action
acids will absorb in acids, bases will absorb in bases
first past effect
drug goes to liver after taking orally
bioavailability
the amount of drug that reaches the target.
what are factors that could affect drug absorption?
taking other drugs, what’s in your gut, certain acidic and non-acidic environments
distribution
describes how drugs are transported through the body to receptor sites. how a drug becomes available to body fluids and body tissues.
what influences distribution?
blood flow, the drugs solubility, the drugs affinity to the tissue, protein binding effect, dehydration, blood viscosity, placental barriers
what is the protein binding effect?
some drugs bind to a protein so they need to be taken with a meal
metabolism
also known as biotransformation. process of chemically converting a drug to a form that is usually removed from the body more easily. makes it more likely to be excreted.
what is the primary site of metabolism?
the liver, kidneys are secondary
what factors might affect metabolism?
hepatitis, diseases that attack or damage the liver, cirrhosis (liver scaring)
excretion
remove drug metabolites from the body and only sometimes the actual drug itself
where are drugs excreted?
usually the kidneys but may also be excreted by the lungs or glands, or into bile (sweat, feces, urine, breast milk)
half life
length of time for 50% of a drug to be absorbed. by knowing the half life we can determine dosing schedules
what can affect the half life?
metabolism and elimination.
therapeutic range
drug concentration between the minimal effective concentration and toxic concentration
agonist
drugs that produces a response the same as the endogenous substances