Pharmacokinetics Flashcards
Define PK
what the human body does to a drug
Define PD
what the drug does to the human body
Define enterohepatic recycling
drugs are transported through the bile from the liver back to the gut where they can be reabsorbed
Define bioavailability
extent to which a drug is absorbed into the systemic circulation
Corrected Ca equation
Ca + [(4-albumin) x 0.8]
Free phenytoin equation
total phenytoin measured/ (0.2 x albumin) +0.1
Define volume of distribution
how large an area in the patient’s body the drug has dristributed into, and is based on the properties of the drug
Vd calculation
amount of drug in body/concentration of drug in plasma
Define first-pass metabolism
hepatic metabolism of a drug before it reaches the systemic circulation, which can dramatically reduce the bioavailability of an oral formulation
Clearance equation
rate of elimination (Re)/ concentration
which drugs don’t follow first order kinetics
phenytoin
theophylline
voriconazole
Define elimination rate constant
is the fraction of the drug that is eliminated per unit of time
Elimination rate constant equation
ke = Cl/Vd
Define half-life
the time required for the drug concentration to decrease by 50%
half-life equation
t1/2 = 0.693/ke