5. Distribution Flashcards
Distribution
The reversible transfer of a drug between compartments
Plasma — interstitial fluid —Intracellular fluid
All 3 are compartments: defined volume of body fluids
Distribution depends on _______ and ______ of the drug.
Molecular size, polarity/Lipophilicity
Very large drugs
Confined to circulation, cannot escape pores
Lipophillic drugs
Enriched in fat, can escape circulation
Very polar Drugs
Hydrophilic - with a charge can escape circulation but do not cross cell membrane because of polarity
Drug evenly distributed
Uncommon
Vd - Volume of distribution
Vd= total amount of drug in body/ concentration of drug in plasma
Expressed in liters
High Vd = low concentration in plasma, drug in tissue
Low Vd = high concentration in plasma
Protein-binding affects drug administration
Protein bound fraction is not available for action
Ex: albumin: certain number of passengers to transport drug, drug can jump off
Drugs may compete for plasma protein binding
Creates drug-drug interaction if drug 2 significantly displaces drug 1s free concentration that drug 1 levels may now be toxic
Blood-Brain Barrier
Prevents distribution of many drugs to the brain
P-glycoproteins in BBB
Certain drugs need to be given intrathecally (through spinal cord) to reach brain
Drugs may be stores in tissues (fat and bone)
Adipose (fat): drug dosing in obese patients difficult because drug can hide out in fate
Teeth (bone): avoid tetracycline antibiotics in children over 8, it can stain teeth.