Pharmacology principles Flashcards
The hypothetical volume into which the administered drug must be uniformly distributed to have its effect
Volume of distribution (amount given mg/plasma concentration mg/L)
Drugs with a low Vd (3-5 liters) likely
Have large molecular weight, are bound extensively to plasma proteins or are highly charged (hydrophilic)
Drugs with Vd ~ 14-16L are likely
Small but hydrophilic
Drugs with very large Vd (~35-40L) are likely
small MW and uncharged (liphophilic)
Which drugs have the greatest volume of distribution
Drugs that can cross the plasma into interstitium (small and hydrophobic)
List 5 CYP450 inducers
Carbamazepine, Phenobarbital, Phenytoin, Rifampin, Griseofulvin
LList 7 CYP450 inhibitors
Cimetidine, Ciprofloxacin, Erythromycin, Azole antifungals, Grapefruit juice, Isoniazid, Ritonavir (protease inhibitors)
A drug that undergoes hepatic metabolism should have which property?
High lipophilicity
Drug that is excreted in urine will have which properties
Low lipophilicity, low Vd
How are drugs with low rate of redistribution eliminated?
Kidneys