pharmacokinetics 2 Flashcards
Distribution
The transfer of drugs in and out of the various tissues of the body
Diffusing across membranes
Only free or unbound drugs are available to diffuse across membranes
Factors affecting drug distributing into various tissues of the body
- The perfusion rate of the tissue (blood flow through the tissue)
- The physiochemical ability of drug to cross membranes
- The nature of the membranes
- The extent to which the drug is bound
Flow rate
Tissues that are well vascularised (plenty of blood vessels) such as the liver and the kidney will receive more of a drug than other parts of the body
Distribution equilibrium
Is when the amount of drug entering the blood compartment is balanced by drug leaving that compartment
Partition co-efficient
Partition coefficient (KP) determines the extent of drug entry into compartments.
It is the measure of a drug lipid solubility.
Unionised drug
When the drug is unionised it readily crosses the membrane due to its lipid solubility
Ionised drug
If drug becomes ionised, it become less lipid soluble and more water soluble, impacting its ability to cross cell membranes. But making it easier to be eliminated in the urine
Basic drugs in a high pH (alkaline or basic environment)
are lipid soluble and therefore readily transported.
Basic drugs in a low pH (acidic environment)
are far less lipid soluble and therefore not readily transported.
Acidic drugs in a high pH (basic or alkaline environment)
are far less lipid soluble and therefore not readily transported.
Acidic drugs in a low pH (acidic environment)
are lipid soluble and therefore readily transported.