pharmacologic principles Flashcards
pharmacokinetics
what the body does to drugs
4 parts of pharmacokinetics
absorption
distribution
metabolism
excretion
pharmacodynamics
study of what drugs do to the body
pharmacodynamics target sites
receptors
ion channels
enzymes
carrier proteins
absorption
method and rate at which drugs leave the site of administration
distribution
occurs when the drug leaves the systemic circulation and enters the intersititium and cells
drugs are redistributed in organs according to their
fat and protein content
psychotropic drugs and fat/protein
most are lipophilic and highly protein bound
only unbound (free) portion is active
so low albumin levels like in malnutrition, aging etc, can experience toxicity due to inc free drug
older adults and psychotropic drugs based on fat/protein
if high fate to lean body mass, like older adults, could have erratic amounts of active drug in system
metabolism
process by which the drug becomes chemically altered in the body
first pass metabolism
process by which the drug is metabolized by CYP450 enzymes in the intestines and liver prior to going to the systemic circulation
elimination
process by which the drug is removed from the body
half life
time needed to clear 50% of the drug from the plasma
also determines the dosing interval and length of time to reach steady state
steady state
point at which the amount of drug eliminated between doses is approximately equal to the dose administered.
drugs usually administered once every half life to achieve steady state
takes about 5 half lives to achieve steady state and 5 to completely eliminate a drug
what can alter pharmacokinetics
p450 can induce or inhibit
10+ whites
20% asians
1st pass in some p450s
enzyme inducers and inhibitors
liver and kidney dz
CYP450 inhibitors
Buproprion
Clomipramine
Cimetidine
Clarithromycin Fluoroquinolones
Grapefruit
Ketoconazole
Nefazodone
SSRIs
CYP450 inducers
Carbamazepine
Hypericum (St. John’s Wort)
Phenytoin
Phenobarbital
Tobacco
types of pharmacodynamic receptor effects
agonist effect
inverse agonist effect
partial agonist effect
antagonist effect
agonist effect
drug bunds to receptors and activates a biological response
inverse agonist effect
drug causes the opposite effect of agonist, binds to same receptor
partial agonist effect
drug does not fully activate the receptors
antagonist effect
drug binds to receptor but does not activate a biological response
NTs and ion channels cause
excitatory or inhibitory response
excitatory response
depolarization
involves the opening of sodium and calcium channels so these ions can go into the cell