pharmacokinetics MT1 Flashcards
(32 cards)
this is the branch of pharmacology concerned with the movement of drugs within the body/what the body does to the drug
pharmacokinetics
what are the factors that determine blood concentration of a drug?
- size of administered dose
- extent of absorption
- rate of absorption
- extent od drug distribution
- extent of elimination
- rate of elimination
this is how much of a drug gets absorbed
extent of absorption
what determines the extent of absorption of a drug
formulation
this is how quickly a drug gets absorbed
rate of absorption
what determines the rate of absorption
route
this is how well a drug spreads and goes into organs
extent of drug distribution
what determines the extent of drug distribution
depends partly on volume/site of distrbution
this is how much and how well a drug can leave the body
extent of elimination
this is how quickly the drug can leave the body
rate of elimination
the manner in which a drug is taken is called a __________. this depends on the therapeutic objectives (e.g. cure, prevention, etc.)
dosage regimen
Managing a proper dosing regimen to treatment of patients with various diseases requires the maintenance of enough drug systematic exposure which in an effective range to have a certain duration and intensity of effect, but doesn’t give adverse effects. It is necessary to keep the dosage regimen within the _______________
therapeutic window
this is a model used in determining drug movement in the body; its the simplest way to view the entry, disposition, and exit of the drug from the body where the body acts like a single, uniform compartment
single compartment open model
the rate of change in concentration over time (dC/dt) in the body (reservoir) in a one compartment open model is dependant on these two factors
- how much drug there is in the body (reservoir)
- how well the drug is eliminated
how much drug there is in the body/reservoir depends on what two factors
- the size of the reservoir for the drug
- the dose given
how well the drug is eliminated depends on what two factors
- rate of elimination
- capacity of the elimination organs to remove the drug
What are the two types of elimination processes?
Zero Order elimination/kinetics and First order elimination/kinetics
this elimination process is the mass of the drug that is eliminated/transferred is constant with respect to time
zero order kinetics
this elimination process is the mass of the drug that is eliminated/transferred is never constant with reprint to time
first order kinetics
for a zero order process, drug transfer is at a constant rate, ______________ of the plasma concentration
independant
for frist order process, the rate of drug transfer is not constant and is _________ of the plasma concentration
dependant - the more drug the faster its eliminated
for first order kinetics, the rate of change of concentration with respect to time depends on what two factors
- how much drug there is initially
- the elimination capacity
zero or first order kinetics?
the number of enzymes/receptors is higher than the amount of drug
first order kinetics
zero or first order kinetics?
accumulation of drug in the body leads to toxicity
zero order kinetics