pharmacology intro Flashcards
What does rate of filtration depend on
Extend of plasma protein binding
How can the solubility of a drug be described?
Limited
How do drugs leave the circulation
filtration through capillaries
What does amphipathic mean?
Having both hydophillic and hydrophobic parts
What are mostly amohipathic
Proteins
What are lipophilic compounds attracted to?
What happens when they attract?
They are attracted to lipophiloc grounds and become loosely bound to protein molecule
How long do drugs bind for
They bind temporarily
What is there an equalibrium between
Bound and free drugs
What do drugs mostly bind to
Mostly to albumin
Then: globulins, glycoproteins and lipoproteins
Do proteins leave the bloodstream
No
What drugs pass into other compartments and how?
Non-bound drugs bind to cellular receptors, pass across the membrane into other compartments
What drugs can be distributed, metabolised and excreted ?
Only non-bound drugs
What happens if a free drug leaves the bloodstream
More free drug will be released from the protein to maintain the equilibrium
What prolongs the time a drug is in the plasma?
Strong protein binding
How many drugs compete for binding sites? Why is this important
Give an example
2 - this is important when giving more than one drug - eg warfarin and asprin