intro to pharmaco pt1 Flashcards
(109 cards)
2 phases of tablets or capsules taken by mouth
PHARMACOKINETICS
PHARMACODYNAMICS
processes of PHARMACOKINETICS (adme)
absorption
distribution
metabolism
excretion
PHARMACODYNAMICS responses
biologic response
physiologic response
process of drug movement throughout the body that is necessary to achieve drug action
pharmacokinetics
refers to the movement of drug into the bloodstream after administration
ABSORPTION
used in drug preparation to allow the drug to take a particular size and shape and to enhance drug dissolution
EXCIPIENTS
simple syrup, vegetable gums and aromatic powders are example of what
EXCIPIENTS
tablet has to be broken down into small particles before it is absorbed
DISINTEGRATION
small particles must combine with a liquid to form a solution
DISSOLUTION
Enteric coated drugs are meant to be absorbed in
small intestine
where does absorption happens
mucosal lining of the small intestine
Does not require energy
PASSIVE TRANSPORT
drug moves across the
cell membrane from an area of higher concentration to lower concentration
Diffusion
relies on a carrier protein to move the drug from an area of higher concentration to lower concentration
Facilitated Diffusion
requires energy
requires a carrier such as an
enzyme or a protein
ACTIVE TRANSPORT
cells carry a drug across their
membrane by engulfing the drug particles into a vesicle
PINOCYTOSIS
drugs that do not pass GIT
parenteral
buccal
inhalation
absorption effect on LIVER
metabolized to an inactive form and are excreted thus reducing the amount of drug available to exert a pharmacologic effect
refers to the percentage of
administered drug available
for activity
Bioavailability
FACTORS THAT ALTER BIOAVAILABILITY
drug form
route of administration
gastric mucosa and motility
administration with food and other drugs
changes in liver metabolism
refers to the movement of the drug from the circulation to body tissues
DISTRIBUTION
influenced by the rate of the blood flow to the tissue, drugs affinity to the tissue and protein binding
DISTRIBUTION
drugs that are 90 % bound to protein
Highly protein-bound drugs
drugs that are less than 10 % bound to protein
Weakly protein-bound drugs