ADME lab Flashcards
organ clearance of a drug is influenced by:
- organ blood flow
- plasma protein binding
- organs intrinsic ability to eliminate the drugs
(so larger drug dose does not change the clearance values)
if a drug has high renal clearance - what does it imply about the filtration through the kidney
will probably be both filtered and actively transported from the blood to the urine
what is the difference between pharmacokinetic half life and the normal half life of a drug
pharmacokinetic half life - the half life of the drug in the plasma
half life - the half life of the drug in the body
if drug A is eliminated from the body slower than drug B, what would you expect the half life of drug A to be compared to drug B
longer
how do we measure drug clearance
(fractional single pass elimination) x (blood flow rate of the organ)
what is the bioavailability of a drug
the proportion of the drug that reaches the systemic circulation in an active form
does oral or IV administration lead to longer lasting drug concentrations and why
oral - because the release is delayed
IV will have higher and faster conc, but oral will have longer effect
what are three ways in which a drug may have bioavailability of less than 100%
- first pass metabolism in the liver
- incomplete drug absorption
- bacterial metabolism in the intestine (if via oral absorption)
what is the volume of distribution
the volume into which the total amount of drug in the body would need to be dissolved to achieve the conc that is observed in the blood