Session 11.2: Pharmacokinetics 4 Flashcards
how does CYP450 become induced
increased transctiption and translation…slower degragation (1-2 weeks)
what happens when CYP450 becomes induced
elimination rate increases and plasma level of drug falls
what is an example of CYP450
CBZ - anti epileptix drug..induced cytochrome p450 enzyme to control epilepsy
what happens if another drug is metabolised at the same time
could inhibit CYP450 (competitive or non competitive) as one maybe metabolised by inhibited isoenzyme…so rate of elimination of other drug reduced
eg: grapefruit juice inhibits an isoenzyme which works to metabolise a drug to treat high BP so increases amount of drug absorbed into blood
what can different efficacies of metabolism of codine cause
codeine into morphine
poor metaboliser = no pain relief as not form morphine
fast metaboliser = morphine intoxication, enhanced therapeutic effect
what are the main processes involved of elimination in the kidney
glomerular filtration
active tubular secretion
passive tubular reabsorption
how else can drugs be eliminated
bile, lung, sweat, tears, genital, saliva, breast milk
how does drug get into glomular filtration
unbound drug enters via bowmans capsulse
what happens during proximal tubular secretion
active secretion of drugs through OAT and OCT (low affinity, high capacity), carry ionised molecules out