Pharmacokinetics and drug formulations Flashcards
Pharmacokinetics definition
what the body does to the drug
pharmacodynamics
what the drug does to the body
what factors can decrease dissolution of a medication in the gut?
- hydrolysis: water destroys the molecule
2. the drug does not dissolve well in acid or the stomach is not acidiec enough
which equation describes the rate of dissolution?
the noyes-whithney equation
where is the major site of drug absorption?
the small intestine
in what PH do enteric formulations get absorbed
in basic environments like in the small intestine
why can AMG no be given PO?
they are polar charged molecules that cant pass through cell walls. The remain in blood more and thats one reason they are nephrotoxic
what are two of the most common protein-bound medications?
phenytoin and warfarin
when is elimination of a medication considered complete?
after 4-5 half lives
what is first order kinetics?
the amount of drug given is proportional to the increase seen in plasma concentration. The more you give of a drug, the higher the drug concentration
what is michaelis menten kinetics?
at first, an increase in drug is proportional to its concentration in the blood. That is until, the metabolizing enzymes become saturated. Then the elimination rate of the drugs becomes independent of the drug concentration: the amount can increase dramatically and lead to toxicty
what are three main examples of drugs that follow michaelis menten kinetics?
phenytoin
voriconazole
theophylline
what are good formulations for people who have trouble swallowing?
orally disintegrating tablets patches some bead formulations sprinkled onto food suppository IV
why are migraine medications in ODT form?
because migraines usually cause nausea and these meds can cause nausea when swallowed. So giving ODT reduces nausea
what formulations are better for patients that are non-adherent?
Long acting formulations