Pharmacokinetics 1 Flashcards
the diffusion coefficient ?
1 / square root of the molecular weight
uptake of molecule into blood
discussion if lipid soluble and uncharged, carrier or channel or pinocytosis if large
ways of administering drug
intravenous - quickest avoids metablism
oral - into gut, metabolism enzymes
rectal - avoid gut
intramuscular - avoid git, e.g. insulin
intrathecal - into CSF e.g. lumbar puncture
inhalation - out and in same way may breath it out
What may affect absorption of drug
site administere, molecular weight, lipid solubility, pH, ionisation
pka?
used to calculate how much drug charged and how much non charged - only uncharged can cross lipid membranes to other compartments
Weak acid drug (aspirin 3.5 pH) in alkaline solution
will dissociate and be trapped in compartment
weak base in an acidic solution
will dissociate and trapped
how do you trap a weak acid in a compartment ?
give sodium carbonate
metformin where is it and what is the transporter
in hepatocytes, transported by OCT1
Ways receptor can be desensitised -
decrease coupling with ligand, no longer produces signal, receptor loss