pharmacokinetics Flashcards
what is absorption
how the drug enters the bloodstream unless through intravenously where the drug typically moves through a semi permeable membrane till it reaches bloodstream
describe the cell membrane
it is semi-permeable and is made up of a bilayer of phospholipids with a hydrophilic head and hydrophobic tail The bilayer is permeable to water and lipid soluble molecules but not large molecules and ions
what is the point of a drug
. replace or act as a substrate for missing chemicals
. increase/ stimulate missing cellular activity
. depress/decrease cellular activity
.interfere with the functioning of foreign cells
factors affecting pharmacokinetics
. age
. sex
. genetics
. organ function
. body composition
passive diffusion
movement from high concentration to low concentration down a concentration gradient and requires no energy
facilitated diffusion
uses plasma membrane proteins either as a channel or carrier protein
leak channel
constantly open for substances to move in and out of
gated channel
open for a brief moment before closing again
carrier protein
molecules bind to the protein and if recognize will open otherwise
active transport
going against a concentration gradient from low to high concentration which requires energy
primary active transport
phosphate from ATP will bind to the molecule to supply it with energy
secondary active transport
energy is supplied when another substance is moving down its concentration gradient
pinocytosis
where fluids and substances are being ‘drank’ by the cell as the cell encloses the fluid or substance and fuses shut to form a vesicle into cell interior. (requires ATP as it is a form of active transport)
why is drug dose form important
it affects rate and extent of absorption i.e. gases are absorbed faster and solid forms must be able to disintegrate for absorption
what are the different form of drugs
.liquids- suspension, elixir and aqueous solutions
.solid- tablets, creams, capsules, ointments
.gases- anesthesia
what is the importance of shape and sizes of drugs
smaller drugs penetrate faster than larger drugs
How does lipid and water solubility affect a drug
most drugs are transported via simple diffusion and formulated to be lipid soluble to be able to penetrate through the phospholipid bilayer
potential ionization
determines the rate at which a drug penetrates a cell membrane which determines the charge
weak acidic drugs
best absorbed in areas with high acidity i.e. stomach
weak base drugs
best absorbed in areas of low acidity i.e. intestine
route of drug
the purpose of a drug is to have the fastest therapeutic effect with minimal side effects.
the onset action of drug
length of time for drug to take affect
Bioavailability
how long the dug stays in the body, rated from 0-100%
First pass metabolism
drugs are metabolized in the liver before it can be distributed into the bloodstream which decreases the concentration of the drug