Principles Flashcards
pharmacokinetics
relationship between drug dosing and [ ] in fluids, tissues and time
Absorption
drug moving from the site of administration to blood
Bioavailability
% of drug administered that reaches systemic circulation
- all oral drugs undergo 1st pass through liver
- sublingual drugs go into SVC and bypass 1st pass
- IV drugs are 100% bioavailable
Distribution
achieved by the blood stream throughout the body
Law of Mass Action
drugs follow mass action
high[plasma] = moves into the tissues
high[tissue] = moves into plasma
Major determinant of end organ drug concentration?
the rate of rise in [ ] = determined by organ perfusion and relative solubility
free vs bound molecules
as free molecules move into tissues -> they are immediately replaced by new unbound molecules that were bound before
lipophilic molecules
they readily transfer between the blood and organs
Context Sensitive half time
time for a 50% decrease of a [drug] after an infusion in stopped
Volume of Distribution
Vd = bolus dose/concentration
Biotransformation
chemical process by which drug molecule is altered in the body
- primarily liver metabolism except for esters
Phase I
oxidation, reduction, hydrolysis
Phase II
conjugation w/ endogenous substrates
Excretion
most are renally cleared
- RBF x renal extraction
Pharmacodynamics
study of how drugs affect the body