F1 ADME & clinical pharmacology 1 Flashcards
What is pharmacokinetics?
the time course of a drug from absorption to elimination
determines the drug regimen for a drug - dose, how often
What does ADME stand for?
Absorption, distribution, metabolism, excretion
What are the 3 mechanisms of drug absorption?
active transport- for drug structurally related to endogenous chemicals
bulk flow of water - small water soluble drug
passive diffusion- movement of most drugs
Are weak acids and bases ionised and absorbed in the stomach?
weak acids - unionised therefore absorbed
weak bases - ionised and not absorbed
Does presence of food increase time of drug in stomach?
yes
Which type of acid drugs have slowed absorption?
acid stable drugs
Why are acid labile drugs more readily broken down?
stay longer in stomach
Why are PPIs given gesture-resistant capsules?
are acid labile
Where is the major site or absorption?
small intestines
Do the small intestines have good blood flow?
yes
Why are most weak acids & bases absorbed in small intestines?
high levels of uncharged drug
What is first pass metabolism?
drug absorbed from small intestines go to liver via hepatic portal vein, some drug metabolised before reaching the systemic circulation
How do you calculate bioavailability F?
F= AUC oral/AUC iv
How do you calculate single dose?
=amount given/ F
What is clearance?
the volume of plasma cleared of a drug in unit time) measure of amount of drug removed by body