module 1 synch Flashcards
pharmacodynamics
what the drug does to the body
pharmacokinetics
what the body does to the drug
pKa
half of drug concentration ionized, half non-ionized
- basic drug in base will stay together
nonionized, lipophilic drugs favored for
oral absorption
weak acids best absorbed
in stomach
weak bases are best absorbed
in small intestine
drugs with low Vd may be
highly protein bound and more likely to remain in plasma
induction and substrates (CYP450)
drugs that are substrates are generally more rapid and extensively metabolized
- reduce concentrations -> dec. drug effect of substrate drug
inhibition and substrates
will generally increase plasma concentrations of drugs that are substrates
- inc. drug effect and possibly toxicity of substrate drugs
CYP450 induction
inc. production of enzyme
dec. degradation
induction by another drug or autoinduction
cyp450 inhibition
incidental or deliberate
competitive inhibition
irreversible inhibition
full agonist
activates receptor with maximal efficacy
partial agonist
activates receptor but not with maximal efficacy
inverse agonist
inactivates constitutively active receptor
maximum effect
further inc. in drug dose will not cause inc. response -> receptor is said to be saturated